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Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1.
Olinger, Eric; Hofmann, Patrick; Kidd, Kendrah; Dufour, Inès; Belge, Hendrica; Schaeffer, Céline; Kipp, Anne; Bonny, Olivier; Deltas, Constantinos; Demoulin, Nathalie; Fehr, Thomas; Fuster, Daniel G; Gale, Daniel P; Goffin, Eric; Hodanová, Katerina; Huynh-Do, Uyen; Kistler, Andreas; Morelle, Johann; Papagregoriou, Gregory; Pirson, Yves; Sandford, Richard; Sayer, John A; Torra, Roser; Venzin, Christina; Venzin, Reto; Vogt, Bruno; Zivná, Martina; Greka, Anna; Dahan, Karin; Rampoldi, Luca; Kmoch, Stanislav; Bleyer, Anthony J; Devuyst, Olivier.
Afiliación
  • Olinger E; Institute of Physiology, University of Zurich, Zurich, Switzerland; Department of Nephrology and Hypertension, Inselspital Bern University Hospital, Bern, Switzerland; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK. Electroni
  • Hofmann P; Institute of Physiology, University of Zurich, Zurich, Switzerland; Department of Internal Medicine, Hospital Uster, Uster, Switzerland.
  • Kidd K; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Dufour I; Institute of Physiology, University of Zurich, Zurich, Switzerland; Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Belge H; Center for Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium.
  • Schaeffer C; Division of Genetics and Cell Biology, San Raffaele Scientific Institute, Milan, Italy.
  • Kipp A; Institute of Physiology, University of Zurich, Zurich, Switzerland.
  • Bonny O; Service of Nephrology, Lausanne University Hospital, Lausanne, Switzerland.
  • Deltas C; Molecular Medicine Research Center, Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus.
  • Demoulin N; Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium; Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, Brussels, Belgium.
  • Fehr T; Institute of Physiology, University of Zurich, Zurich, Switzerland; Department of Internal Medicine, Cantonal Hospital Graubuenden, Chur, Switzerland.
  • Fuster DG; Department of Nephrology and Hypertension, Inselspital Bern University Hospital, Bern, Switzerland.
  • Gale DP; Department of Nephrology, University College of London, London, UK.
  • Goffin E; Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium; Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, Brussels, Belgium.
  • Hodanová K; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Huynh-Do U; Department of Nephrology and Hypertension, Inselspital Bern University Hospital, Bern, Switzerland.
  • Kistler A; Department of Internal Medicine, Cantonal Hospital Frauenfeld, Frauenfeld, Switzerland.
  • Morelle J; Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium; Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, Brussels, Belgium.
  • Papagregoriou G; Molecular Medicine Research Center, Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus.
  • Pirson Y; Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Sandford R; Department of Medical Genetics, Cambridge Biomedical Campus, Cambridge, UK.
  • Sayer JA; Renal Services, Newcastle upon Tyne Hospitals National Health Service Trust, Newcastle upon Tyne, UK; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Torra R; Inherited Renal Disorders, Nephrology Department, Fundació Puigvert, Spanish Renal Research Network (REDinREN), Instituto de Investigaciones Biomédicas Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Venzin C; Division of Nephrology, Department of Internal Medicine, Hospital Davos, Davos, Switzerland.
  • Venzin R; Division of Nephrology, Department of Internal Medicine, Cantonal Hospital Graubuenden, Chur, Switzerland.
  • Vogt B; Department of Nephrology and Hypertension, Inselspital Bern University Hospital, Bern, Switzerland.
  • Zivná M; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Greka A; Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA; Broad Institute of MIT and Harvard, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
  • Dahan K; Center for Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium.
  • Rampoldi L; Division of Genetics and Cell Biology, San Raffaele Scientific Institute, Milan, Italy.
  • Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Bleyer AJ; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic. Electronic address: ableyer@wakehealth.edu.
  • Devuyst O; Institute of Physiology, University of Zurich, Zurich, Switzerland; Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium. Electronic address: olivier.devuyst@uzh.ch.
Kidney Int ; 98(3): 717-731, 2020 09.
Article en En | MEDLINE | ID: mdl-32450155
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Riñón Poliquístico Autosómico Dominante Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: Kidney Int Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Riñón Poliquístico Autosómico Dominante Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: Kidney Int Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos