Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary Diversion-Reference-Cited by-同舟云学术

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Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary Diversion

Published:2008-10-20 Issue:1 Volume:8 Page:
ISSN:1471-230X
Container-title:BMC Gastroenterology
language:en
Short-container-title:BMC Gastroenterol

Author:

Emerick Karan M,Elias Marc S,Melin-Aldana Hector,Strautnieks Sandra,Thompson Richard J,Bull Laura N,Knisely AS,Whitington Peter F,Green Richard M

Publisher

Springer Science and Business Media LLC

Subject

Gastroenterology,General Medicine

Link

http://link.springer.com/article/10.1186/1471-230X-8-47/fulltext.html

Reference37 articles.

1. McDaniell R, Warthen DM, Sanchez-Lara PA, Pai A, Krantz ID, Piccoli DA, Spinner NB: Notch2 mutations cause alagille syndrome, a heterogeneous disorder of the notch signaling pathway. Am J Hum Genet. 2006, 79: 169-173. 10.1086/505332.

2. Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, Piccoli DA, Meltzer PS, Spinner NB, Collins FS, Chandrasekharappa SC: Mutations in the human jagged1 gene are responsible for alagille syndrome. Nat Genet. 1997, 16: 235-242. 10.1038/ng0797-235.

3. Carlton VE, Pawlikowska L, Bull LN: Molecular basis of intrahepatic cholestasis. Ann Med. 2004, 36: 606-617.

4. Whitington PF, Freese DK, Alonso EM, Schwarzenberg SJ, Sharp HL: Clinical and biochemical findings in progressive familial intrahepatic cholestasis. J Pediatr Gastroenterol Nutr. 1994, 18: 134-141.

5. Bull LN, van Eijk MJ, Pawlikowska L, DeYoung JA, Juijn JA, Liao M, Klomp LW, Lomri N, Berger R, Scharschmidt BF, Knisely AS, Houwen RH, Freimer NB: A gene encoding a p-type atpase mutated in two forms of hereditary cholestasis. Nat Genet. 1998, 18: 219-224. 10.1038/ng0398-219.

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4. Biliary diversion in progressive familial intrahepatic cholestasis: a systematic review and meta-analysis;Expert Review of Gastroenterology & Hepatology;2022-02-01

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