Cochat P - Search Results

1

Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours.

Heidet L, Dahan K, Zhou J, Xu Z, Cochat P, Gould JD, Leppig KA, Proesmans W, Guyot C, Guillot M, et al. Heidet L, et al. Among authors: cochat p. Hum Mol Genet. 1995 Jan;4(1):99-108. doi: 10.1093/hmg/4.1.99. Hum Mol Genet. 1995. PMID: 7711741

2

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

Boye E, Mollet G, Forestier L, Cohen-Solal L, Heidet L, Cochat P, Grünfeld JP, Palcoux JB, Gubler MC, Antignac C. Boye E, et al. Among authors: cochat p. Am J Hum Genet. 1998 Nov;63(5):1329-40. doi: 10.1086/302106. Am J Hum Genet. 1998. PMID: 9792860 Free PMC article.

3

Alport syndrome and diffuse leiomyomatosis: deletions in the 5' end of the COL4A5 collagen gene.

Antignac C, Zhou J, Sanak M, Cochat P, Roussel B, Deschênes G, Gros F, Knebelmann B, Hors-Cayla MC, Tryggvason K, et al. Antignac C, et al. Among authors: cochat p. Kidney Int. 1992 Nov;42(5):1178-83. doi: 10.1038/ki.1992.402. Kidney Int. 1992. PMID: 1453602 Free article.

4

Pathological case of the month. Alport syndrome and diffuse leiomyomatosis.

Cochat P, Guyot C, Antignac C, Pracros JP, Bouvier R, Chappuis JP, Gilbert-Barness E. Cochat P, et al. Am J Dis Child. 1993 Jul;147(7):791-2. Am J Dis Child. 1993. PMID: 8322755 No abstract available.

5

Risk factors for chronic rejection in pediatric renal allograft recipients.

Guyot C, Nguyen JM, Cochat P, Foulard M, Bouissou F, Van Damme-Lombaerts R, Loirat C, Janssen F, Bensman A, Nivet H, Fischbach M, Guignard JP, André JL. Guyot C, et al. Among authors: cochat p. Pediatr Nephrol. 1996 Dec;10(6):723-7. doi: 10.1007/s004670050199. Pediatr Nephrol. 1996. PMID: 8971889 Clinical Trial.

6

Diffuse leiomyomatosis in Alport syndrome.

Cochat P, Guibaud P, Garcia Torres R, Roussel B, Guarner V, Larbre F. Cochat P, et al. J Pediatr. 1988 Aug;113(2):339-43. doi: 10.1016/s0022-3476(88)80280-4. J Pediatr. 1988. PMID: 3294362 Review. No abstract available.

7

Partial deletion of the AGXT gene (EX1_EX7del): A new genotype in hyperoxaluria type 1.

Nogueira PK, Vuong TS, Bouton O, Maillard A, Marchand M, Rolland MO, Cochat P, Bozon D. Nogueira PK, et al. Among authors: cochat p. Hum Mutat. 2000 Apr;15(4):384-5. doi: 10.1002/(SICI)1098-1004(200004)15:4<384::AID-HUMU20>3.0.CO;2-J. Hum Mutat. 2000. PMID: 10737993

8

Long-term results of rhGH treatment in children with renal failure: experience of the French Society of Pediatric Nephrology.

Bérard E, André JL, Guest G, Berthier F, Afanetti M, Cochat P, Broyer M; French Society for Pediatric Nephrology. Bérard E, et al. Among authors: cochat p. Pediatr Nephrol. 2008 Nov;23(11):2031-8. doi: 10.1007/s00467-008-0849-3. Epub 2008 Jun 27. Pediatr Nephrol. 2008. PMID: 18584215

9

Schimke immunoosseous dysplasia: suggestions of genetic diversity.

Clewing JM, Fryssira H, Goodman D, Smithson SF, Sloan EA, Lou S, Huang Y, Choi K, Lücke T, Alpay H, André JL, Asakura Y, Biebuyck-Gouge N, Bogdanovic R, Bonneau D, Cancrini C, Cochat P, Cockfield S, Collard L, Cordeiro I, Cormier-Daire V, Cransberg K, Cutka K, Deschenes G, Ehrich JH, Fründ S, Georgaki H, Guillen-Navarro E, Hinkelmann B, Kanariou M, Kasap B, Kilic SS, Lama G, Lamfers P, Loirat C, Majore S, Milford D, Morin D, Ozdemir N, Pontz BF, Proesmans W, Psoni S, Reichenbach H, Reif S, Rusu C, Saraiva JM, Sakallioglu O, Schmidt B, Shoemaker L, Sigaudy S, Smith G, Sotsiou F, Stajic N, Stein A, Stray-Pedersen A, Taha D, Taque S, Tizard J, Tsimaratos M, Wong NA, Boerkoel CF. Clewing JM, et al. Among authors: cochat p. Hum Mutat. 2007 Mar;28(3):273-83. doi: 10.1002/humu.20432. Hum Mutat. 2007. PMID: 17089404

10

Identification of 5 novel mutations in the AGXT gene.

Basmaison O, Rolland MO, Cochat P, Bozon D. Basmaison O, et al. Among authors: cochat p. Hum Mutat. 2000 Jun;15(6):577. doi: 10.1002/1098-1004(200006)15:6<577::AID-HUMU9>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10862087

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