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Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysis.
Leenen, Esther; Erger, Florian; Altmüller, Janine; Wenzel, Andrea; Thiele, Holger; Harth, Ana; Tschernoster, Nikolai; Lokhande, Shanti; Joerres, Achim; Becker, Jan-Ulrich; Ekici, Arif; Huettel, Bruno; Beck, Bodo; Weidemann, Alexander.
Afiliación
  • Leenen E; Department of Medicine I-Nephrology, Transplantation & Medical Intensive Care, University Witten/Herdecke, Medical Center Cologne-Merheim, Germany.
  • Erger F; Institute of Human Genetics, Center for Molecular Medicine Cologne and Center for Rare and Hereditary Kidney Disease, Cologne, University Hospital of Cologne, Cologne, Germany.
  • Altmüller J; Berlin Institute of Health at Charité-Universitätsmedizin Berlin, Core Facility Genomics, Berlin, Germany.
  • Wenzel A; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Thiele H; Institute of Human Genetics, Center for Molecular Medicine Cologne and Center for Rare and Hereditary Kidney Disease, Cologne, University Hospital of Cologne, Cologne, Germany.
  • Harth A; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Tschernoster N; Department of Medicine I-Nephrology, Transplantation & Medical Intensive Care, University Witten/Herdecke, Medical Center Cologne-Merheim, Germany.
  • Lokhande S; Institute of Human Genetics, Center for Molecular Medicine Cologne and Center for Rare and Hereditary Kidney Disease, Cologne, University Hospital of Cologne, Cologne, Germany.
  • Joerres A; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Becker JU; Department of Medicine I-Nephrology, Transplantation & Medical Intensive Care, University Witten/Herdecke, Medical Center Cologne-Merheim, Germany.
  • Ekici A; Department of Medicine I-Nephrology, Transplantation & Medical Intensive Care, University Witten/Herdecke, Medical Center Cologne-Merheim, Germany.
  • Huettel B; Institute of Pathology, University Hospital of Cologne, Cologne, Germany.
  • Beck B; Institute of Human Genetics, University Hospital Erlangen, Erlangen, Germany.
  • Weidemann A; Max-Plank-Genome-Centre Cologne (MP-GC), Cologne, Germany.
Nephrol Dial Transplant ; 37(10): 1895-1905, 2022 09 22.
Article en En | MEDLINE | ID: mdl-35485766
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fallo Renal Crónico / Enfermedades Renales Poliquísticas / Nefritis Hereditaria Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nephrol Dial Transplant Asunto de la revista: NEFROLOGIA / TRANSPLANTE Año: 2022 Tipo del documento: Article País de afiliación: Alemania
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fallo Renal Crónico / Enfermedades Renales Poliquísticas / Nefritis Hereditaria Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nephrol Dial Transplant Asunto de la revista: NEFROLOGIA / TRANSPLANTE Año: 2022 Tipo del documento: Article País de afiliación: Alemania