Skip to main content

Main menu

  • Home
  • Content
    • Published Ahead of Print
    • Current Issue
    • Podcasts
    • Subject Collections
    • Archives
    • ASN Meeting Abstracts
    • Saved Searches
  • Authors
    • Submit a Manuscript
    • Author Resources
    • Reprint Information
  • Trainees
    • Peer Review Program
    • Prize Competition
  • About CJASN
    • About CJASN
    • Editorial Team
    • CJASN Impact
    • CJASN Recognitions
  • More
    • Alerts
    • Advertising
    • Reprint Information
    • Subscriptions
    • Feedback
  • ASN Kidney News
  • Other
    • JASN
    • Kidney360
    • Kidney News Online
    • American Society of Nephrology

User menu

  • Subscribe
  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
American Society of Nephrology
  • Other
    • JASN
    • Kidney360
    • Kidney News Online
    • American Society of Nephrology
  • Subscribe
  • My alerts
  • Log in
  • My Cart
Advertisement
American Society of Nephrology

Advanced Search

  • Home
  • Content
    • Published Ahead of Print
    • Current Issue
    • Podcasts
    • Subject Collections
    • Archives
    • ASN Meeting Abstracts
    • Saved Searches
  • Authors
    • Submit a Manuscript
    • Author Resources
    • Reprint Information
  • Trainees
    • Peer Review Program
    • Prize Competition
  • About CJASN
    • About CJASN
    • Editorial Team
    • CJASN Impact
    • CJASN Recognitions
  • More
    • Alerts
    • Advertising
    • Reprint Information
    • Subscriptions
    • Feedback
  • ASN Kidney News
  • Visit ASN on Facebook
  • Follow CJASN on Twitter
  • CJASN RSS
  • Community Forum

Index by author

April 01, 2010; Volume 5,Issue 4
  • A
  • B
  • C
  • D
  • E
  • F
  • G
  • H
  • I
  • J
  • K
  • L
  • M
  • N
  • O
  • P
  • Q
  • R
  • S
  • T
  • U
  • V
  • W
  • X
  • Y
  • Z

A

  1. Acurcio, Francisco de Assis

    1. You have accessRestricted Access
      Allocation of Initial Modality for Renal Replacement Therapy in Brazil
      Mônica Viegas Andrade, Jaume Puig Junoy, Eli Iola Gurgel Andrade, Francisco de Assis Acurcio, Ricardo Sesso, Odilon Vanni de Queiroz, Daniele Araújo Szuster, Isabel Cristina Gomes, Alessandra Maciel Almeida and Mariangela Leal Cherchiglia
      CJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
      Add to Selected Citations
  2. Adams, JN

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  3. Alamovitch, S

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  4. Almeida, Alessandra Maciel

    1. You have accessRestricted Access
      Allocation of Initial Modality for Renal Replacement Therapy in Brazil
      Mônica Viegas Andrade, Jaume Puig Junoy, Eli Iola Gurgel Andrade, Francisco de Assis Acurcio, Ricardo Sesso, Odilon Vanni de Queiroz, Daniele Araújo Szuster, Isabel Cristina Gomes, Alessandra Maciel Almeida and Mariangela Leal Cherchiglia
      CJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
      Add to Selected Citations
  5. Andrade, Eli Iola Gurgel

    1. You have accessRestricted Access
      Allocation of Initial Modality for Renal Replacement Therapy in Brazil
      Mônica Viegas Andrade, Jaume Puig Junoy, Eli Iola Gurgel Andrade, Francisco de Assis Acurcio, Ricardo Sesso, Odilon Vanni de Queiroz, Daniele Araújo Szuster, Isabel Cristina Gomes, Alessandra Maciel Almeida and Mariangela Leal Cherchiglia
      CJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
      Add to Selected Citations
  6. Andrade, Mônica Viegas

    1. You have accessRestricted Access
      Allocation of Initial Modality for Renal Replacement Therapy in Brazil
      Mônica Viegas Andrade, Jaume Puig Junoy, Eli Iola Gurgel Andrade, Francisco de Assis Acurcio, Ricardo Sesso, Odilon Vanni de Queiroz, Daniele Araújo Szuster, Isabel Cristina Gomes, Alessandra Maciel Almeida and Mariangela Leal Cherchiglia
      CJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
      Add to Selected Citations
  7. Antignac, C

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  8. Aronoff, George R.

    1. You have accessRestricted Access
      Iron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic Response
      Adam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. Aronoff
      CJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
      Add to Selected Citations
  9. Artifoni, Lina

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations

B

  1. Barash, Irina

    1. You have accessRestricted Access
      A Pilot Clinical Study to Evaluate Changes in Urine Osmolality and Urine cAMP in Response to Acute and Chronic Water Loading in Autosomal Dominant Polycystic Kidney Disease
      Irina Barash, Manish P. Ponda, David S. Goldfarb and Edward Y. Skolnik
      CJASN April 2010, 5 (4) 693-697; DOI: https://doi.org/10.2215/CJN.04180609
      Add to Selected Citations
  2. Baresova, V

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  3. Barreto, Daniela V.

    1. You have accessRestricted Access
      The Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary Report
      Leon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. Massy
      CJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
      Add to Selected Citations
  4. Barreto, Fellype C.

    1. You have accessRestricted Access
      The Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary Report
      Leon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. Massy
      CJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
      Add to Selected Citations
  5. Becker, DJ

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  6. Begelman, Susan M.

    1. You have accessRestricted Access
      A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3
      James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. Begelman
      CJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
      Add to Selected Citations
  7. Benetti, Elisa

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations
  8. Benner, Debbie

    1. You have accessRestricted Access
      Association of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis Patients
      Nazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. Kopple
      CJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
      Add to Selected Citations
  9. Bergrem, Harald

    1. You have accessRestricted Access
      Undiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding Strategy
      Henrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond Jenssen
      CJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
      Add to Selected Citations
  10. Bergrem, Henrik Andreas

    1. You have accessRestricted Access
      Undiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding Strategy
      Henrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond Jenssen
      CJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
      Add to Selected Citations
  11. Bernstein, Keevin

    1. You have accessRestricted Access
      Model for Equitable Care and Outcomes for Remote Full Care Hemodialysis Units
      Keevin Bernstein, James Zacharias, James F. Blanchard, B. Nancy Yu and Souradet Y. Shaw
      CJASN April 2010, 5 (4) 645-651; DOI: https://doi.org/10.2215/CJN.04550709
      Add to Selected Citations
  12. Blanchard, James F.

    1. You have accessRestricted Access
      Model for Equitable Care and Outcomes for Remote Full Care Hemodialysis Units
      Keevin Bernstein, James Zacharias, James F. Blanchard, B. Nancy Yu and Souradet Y. Shaw
      CJASN April 2010, 5 (4) 645-651; DOI: https://doi.org/10.2215/CJN.04550709
      Add to Selected Citations
  13. Blaney, Martha

    1. You have accessRestricted Access
      A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3
      James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. Begelman
      CJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
      Add to Selected Citations
  14. Blazkova, H

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  15. Bleyer, AJ

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  16. Bloom, Roy D.

    1. You have accessRestricted Access
      Transplant-Associated Hyperglycemia: Shedding Light on the Mechanisms
      Peter P. Reese and Roy D. Bloom
      CJASN April 2010, 5 (4) 560-562; DOI: https://doi.org/10.2215/CJN.01430210
      Add to Selected Citations
  17. Booth, Sarah L.

    1. You have accessRestricted Access
      Vitamins K and D Status in Stages 3–5 Chronic Kidney Disease
      Rachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. Booth
      CJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
      Add to Selected Citations
  18. Bostom, Andrew G.

    1. You have accessRestricted Access
      Hypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized Trial
      Darbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. Bostom
      CJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
      Add to Selected Citations
  19. Bowers, Peter

    1. You have accessRestricted Access
      A Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with Anemia
      Pablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter Bowers
      CJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
      Add to Selected Citations
  20. Bradbury, Brian D.

    1. You have accessRestricted Access
      Transfusion Burden among Patients with Chronic Kidney Disease and Anemia
      Elizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. Gagnon
      CJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
      Add to Selected Citations
  21. Brier, Michael E.

    1. You have accessRestricted Access
      Iron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic Response
      Adam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. Aronoff
      CJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
      Add to Selected Citations
  22. Bross, Rachelle

    1. You have accessRestricted Access
      Association of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis Patients
      Nazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. Kopple
      CJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
      Add to Selected Citations
  23. Brown, EJ

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  24. Budde, Klemens

    1. You have accessRestricted Access
      Increased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant Recipients
      Michael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens Budde
      CJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
      Add to Selected Citations

C

  1. Caridi, Gianluca

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations
  2. Chao, MC

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  3. Chaudhary, Kunal

    1. You have accessRestricted Access
      Biocompatible Peritoneal Dialysis Solutions: Do We Have One?
      Kunal Chaudhary and Ramesh Khanna
      CJASN April 2010, 5 (4) 723-732; DOI: https://doi.org/10.2215/CJN.05720809
      Add to Selected Citations
  4. Chen, Z

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  5. Cheng, Yuk Lun

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations
  6. Cherchiglia, Mariangela Leal

    1. You have accessRestricted Access
      Allocation of Initial Modality for Renal Replacement Therapy in Brazil
      Mônica Viegas Andrade, Jaume Puig Junoy, Eli Iola Gurgel Andrade, Francisco de Assis Acurcio, Ricardo Sesso, Odilon Vanni de Queiroz, Daniele Araújo Szuster, Isabel Cristina Gomes, Alessandra Maciel Almeida and Mariangela Leal Cherchiglia
      CJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
      Add to Selected Citations
  7. Chiang, SC

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  8. Chien, YH

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  9. Choukroun, Gabriel

    1. You have accessRestricted Access
      The Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary Report
      Leon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. Massy
      CJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
      Add to Selected Citations
  10. Chow, Kai Ming

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations
  11. Christensen, Karl Bang

    1. You have accessRestricted Access
      New-Onset Diabetes Mellitus after Kidney Transplantation in Denmark
      Mads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-Rasmussen
      CJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
      Add to Selected Citations
  12. Claes, K

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  13. Clemessy, M

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  14. Coresh, Josef

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  15. Coyne, Daniel W.

    1. You have accessRestricted Access
      It's Time to Compare Anemia Management Strategies in Hemodialysis
      Daniel W. Coyne
      CJASN April 2010, 5 (4) 740-742; DOI: https://doi.org/10.2215/CJN.02490409
      Add to Selected Citations
  16. Crews, Deidra C.

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  17. Cuerden, Meaghan

    1. You have accessRestricted Access
      Attitudes to Sharing Personal Health Information in Living Kidney Donation
      Patricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) Network
      CJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
      Add to Selected Citations
  18. Curhan, Gary C.

    1. You have accessRestricted Access
      Prediabetes, Prehypertension … Is It Time for Pre-CKD?
      Gary C. Curhan
      CJASN April 2010, 5 (4) 557-559; DOI: https://doi.org/10.2215/CJN.01650210
      Add to Selected Citations

D

  1. D'Agati, Vivette D.

    1. You have accessRestricted Access
      Treatment with IFN-α, -β, or -γ Is Associated with Collapsing Focal Segmental Glomerulosclerosis
      Glen S. Markowitz, Samih H. Nasr, M. Barry Stokes and Vivette D. D'Agati
      CJASN April 2010, 5 (4) 607-615; DOI: https://doi.org/10.2215/CJN.07311009
      Add to Selected Citations
  2. Dagnino, Monica

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations
  3. Day, Andrew G.

    1. You have accessRestricted Access
      Vitamins K and D Status in Stages 3–5 Chronic Kidney Disease
      Rachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. Booth
      CJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
      Add to Selected Citations
  4. Dekker, HM

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  5. De Man, RA

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  6. Desnick, RJ

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  7. Diekmann, Fritz

    1. You have accessRestricted Access
      Increased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant Recipients
      Michael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens Budde
      CJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
      Add to Selected Citations
  8. Dobrovolny, R

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  9. Dragun, Duska

    1. You have accessRestricted Access
      Increased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant Recipients
      Michael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens Budde
      CJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
      Add to Selected Citations
  10. Drenth, JPH

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  11. Duerr, Michael

    1. You have accessRestricted Access
      Increased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant Recipients
      Michael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens Budde
      CJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
      Add to Selected Citations

E

  1. Eberhardt, Mark S.

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  2. Elleder, M

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations

F

  1. Favrole, P

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  2. Feldt-Rasmussen, Bo

    1. You have accessRestricted Access
      New-Onset Diabetes Mellitus after Kidney Transplantation in Denmark
      Mads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-Rasmussen
      CJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
      Add to Selected Citations
  3. Fok, Queenie Wing-Yi

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations
  4. Fonda, Jennifer R.

    1. You have accessRestricted Access
      Transfusion Burden among Patients with Chronic Kidney Disease and Anemia
      Elizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. Gagnon
      CJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
      Add to Selected Citations
  5. Fryns, JP

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  6. Fu, Min

    1. You have accessRestricted Access
      A Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with Anemia
      Pablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter Bowers
      CJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
      Add to Selected Citations
  7. Fujii, Hisako

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  8. Fukuda, Sanae

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations

G

  1. Gagnon, David R.

    1. You have accessRestricted Access
      Transfusion Burden among Patients with Chronic Kidney Disease and Anemia
      Elizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. Gagnon
      CJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
      Add to Selected Citations
  2. Garg, Amit X.

    1. You have accessRestricted Access
      Attitudes to Sharing Personal Health Information in Living Kidney Donation
      Patricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) Network
      CJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
      Add to Selected Citations
  3. Garland, Jocelyn S.

    1. You have accessRestricted Access
      Vitamins K and D Status in Stages 3–5 Chronic Kidney Disease
      Rachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. Booth
      CJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
      Add to Selected Citations
  4. Gartenberg, Gary

    1. You have accessRestricted Access
      A Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with Anemia
      Pablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter Bowers
      CJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
      Add to Selected Citations
  5. Gasc, JM

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  6. Gaweda, Adam E.

    1. You have accessRestricted Access
      Iron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic Response
      Adam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. Aronoff
      CJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
      Add to Selected Citations
  7. Gaziano, J. Michael

    1. You have accessRestricted Access
      Transfusion Burden among Patients with Chronic Kidney Disease and Anemia
      Elizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. Gagnon
      CJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
      Add to Selected Citations
  8. Ghiggeri, Gian Marco

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations
  9. Gillespie, Barbara S.

    1. You have accessRestricted Access
      A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3
      James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. Begelman
      CJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
      Add to Selected Citations
  10. Glander, Petra

    1. You have accessRestricted Access
      Increased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant Recipients
      Michael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens Budde
      CJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
      Add to Selected Citations
  11. Goldfarb, David S.

    1. You have accessRestricted Access
      A Pilot Clinical Study to Evaluate Changes in Urine Osmolality and Urine cAMP in Response to Acute and Chronic Water Loading in Autosomal Dominant Polycystic Kidney Disease
      Irina Barash, Manish P. Ponda, David S. Goldfarb and Edward Y. Skolnik
      CJASN April 2010, 5 (4) 693-697; DOI: https://doi.org/10.2215/CJN.04180609
      Add to Selected Citations
  12. Goldman, Jesse

    1. You have accessRestricted Access
      A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3
      James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. Begelman
      CJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
      Add to Selected Citations
  13. Goldsmith, Linda J.

    1. You have accessRestricted Access
      Iron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic Response
      Adam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. Aronoff
      CJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
      Add to Selected Citations
  14. Gomes, Isabel Cristina

    1. You have accessRestricted Access
      Allocation of Initial Modality for Renal Replacement Therapy in Brazil
      Mônica Viegas Andrade, Jaume Puig Junoy, Eli Iola Gurgel Andrade, Francisco de Assis Acurcio, Ricardo Sesso, Odilon Vanni de Queiroz, Daniele Araújo Szuster, Isabel Cristina Gomes, Alessandra Maciel Almeida and Mariangela Leal Cherchiglia
      CJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
      Add to Selected Citations
  15. Grimbert, P

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  16. Grünfeld, Jean-Pierre

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  17. Gubler, MC

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations

H

  1. Hanlon, William A.

    1. You have accessRestricted Access
      Hypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized Trial
      Darbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. Bostom
      CJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
      Add to Selected Citations
  2. Hansen, Jesper Melchior

    1. You have accessRestricted Access
      New-Onset Diabetes Mellitus after Kidney Transplantation in Denmark
      Mads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-Rasmussen
      CJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
      Add to Selected Citations
  3. Hart, PS

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  4. Hart, TC

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  5. Hartmann, Anders

    1. You have accessRestricted Access
      Undiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding Strategy
      Henrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond Jenssen
      CJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
      Add to Selected Citations
  6. Hedgeman, Elizabeth

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  7. Hemmelgarn, Brenda R.

    1. You have accessRestricted Access
      Cardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-Analysis
      Davina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease Network
      CJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
      Add to Selected Citations
  8. Henderson, JM

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  9. Higgs, HN

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  10. Hirayama, Yoshinobu

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  11. Hizo-Abes, Patricia

    1. You have accessRestricted Access
      Attitudes to Sharing Personal Health Information in Living Kidney Donation
      Patricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) Network
      CJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
      Add to Selected Citations
  12. Hjelmesæth, Jøran

    1. You have accessRestricted Access
      Undiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding Strategy
      Henrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond Jenssen
      CJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
      Add to Selected Citations
  13. Hodanova, K

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  14. Hoffmann, AL

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  15. Holden, Rachel M.

    1. You have accessRestricted Access
      Vitamins K and D Status in Stages 3–5 Chronic Kidney Disease
      Rachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. Booth
      CJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
      Add to Selected Citations
  16. Hornum, Mads

    1. You have accessRestricted Access
      New-Onset Diabetes Mellitus after Kidney Transplantation in Denmark
      Mads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-Rasmussen
      CJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
      Add to Selected Citations
  17. Hsu, LW

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  18. Huang, AC

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  19. Hulkova, H

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  20. Hwu, WL

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations

I

  1. Inaba, Masaaki

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  2. Ivanek, R

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations

J

  1. Jacobs, Joan

    1. You have accessRestricted Access
      A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3
      James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. Begelman
      CJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
      Add to Selected Citations
  2. James, Matthew T.

    1. You have accessRestricted Access
      Cardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-Analysis
      Davina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease Network
      CJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
      Add to Selected Citations
  3. Jenssen, Trond

    1. You have accessRestricted Access
      Undiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding Strategy
      Henrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond Jenssen
      CJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
      Add to Selected Citations
  4. Jørgensen, Kaj Anker

    1. You have accessRestricted Access
      New-Onset Diabetes Mellitus after Kidney Transplantation in Denmark
      Mads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-Rasmussen
      CJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
      Add to Selected Citations
  5. Junoy, Jaume Puig

    1. You have accessRestricted Access
      Allocation of Initial Modality for Renal Replacement Therapy in Brazil
      Mônica Viegas Andrade, Jaume Puig Junoy, Eli Iola Gurgel Andrade, Francisco de Assis Acurcio, Ricardo Sesso, Odilon Vanni de Queiroz, Daniele Araújo Szuster, Isabel Cristina Gomes, Alessandra Maciel Almeida and Mariangela Leal Cherchiglia
      CJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
      Add to Selected Citations

K

  1. Kalantar-Zadeh, Kamyar

    1. You have accessRestricted Access
      Association of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis Patients
      Nazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. Kopple
      CJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
      Add to Selected Citations
  2. Kalbacova, M

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  3. Kapp, K

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  4. Khanna, Ramesh

    1. You have accessRestricted Access
      Biocompatible Peritoneal Dialysis Solutions: Do We Have One?
      Kunal Chaudhary and Ramesh Khanna
      CJASN April 2010, 5 (4) 723-732; DOI: https://doi.org/10.2215/CJN.05720809
      Add to Selected Citations
  5. Kitagawa, T

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  6. Kmoch, S

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  7. Kopple, Joel D.

    1. You have accessRestricted Access
      Association of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis Patients
      Nazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. Kopple
      CJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
      Add to Selected Citations
  8. Kovesdy, Csaba P.

    1. You have accessRestricted Access
      Association of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis Patients
      Nazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. Kopple
      CJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
      Add to Selected Citations
  9. Koyama, Hidenori

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  10. Kuratsune, Hirohiko

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  11. Kuznetsova, Olga

    1. You have accessRestricted Access
      Hypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized Trial
      Darbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. Bostom
      CJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
      Add to Selected Citations
  12. Kwan, Bonnie Ching-Ha

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations

L

  1. Lawler, Elizabeth V.

    1. You have accessRestricted Access
      Transfusion Burden among Patients with Chronic Kidney Disease and Anemia
      Elizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. Gagnon
      CJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
      Add to Selected Citations
  2. Lee, NC

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  3. Leivestad, Torbjørn

    1. You have accessRestricted Access
      Undiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding Strategy
      Henrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond Jenssen
      CJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
      Add to Selected Citations
  4. Leonardi, Emanuela

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations
  5. Lerut, E

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  6. Leung, Chi Bon

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations
  7. Li, Philip Kam-Tao

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations
  8. Liabeuf, Sophie

    1. You have accessRestricted Access
      The Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary Report
      Leon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. Massy
      CJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
      Add to Selected Citations
  9. Lim, Thomas W.

    1. You have accessRestricted Access
      Cardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-Analysis
      Davina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease Network
      CJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
      Add to Selected Citations
  10. Lin, SJ

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations

M

  1. Maccubbin, Darbie

    1. You have accessRestricted Access
      Hypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized Trial
      Darbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. Bostom
      CJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
      Add to Selected Citations
  2. Magdeleyns, Elke J.

    1. You have accessRestricted Access
      The Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary Report
      Leon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. Massy
      CJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
      Add to Selected Citations
  3. Malaventura, Cristina

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations
  4. Manns, Braden J.

    1. You have accessRestricted Access
      Cardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-Analysis
      Davina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease Network
      CJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
      Add to Selected Citations
  5. Markowitz, Glen S.

    1. You have accessRestricted Access
      Treatment with IFN-α, -β, or -γ Is Associated with Collapsing Focal Segmental Glomerulosclerosis
      Glen S. Markowitz, Samih H. Nasr, M. Barry Stokes and Vivette D. D'Agati
      CJASN April 2010, 5 (4) 607-615; DOI: https://doi.org/10.2215/CJN.07311009
      Add to Selected Citations
  6. Marro, B

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  7. Massy, Ziad A.

    1. You have accessRestricted Access
      The Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary Report
      Leon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. Massy
      CJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
      Add to Selected Citations
  8. Mathiesen, Elisabeth R.

    1. You have accessRestricted Access
      New-Onset Diabetes Mellitus after Kidney Transplantation in Denmark
      Mads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-Rasmussen
      CJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
      Add to Selected Citations
  9. Matignon, M

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  10. McFarlane, Phil

    1. You have accessRestricted Access
      Attitudes to Sharing Personal Health Information in Living Kidney Donation
      Patricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) Network
      CJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
      Add to Selected Citations
  11. Miller, Edgar R.

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  12. Morton, A. Ross

    1. You have accessRestricted Access
      Vitamins K and D Status in Stages 3–5 Chronic Kidney Disease
      Rachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. Booth
      CJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
      Add to Selected Citations
  13. Murer, Luisa

    1. You have accessRestricted Access
      A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis
      Elisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa Murer
      CJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
      Add to Selected Citations

N

  1. Nasr, Samih H.

    1. You have accessRestricted Access
      Treatment with IFN-α, -β, or -γ Is Associated with Collapsing Focal Segmental Glomerulosclerosis
      Glen S. Markowitz, Samih H. Nasr, M. Barry Stokes and Vivette D. D'Agati
      CJASN April 2010, 5 (4) 607-615; DOI: https://doi.org/10.2215/CJN.07311009
      Add to Selected Citations
  2. Neumayer, Hans-H.

    1. You have accessRestricted Access
      Increased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant Recipients
      Michael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens Budde
      CJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
      Add to Selected Citations
  3. Nevens, F

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  4. Ng, Esther Siu-Chun

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations
  5. Nielsen, Finn Thomsen

    1. You have accessRestricted Access
      New-Onset Diabetes Mellitus after Kidney Transplantation in Denmark
      Mads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-Rasmussen
      CJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
      Add to Selected Citations
  6. Nishizawa, Yoshiki

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  7. Noori, Nazanin

    1. You have accessRestricted Access
      Association of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis Patients
      Nazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. Kopple
      CJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
      Add to Selected Citations
  8. Ntoso, K. Adu

    1. You have accessRestricted Access
      A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3
      James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. Begelman
      CJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
      Add to Selected Citations

O

  1. Okada, Shigeki

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  2. Okamura, Mikio

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations
  3. Okuno, Senji

    1. You have accessRestricted Access
      Fatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing Hemodialysis
      Hidenori Koyama, Sanae Fukuda, Tetsuo Shoji, Masaaki Inaba, Yoshihiro Tsujimoto, Tsutomu Tabata, Senji Okuno, Tomoyuki Yamakawa, Shigeki Okada, Mikio Okamura, Hirohiko Kuratsune, Hisako Fujii, Yoshinobu Hirayama, Yasuyoshi Watanabe and Yoshiki Nishizawa
      CJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
      Add to Selected Citations

P

  1. Pavkov, Meda

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  2. Pavlov, Andrey

    1. You have accessRestricted Access
      Vitamins K and D Status in Stages 3–5 Chronic Kidney Disease
      Rachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. Booth
      CJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
      Add to Selected Citations
  3. Pawtowski, A

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  4. Pergola, Pablo E.

    1. You have accessRestricted Access
      A Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with Anemia
      Pablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter Bowers
      CJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
      Add to Selected Citations
  5. Plaisier, E

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  6. Plantinga, Laura C.

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  7. Pollak, MR

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens, R Vanslembrouck, GH Van Oijen, AL Hoffmann, HM Dekker, RA De Man, JPH Drenth, E Plaisier, P Favrole, C Prost, Z Chen, T Van Agrmael, B Marro, P Ronco, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch, JS Schlöndorff, DJ Becker, H Tsukaguchi, AL Uschinski, HN Higgs, JM Henderson and MR Pollak
      CJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
      Add to Selected Citations
  8. Ponda, Manish P.

    1. You have accessRestricted Access
      A Pilot Clinical Study to Evaluate Changes in Urine Osmolality and Urine cAMP in Response to Acute and Chronic Water Loading in Autosomal Dominant Polycystic Kidney Disease
      Irina Barash, Manish P. Ponda, David S. Goldfarb and Edward Y. Skolnik
      CJASN April 2010, 5 (4) 693-697; DOI: https://doi.org/10.2215/CJN.04180609
      Add to Selected Citations
  9. Poon, Yuet Ling

    1. You have accessRestricted Access
      Effect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized Trial
      Philip Kam-Tao Li, Yuk Lun Cheng, Chi Bon Leung, Cheuk Chun Szeto, Kai Ming Chow, Bonnie Ching-Ha Kwan, Esther Siu-Chun Ng, Queenie Wing-Yi Fok, Yuet Ling Poon and Alex Wai-Yin Yu
      CJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
      Add to Selected Citations
  10. Powe, Neil R.

    1. You have accessRestricted Access
      Prevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or Prediabetes
      Laura C. Plantinga, Deidra C. Crews, Josef Coresh, Edgar R. Miller, Rajiv Saran, Jerry Yee, Elizabeth Hedgeman, Meda Pavkov, Mark S. Eberhardt, Desmond E. Williams, Neil R. Powe and for the CDC CKD Surveillance Team
      CJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
      Add to Selected Citations
  11. Prost, C

    1. You have accessRestricted Access
      More on Clinical Renal GeneticsNewborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset mutation c.936+919G>A (IVS4+919G>A). Hum Mutat 30: 1397–1405, 2009Lanreotide reduces the volume of polycystic liver: A randomized, double-blind, placebo-controlled trial. Gastroenterology 137: 1661–1668, 2009Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome. Neurology 73: 1873–1882, 2009Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic renal failure. Am J Hum Genet 85: 204–213, 2009Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat Genet 42: 72–76, 2009
      Jean-Pierre Grünfeld, WL Hwu, L Van Keimpema, S Alamovitch, M Zivna, EJ Brown, YH Chien, NC Lee, SC Chiang, R Dobrovolny, AC Huang, HY Yeh, MC Chao, SJ Lin, T Kitagawa, RJ Desnick, LW Hsu, F Nevens,