Hadchouel M - Search Results

1

Homozygosity mapping of a locus for a novel syndromic ichthyosis to chromosome 3q27-q28.

Baala L, Hadj-Rabia S, Hamel-Teillac D, Hadchouel M, Prost C, Leal SM, Jacquemin E, Sefiani A, De Prost Y, Courtois G, Munnich A, Lyonnet S, Vabres P. Baala L, et al. Among authors: hadchouel m. J Invest Dermatol. 2002 Jul;119(1):70-6. doi: 10.1046/j.1523-1747.2002.01809.x. J Invest Dermatol. 2002. PMID: 12164927 Free PMC article.

2

Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: a tight junction disease.

Hadj-Rabia S, Baala L, Vabres P, Hamel-Teillac D, Jacquemin E, Fabre M, Lyonnet S, De Prost Y, Munnich A, Hadchouel M, Smahi A. Hadj-Rabia S, et al. Among authors: hadchouel m. Gastroenterology. 2004 Nov;127(5):1386-90. doi: 10.1053/j.gastro.2004.07.022. Gastroenterology. 2004. PMID: 15521008

3

Genetic basis of progressive familial intrahepatic cholestasis.

Jacquemin E, Hadchouel M. Jacquemin E, et al. Among authors: hadchouel m. J Hepatol. 1999 Aug;31(2):377-81. doi: 10.1016/s0168-8278(99)80240-2. J Hepatol. 1999. PMID: 10453956 Review. No abstract available.

4

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: hadchouel m. J Pediatr. 1997 May;130(5):817-22. doi: 10.1016/s0022-3476(97)80027-3. J Pediatr. 1997. PMID: 9152294

5

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: hadchouel m. Hum Genet. 1994 Dec;94(6):693-7. doi: 10.1007/BF00206965. Hum Genet. 1994. PMID: 7989045

6

Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease).

Jacquemin E, Dumont M, Bernard O, Erlinger S, Hadchouel M. Jacquemin E, et al. Among authors: hadchouel m. Eur J Pediatr. 1994 Jun;153(6):424-8. doi: 10.1007/BF01983406. Eur J Pediatr. 1994. PMID: 8088298

7

Transient neonatal cholestasis: origin and outcome.

Jacquemin E, Lykavieris P, Chaoui N, Hadchouel M, Bernard O. Jacquemin E, et al. Among authors: hadchouel m. J Pediatr. 1998 Oct;133(4):563-7. doi: 10.1016/s0022-3476(98)70070-8. J Pediatr. 1998. PMID: 9787700

8

Pattern of expression of gamma-glutamyl transpeptidase in rat liver and kidney during development: study by immunochemistry and in situ hybridization.

Jacquemin E, Bulle F, Bernaudin JF, Wellman M, Hugon RN, Guellaen G, Hadchouel M. Jacquemin E, et al. Among authors: hadchouel m. J Pediatr Gastroenterol Nutr. 1990 Jul;11(1):89-95. doi: 10.1097/00005176-199007000-00018. J Pediatr Gastroenterol Nutr. 1990. PMID: 1974921

9

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: hadchouel m. Hepatology. 1997 Mar;25(3):519-23. doi: 10.1002/hep.510250303. Hepatology. 1997. PMID: 9049190

10

CFCI gene mutation and biliary atresia with polysplenia syndrome.

Jacquemin E, Cresteil D, Raynaud N, Hadchouel M. Jacquemin E, et al. Among authors: hadchouel m. J Pediatr Gastroenterol Nutr. 2002 Mar;34(3):326-7. doi: 10.1097/00005176-200203000-00026. J Pediatr Gastroenterol Nutr. 2002. PMID: 11964968 No abstract available.

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