Infections urinaires de l'enfant et de l'adulte. LeucocyturieBARBET, Christelle; NIVET, Hubert.La Revue du praticien (Paris). 2006, Vol 56, Num 18, pp 2073-2078, issn 0035-2640, 6 p.Article

Protéinurie et syndrome néphrotique chez l'enfant et l'adulte : Orientation diagnostique = Proteinuria and nephrotic syndrom in the child and the adultVALENTIN, Jean Francois; HALIMI, Jean-Michel; NIVET, Hubert et al.La Revue du praticien (Paris). 2003, Vol 53, Num 2, pp 223-228, issn 0035-2640, 6 p.Article

Plasma therapy in von Willebrand factor protease deficiencyDESCHENES, Georges; VEYRADIER, Agnès; CLOAREC, Sylvie et al.Pediatric nephrology (Berlin, West). 2002, Vol 17, Num 10, pp 867-870, issn 0931-041XArticle

Transplantation rénale pour polykystose rénale autosomique dominante : spécificités de la préparation et du suivi des patients = Renal transplantation in patients with autosomal dominant polycystic kidney disease : pre-transplantation evaluation and follow-upBRETAGNOL, Anne; BÜCHLER, Matthias; BOUTIN, Jean-Michel et al.Néphrologie & thérapeutique. 2007, Vol 3, Num 7, pp 449-455, issn 1769-7255, 7 p.Article

In vitro decrease of glomerular heparan sulfate by lymphocytes from idiopathic nephrotic syndrome patientsBIRMELE, Beatrice; THIBAULT, Gilles; NIVET, Hubert et al.Kidney international. 2001, Vol 59, Num 3, pp 913-922, issn 0085-2538Article

Mutations of NPHP2 and NPHP3 in infantile nephronophthisisTORY, Kalman; ROUSSET-ROUVIERE, Caroline; DESCHENES, Georges et al.Kidney international. 2009, Vol 75, Num 8, pp 839-847, issn 0085-2538, 9 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

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

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

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndromeFREMEAUX-BACCHI, Veronique; MILLER, Elizabeth C; KAPUR, Gaurav et al.Blood. 2008, Vol 112, Num 13, pp 4948-4952, issn 0006-4971, 5 p.Article

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndromeVEYRADIER, Agnès; OBERT, Bernadette; GIRMA, Jean-Pierre et al.The Journal of pediatrics. 2003, Vol 142, Num 3, pp 310-317, issn 0022-3476, 8 p.Article

Doubling of Serum Creatinine in Clinical Trials, Cost-Effectiveness Studies, and Individual Patients: Adequate Use in Renal TransplantationGATAULT, Philippe; AL-NAJJAR, Azmi; LEBRANCHU, Yvon et al.Transplantation. 2011, Vol 92, Num 9, pp 1012-1017, issn 0041-1337, 6 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

Recipient age and mycophenolate mofetil as the main determinants of outcome after steroid withdrawal : Analysis of long-term follow-up in renal transplantationLAOUAD, Inass; HALIMI, Jean-Michel; BÜCHLER, Matthias et al.Transplantation. 2005, Vol 80, Num 6, pp 872-874, issn 0041-1337, 3 p.Article

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationOTTO, Edgar A; SCHERMER, Bernhard; FOREMAN, John W et al.Nature genetics. 2003, Vol 34, Num 4, pp 413-420, issn 1061-4036, 8 p.Article

Papillary stones with Randall's plaques in children: clinicobiological features and outcomeBOUCHIREB, Karim; BOYER, Olivia; DAUDON, Michel et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 4, pp 1529-1534, issn 0931-0509, 6 p.Article

Spectrum of Mutations in Gitelman SyndromeVARGAS-POUSSOU, Rosa; DAHAN, Karin; HAYMANN, Jean-Philippe et al.Journal of the American Society of Nephrology. 2011, Vol 22, Num 4, pp 693-703, issn 1046-6673, 11 p.Article

Respective predictive role of urinary albumin excretion and nonalbumin proteinuria on graft loss and death in renal transplant recipientsHALIMI, Jean-Michel; BUCHLER, Matthias; AL-NAJJAR, Azmi et al.American journal of transplantation (Print). 2007, Vol 7, Num 12, pp 2775-2781, issn 1600-6135, 7 p.Article

Occupational exposure in ANCA-positive patients : A case-control studyBEAUDREUIL, Séverine; LASFARGUES, Gérard; LAUERIERE, Laurence et al.Kidney international. 2005, Vol 67, Num 5, pp 1961-1966, issn 0085-2538, 6 p.Article

Association of donor TNFRSF6 (FAS) gene polymorphism with acute rejection in renal transplant patients: a case-control studyCAPPELLESSO, Sandrine; VALENTIN, Jean-Francois; WATIER, Hervé et al.Nephrology, dialysis, transplantation (Print). 2004, Vol 19, Num 2, pp 439-443, issn 0931-0509, 5 p.Article

The risk of hypertension in men: direct and indirect effects of chronic smoking. CommentaryHALIMI, Jean-Michel; GIRAUDEAU, Bruno; VOL, Sylviane et al.Journal of hypertension. 2002, Vol 20, Num 2, pp 171-172, issn 0263-6352, 9 p.Article

Interferon gamma licensing of human dendritic cells in T-helper-independent CD8⁺ alloimmunityLEMOINE, Roxane; VELGE-ROUSSEL, Florence; HERR, Florence et al.Blood. 2010, Vol 116, Num 16, pp 3089-3098, issn 0006-4971, 10 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

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