Hypertension artérielle chez l'enfant : Hypertension artérielle = Hypertension in childrenSALOMON, Rémi.La Presse médicale (1983). 2006, Vol 35, Num 6, pp 1072-1076, issn 0755-4982, 5 p., CAH2Conference Paper

Néphronophtise = NephronophtisisNIAUDET, Patrick; SALOMON, Rémi.Néphrologie & thérapeutique. 2006, Vol 2, Num 4, pp 200-206, issn 1769-7255, 7 p.Article

Génétique et maladie de Hirschsprung : Diagnostic de la maladie de Crohn chez l'enfant = Genetics in Hirschsprung diseaseSALOMON, Rémi; AMIEL, Jeanne; JAN, Dominique et al.MTP. Médecine thérapeutique pédiatrie. 2001, Vol 4, Num 4, pp 273-277, issn 1286-5494Article

Intravenous cyclosporine therapy in recurrent nephrotic syndrome after renal transplantation in childrenSALOMON, Rémi; GAGNADOUX, Marie-France; NIAUDET, Patrick et al.Transplantation. 2003, Vol 75, Num 6, pp 810-814, issn 0041-1337, 5 p.Article

PAX2 Mutations in Fetal Renal HypodysplasiaMARTINOVIC-BOURIEL, Jelena; BENACHI, Alexandra; ATTIE-BITACH, Tania et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 4, pp 830-835, issn 1552-4825, 6 p.Article

Primary glomerulonephritis with isolated C3 deposits : a new entity which shares common genetic risk factors with haemolytic uraemic syndromeSERVAIS, Aude; FREMEAUX-BACCHI, Véronique; LEQUINTREC, Moglie et al.Journal of medical genetics. 2007, Vol 44, Num 3, pp 193-199, issn 0022-2593, 7 p.Article

BBS10 mutations are common in 'Meckel'-type cystic kidneysPUTOUX, Audrey; MOUGOU-ZERELLI, Soumaya; DELEZOIDE, Anne-Lise et al.Journal of medical genetics. 2010, Vol 47, Num 12, pp 848-852, issn 0022-2593, 5 p.Article

Increased β-2 microglobulinuria in human immunodeficiency virus-1-infected children and adolescents treated with tenofovirPAPALEO, Andrea; WARSZAWSKI, Josiane; SALOMON, Rémi et al.The Pediatric infectious disease journal. 2007, Vol 26, Num 10, pp 949-951, issn 0891-3668, 3 p.Article

The meckel-gruber syndrome gene, MKS3, is mutated in joubert syndromeBAALA, Lekbir; ROMANO, Stéphane; MUNNICH, Arnold et al.American journal of human genetics. 2007, Vol 80, Num 1, pp 186-194, issn 0002-9297, 9 p.Article

ANCA-Associated Glomerulonephritis in Systemic-Onset Juvenile Idiopathic ArthritisBELOT, Alexandre; BADER-MEUNIER, Brigitte; NIAUDET, Patrick et al.American journal of kidney diseases. 2012, Vol 59, Num 3, pp 439-443, issn 0272-6386, 5 p.Article

Recurrence of nephrotic syndrome after transplantation in a mixed population of children and adults: course of glomerular lesions and value of the Columbia classification of histological variants of focal and segmental glomerulosclerosis (FSGS)CANAUD, Guillaume; DION, Daniel; LEGENDRE, Christophe et al.Nephrology, dialysis, transplantation (Print). 2010, Vol 25, Num 4, pp 1321-1328, issn 0931-0509, 8 p.Article

Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6DELOUS, Marion; HELLMAN, Nathan E; GAUDE, Helori-Maël et al.Human molecular genetics (Print). 2009, Vol 18, Num 24, pp 4711-4723, issn 0964-6906, 13 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

Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adultsBOLLEE, Guillaume; FAKHOURI, Fadi; KARRAS, Alexandre et al.Nephrology, dialysis, transplantation (Print). 2006, Vol 21, Num 9, pp 2660-2663, issn 0931-0509, 4 p.Article

Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomesMOLLET, Géraldine; SILBERMANN, Flora; DELOUS, Marion et al.Human molecular genetics (Print). 2005, Vol 14, Num 5, pp 645-656, issn 0964-6906, 12 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

FGF9 and FGF20 Maintain the Stemness of Nephron Progenitors in Mice and ManBARAK, Hila; HUH, Sung-Ho; ORNITZ, David M et al.Developmental cell. 2012, Vol 22, Num 6, pp 1191-1207, issn 1534-5807, 17 p.Article

Control of the Wnt pathways by nephrocystin-4 is required for morphogenesis of the zebrafish pronephrosBURCKLE, Céline; GAUDE, Helori-Mael; VESQUE, Christine et al.Human molecular genetics (Print). 2011, Vol 20, Num 13, pp 2611-2627, issn 0964-6906, 17 p.Article

Bleeding disorders in Lowe syndrome patients: evidence for a link between OCRL mutations and primary haemostasis disordersLASNE, Dominique; BAUJAT, Geneviève; MIRAULT, Tristan et al.British journal of haematology. 2010, Vol 150, Num 6, pp 685-688, issn 0007-1048, 4 p.Article

Different inactivating mutations of the mineralocorticoid receptor in fourteen families affected by type I pseudohypoaldosteronism : Cardiovascular endocrinology: Original articlesSARTORATO, Paola; LAPEYRAQUE, Anne-Laure; BOSIO, Maurizio et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 6, pp 2508-2517, issn 0021-972X, 10 p.Article

Clinical features and management of arterial hypertension in children with Williams―Beuren syndromeBOUCHIREB, Karim; BOYER, Olivia; BONNET, Damien et al.Nephrology, dialysis, transplantation (Print). 2010, Vol 25, Num 2, pp 434-438, issn 0931-0509, 5 p.Article

Pulse Cyclophosphamide Therapy and Clinical Remission in Atypical Hemolytic Uremic Syndrome With Anti-Complement Factor H AutoantibodiesBOYER, Olivia; BALZAMO, Eve; CHARBIT, Marina et al.American journal of kidney diseases. 2010, Vol 55, Num 5, pp 923-927, issn 0272-6386, 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

Segregation at three loci explains familial and population risk in Hirschsprung diseaseGABRIEL, Stacey Bolk; SALOMON, Rémi; STEFFANN, Julie et al.Nature genetics. 2002, Vol 31, Num 1, pp 89-93, issn 1061-4036Article

PAX2 mutations in oligomeganephroniaSALOMON, Rémi; TELLIER, Anne-Lorraine; ATTIE-BITACH, Tania et al.Kidney international. 2001, Vol 59, Num 2, pp 457-462, issn 0085-2538Article