Showing results (21-30 of 73) with videos related to
Sort By:
Pageof 8
Journal of the American Society of Nephrology : JASN|March 3, 2007
Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndromeEva Riveira-Munoz, Qing Chang, Nathalie Godefroid, et al.Pediatric Nephrology (Berlin, Germany)|January 16, 2023
Severe parental phenotype associates with hypertension in children with ADPKDNathalie Demoulin, Elliott Van Regemorter, Karin Dahan, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 8, 2002
Polymicrogyria in chromosome 22q11 deletion syndromeSophie Ghariani, Karin Dahan, Christine Saint-Martin, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 9, 2016
Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndromeHendrica Belge, Karin Dahan, Jean-François Cambier, et al.Journal of Pediatric Hematology/Oncology|July 1, 2009
Multiple neoplasia in a 15-year-old girl with familial adenomatous polyposisBenoit Brasseur, Karin Dahan, Véronique Beauloye, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 2, 2011
Association of PKD2 (polycystin 2) mutations with left-right laterality defectsStanislas Bataille, Nathalie Demoulin, Olivier Devuyst, et al.Nature Chemical Biology|January 5, 2021
Molecular basis for arginine C-terminal degron recognition by Cul2FEM1 E3 ligaseXinyan Chen, Shanhui Liao, Yaara Makaros, et al.Journal of the American Society of Nephrology : JASN|October 25, 2001
Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: two facets of the same disease?Karin Dahan, Arno Fuchshuber, Stavroula Adamis, et al.Clinical Journal of the American Society of Nephrology : CJASN|August 27, 2011
Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutationsGuillaume Bollée, Karin Dahan, Martin Flamant, et al.Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|July 8, 2005
[Rupture of the renal artery and renal parenchyma in a pregnant woman with vascular form of Ehlers-Danlos syndrome]Benoît Debie, Frank Hammer, Karin Dahan, et al.Pageof 8