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Journal of the American Society of Nephrology : JASN|March 19, 2011
Spectrum of mutations in Gitelman syndromeRosa Vargas-Poussou, Karin Dahan, Diana Kahila, et al.Nature Genetics|July 23, 2003
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationEdgar A Otto, Bernhard Schermer, Tomoko Obara, et al.European Radiology|July 5, 2020
COVID-19 impact assessment on the French radiological centers: a nationwide surveyGuillaume Herpe, Mathieu Naudin, Mathieu Léderlin, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 14, 2015
Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide studyAnne-Sylvia Sacri, Tristan Chambaraud, Bruno Ranchin, et al.Journal of the American Society of Nephrology : JASN|April 14, 2006
Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 geneRosa Vargas-Poussou, Pascal Houillier, Nelly Le Pottier, et al.Blood|September 18, 2008
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndromeVeronique Frémeaux-Bacchi, Elizabeth C Miller, M Kathryn Liszewski, et al.Nature Genetics|June 15, 2007
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeMarion Delous, Lekbir Baala, Rémi Salomon, et al.Pediatric Nephrology (Berlin, Germany)|October 24, 2017
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndromeGuillaume Dorval, Olivier Gribouval, Vanesa Martinez-Barquero, et al.Human Mutation|April 25, 2015
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1Lamisse Mansour-Hendili, Anne Blanchard, Nelly Le Pottier, et al.Pageof 5