Index by author
April 01, 2010; Volume 5,Issue 4
A
Acurcio, Francisco de Assis
- You have accessRestricted AccessAllocation of Initial Modality for Renal Replacement Therapy in BrazilMônica 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 CherchigliaCJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
Adams, JN
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Alamovitch, S
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Almeida, Alessandra Maciel
- You have accessRestricted AccessAllocation of Initial Modality for Renal Replacement Therapy in BrazilMônica 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 CherchigliaCJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
Andrade, Eli Iola Gurgel
- You have accessRestricted AccessAllocation of Initial Modality for Renal Replacement Therapy in BrazilMônica 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 CherchigliaCJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
Andrade, Mônica Viegas
- You have accessRestricted AccessAllocation of Initial Modality for Renal Replacement Therapy in BrazilMônica 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 CherchigliaCJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
Antignac, C
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Aronoff, George R.
- You have accessRestricted AccessIron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic ResponseAdam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. AronoffCJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
Artifoni, Lina
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
B
Barash, Irina
- You have accessRestricted AccessA 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 DiseaseIrina Barash, Manish P. Ponda, David S. Goldfarb and Edward Y. SkolnikCJASN April 2010, 5 (4) 693-697; DOI: https://doi.org/10.2215/CJN.04180609
Baresova, V
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Barreto, Daniela V.
- You have accessRestricted AccessThe Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary ReportLeon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. MassyCJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
Barreto, Fellype C.
- You have accessRestricted AccessThe Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary ReportLeon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. MassyCJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
Becker, DJ
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Begelman, Susan M.
- You have accessRestricted AccessA Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. BegelmanCJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
Benetti, Elisa
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
Benner, Debbie
- You have accessRestricted AccessAssociation of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis PatientsNazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. KoppleCJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
Bergrem, Harald
- You have accessRestricted AccessUndiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding StrategyHenrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond JenssenCJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
Bergrem, Henrik Andreas
- You have accessRestricted AccessUndiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding StrategyHenrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond JenssenCJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
Bernstein, Keevin
- You have accessRestricted AccessModel for Equitable Care and Outcomes for Remote Full Care Hemodialysis UnitsKeevin Bernstein, James Zacharias, James F. Blanchard, B. Nancy Yu and Souradet Y. ShawCJASN April 2010, 5 (4) 645-651; DOI: https://doi.org/10.2215/CJN.04550709
Blanchard, James F.
- You have accessRestricted AccessModel for Equitable Care and Outcomes for Remote Full Care Hemodialysis UnitsKeevin Bernstein, James Zacharias, James F. Blanchard, B. Nancy Yu and Souradet Y. ShawCJASN April 2010, 5 (4) 645-651; DOI: https://doi.org/10.2215/CJN.04550709
Blaney, Martha
- You have accessRestricted AccessA Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. BegelmanCJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
Blazkova, H
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Bleyer, AJ
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Bloom, Roy D.
- You have accessRestricted AccessTransplant-Associated Hyperglycemia: Shedding Light on the MechanismsPeter P. Reese and Roy D. BloomCJASN April 2010, 5 (4) 560-562; DOI: https://doi.org/10.2215/CJN.01430210
Booth, Sarah L.
- You have accessRestricted AccessVitamins K and D Status in Stages 3–5 Chronic Kidney DiseaseRachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. BoothCJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
Bostom, Andrew G.
- You have accessRestricted AccessHypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized TrialDarbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. BostomCJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
Bowers, Peter
- You have accessRestricted AccessA Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with AnemiaPablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter BowersCJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
Bradbury, Brian D.
- You have accessRestricted AccessTransfusion Burden among Patients with Chronic Kidney Disease and AnemiaElizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. GagnonCJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
Brier, Michael E.
- You have accessRestricted AccessIron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic ResponseAdam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. AronoffCJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
Bross, Rachelle
- You have accessRestricted AccessAssociation of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis PatientsNazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. KoppleCJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
Brown, EJ
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Budde, Klemens
- You have accessRestricted AccessIncreased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant RecipientsMichael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens BuddeCJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
C
Caridi, Gianluca
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
Chao, MC
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Chaudhary, Kunal
- You have accessRestricted AccessBiocompatible Peritoneal Dialysis Solutions: Do We Have One?Kunal Chaudhary and Ramesh KhannaCJASN April 2010, 5 (4) 723-732; DOI: https://doi.org/10.2215/CJN.05720809
Chen, Z
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Cheng, Yuk Lun
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
Cherchiglia, Mariangela Leal
- You have accessRestricted AccessAllocation of Initial Modality for Renal Replacement Therapy in BrazilMônica 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 CherchigliaCJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
Chiang, SC
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Chien, YH
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Choukroun, Gabriel
- You have accessRestricted AccessThe Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary ReportLeon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. MassyCJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
Chow, Kai Ming
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
Christensen, Karl Bang
- You have accessRestricted AccessNew-Onset Diabetes Mellitus after Kidney Transplantation in DenmarkMads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-RasmussenCJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
Claes, K
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Clemessy, M
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Coresh, Josef
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Coyne, Daniel W.
- You have accessRestricted AccessIt's Time to Compare Anemia Management Strategies in HemodialysisDaniel W. CoyneCJASN April 2010, 5 (4) 740-742; DOI: https://doi.org/10.2215/CJN.02490409
Crews, Deidra C.
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Cuerden, Meaghan
- You have accessRestricted AccessAttitudes to Sharing Personal Health Information in Living Kidney DonationPatricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) NetworkCJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
Curhan, Gary C.
- You have accessRestricted AccessPrediabetes, Prehypertension … Is It Time for Pre-CKD?Gary C. CurhanCJASN April 2010, 5 (4) 557-559; DOI: https://doi.org/10.2215/CJN.01650210
D
D'Agati, Vivette D.
- You have accessRestricted AccessTreatment with IFN-α, -β, or -γ Is Associated with Collapsing Focal Segmental GlomerulosclerosisGlen S. Markowitz, Samih H. Nasr, M. Barry Stokes and Vivette D. D'AgatiCJASN April 2010, 5 (4) 607-615; DOI: https://doi.org/10.2215/CJN.07311009
Dagnino, Monica
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
Day, Andrew G.
- You have accessRestricted AccessVitamins K and D Status in Stages 3–5 Chronic Kidney DiseaseRachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. BoothCJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
Dekker, HM
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
De Man, RA
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Desnick, RJ
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Diekmann, Fritz
- You have accessRestricted AccessIncreased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant RecipientsMichael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens BuddeCJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
Dobrovolny, R
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Dragun, Duska
- You have accessRestricted AccessIncreased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant RecipientsMichael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens BuddeCJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
Drenth, JPH
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Duerr, Michael
- You have accessRestricted AccessIncreased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant RecipientsMichael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens BuddeCJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
E
Eberhardt, Mark S.
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Elleder, M
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
F
Favrole, P
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Feldt-Rasmussen, Bo
- You have accessRestricted AccessNew-Onset Diabetes Mellitus after Kidney Transplantation in DenmarkMads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-RasmussenCJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
Fok, Queenie Wing-Yi
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
Fonda, Jennifer R.
- You have accessRestricted AccessTransfusion Burden among Patients with Chronic Kidney Disease and AnemiaElizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. GagnonCJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
Fryns, JP
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Fu, Min
- You have accessRestricted AccessA Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with AnemiaPablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter BowersCJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
Fujii, Hisako
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Fukuda, Sanae
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
G
Gagnon, David R.
- You have accessRestricted AccessTransfusion Burden among Patients with Chronic Kidney Disease and AnemiaElizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. GagnonCJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
Garg, Amit X.
- You have accessRestricted AccessAttitudes to Sharing Personal Health Information in Living Kidney DonationPatricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) NetworkCJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
Garland, Jocelyn S.
- You have accessRestricted AccessVitamins K and D Status in Stages 3–5 Chronic Kidney DiseaseRachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. BoothCJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
Gartenberg, Gary
- You have accessRestricted AccessA Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with AnemiaPablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter BowersCJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
Gasc, JM
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Gaweda, Adam E.
- You have accessRestricted AccessIron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic ResponseAdam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. AronoffCJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
Gaziano, J. Michael
- You have accessRestricted AccessTransfusion Burden among Patients with Chronic Kidney Disease and AnemiaElizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. GagnonCJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
Ghiggeri, Gian Marco
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
Gillespie, Barbara S.
- You have accessRestricted AccessA Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. BegelmanCJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
Glander, Petra
- You have accessRestricted AccessIncreased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant RecipientsMichael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens BuddeCJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
Goldfarb, David S.
- You have accessRestricted AccessA 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 DiseaseIrina Barash, Manish P. Ponda, David S. Goldfarb and Edward Y. SkolnikCJASN April 2010, 5 (4) 693-697; DOI: https://doi.org/10.2215/CJN.04180609
Goldman, Jesse
- You have accessRestricted AccessA Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. BegelmanCJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
Goldsmith, Linda J.
- You have accessRestricted AccessIron, Inflammation, Dialysis Adequacy, Nutritional Status, and Hyperparathyroidism Modify Erythropoietic ResponseAdam E. Gaweda, Linda J. Goldsmith, Michael E. Brier and George R. AronoffCJASN April 2010, 5 (4) 576-581; DOI: https://doi.org/10.2215/CJN.04710709
Gomes, Isabel Cristina
- You have accessRestricted AccessAllocation of Initial Modality for Renal Replacement Therapy in BrazilMônica 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 CherchigliaCJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
Grimbert, P
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Grünfeld, Jean-Pierre
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Gubler, MC
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
H
Hanlon, William A.
- You have accessRestricted AccessHypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized TrialDarbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. BostomCJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
Hansen, Jesper Melchior
- You have accessRestricted AccessNew-Onset Diabetes Mellitus after Kidney Transplantation in DenmarkMads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-RasmussenCJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
Hart, PS
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Hart, TC
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Hartmann, Anders
- You have accessRestricted AccessUndiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding StrategyHenrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond JenssenCJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
Hedgeman, Elizabeth
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Hemmelgarn, Brenda R.
- You have accessRestricted AccessCardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-AnalysisDavina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease NetworkCJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
Henderson, JM
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Higgs, HN
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Hirayama, Yoshinobu
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Hizo-Abes, Patricia
- You have accessRestricted AccessAttitudes to Sharing Personal Health Information in Living Kidney DonationPatricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) NetworkCJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
Hjelmesæth, Jøran
- You have accessRestricted AccessUndiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding StrategyHenrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond JenssenCJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
Hodanova, K
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Hoffmann, AL
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Holden, Rachel M.
- You have accessRestricted AccessVitamins K and D Status in Stages 3–5 Chronic Kidney DiseaseRachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. BoothCJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
Hornum, Mads
- You have accessRestricted AccessNew-Onset Diabetes Mellitus after Kidney Transplantation in DenmarkMads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-RasmussenCJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
Hsu, LW
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Huang, AC
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Hulkova, H
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Hwu, WL
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
I
Inaba, Masaaki
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Ivanek, R
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
J
Jacobs, Joan
- You have accessRestricted AccessA Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. BegelmanCJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
James, Matthew T.
- You have accessRestricted AccessCardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-AnalysisDavina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease NetworkCJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
Jenssen, Trond
- You have accessRestricted AccessUndiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding StrategyHenrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond JenssenCJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
Jørgensen, Kaj Anker
- You have accessRestricted AccessNew-Onset Diabetes Mellitus after Kidney Transplantation in DenmarkMads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-RasmussenCJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
Junoy, Jaume Puig
- You have accessRestricted AccessAllocation of Initial Modality for Renal Replacement Therapy in BrazilMônica 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 CherchigliaCJASN April 2010, 5 (4) 637-644; DOI: https://doi.org/10.2215/CJN.04840709
K
Kalantar-Zadeh, Kamyar
- You have accessRestricted AccessAssociation of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis PatientsNazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. KoppleCJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
Kalbacova, M
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Kapp, K
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Khanna, Ramesh
- You have accessRestricted AccessBiocompatible Peritoneal Dialysis Solutions: Do We Have One?Kunal Chaudhary and Ramesh KhannaCJASN April 2010, 5 (4) 723-732; DOI: https://doi.org/10.2215/CJN.05720809
Kitagawa, T
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Kmoch, S
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Kopple, Joel D.
- You have accessRestricted AccessAssociation of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis PatientsNazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. KoppleCJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
Kovesdy, Csaba P.
- You have accessRestricted AccessAssociation of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis PatientsNazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. KoppleCJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
Koyama, Hidenori
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Kuratsune, Hirohiko
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Kuznetsova, Olga
- You have accessRestricted AccessHypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized TrialDarbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. BostomCJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
Kwan, Bonnie Ching-Ha
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
L
Lawler, Elizabeth V.
- You have accessRestricted AccessTransfusion Burden among Patients with Chronic Kidney Disease and AnemiaElizabeth V. Lawler, Brian D. Bradbury, Jennifer R. Fonda, J. Michael Gaziano and David R. GagnonCJASN April 2010, 5 (4) 667-672; DOI: https://doi.org/10.2215/CJN.06020809
Lee, NC
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Leivestad, Torbjørn
- You have accessRestricted AccessUndiagnosed Diabetes in Kidney Transplant Candidates: A Case-Finding StrategyHenrik Andreas Bergrem, Tone Gretland Valderhaug, Anders Hartmann, Jøran Hjelmesæth, Torbjørn Leivestad, Harald Bergrem and Trond JenssenCJASN April 2010, 5 (4) 616-622; DOI: https://doi.org/10.2215/CJN.07501009
Leonardi, Emanuela
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
Lerut, E
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Leung, Chi Bon
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
Li, Philip Kam-Tao
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
Liabeuf, Sophie
- You have accessRestricted AccessThe Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary ReportLeon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. MassyCJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
Lim, Thomas W.
- You have accessRestricted AccessCardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-AnalysisDavina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease NetworkCJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
Lin, SJ
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
M
Maccubbin, Darbie
- You have accessRestricted AccessHypophosphatemic Effect of Niacin in Patients without Renal Failure: A Randomized TrialDarbie Maccubbin, Diane Tipping, Olga Kuznetsova, William A. Hanlon and Andrew G. BostomCJASN April 2010, 5 (4) 582-589; DOI: https://doi.org/10.2215/CJN.07341009
Magdeleyns, Elke J.
- You have accessRestricted AccessThe Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary ReportLeon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. MassyCJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
Malaventura, Cristina
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
Manns, Braden J.
- You have accessRestricted AccessCardiovascular Effects of Angiotensin Converting Enzyme Inhibition or Angiotensin Receptor Blockade in Hemodialysis: A Meta-AnalysisDavina J. Tai, Thomas W. Lim, Matthew T. James, Braden J. Manns, Marcello Tonelli, Brenda R. Hemmelgarn and for the Alberta Kidney Disease NetworkCJASN April 2010, 5 (4) 623-630; DOI: https://doi.org/10.2215/CJN.07831109
Markowitz, Glen S.
- You have accessRestricted AccessTreatment with IFN-α, -β, or -γ Is Associated with Collapsing Focal Segmental GlomerulosclerosisGlen S. Markowitz, Samih H. Nasr, M. Barry Stokes and Vivette D. D'AgatiCJASN April 2010, 5 (4) 607-615; DOI: https://doi.org/10.2215/CJN.07311009
Marro, B
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Massy, Ziad A.
- You have accessRestricted AccessThe Circulating Inactive Form of Matrix Gla Protein Is a Surrogate Marker for Vascular Calcification in Chronic Kidney Disease: A Preliminary ReportLeon J. Schurgers, Daniela V. Barreto, Fellype C. Barreto, Sophie Liabeuf, Cédric Renard, Elke J. Magdeleyns, Cees Vermeer, Gabriel Choukroun and Ziad A. MassyCJASN April 2010, 5 (4) 568-575; DOI: https://doi.org/10.2215/CJN.07081009
Mathiesen, Elisabeth R.
- You have accessRestricted AccessNew-Onset Diabetes Mellitus after Kidney Transplantation in DenmarkMads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-RasmussenCJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
Matignon, M
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
McFarlane, Phil
- You have accessRestricted AccessAttitudes to Sharing Personal Health Information in Living Kidney DonationPatricia Hizo-Abes, Ann Young, Peter P. Reese, Phil McFarlane, Linda Wright, Meaghan Cuerden, Amit X. Garg and for the Donor Nephrectomy Outcomes Research (DONOR) NetworkCJASN April 2010, 5 (4) 717-722; DOI: https://doi.org/10.2215/CJN.06130809
Miller, Edgar R.
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Morton, A. Ross
- You have accessRestricted AccessVitamins K and D Status in Stages 3–5 Chronic Kidney DiseaseRachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. BoothCJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
Murer, Luisa
- You have accessRestricted AccessA Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental GlomerulosclerosisElisa Benetti, Gianluca Caridi, Cristina Malaventura, Monica Dagnino, Emanuela Leonardi, Lina Artifoni, Gian Marco Ghiggeri, Silvio C.E. Tosatto and Luisa MurerCJASN April 2010, 5 (4) 698-702; DOI: https://doi.org/10.2215/CJN.05670809
N
Nasr, Samih H.
- You have accessRestricted AccessTreatment with IFN-α, -β, or -γ Is Associated with Collapsing Focal Segmental GlomerulosclerosisGlen S. Markowitz, Samih H. Nasr, M. Barry Stokes and Vivette D. D'AgatiCJASN April 2010, 5 (4) 607-615; DOI: https://doi.org/10.2215/CJN.07311009
Neumayer, Hans-H.
- You have accessRestricted AccessIncreased Incidence of Angioedema with ACE Inhibitors in Combination with mTOR Inhibitors in Kidney Transplant RecipientsMichael Duerr, Petra Glander, Fritz Diekmann, Duska Dragun, Hans-H. Neumayer and Klemens BuddeCJASN April 2010, 5 (4) 703-708; DOI: https://doi.org/10.2215/CJN.07371009
Nevens, F
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Ng, Esther Siu-Chun
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
Nielsen, Finn Thomsen
- You have accessRestricted AccessNew-Onset Diabetes Mellitus after Kidney Transplantation in DenmarkMads Hornum, Kaj Anker Jørgensen, Jesper Melchior Hansen, Finn Thomsen Nielsen, Karl Bang Christensen, Elisabeth R. Mathiesen and Bo Feldt-RasmussenCJASN April 2010, 5 (4) 709-716; DOI: https://doi.org/10.2215/CJN.05360709
Nishizawa, Yoshiki
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Noori, Nazanin
- You have accessRestricted AccessAssociation of Dietary Phosphorus Intake and Phosphorus to Protein Ratio with Mortality in Hemodialysis PatientsNazanin Noori, Kamyar Kalantar-Zadeh, Csaba P. Kovesdy, Rachelle Bross, Debbie Benner and Joel D. KoppleCJASN April 2010, 5 (4) 683-692; DOI: https://doi.org/10.2215/CJN.08601209
Ntoso, K. Adu
- You have accessRestricted AccessA Phase III, Randomized, Double-Blind, Placebo-Controlled Study of Tenecteplase for Improvement of Hemodialysis Catheter Function: TROPICS 3James Tumlin, Jesse Goldman, David M. Spiegel, David Roer, K. Adu Ntoso, Martha Blaney, Joan Jacobs, Barbara S. Gillespie and Susan M. BegelmanCJASN April 2010, 5 (4) 631-636; DOI: https://doi.org/10.2215/CJN.06520909
O
Okada, Shigeki
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Okamura, Mikio
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
Okuno, Senji
- You have accessRestricted AccessFatigue Is a Predictor for Cardiovascular Outcomes in Patients Undergoing HemodialysisHidenori 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 NishizawaCJASN April 2010, 5 (4) 659-666; DOI: https://doi.org/10.2215/CJN.08151109
P
Pavkov, Meda
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Pavlov, Andrey
- You have accessRestricted AccessVitamins K and D Status in Stages 3–5 Chronic Kidney DiseaseRachel M. Holden, A. Ross Morton, Jocelyn S. Garland, Andrey Pavlov, Andrew G. Day and Sarah L. BoothCJASN April 2010, 5 (4) 590-597; DOI: https://doi.org/10.2215/CJN.06420909
Pawtowski, A
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Pergola, Pablo E.
- You have accessRestricted AccessA Randomized Controlled Study Comparing Once-Weekly to Every-2-Week and Every-4-Week Dosing of Epoetin Alfa in CKD Patients with AnemiaPablo E. Pergola, Gary Gartenberg, Min Fu, Steven Sun, Marsha Wolfson and Peter BowersCJASN April 2010, 5 (4) 598-606; DOI: https://doi.org/10.2215/CJN.06770909
Plaisier, E
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Plantinga, Laura C.
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Pollak, MR
- You have accessRestricted AccessMore 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, 2009Jean-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 PollakCJASN April 2010, 5 (4) 563-567; DOI: https://doi.org/10.2215/CJN.01720210
Ponda, Manish P.
- You have accessRestricted AccessA 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 DiseaseIrina Barash, Manish P. Ponda, David S. Goldfarb and Edward Y. SkolnikCJASN April 2010, 5 (4) 693-697; DOI: https://doi.org/10.2215/CJN.04180609
Poon, Yuet Ling
- You have accessRestricted AccessEffect of Membrane Permeability on Inflammation and Arterial Stiffness: A Randomized TrialPhilip 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 YuCJASN April 2010, 5 (4) 652-658; DOI: https://doi.org/10.2215/CJN.05620809
Powe, Neil R.
- You have accessRestricted AccessPrevalence of Chronic Kidney Disease in US Adults with Undiagnosed Diabetes or PrediabetesLaura 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 TeamCJASN April 2010, 5 (4) 673-682; DOI: https://doi.org/10.2215/CJN.07891109
Prost, C
- You have accessRestricted AccessMore 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, 2009Jean-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,