Index by author

April 01, 2010; Volume 5,Issue 4

A

  1. Acurcio, Francisco de Assis

    1. 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

  2. Adams, JN

    1. 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

  3. Alamovitch, S

    1. 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

  4. Almeida, Alessandra Maciel

    1. 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

  5. Andrade, Eli Iola Gurgel

    1. 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

  6. Andrade, Mônica Viegas

    1. 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

  7. Antignac, C

    1. 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

  8. Aronoff, George R.

    1. 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

  9. Artifoni, Lina

    1. 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

B

  1. Barash, Irina

    1. 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

  2. Baresova, V

    1. 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

  3. Barreto, Daniela V.

    1. 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

  4. Barreto, Fellype C.

    1. 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

  5. Becker, DJ

    1. 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

  6. Begelman, Susan M.

    1. 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

  7. Benetti, Elisa

    1. 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

  8. Benner, Debbie

    1. 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

  9. Bergrem, Harald

    1. 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

  10. Bergrem, Henrik Andreas

    1. 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

  11. Bernstein, Keevin

    1. 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

  12. Blanchard, James F.

    1. 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

  13. Blaney, Martha

    1. 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

  14. Blazkova, H

    1. 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

  15. Bleyer, AJ

    1. 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

  16. Bloom, Roy D.

    1. 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

  17. Booth, Sarah L.

    1. 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

  18. Bostom, Andrew G.

    1. 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

  19. Bowers, Peter

    1. 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

  20. Bradbury, Brian D.

    1. 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

  21. Brier, Michael E.

    1. 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

  22. Bross, Rachelle

    1. 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

  23. Brown, EJ

    1. 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

  24. Budde, Klemens

    1. 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

C

  1. Caridi, Gianluca

    1. 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

  2. Chao, MC

    1. 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

  3. Chaudhary, Kunal

    1. 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

  4. Chen, Z

    1. 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

  5. Cheng, Yuk Lun

    1. 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

  6. Cherchiglia, Mariangela Leal

    1. 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

  7. Chiang, SC

    1. 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

  8. Chien, YH

    1. 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

  9. Choukroun, Gabriel

    1. 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

  10. Chow, Kai Ming

    1. 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

  11. Christensen, Karl Bang

    1. 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

  12. Claes, K

    1. 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

  13. Clemessy, M

    1. 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

  14. Coresh, Josef

    1. 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

  15. Coyne, Daniel W.

    1. 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

  16. Crews, Deidra C.

    1. 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

  17. Cuerden, Meaghan

    1. 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

  18. Curhan, Gary C.

    1. 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

D

  1. D'Agati, Vivette D.

    1. 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

  2. Dagnino, Monica

    1. 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

  3. Day, Andrew G.

    1. 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

  4. Dekker, HM

    1. 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

  5. De Man, RA

    1. 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

  6. Desnick, RJ

    1. 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

  7. Diekmann, Fritz

    1. 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

  8. Dobrovolny, R

    1. 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

  9. Dragun, Duska

    1. 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

  10. Drenth, JPH

    1. 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

  11. Duerr, Michael

    1. 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

E

  1. Eberhardt, Mark S.

    1. 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

  2. Elleder, M

    1. 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

F

  1. Favrole, P

    1. 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

  2. Feldt-Rasmussen, Bo

    1. 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

  3. Fok, Queenie Wing-Yi

    1. 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

  4. Fonda, Jennifer R.

    1. 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

  5. Fryns, JP

    1. 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

  6. Fu, Min

    1. 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

  7. Fujii, Hisako

    1. 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

  8. Fukuda, Sanae

    1. 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

G

  1. Gagnon, David R.

    1. 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

  2. Garg, Amit X.

    1. 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

  3. Garland, Jocelyn S.

    1. 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

  4. Gartenberg, Gary

    1. 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

  5. Gasc, JM

    1. 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

  6. Gaweda, Adam E.

    1. 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

  7. Gaziano, J. Michael

    1. 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

  8. Ghiggeri, Gian Marco

    1. 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

  9. Gillespie, Barbara S.

    1. 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

  10. Glander, Petra

    1. 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

  11. Goldfarb, David S.

    1. 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

  12. Goldman, Jesse

    1. 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

  13. Goldsmith, Linda J.

    1. 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

  14. Gomes, Isabel Cristina

    1. 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

  15. Grimbert, P

    1. 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

  16. Grünfeld, Jean-Pierre

    1. 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

  17. Gubler, MC

    1. 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

H

  1. Hanlon, William A.

    1. 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

  2. Hansen, Jesper Melchior

    1. 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

  3. Hart, PS

    1. 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

  4. Hart, TC

    1. 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

  5. Hartmann, Anders

    1. 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

  6. Hedgeman, Elizabeth

    1. 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

  7. Hemmelgarn, Brenda R.

    1. 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

  8. Henderson, JM

    1. 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

  9. Higgs, HN

    1. 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

  10. Hirayama, Yoshinobu

    1. 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

  11. Hizo-Abes, Patricia

    1. 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

  12. Hjelmesæth, Jøran

    1. 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

  13. Hodanova, K

    1. 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

  14. Hoffmann, AL

    1. 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

  15. Holden, Rachel M.

    1. 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

  16. Hornum, Mads

    1. 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

  17. Hsu, LW

    1. 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

  18. Huang, AC

    1. 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

  19. Hulkova, H

    1. 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

  20. Hwu, WL

    1. 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

I

  1. Inaba, Masaaki

    1. 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

  2. Ivanek, R

    1. 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

J

  1. Jacobs, Joan

    1. 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

  2. James, Matthew T.

    1. 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

  3. Jenssen, Trond

    1. 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

  4. Jørgensen, Kaj Anker

    1. 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

  5. Junoy, Jaume Puig

    1. 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

K

  1. Kalantar-Zadeh, Kamyar

    1. 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

  2. Kalbacova, M

    1. 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

  3. Kapp, K

    1. 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

  4. Khanna, Ramesh

    1. 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

  5. Kitagawa, T

    1. 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

  6. Kmoch, S

    1. 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

  7. Kopple, Joel D.

    1. 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

  8. Kovesdy, Csaba P.

    1. 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

  9. Koyama, Hidenori

    1. 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

  10. Kuratsune, Hirohiko

    1. 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

  11. Kuznetsova, Olga

    1. 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

  12. Kwan, Bonnie Ching-Ha

    1. 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

L

  1. Lawler, Elizabeth V.

    1. 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

  2. Lee, NC

    1. 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

  3. Leivestad, Torbjørn

    1. 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

  4. Leonardi, Emanuela

    1. 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

  5. Lerut, E

    1. 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

  6. Leung, Chi Bon

    1. 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

  7. Li, Philip Kam-Tao

    1. 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

  8. Liabeuf, Sophie

    1. 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

  9. Lim, Thomas W.

    1. 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

  10. Lin, SJ

    1. 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

M

  1. Maccubbin, Darbie

    1. 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

  2. Magdeleyns, Elke J.

    1. 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

  3. Malaventura, Cristina

    1. 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

  4. Manns, Braden J.

    1. 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

  5. Markowitz, Glen S.

    1. 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

  6. Marro, B

    1. 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

  7. Massy, Ziad A.

    1. 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

  8. Mathiesen, Elisabeth R.

    1. 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

  9. Matignon, M

    1. 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

  10. McFarlane, Phil

    1. 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

  11. Miller, Edgar R.

    1. 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

  12. Morton, A. Ross

    1. 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

  13. Murer, Luisa

    1. 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

N

  1. Nasr, Samih H.

    1. 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

  2. Neumayer, Hans-H.

    1. 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

  3. Nevens, F

    1. 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

  4. Ng, Esther Siu-Chun

    1. 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

  5. Nielsen, Finn Thomsen

    1. 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

  6. Nishizawa, Yoshiki

    1. 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

  7. Noori, Nazanin

    1. 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

  8. Ntoso, K. Adu

    1. 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

O

  1. Okada, Shigeki

    1. 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

  2. Okamura, Mikio

    1. 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

  3. Okuno, Senji

    1. 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

P

  1. Pavkov, Meda

    1. 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

  2. Pavlov, Andrey

    1. 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

  3. Pawtowski, A

    1. 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

  4. Pergola, Pablo E.

    1. 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

  5. Plaisier, E

    1. 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

  6. Plantinga, Laura C.

    1. 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

  7. Pollak, MR

    1. 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

  8. Ponda, Manish P.

    1. 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

  9. Poon, Yuet Ling

    1. 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

  10. Powe, Neil R.

    1. 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

  11. Prost, C

    1. 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