157 related articles for article (PubMed ID: 16226694)
1. Molecular basis of cholestatic diseases of surgical interest.
Alvarez L; Jara P; Hierro L; Sánchez-Sabaté E; Martínez-Fernández P; López-Santamaría M
Semin Pediatr Surg; 2005 Nov; 14(4):200-5. PubMed ID: 16226694
[TBL] [Abstract][Full Text] [Related]
2. Molecular basis of intrahepatic cholestasis.
Carlton VE; Pawlikowska L; Bull LN
Ann Med; 2004; 36(8):606-17. PubMed ID: 15768832
[TBL] [Abstract][Full Text] [Related]
3. Novel resequencing chip customized to diagnose mutations in patients with inherited syndromes of intrahepatic cholestasis.
Liu C; Aronow BJ; Jegga AG; Wang N; Miethke A; Mourya R; Bezerra JA
Gastroenterology; 2007 Jan; 132(1):119-26. PubMed ID: 17241866
[TBL] [Abstract][Full Text] [Related]
4. Alagille Syndrome Mimicking Biliary Atresia in Early Infancy.
Dědič T; Jirsa M; Keil R; Rygl M; Šnajdauf J; Kotalová R
PLoS One; 2015; 10(11):e0143939. PubMed ID: 26618708
[TBL] [Abstract][Full Text] [Related]
5. Advances in familial and congenital cholestatic diseases. Clinical and diagnostic implications.
Colombo C; Okolicsanyi L; Strazzabosco M
Dig Liver Dis; 2000 Mar; 32(2):152-9. PubMed ID: 10975791
[TBL] [Abstract][Full Text] [Related]
6. Reduced hepatic expression of farnesoid X receptor in hereditary cholestasis associated to mutation in ATP8B1.
Alvarez L; Jara P; Sánchez-Sabaté E; Hierro L; Larrauri J; Díaz MC; Camarena C; De la Vega A; Frauca E; López-Collazo E; Lapunzina P
Hum Mol Genet; 2004 Oct; 13(20):2451-60. PubMed ID: 15317749
[TBL] [Abstract][Full Text] [Related]
7. Alagille syndrome with a previously undescribed mutation.
Bhatia V; Kumar P
Indian Pediatr; 2014 Apr; 51(4):314-6. PubMed ID: 24825276
[TBL] [Abstract][Full Text] [Related]
8. Childhood Cholestatic Liver Diseases that Persist Into Adulthood: Lessons for the Adult Gastroenterologist.
Chan AP; Venick RS
J Clin Gastroenterol; 2023 Aug; 57(7):686-693. PubMed ID: 37022007
[TBL] [Abstract][Full Text] [Related]
9. Progressive familial intrahepatic cholestasis.
Jacquemin E
Clin Res Hepatol Gastroenterol; 2012 Sep; 36 Suppl 1():S26-35. PubMed ID: 23141890
[TBL] [Abstract][Full Text] [Related]
10. Liver transplantation for progressive familial intrahepatic cholestasis: the evolving role of genotyping.
Shneider BL
Liver Transpl; 2009 Jun; 15(6):565-6. PubMed ID: 19479788
[No Abstract] [Full Text] [Related]
11. Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.
van der Woerd WL; van Mil SW; Stapelbroek JM; Klomp LW; van de Graaf SF; Houwen RH
Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):541-53. PubMed ID: 20955958
[TBL] [Abstract][Full Text] [Related]
12. Progressive familial intrahepatic cholestasis (PFIC) type 1, 2, and 3: a review of the liver pathology findings.
Morotti RA; Suchy FJ; Magid MS
Semin Liver Dis; 2011 Feb; 31(1):3-10. PubMed ID: 21344347
[TBL] [Abstract][Full Text] [Related]
13. The significance of human jagged 1 mutations detected in severe cases of extrahepatic biliary atresia.
Kohsaka T; Yuan ZR; Guo SX; Tagawa M; Nakamura A; Nakano M; Kawasasaki H; Inomata Y; Tanaka K; Miyauchi J
Hepatology; 2002 Oct; 36(4 Pt 1):904-12. PubMed ID: 12297837
[TBL] [Abstract][Full Text] [Related]
14. Variable expression of Alagille syndrome in a family with a new JAG1 gene mutation.
Ziesenitz VC; Loukanov T; Gläser C; Gorenflo M
Cardiol Young; 2016 Jan; 26(1):164-7. PubMed ID: 25613755
[TBL] [Abstract][Full Text] [Related]
15. Cholestatic liver disease in children.
Santos JL; Choquette M; Bezerra JA
Curr Gastroenterol Rep; 2010 Feb; 12(1):30-9. PubMed ID: 20425482
[TBL] [Abstract][Full Text] [Related]
16. The genetic basis of the Alagille syndrome.
Rand EB
J Pediatr Gastroenterol Nutr; 1998 Feb; 26(2):234-6. PubMed ID: 9481647
[No Abstract] [Full Text] [Related]
17. Alagille syndrome: A nutritional niche for Notch.
Sokol RJ
J Pediatr; 1999 Feb; 134(2):136-8. PubMed ID: 9931516
[No Abstract] [Full Text] [Related]
18. Diagnostic Yield of an Algorithm for Neonatal and Infantile Cholestasis Integrating Next-Generation Sequencing.
Nicastro E; Di Giorgio A; Marchetti D; Barboni C; Cereda A; Iascone M; D'Antiga L
J Pediatr; 2019 Aug; 211():54-62.e4. PubMed ID: 31160058
[TBL] [Abstract][Full Text] [Related]
19. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
Marchetti D; Iascone MR; Pezzoli L
Hum Genet; 2009 Aug; 126(2):350-1. PubMed ID: 19694056
[No Abstract] [Full Text] [Related]
20. NR1H4 analysis in patients with progressive familial intrahepatic cholestasis, drug-induced cholestasis or intrahepatic cholestasis of pregnancy unrelated to ATP8B1, ABCB11 and ABCB4 mutations.
Davit-Spraul A; Gonzales E; Jacquemin E
Clin Res Hepatol Gastroenterol; 2012 Dec; 36(6):569-73. PubMed ID: 23142591
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
