72 related articles for article (PubMed ID: 22343912)
21. Genotype correlates with clinical course and outcome of children with tight junction protein 2 (TJP2) deficiency-related cholestasis.
Lal BB; Alam S; Sibal A; Kumar K; Hosaagrahara Ramakrishna S; Shah V; Dheivamani N; Bavdekar A; Nagral A; Wadhwa N; Maria A; Shah A; Shah I; Nalwalla Z; Snehavardhan P; Srikanth KP; Gupta S; Sivaramakrishnan VM; Waikar Y; Suchismita A; Ashritha A; Sood V; Khanna R;
Hepatology; 2024 Mar; ():. PubMed ID: 38447037
[TBL] [Abstract][Full Text] [Related]
22. Clinical characteristics and genetic profiles of young and adult patients with cholestatic liver disease.
Huynh MT; Nguyen TT; Grison S; Lascols O; Fernandez E; Barbu V
Rev Esp Enferm Dig; 2019 Oct; 111(10):775-788. PubMed ID: 31538484
[TBL] [Abstract][Full Text] [Related]
23. A novel heterozygous deletion in ABCB4 gene in a Chinese family with intrahepatic cholestasis of pregnancy, neonatal hyperbilirubinemia, and cholelithiasis: Case reports and literature review.
Zheng Y; Rao Q; Han Y; He J
Mol Genet Genomic Med; 2024 Jan; 12(1):e2291. PubMed ID: 37787087
[TBL] [Abstract][Full Text] [Related]
24. Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy.
Gonzales E; Gardin A; Almes M; Darmellah-Remil A; Seguin H; Mussini C; Franchi-Abella S; Duché M; Ackermann O; Thébaut A; Habes D; Hermeziu B; Lapalus M; Falguières T; Combal JP; Benichou B; Valero S; Davit-Spraul A; Jacquemin E
JHEP Rep; 2023 Oct; 5(10):100844. PubMed ID: 37701337
[TBL] [Abstract][Full Text] [Related]
25. Clinical characteristics and prognosis of primary hepatolithiasis in hospitalized children.
Yan J; Zhang Z; Guo J; Lv C; Chen Y
Eur J Pediatr; 2023 Jul; 182(7):3195-3202. PubMed ID: 37129614
[TBL] [Abstract][Full Text] [Related]
26. Clinical and genetic characterization of pediatric patients with progressive familial intrahepatic cholestasis type 3 (PFIC3): identification of 14 novel ABCB4 variants and review of the literatures.
Chen R; Yang FX; Tan YF; Deng M; Li H; Xu Y; Ouyang WX; Song YZ
Orphanet J Rare Dis; 2022 Dec; 17(1):445. PubMed ID: 36550572
[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. Phenotypic spectrum and diagnostic pitfalls of ABCB4 deficiency depending on age of onset.
Schatz SB; Jüngst C; Keitel-Anselmo V; Kubitz R; Becker C; Gerner P; Pfister ED; Goldschmidt I; Junge N; Wenning D; Gehring S; Arens S; Bretschneider D; Grothues D; Engelmann G; Lammert F; Baumann U
Hepatol Commun; 2018 May; 2(5):504-514. PubMed ID: 29761167
[TBL] [Abstract][Full Text] [Related]
29. A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions.
Wang NL; Lu YL; Zhang P; Zhang MH; Gong JY; Lu Y; Xie XB; Qiu YL; Yan YY; Wu BB; Wang JS
PLoS One; 2016; 11(10):e0164058. PubMed ID: 27706244
[TBL] [Abstract][Full Text] [Related]
30. The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency.
Wang NL; Li LT; Wu BB; Gong JY; Abuduxikuer K; Li G; Wang JS
PLoS One; 2016; 11(4):e0153114. PubMed ID: 27050426
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. ABCB4 disease: Many faces of one gene deficiency.
Sticova E; Jirsa M
Ann Hepatol; 2020; 19(2):126-133. PubMed ID: 31759867
[TBL] [Abstract][Full Text] [Related]
33. Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutations.
Fang LJ; Wang XH; Knisely AS; Yu H; Lu Y; Liu LY; Wang JS
J Pediatr Gastroenterol Nutr; 2012 Aug; 55(2):150-6. PubMed ID: 22343912
[TBL] [Abstract][Full Text] [Related]
34. A new splicing site mutation of the ABCB4 gene in intrahepatic cholestasis of pregnancy with raised serum gamma-GT.
Tavian D; Degiorgio D; Roncaglia N; Vergani P; Cameroni I; Colombo R; Coviello DA
Dig Liver Dis; 2009 Sep; 41(9):671-5. PubMed ID: 19261551
[TBL] [Abstract][Full Text] [Related]
35. A female of progressive familial intrahepatic cholestasis type 3 caused by heterozygous mutations of ABCB4 gene and her cirrhosis improved after treatment of ursodeoxycholic acid: a case report.
Qiao F; Ren F; Lu W; Yang H; Mo G; Wang S; Liu L; Xu X
BMC Med Genomics; 2023 Jul; 16(1):171. PubMed ID: 37488596
[TBL] [Abstract][Full Text] [Related]
36. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort.
Mínguez Rodríguez B; Molera Busoms C; Martorell Sampol L; García Romero R; Colomé Rivero G; Martín de Carpi J
Gastroenterol Hepatol; 2022 Oct; 45(8):585-592. PubMed ID: 34942279
[TBL] [Abstract][Full Text] [Related]
37.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
38.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
39.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
