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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Sadowski, Carolin E; Lovric, Svjetlana; Ashraf, Shazia; Pabst, Werner L; Gee, Heon Yung; Kohl, Stefan; Engelmann, Susanne; Vega-Warner, Virginia; Fang, Humphrey; Halbritter, Jan; Somers, Michael J; Tan, Weizhen; Shril, Shirlee; Fessi, Inès; Lifton, Richard P; Bockenhauer, Detlef; El-Desoky, Sherif; Kari, Jameela A; Zenker, Martin; Kemper, Markus J; Mueller, Dominik; Fathy, Hanan M; Soliman, Neveen A; Hildebrandt, Friedhelm.
Afiliação
  • Sadowski CE; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Lovric S; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Ashraf S; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Pabst WL; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Gee HY; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Kohl S; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Engelmann S; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Vega-Warner V; Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan;
  • Fang H; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Halbritter J; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Somers MJ; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Tan W; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Shril S; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Fessi I; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
  • Lifton RP; Department of Genetics and Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut;
  • Bockenhauer D; Institute of Child Health, University College London, London, United Kingdom;
  • El-Desoky S; Pediatric Nephrology Unit, King Abdulaziz University Hospital, Jeddah, Kingdom of Saudi Arabia;
  • Kari JA; Pediatric Nephrology Unit, King Abdulaziz University Hospital, Jeddah, Kingdom of Saudi Arabia;
  • Zenker M; Department of Human Genetics, Otto von Guericke University, Magdeburg, Germany;
  • Kemper MJ; Department of Pediatrics, University Hospital Hamburg-Eppendorf, Hamburg, Germany;
  • Mueller D; Department of Pediatric Nephrology, Medical Faculty of the Charité, Berlin, Germany;
  • Fathy HM; The Pediatric Nephrology Unit, Alexandria University, Alexandria, Egypt;
  • Soliman NA; Department of Pediatrics, Center of Pediatric Nephrology & Transplantation, Kasr Al Ainy School of Medicine, Cairo University, Cairo, Egypt; Egyptian Group for Orphan Renal Diseases, Cairo, Egypt; and.
  • Hildebrandt F; Division of Nephrology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Howard Hughes Medical Institute, Chevy Chase, Maryland friedhelm.hildebrandt@childrens.harvard.edu.
J Am Soc Nephrol ; 26(6): 1279-89, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25349199
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Peptídeos e Proteínas de Sinalização Intracelular / Proteínas de Membrana / Síndrome Nefrótica Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Peptídeos e Proteínas de Sinalização Intracelular / Proteínas de Membrana / Síndrome Nefrótica Idioma: En Ano de publicação: 2015 Tipo de documento: Article