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Clinical Genetics|June 1, 1989
X-linked hypohidrotic ectodermal dysplasia and t(X;12) in a femaleC Turleau, P Niaudet, M O Cabanis, et al.Journal of the American Society of Nephrology : JASN|December 24, 1997
Mutations in the vasopressin V2 receptor and aquaporin-2 genes in 12 families with congenital nephrogenic diabetes insipidusR Vargas-Poussou, L Forestier, M D Dautzenberg, et al.Presse Medicale (Paris, France : 1983)|April 16, 1994
[Hemolytic anemia after kidney transplantation]J Cartron, S Blesson, J L Celton, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1984
[Captopril treatment of arterial hypertension in children after renal transplantation]M F Gagnadoux, C Antignac, J L Bacri, et al.European Journal of Pediatrics|September 15, 1999
Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiencyP Labrune, J Zittoun, I Duvaltier, et al.Pediatric Nephrology (Berlin, Germany)|April 1, 1996
Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish populationA Fuchshuber, P Niaudet, O Gribouval, et al.Virchows Archiv. A, Pathological Anatomy and Histology|January 1, 1982
Tumor cell line characterization of a malignant histiocytosis transplanted into nude miceM F Rousseau-Merck, F Jaubert, M A Bach, et al.Pediatric Nephrology (Berlin, Germany)|April 16, 1998
Renovascular hypertension and vascular anomalies in Alagille syndromeE Bérard, J Sarles, V Triolo, et al.Pediatric Nephrology (Berlin, Germany)|April 1, 1994
Deletion of the mitochondrial DNA in a case of de Toni-Debré-Fanconi syndrome and Pearson syndromeP Niaudet, L Heidet, A Munnich, et al.The Journal of Pediatrics|July 1, 1992
Impairment of lung diffusion capacity in Schönlein-Henoch purpuraM Chaussain, D de Boissieu, G Kalifa, et al.Pageof 14