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Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndromeKWON, Theresa; DRAGON-DUREY, Marie-Agnes; MACHER, Marie-Alice et al.Nephrology, dialysis, transplantation (Print). 2008, Vol 23, Num 6, pp 2088-2090, issn 0931-0509, 3 p.Article

Developmental toxicity of the angiotensin II type 1 receptor antagonists during human pregnancy : a report of 10 casesSERREAU, Raphael; LUTON, Dominique; MACHER, Marie-Alice et al.BJOG (Oxford. Print). 2005, Vol 112, Num 6, pp 710-712, issn 1470-0328, 3 p.Article

Rituximab in steroid-dependent idiopathic nephrotic syndrome in childhood—follow—up after CD19 recoverySELLIER-LECLERC, Anne-Laure; BAUDOUIN, Veronique; KWON, Theresa et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 3, pp 1083-1089, issn 0931-0509, 7 p.Article

A humanized mouse model of idiopathic nephrotic syndrome suggests a pathogenic role for immature cellsSELLIER-LECLERC, Anne-Laure; DUVAL, Arnaud; HADDAD, Elie et al.Journal of the American Society of Nephrology. 2007, Vol 18, Num 10, pp 2732-2739, issn 1046-6673, 8 p.Article

High NPHP1 and NPHP6 mutation rate in patients with joubert syndrome and nephronophthisis : Potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutationsTORY, Kalman; LACOSTE, Tiphanie; ANTIGNAC, Corinne et al.Journal of the American Society of Nephrology. 2007, Vol 18, Num 5, pp 1566-1575, issn 1046-6673, 10 p.Article

Effect of Hydrochlorothiazide on Urinary Calcium Excretion in Dent Disease : An Uncontrolled TrialBLANCHARD, Anne; VARGAS-POUSSOU, Rosa; MACHER, Marie-Alice et al.American journal of kidney diseases. 2008, Vol 52, Num 6, pp 1084-1095, issn 0272-6386, 12 p.Article

Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulationLOIRAT, Chantal; MACHER, Marie-Alice; MORET, Jacques et al.Nephrology, dialysis, transplantation (Print). 2010, Vol 25, Num 10, pp 3421-3425, issn 0931-0509, 5 p.Article

Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1FARGUE, Sonia; HARAMBAT, Jérôme; MACHER, Marie-Alice et al.Kidney international. 2009, Vol 76, Num 7, pp 767-773, issn 0085-2538, 7 p.Article

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndromeBROCHARD, Karine; BOYER, Olivia; MORIN, Denis et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 5, pp 1455-1464, issn 0931-0509, 10 p.Article

Anti-factor H autoantibodies associated with atypical hemolytic uremic syndromeDRAGON-DUREY, Marie-Agnès; LOIRAT, Chantal; CLOAREC, Sylvie et al.Journal of the American Society of Nephrology. 2005, Vol 16, Num 2, pp 555-563, issn 1046-6673, 9 p.Article

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathiesSERVAIS, Aude; NOËL, Laure-Hélène; MOULIN, Bruno et al.Kidney international. 2012, Vol 82, Num 4, pp 454-464, issn 0085-2538, 11 p.Article

Genotype―phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcomeHARAMBAT, Jérôme; FARGUE, Sonia; DURRBACH, Antoine et al.Kidney international. 2010, Vol 77, Num 5, pp 443-449, issn 0085-2538, 7 p.Article

Enhanced expression of the CD71 mesangial iga1 receptor in Berger disease and Henoch-Schönlein nephritis: Association between CD71 expression and IgA depositsHADDAD, Elie; MOURA, Ivan C; ARCOS-FAJARDO, Michelle et al.Journal of the American Society of Nephrology. 2003, Vol 14, Num 2, pp 327-337, issn 1046-6673, 11 p.Article

Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndromeBOYER, Olivia; BENOIT, Geneviève; MACHER, Marie-Alice et al.Journal of medical genetics. 2010, Vol 47, Num 7, pp 445-452, issn 0022-2593, 8 p.Article

Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndromeROUMENINA, Lubka T; JABLONSKI, Mathieu; MOULONGUET, Luc et al.Blood. 2009, Vol 114, Num 13, pp 2837-2845, issn 0006-4971, 9 p.Article

Long-Term Outcome of Prenatally Detected Posterior Urethral Valves : Single Center Study of 65 Cases Managed by Primary Valve AblationSARHAN, Osama; ZACCARIA, Isabelle; HENSLE, Terry W et al.The Journal of urology. 2008, Vol 179, Num 1, pp 307-313, issn 0022-5347, 7 p.Article

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndromeSELLIER-LEDERC, Anne-Laure; FREMEAUX-BACCHI, Veronique; TSIMARATOS, Michel et al.Journal of the American Society of Nephrology. 2007, Vol 18, Num 8, pp 2392-2400, issn 1046-6673, 9 p.Article

Genetic investigation of autosomal recessive distal renal tubular acidosis : Evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 geneVARGAS-POUSSOU, Rosa; HOUILLIER, Pascal; ECKART, Philippe et al.Journal of the American Society of Nephrology. 2006, Vol 17, Num 5, pp 1437-1443, issn 1046-6673, 7 p.Article

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeDELOUS, Marion; BAALA, Lekbir; MOUTKINE, Imane et al.Nature genetics. 2007, Vol 39, Num 7, pp 875-881, issn 1061-4036, 7 p.Article