The Renal Lesions of Alport SyndromeHEIDET, Laurence; GUBLER, Marie-Claire.Journal of the American Society of Nephrology. 2009, Vol 20, Num 6, pp 1210-1215, issn 1046-6673, 6 p.Article

Syndrome d'Alport ou néphropathie héréditaire hématurique progressive avec surdité = Alport syndrome or progressive hereditary nephritis with hearing lossGABIER, Marie-Claire; HEIDET, Laurence; ANTIGNAC, Corinne et al.Néphrologie & thérapeutique. 2007, Vol 3, Num 3, pp 113-120, issn 1769-7255, 8 p.Article

A murine model of Denys―Drash syndrome reveals novel transcriptional targets of WT1 in podocytesRATELADE, Julien; ARRONDEL, Christelle; ANTIGNAC, Corinne et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, pp 1-15, issn 0964-6906, 15 p.Article

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutationsTEMME, Johanna; PETERS, Frederick; GROSS, Oliver et al.Kidney international. 2012, Vol 81, Num 8, pp 779-783, issn 0085-2538, 5 p.Article

Stem cell therapy for Alport syndrome : the hope beyond the hypeGROSS, Oliver; BORZA, Dorin-Bogdan; COSGROVE, Dominic et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 3, pp 731-734, issn 0931-0509, 4 p.Article

COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndromeLONGO, Ilaria; PORCEDDA, Paola; ROCCATELLO, Dario et al.Kidney international. 2002, Vol 61, Num 6, pp 1947-1956, issn 0085-2538Article

Alport syndrome associated with diffuse leiomyomatosis: COL4A5-COL4A6 deletion associated with a mild form of Alport nephropathyMOTHES, Henning; HEIDET, Laurence; ARRONDEL, Christelle et al.Nephrology, dialysis, transplantation (Print). 2002, Vol 17, Num 1, pp 70-74, issn 0931-0509Article

Mutations in the COL4A4 and COL4A3 genes cause familial benign hematuriaBADENAS, Cèlia; PRAGA, Manuel; DAVILA, Sonia et al.Journal of the American Society of Nephrology. 2002, Vol 13, Num 5, pp 1248-1254, issn 1046-6673Article

Benign familial hematuria associated with a novel COL4A4 mutationOZEN, Seza; ERTOY, Dilek; HEIDET, Laurence et al.Pediatric nephrology (Berlin, West). 2001, Vol 16, Num 11, pp 874-877, issn 0931-041XConference Paper

In vivo expression of putative LMW1B targets in nail-patella syndrome kidneysHEIDET, Laurence; BONGERS, Ernie M. H. F; KNOERS, Nine V. A. M et al.The American journal of pathology. 2003, Vol 163, Num 1, pp 145-155, issn 0002-9440, 11 p.Article

A human-mouse chimera of the α3α4α5(IV) collagen protomer rescues the renal phenotype in Col4a3^-/- Alport miceHEIDET, Laurence; BORZA, Dorin-Bogdan; JOUIN, Mélanie et al.The American journal of pathology. 2003, Vol 163, Num 4, pp 1633-1644, issn 0002-9440, 12 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

A large tandem duplication within the COL4A5 gene is responsible for the high prevalence of Alport syndrome in French PolynesiaARRONDEL, Christelle; DESCHENES, Georges; LE MEUR, Yannick et al.Kidney international. 2004, Vol 65, Num 6, pp 2030-2040, issn 0085-2538, 11 p.Article

In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutationZHANG, Shao-Yu; MARLIER, Arnaud; GRIBOUVAL, Olivier et al.Kidney international. 2004, Vol 66, Num 3, pp 945-954, issn 0085-2538, 10 p.Article

Diffuse esophageal leiomyomatosis with perirectal involvement mimicking Hirschsprung diseaseGUILLEM, Philippe; DELCAMBRE, Frédéric; COHEN-SOLAL, Lola et al.Gastroenterology (New York, NY. 1943). 2001, Vol 120, Num 1, pp 216-220, issn 0016-5085Article

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutationVAN DER LOOP, Frank T. L; HEIDET, Laurence; SMEETS, Hubert J. M et al.Kidney international. 2000, Vol 58, Num 5, pp 1870-1875, issn 0085-2538Article

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

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defectsJEANPIERRE, Cécile; MACE, Guillaume; LOGET, Philippe et al.Journal of medical genetics. 2011, Vol 48, Num 7, pp 497-504, issn 0022-2593, 8 p.Article

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndromeHEIDET, Laurence; ARRONDEL, Christelle; FORESTIER, Lionel et al.Journal of the American Society of Nephrology. 2000, Vol 12, Num 1, pp 97-106, issn 1046-6673Article