Épidémiologie de la lithiase urinaire : LITHIASE URINAIRE = Epidemiology of urolithiasisDAUDON, Michel; KNEBELMANN, Bertrand.La Revue du praticien (Paris). 2011, Vol 61, Num 3, issn 0035-2640, 372-375, 377-378 [6 p.]Article

Lithiase oxalocalcique : LITHIASE URINAIRE = Calcium oxalate urolithiasisDAUDON, Michel; KNEBELMANN, Bertrand.La Revue du praticien (Paris). 2011, Vol 61, Num 3, pp 385-388, issn 0035-2640, 4 p.Article

Ciliary function of polycystins: a new model for cystogenesisJOLY, Dominique; HUMMEL, Aurélie; RUELLO, Antonella et al.Nephrology, dialysis, transplantation (Print). 2003, Vol 18, Num 9, pp 1689-1692, issn 0931-0509, 4 p.Article

Lithiase calcique primitiveJUNGERS, Paul; KNEBELMANN, Bertrand; DAUDON, Michel et al.L' Eurobiologiste (Paris). 2001, Vol 35, Num 254, pp 12-17, issn 0999-5749Article

Polykystose rénale autosomique dominante: la lumière au bout du tunnel ? = Autosomal dominant polycystic kidney disease: Light at the end of the tunnel?MELANDER, Catherine; JOLY, Dominique; KNEBELMANN, Bertrand et al.Néphrologie & thérapeutique. 2010, Vol 6, Num 4, pp 226-231, issn 1769-7255, 6 p.Article

Lithiases calciques secondairesJUNGERS, Paul; KNEBELMANN, Bertrand; JOLY, Dominique et al.L' Eurobiologiste (Paris). 2001, Vol 35, Num 254, pp 3-11, issn 0999-5749Article

Lithiase cystiniqueJUNGERS, Paul; KNEBELMANN, Bertrand; JOLY, Dominique et al.L' Eurobiologiste (Paris). 2001, Vol 35, Num 254, pp 29-33, issn 0999-5749Article

Exploitation biologique des lithiases urinaires = Biological investigation of urinary lithiasisJUNGERS, Paul; KNEBELMANN, Bertrand; DAUDON, Michel et al.L' Eurobiologiste (Paris). 2001, Vol 35, Num 253, pp 48-55, issn 0999-5749Article

Lithiases d'infectionJUNGERS, Paul; RIEU, Philippe; MERIA, Paul et al.L' Eurobiologiste (Paris). 2001, Vol 35, Num 254, pp 23-28, issn 0999-5749Article

Hereditary nephritis with macrothrombocytopenia : no longer an Alport syndrome variantKNEBELMANN, Bertrand; FAKHOURI, Fadi; GRÜNFELD, Jean-Pierre et al.Nephrology, dialysis, transplantation (Print). 2001, Vol 16, Num 6, pp 1101-1103, issn 0931-0509Conference Paper

Lithiases rénales héréditaires monogéniques : récents acquis diagnostiques et thérapeutiques = Inherited monogenic kidney stone diseases : Recent diagnostic and therapeutic advancesJUNGERS, Paul; JOLY, Dominique; BLANCHARD, Anne et al.Néphrologie & thérapeutique. 2008, Vol 4, Num 4, pp 231-255, issn 1769-7255, 25 p.Article

Thrombotic microangiopathy secondary to VEGF pathway inhibition by sunitinibBOLLEE, Guillaume; PATEY, Natacha; CAZAJOUS, Géraldine et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 2, pp 682-685, issn 0931-0509, 4 p.Article

Post-allogeneic haematopoietic stem cell transplantation membranous nephropathy : clinical presentation, outcome and pathogenic aspectsTERRIER, Benjamin; DELMAS, Yahsou; PATEY-MARIAUD DE SERRE, Natahlie et al.Nephrology, dialysis, transplantation (Print). 2007, Vol 22, Num 5, pp 1369-1376, issn 0931-0509, 8 p.Article

Phenotype and Genotype Characterization of Adenine Phosphoribosyltransferase DeficiencyBOLLEE, Guillaume; DOLLINGER, Cécile; BOUTAUD, Lucile et al.Journal of the American Society of Nephrology. 2010, Vol 21, Num 4, pp 679-688, issn 1046-6673, 10 p.Article

Complete Remission of Lupus Nephritis With Rituximab and Steroids for Induction and Rituximab Alone for Maintenance TherapyCAMOUS, Laurent; MELANDER, Catherine; VALLET, Marion et al.American journal of kidney diseases. 2008, Vol 52, Num 2, pp 346-352, issn 0272-6386, 7 p.Article

β₄ Integrin and laminin 5 are aberrantly expressed in Polycystic Kidney Disease: Role in increased cell adhesion and migrationJOLY, Dominique; MOREL, Viviane; HUMMEL, Aurélie et al.The American journal of pathology. 2003, Vol 163, Num 5, pp 1791-1800, issn 0002-9440, 10 p.Article

Maladie de Fabry : propositions d'un groupe d'experts français concernant le diagnostic, le traitement et le suivi des patients = Fabry disease : proposed guidelines for its diagnosis, treatment and follow-upLIDOVE, Olivier; BEKRI, Soumeya; JAUSSAUD, Roland et al.La Presse médicale (1983). 2007, Vol 36, Num 7-8, pp 1084-1097, issn 0755-4982, 14 p.Article

Reversible paraparesis in multiple myeloma with renal failure. CommentaryZEIER, M. G; TERRIER, Benjamin; JOLY, Dominique et al.Nephrology, dialysis, transplantation (Print). 2006, Vol 21, Num 5, pp 1439-1440, issn 0931-0509, 2 p.Article

Steroid-sensitive nephrotic syndrome: From childhood to adulthoodFAKHOURI, Fadi; BOCQUET, Nathalie; GRÜNFELD, Jean-Pierre et al.American journal of kidney diseases. 2003, Vol 41, Num 3, pp 550-557, issn 0272-6386, 8 p.Article

Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromesARRONDEL, Christelle; VODOVAR, Nicolas; KNEBELMANN, Bertrand et al.Journal of the American Society of Nephrology. 2002, Vol 13, Num 1, pp 65-74, issn 1046-6673Article

Mesangial IgG glomerulonephritis: A distinct type of primary glomerulonephritisFAKHOURI, Fadi; DARRE, Silvina; KNEBELMANN, Bertrand et al.Journal of the American Society of Nephrology. 2002, Vol 13, Num 2, pp 379-387, issn 1046-6673Article

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancyGROSS, Oliver; LICHT, Christoph; KONRAD, Martin et al.Kidney international. 2012, Vol 81, Num 5, pp 494-501, issn 0085-2538, 8 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

X-linked Alport syndrome: Natural history and genotype-phenotype correlations in girls and women belonging to 195 families: A European Community Alport Syndrome Concerted Action StudyJAIS, Jean Philippe; KNEBELMANN, Bertrand; PIRSON, Yves et al.Journal of the American Society of Nephrology. 2003, Vol 14, Num 10, pp 2603-2610, issn 1046-6673, 8 p.Article

Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndromeFAKHOURI, Fadi; JABLONSKI, Mathieu; FREMEAUX-BACCHI, Véronique et al.Blood. 2008, Vol 112, Num 12, pp 4542-4545, issn 0006-4971, 4 p.Article