Collapsing glomerulopathy in Galloway–Mowat syndrome: A case report and review of the literature-Reference-Cited by-同舟云学术

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Collapsing glomerulopathy in Galloway–Mowat syndrome: A case report and review of the literature

Published:2008-06 Issue:6 Volume:204 Page:401-406
ISSN:0344-0338
Container-title:Pathology - Research and Practice
language:en
Short-container-title:Pathology - Research and Practice

Author:

Sartelet Hervé,Pietrement Christine,Noel Laure-Hélène,Sabouraud Pascal,Birembaut Philippe,Oligny Luc Laurier,Roussel Bernard,Doco-Fenzy Martine

Publisher

Elsevier BV

Subject

Cell Biology,Pathology and Forensic Medicine

Reference38 articles.

1. Posttransplantation relapse of FSGS is characterized by glomerular epithelial cell transdifferentiation;Bariety;J. Am. Soc. Nephrol.,2001

2. The dysregulated podocyte phenotype;Barisoni;J. Am. Soc. Nephrol.,1999

3. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome;Boute;Nat. Genet.,2000

4. Prenatal magnetic resonance imaging of Galloway–Mowat syndrome;Chen;Prenatal Diagn.,2005

5. Kidney in Galloway–Mowat syndrome: clinical spectrum with description of pathology;Cohen;Kidney Int.,1994

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1. Novel LAGE3 Pathogenic Variants Combined with TRPC6 and NUP160 Variants in Galloway-Mowat Syndrome: A Case Report;Case Reports in Nephrology and Dialysis;2023-09-25

2. WDR73 Depletion Destabilizes PIP4K2C Activity and Impairs Focal Adhesion Formation in Galloway–Mowat Syndrome;Biology;2022-09-25

3. Clinical Aspects of Genetic Forms of Nephrotic Syndrome;Pediatric Nephrology;2022

4. Clinical Aspects of Genetic Forms of Nephrotic Syndrome;Pediatric Nephrology;2021

5. An unusual kidney presentation of severe proteinuria in a 2-year-old girl: Answers;Pediatric Nephrology;2020-08-12

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