Bernard O - Search Results

1

Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases.

Labrune P, Myara A, Hadchouel M, Ronchi F, Bernard O, Trivin F, Chowdhury NR, Chowdhury JR, Munnich A, Odièvre M. Labrune P, et al. Among authors: bernard o. Hum Genet. 1994 Dec;94(6):693-7. doi: 10.1007/BF00206965. Hum Genet. 1994. PMID: 7989045

2

Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome.

Crosnier C, Driancourt C, Raynaud N, Dhorne-Pollet S, Pollet N, Bernard O, Hadchouel M, Meunier-Rotival M. Crosnier C, et al. Among authors: bernard o. Gastroenterology. 1999 May;116(5):1141-8. doi: 10.1016/s0016-5085(99)70017-x. Gastroenterology. 1999. PMID: 10220506

3

Identification of three novel mutations (Q54P, W70X and T108I) in the glucose-6-phosphatase gene of patients with glycogen storage disease type Ia. Mutation in brief no. 256. Online.

Trioche P, Francoual J, Chalas J, Capel L, Bernard O, Labrune P. Trioche P, et al. Among authors: bernard o. Hum Mutat. 1999;14(1):91. doi: 10.1002/(SICI)1098-1004(1999)14:1<91::AID-HUMU21>3.0.CO;2-B. Hum Mutat. 1999. PMID: 10447271

4

Liver transplantation in children with Alagille syndrome--a study of twelve cases.

Cardona J, Houssin D, Gauthier F, Devictor D, Losay J, Hadchouel M, Bernard O. Cardona J, et al. Among authors: bernard o. Transplantation. 1995 Aug 27;60(4):339-42. doi: 10.1097/00007890-199508270-00007. Transplantation. 1995. PMID: 7652762

5

[Renal involvement in the Alagille syndrome].

Dommergues JP, Gubler MC, Habib R, Hadchouel M, Odièvre M, Bernard O, Alagille D. Dommergues JP, et al. Among authors: bernard o. Arch Pediatr. 1994 Apr;1(4):411-3. Arch Pediatr. 1994. PMID: 7842097 French. No abstract available.

6

Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis.

Jacquemin E, Hermans D, Myara A, Habes D, Debray D, Hadchouel M, Sokal EM, Bernard O. Jacquemin E, et al. Among authors: bernard o. Hepatology. 1997 Mar;25(3):519-23. doi: 10.1002/hep.510250303. Hepatology. 1997. PMID: 9049190

7

Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylation.

Cormier-Daire V, Chretien D, Rustin P, Rötig A, Dubuisson C, Jacquemin E, Hadchouel M, Bernard O, Munnich A. Cormier-Daire V, et al. Among authors: bernard o. J Pediatr. 1997 May;130(5):817-22. doi: 10.1016/s0022-3476(97)80027-3. J Pediatr. 1997. PMID: 9152294

8

Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acid.

Labrune P, Fabre M, Trioche P, Estournet-Mathiaud B, Grangeponte MC, Rambaud C, Maurage C, Bernard O. Labrune P, et al. Among authors: bernard o. Am J Med Genet. 1999 Dec 3;87(4):324-8. doi: 10.1002/(sici)1096-8628(19991203)87:4<324::aid-ajmg8>3.0.co;2-u. Am J Med Genet. 1999. PMID: 10588838

9

Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years.

Laurent J, Gauthier F, Bernard O, Hadchouel M, Odièvre M, Valayer J, Alagille D. Laurent J, et al. Among authors: bernard o. Gastroenterology. 1990 Dec;99(6):1793-7. doi: 10.1016/0016-5085(90)90489-n. Gastroenterology. 1990. PMID: 2227293

10

Incidence of cirrhosis in children with chronic hepatitis.

Vajro P, Hadchouel P, Hadchouel M, Bernard O, Alagille D. Vajro P, et al. Among authors: bernard o. J Pediatr. 1990 Sep;117(3):392-6. doi: 10.1016/s0022-3476(05)81078-9. J Pediatr. 1990. PMID: 2391593

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