110 related articles for article (PubMed ID: 22766396)
21. [The MDR3 gene mutation: a rare cause of progressive familial intrahepatic cholestasis (PFIC)].
Maisonnette F; Abita T; Barriere E; Pichon N; Vincensini JF; Descottes B
Ann Chir; 2005 Oct; 130(9):581-3. PubMed ID: 16199000
[TBL] [Abstract][Full Text] [Related]
22. Elevation of gamma-glutamyl transferase in adult: Should we think about progressive familiar intrahepatic cholestasis?
Oliveira HM; Pereira C; Santos Silva E; Pinto-Basto J; Pessegueiro Miranda H
Dig Liver Dis; 2016 Feb; 48(2):203-5. PubMed ID: 26699824
[TBL] [Abstract][Full Text] [Related]
23. Effects of bezafibrate on dyslipidemia with cholestasis in children with familial intrahepatic cholestasis-1 deficiency manifesting progressive familial intrahepatic cholestasis.
Nagasaka H; Yorifuji T; Hirano K; Ota A; Toyama-Nakagawa Y; Takatani T; Tsukahara H; Kobayashi K; Takayanagi M; Inomata Y; Uemoto S; Miida T
Metabolism; 2009 Jan; 58(1):48-54. PubMed ID: 19059530
[TBL] [Abstract][Full Text] [Related]
24. Ductopenia and cirrhosis in a 32-year-old woman with progressive familial intrahepatic cholestasis type 3: A case report and review of the literature.
Tan YW; Ji HL; Lu ZH; Ge GH; Sun L; Zhou XB; Sheng JH; Gong YH
World J Gastroenterol; 2018 Nov; 24(41):4716-4720. PubMed ID: 30416319
[TBL] [Abstract][Full Text] [Related]
25. Paucity of Interlobular Bile Ducts in Multidrug-Resistant P-Glycoprotein 3 (MDR3) Deficiency.
Vij M; Valamparampil J; Shanmugum N; Reddy SM; Rajindrajith S; Rela M
Int J Surg Pathol; 2019 May; 27(3):343-347. PubMed ID: 30222019
[TBL] [Abstract][Full Text] [Related]
26. Two novel mutations in African and Asian children with progressive familial intrahepatic cholestasis type 3.
Giovannoni I; Santorelli FM; Candusso M; Di Rocco M; Bellacchio E; Callea F; Francalanci P
Dig Liver Dis; 2011 Jul; 43(7):567-70. PubMed ID: 21514256
[TBL] [Abstract][Full Text] [Related]
27. Novel ABCB4 mutation in a Chinese female patient with progressive familial intrahepatic cholestasis type 3: a case report.
Wu Z; Zhang S; Zhang L; Li M
Diagn Pathol; 2020 Apr; 15(1):39. PubMed ID: 32321542
[TBL] [Abstract][Full Text] [Related]
28. Hepatobiliary phospholipid transporter ABCB4, MDR3 gene variants in a large cohort of Italian women with intrahepatic cholestasis of pregnancy.
Floreani A; Carderi I; Paternoster D; Soardo G; Azzaroli F; Esposito W; Montagnani M; Marchesoni D; Variola A; Rosa Rizzotto E; Braghin C; Mazzella G
Dig Liver Dis; 2008 May; 40(5):366-70. PubMed ID: 18083082
[TBL] [Abstract][Full Text] [Related]
29. Phosphorylation of ABCB4 impacts its function: insights from disease-causing mutations.
Gautherot J; Delautier D; Maubert MA; Aït-Slimane T; Bolbach G; Delaunay JL; Durand-Schneider AM; Firrincieli D; Barbu V; Chignard N; Housset C; Maurice M; Falguières T
Hepatology; 2014 Aug; 60(2):610-21. PubMed ID: 24723470
[TBL] [Abstract][Full Text] [Related]
30. Progressive familial intrahepatic cholestasis and inborn errors of bile acid synthesis.
Jankowska I; Socha P
Clin Res Hepatol Gastroenterol; 2012 Jun; 36(3):271-4. PubMed ID: 22609295
[TBL] [Abstract][Full Text] [Related]
31. Heterozygous ABCB4 mutations in children with cholestatic liver disease.
Gordo-Gilart R; Hierro L; Andueza S; Muñoz-Bartolo G; López C; Díaz C; Jara P; Álvarez L
Liver Int; 2016 Feb; 36(2):258-67. PubMed ID: 26153658
[TBL] [Abstract][Full Text] [Related]
32. Role of multidrug resistance 3 deficiency in pediatric and adult liver disease: one gene for three diseases.
Jacquemin E
Semin Liver Dis; 2001 Nov; 21(4):551-62. PubMed ID: 11745043
[TBL] [Abstract][Full Text] [Related]
33. [Progressive familial intrahepatic cholestasis and hereditary anomalies lf hepatocellular metabolism of bile acids].
Jacquemin E
Arch Pediatr; 1998 Jan; 5(1):45-53. PubMed ID: 10223112
[TBL] [Abstract][Full Text] [Related]
34. [Clinical and genetic analysis of a family affected by progressive familial intraphepatic cholestasis type 3].
Deng M; Guo L; Song Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct; 35(5):686-690. PubMed ID: 30298496
[TBL] [Abstract][Full Text] [Related]
35. The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood.
Jacquemin E; De Vree JM; Cresteil D; Sokal EM; Sturm E; Dumont M; Scheffer GL; Paul M; Burdelski M; Bosma PJ; Bernard O; Hadchouel M; Elferink RP
Gastroenterology; 2001 May; 120(6):1448-58. PubMed ID: 11313315
[TBL] [Abstract][Full Text] [Related]
36. Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis.
Deleuze JF; Jacquemin E; Dubuisson C; Cresteil D; Dumont M; Erlinger S; Bernard O; Hadchouel M
Hepatology; 1996 Apr; 23(4):904-8. PubMed ID: 8666348
[TBL] [Abstract][Full Text] [Related]
37. Case report: progressive familial intrahepatic cholestasis type 3 with compound heterozygous ABCB4 variants diagnosed 15 years after liver transplantation.
Goubran M; Aderibigbe A; Jacquemin E; Guettier C; Girgis S; Bain V; Mason AL
BMC Med Genet; 2020 Nov; 21(1):238. PubMed ID: 33256620
[TBL] [Abstract][Full Text] [Related]
38. Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model Organisms.
Pham DH; Kudira R; Xu L; Valencia CA; Ellis JL; Shi T; Evason KJ; Osuji I; Matuschek N; Pfuhler L; Mullen M; Mohanty SK; Husami A; Bull LN; Zhang K; Wali S; Yin C; Miethke A
Gastroenterology; 2021 Jul; 161(1):287-300.e16. PubMed ID: 33771553
[TBL] [Abstract][Full Text] [Related]
39. Functional characterization of ABCB4 mutations found in progressive familial intrahepatic cholestasis type 3.
Park HJ; Kim TH; Kim SW; Noh SH; Cho KJ; Choi C; Kwon EY; Choi YJ; Gee HY; Choi JH
Sci Rep; 2016 Jun; 6():26872. PubMed ID: 27256251
[TBL] [Abstract][Full Text] [Related]
40. Functional variants of the central bile acid sensor FXR identified in intrahepatic cholestasis of pregnancy.
Van Mil SW; Milona A; Dixon PH; Mullenbach R; Geenes VL; Chambers J; Shevchuk V; Moore GE; Lammert F; Glantz AG; Mattsson LA; Whittaker J; Parker MG; White R; Williamson C
Gastroenterology; 2007 Aug; 133(2):507-16. PubMed ID: 17681172
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
