Detalhe da pesquisa
1.
Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency.
Hepatology
; 74(2): 892-906, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33666275
2.
Effects of new and emerging therapies on gastrointestinal outcomes in cystic fibrosis.
Curr Opin Pulm Med
; 23(6): 551-555, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28787381
3.
Rescue of defective ATP8B1 trafficking by CFTR correctors as a therapeutic strategy for familial intrahepatic cholestasis.
J Hepatol
; 64(6): 1339-47, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26879107
4.
Analysis of aberrant pre-messenger RNA splicing resulting from mutations in ATP8B1 and efficient in vitro rescue by adapted U1 small nuclear RNA.
Hepatology
; 61(4): 1382-91, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25421123
5.
Interim results from an ongoing, open-label, single-arm trial of odevixibat in progressive familial intrahepatic cholestasis.
JHEP Rep
; 5(8): 100782, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37456676
6.
Current and future therapies for inherited cholestatic liver diseases.
World J Gastroenterol
; 23(5): 763-775, 2017 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28223721
7.
Total biliary diversion as a treatment option for patients with progressive familial intrahepatic cholestasis and Alagille syndrome.
J Pediatr Surg
; 50(11): 1846-9, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26319776
8.
Mutational analysis of ATP8B1 in patients with chronic pancreatitis.
PLoS One
; 8(11): e80553, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24260417
9.
Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.
Best Pract Res Clin Gastroenterol
; 24(5): 541-53, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20955958
10.
Neo-aortic valvar function after the arterial switch.
Cardiol Young
; 16(5): 481-9, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16984700
11.
Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11.
Gastroenterology
; 127(2): 379-84, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15300568