Jacquemin E - Search Results

1

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: jacquemin e. Gastroenterology. 2004 Nov;127(5):1386-90. doi: 10.1053/j.gastro.2004.07.022. Gastroenterology. 2004. PMID: 15521008

2

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. J Pediatr Gastroenterol Nutr. 1990 Jul;11(1):89-95. doi: 10.1097/00005176-199007000-00018. J Pediatr Gastroenterol Nutr. 1990. PMID: 1974921

3

A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiency.

Jacquemin E, Setchell KD, O'Connell NC, Estrada A, Maggiore G, Schmitz J, Hadchouel M, Bernard O. Jacquemin E, et al. J Pediatr. 1994 Sep;125(3):379-84. doi: 10.1016/s0022-3476(05)83280-9. J Pediatr. 1994. PMID: 7915305

4

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. Eur J Pediatr. 1994 Jun;153(6):424-8. doi: 10.1007/BF01983406. Eur J Pediatr. 1994. PMID: 8088298

5

Ontogenic expression of the Na(+)-independent organic anion transporting polypeptide (oatp) in rat liver and kidney.

Dubuisson C, Cresteil D, Desrochers M, Decimo D, Hadchouel M, Jacquemin E. Dubuisson C, et al. Among authors: jacquemin e. J Hepatol. 1996 Dec;25(6):932-40. doi: 10.1016/s0168-8278(96)80299-6. J Hepatol. 1996. PMID: 9007723

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

8

Expression of the liver Na+-independent organic anion transporting polypeptide (oatp-1) in rats with bile duct ligation.

Dumont M, Jacquemin E, D'Hont C, Descout C, Cresteil D, Haouzi D, Desrochers M, Stieger B, Hadchouel M, Erlinger S. Dumont M, et al. Among authors: jacquemin e. J Hepatol. 1997 Dec;27(6):1051-6. doi: 10.1016/s0168-8278(97)80149-3. J Hepatol. 1997. PMID: 9453431

9

Transient neonatal cholestasis: origin and outcome.

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

10

Genetic basis of progressive familial intrahepatic cholestasis.

Jacquemin E, Hadchouel M. Jacquemin E, et al. 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.

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