Detalhe da pesquisa
1.
Ferric Carboxymaltose Versus Ferrous Fumarate in Anemic Children with Inflammatory Bowel Disease: The POPEYE Randomized Controlled Clinical Trial.
J Pediatr
; 256: 113-119.e4, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36563900
2.
Fatigue and Physical Activity Patterns in Children With Inflammatory Bowel Disease.
J Pediatr Gastroenterol Nutr
; 77(5): 628-633, 2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37494540
3.
First-line treatment with infliximab versus conventional treatment in children with newly diagnosed moderate-to-severe Crohn's disease: an open-label multicentre randomised controlled trial.
Gut
; 71(1): 34-42, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33384335
4.
Safety of Thioguanine in Pediatric Inflammatory Bowel Disease: A Multi-Center Case Series.
J Pediatr Gastroenterol Nutr
; 75(6): e111-e115, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36136124
5.
Paraneoplastic pemphigus associated with post-transplant lymphoproliferative disorder after small bowel transplantation.
Pediatr Transplant
; 25(6): e14023, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34014017
6.
Loss of syntaxin 3 causes variant microvillus inclusion disease.
Gastroenterology
; 147(1): 65-68.e10, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24726755
7.
Randomised clinical trial: First-line infliximab biosimilar is cost-effective compared to conventional treatment in paediatric Crohn's disease.
Aliment Pharmacol Ther
; 59(12): 1510-1520, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38644588
8.
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.
Nat Genet
; 36(4): 400-4, 2004 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15052268
9.
ATP8B1 is essential for maintaining normal hearing.
Proc Natl Acad Sci U S A
; 106(24): 9709-14, 2009 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-19478059
10.
Neither inflammatory bowel disease nor immunosuppressants are associated with an increased risk of severe COVID-19: an observational Dutch cohort study.
Clin Exp Med
; 22(3): 465-476, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34542781
11.
Folding defects in P-type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4-phenylbutyrate.
Hepatology
; 51(1): 286-96, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19918981
12.
Liver disease associated with canalicular transport defects: current and future therapies.
J Hepatol
; 52(2): 258-71, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20034695
13.
Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin.
Hepatology
; 50(6): 1783-95, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19937698
14.
Mutational analysis of ATP8B1 in patients with chronic pancreatitis.
PLoS One
; 8(11): e80553, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24260417
15.
Farnesoid X receptor (FXR) activation and FXR genetic variation in inflammatory bowel disease.
PLoS One
; 6(8): e23745, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21887309
16.
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
17.
Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis.
Hepatology
; 43(1): 51-3, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16374853
18.
The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis.
J Hepatol
; 41(5): 758-63, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15519648