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Items: 1 to 20 of 555

1.

Progressive Familial Intrahepatic Cholestasis.

Bull LN, Thompson RJ.

Clin Liver Dis. 2018 Nov;22(4):657-669. doi: 10.1016/j.cld.2018.06.003. Epub 2018 Aug 3. Review.

2.

Identification of novel loci for pediatric cholestatic liver disease defined by KIF12, PPM1F, USP53, LSR, and WDR83OS pathogenic variants.

Maddirevula S, Alhebbi H, Alqahtani A, Algoufi T, Alsaif HS, Ibrahim N, Abdulwahab F, Barr M, Alzaidan H, Almehaideb A, AlSasi O, Alhashem A, Hussaini HA, Wali S, Alkuraya FS.

Genet Med. 2018 Sep 25. doi: 10.1038/s41436-018-0288-x. [Epub ahead of print]

PMID:
30250217
3.

Systematic review of progressive familial intrahepatic cholestasis.

Baker A, Kerkar N, Todorova L, Kamath BM, Houwen RHJ.

Clin Res Hepatol Gastroenterol. 2018 Sep 17. pii: S2210-7401(18)30149-9. doi: 10.1016/j.clinre.2018.07.010. [Epub ahead of print]

PMID:
30236549
4.

[Clinical and genetic analysis of an infant with progressive familial intrahepatic cholestasis type II].

Lin GZ, Qiu JW, Cheng Y, Lin WX, Song YZ.

Zhongguo Dang Dai Er Ke Za Zhi. 2018 Sep;20(9):758-764. Chinese.

5.

New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical Implications.

Sticova E, Jirsa M, Pawłowska J.

Can J Gastroenterol Hepatol. 2018 Jul 26;2018:2313675. doi: 10.1155/2018/2313675. eCollection 2018. Review.

6.

The role of ABC transporters' gene polymorphism in the etiology of intrahepatic cholestasis of pregnancy.

Piątek K, Kurzawińska G, Magiełda J, Drews K, Barlik M, Malewski Z, Ożarowski M, Maciejewska M, Seremak-Mrozikiewicz A.

Ginekol Pol. 2018;89(7):393-397. doi: 10.5603/GP.a2018.0067.

7.

The ileum-liver Farnesoid X Receptor signaling axis mediates the compensatory mechanism of 17α-ethynylestradiol-induced cholestasis via increasing hepatic biosynthesis of chenodeoxycholic acids in rats.

Zhang F, Xi L, Duan Y, Qin H, Wei M, Wu Y, Li B, Zhou Y, Wu X.

Eur J Pharm Sci. 2018 Oct 15;123:404-415. doi: 10.1016/j.ejps.2018.08.005. Epub 2018 Aug 2.

PMID:
30077711
8.

Phenotypic variability in Tunisian PFIC3 patients harboring a complex genotype with a differential clinical outcome of UDCA treatment.

Khabou B, Mahjoub B, Barbu V, Balhoudi N, Wardani A, Sfar MT, Fakhfakh F.

Clin Chim Acta. 2018 Nov;486:122-128. doi: 10.1016/j.cca.2018.07.035. Epub 2018 Jul 20.

PMID:
30036524
9.

A Complex Case of Cholestasis in a Patient with ABCB4 and ABCB11 Mutations.

Cardoso MF, E Branco JC, Anapaz V, Rodrigues CG, Carvalho R, Horta D, Martins A, Reis J.

GE Port J Gastroenterol. 2018 Jun;25(4):189-194. doi: 10.1159/000484612. Epub 2017 Nov 25.

10.

Biliary transporter gene mutations in severe intrahepatic cholestasis of pregnancy: Diagnostic and management implications.

Yeap SP, Harley H, Thompson R, Williamson KD, Bate J, Sethna F, Farrell G, Hague WB.

J Gastroenterol Hepatol. 2018 Jul 10. doi: 10.1111/jgh.14376. [Epub ahead of print]

PMID:
29992621
11.

Spectrum of genomic variations in Indian patients with progressive familial intrahepatic cholestasis.

Sharma A, Poddar U, Agnihotry S, Phadke SR, Yachha SK, Aggarwal R.

BMC Gastroenterol. 2018 Jul 4;18(1):107. doi: 10.1186/s12876-018-0835-6.

12.

Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital Hypopituitarism.

Grammatikopoulos T, Deheragoda M, Strautnieks S, Neves Souza L, Hinds R, Thompson RJ, Hadzic N.

J Pediatr. 2018 Sep;200:181-187. doi: 10.1016/j.jpeds.2018.05.009. Epub 2018 Jun 20.

PMID:
29935878
13.

Allogeneic haematopoietic stem cell transplantation eliminates alloreactive inhibitory antibodies after liver transplantation for bile salt export pump deficiency.

Brinkert F, Pukite I, Krebs-Schmitt D, Briem-Richter A, Stindt J, Häussinger D, Keitel V, Müller I, Grabhorn E.

J Hepatol. 2018 Oct;69(4):961-965. doi: 10.1016/j.jhep.2018.06.003. Epub 2018 Jun 21.

PMID:
29935200
14.

Long-term outcomes after cholecystocolostomy for progressive familial intrahepatic cholestasis.

Chen L, Xiao H, Ren XH, Li L.

Hepatol Res. 2018 Jun 22. doi: 10.1111/hepr.13222. [Epub ahead of print]

PMID:
29934967
15.

[Relationship between phenotype and genotype of ABCB11 deficiency in siblings and literature review].

Peng XR, Lu Y, Zhang MH, Li LT, Xie XB, Gong JY, Wang JS.

Zhonghua Er Ke Za Zhi. 2018 Jun 2;56(6):440-444. doi: 10.3760/cma.j.issn.0578-1310.2018.06.007. Chinese.

PMID:
29886607
16.

Omics-based responses induced by bosentan in human hepatoma HepaRG cell cultures.

Rodrigues RM, Kollipara L, Chaudhari U, Sachinidis A, Zahedi RP, Sickmann A, Kopp-Schneider A, Jiang X, Keun H, Hengstler J, Oorts M, Annaert P, Hoeben E, Gijbels E, De Kock J, Vanhaecke T, Rogiers V, Vinken M.

Arch Toxicol. 2018 May 14;92(6):1939-1952. doi: 10.1007/s00204-018-2214-z. [Epub ahead of print]

17.

Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies.

Bull LN, Pawlikowska L, Strautnieks S, Jankowska I, Czubkowski P, Dodge JL, Emerick K, Wanty C, Wali S, Blanchard S, Lacaille F, Byrne JA, van Eerde AM, Kolho KL, Houwen R, Lobritto S, Hupertz V, McClean P, Mieli-Vergani G, Sokal E, Rosenthal P, Whitington PF, Pawlowska J, Thompson RJ.

Hepatol Commun. 2018 Mar 30;2(5):515-528. doi: 10.1002/hep4.1168. eCollection 2018 May.

18.

Xenobiotic Nuclear Receptor Signaling Determines Molecular Pathogenesis of Progressive Familial Intrahepatic Cholestasis.

Kim KH, Choi JM, Li F, Arizpe A, Wooton-Kee CR, Anakk S, Jung SY, Finegold MJ, Moore DD.

Endocrinology. 2018 Jun 1;159(6):2435-2446. doi: 10.1210/en.2018-00110.

PMID:
29718219
19.

Drug-induced Cholestasis: Mechanisms, Models, and Markers.

Chatterjee S, Annaert P.

Curr Drug Metab. 2018;19(10):808-818. doi: 10.2174/1389200219666180427165035. Review.

PMID:
29708070
20.

Variants Associated with Infantile Cholestatic Syndromes Detected in Extrahepatic Biliary Atresia by Whole Exome Studies: A 20-Case Series from Thailand.

Sangkhathat S, Laochareonsuk W, Maneechay W, Kayasut K, Chiengkriwate P.

J Pediatr Genet. 2018 Jun;7(2):67-73. doi: 10.1055/s-0038-1632395. Epub 2018 Feb 16.

PMID:
29707407

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