246 related articles for article (PubMed ID: 29761168)
1. 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 May; 2(5):515-528. PubMed ID: 29761168
[TBL] [Abstract][Full Text] [Related]
2. Differences in presentation and progression between severe FIC1 and BSEP deficiencies.
Pawlikowska L; Strautnieks S; Jankowska I; Czubkowski P; Emerick K; Antoniou A; Wanty C; Fischler B; Jacquemin E; Wali S; Blanchard S; Nielsen IM; Bourke B; McQuaid S; Lacaille F; Byrne JA; van Eerde AM; Kolho KL; Klomp L; Houwen R; Bacchetti P; Lobritto S; Hupertz V; McClean P; Mieli-Vergani G; Shneider B; Nemeth A; Sokal E; Freimer NB; Knisely AS; Rosenthal P; Whitington PF; Pawlowska J; Thompson RJ; Bull LN
J Hepatol; 2010 Jul; 53(1):170-8. PubMed ID: 20447715
[TBL] [Abstract][Full Text] [Related]
3. Clinical outcomes of surgical management for rare types of progressive familial intrahepatic cholestasis: a case series.
Masahata K; Ueno T; Bessho K; Kodama T; Tsukada R; Saka R; Tazuke Y; Miyagawa S; Okuyama H
Surg Case Rep; 2022 Jan; 8(1):10. PubMed ID: 35024979
[TBL] [Abstract][Full Text] [Related]
4. Sequencing of FIC1, BSEP and MDR3 in a large cohort of patients with cholestasis revealed a high number of different genetic variants.
Dröge C; Bonus M; Baumann U; Klindt C; Lainka E; Kathemann S; Brinkert F; Grabhorn E; Pfister ED; Wenning D; Fichtner A; Gotthardt DN; Weiss KH; McKiernan P; Puri RD; Verma IC; Kluge S; Gohlke H; Schmitt L; Kubitz R; Häussinger D; Keitel V
J Hepatol; 2017 Dec; 67(6):1253-1264. PubMed ID: 28733223
[TBL] [Abstract][Full Text] [Related]
5. Analysis of surgical interruption of the enterohepatic circulation as a treatment for pediatric cholestasis.
Wang KS; Tiao G; Bass LM; Hertel PM; Mogul D; Kerkar N; Clifton M; Azen C; Bull L; Rosenthal P; Stewart D; Superina R; Arnon R; Bozic M; Brandt ML; Dillon PA; Fecteau A; Iyer K; Kamath B; Karpen S; Karrer F; Loomes KM; Mack C; Mattei P; Miethke A; Soltys K; Turmelle YP; West K; Zagory J; Goodhue C; Shneider BL;
Hepatology; 2017 May; 65(5):1645-1654. PubMed ID: 28027587
[TBL] [Abstract][Full Text] [Related]
6. Progressive familial intrahepatic cholestasis.
Srivastava A
J Clin Exp Hepatol; 2014 Mar; 4(1):25-36. PubMed ID: 25755532
[TBL] [Abstract][Full Text] [Related]
7. Progressive Familial Intrahepatic Cholestasis: A Study in Children From a Liver Transplant Center in India.
Mehta S; Kumar K; Bhardwaj R; Malhotra S; Goyal N; Sibal A
J Clin Exp Hepatol; 2022; 12(2):454-460. PubMed ID: 35535061
[TBL] [Abstract][Full Text] [Related]
8. Mutation Analysis and Disease Features at Presentation in a Multi-Center Cohort of Children With Monogenic Cholestasis.
Hertel PM; Bull LN; Thompson RJ; Goodrich NP; Ye W; Magee JC; Squires RH; Bass LM; Heubi JE; Kim GE; Ranganathan S; Schwarz KB; Bozic MA; Horslen SP; Clifton MS; Turmelle YP; Suchy FJ; Superina RA; Wang KS; Loomes KM; Kamath BM; Sokol RJ; Shneider BL;
J Pediatr Gastroenterol Nutr; 2021 Aug; 73(2):169-177. PubMed ID: 34016879
[TBL] [Abstract][Full Text] [Related]
9. ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): phenotypic differences between PFIC1 and PFIC2 and natural history.
Davit-Spraul A; Fabre M; Branchereau S; Baussan C; Gonzales E; Stieger B; Bernard O; Jacquemin E
Hepatology; 2010 May; 51(5):1645-55. PubMed ID: 20232290
[TBL] [Abstract][Full Text] [Related]
10. Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency.
Felzen A; van Wessel DBE; Gonzales E; Thompson RJ; Jankowska I; Shneider BL; Sokal E; Grammatikopoulos T; Kadaristiana A; Jacquemin E; Spraul A; Lipiński P; Czubkowski P; Rock N; Shagrani M; Broering D; Nicastro E; Kelly D; Nebbia G; Arnell H; Fischler B; Hulscher JBF; Serranti D; Arikan C; Polat E; Debray D; Lacaille F; Goncalves C; Hierro L; Muñoz Bartolo G; Mozer-Glassberg Y; Azaz A; Brecelj J; Dezsőfi A; Calvo PL; Grabhorn E; Hartleif S; van der Woerd WJ; Kamath BM; Wang JS; Li L; Durmaz Ö; Kerkar N; Jørgensen MH; Fischer R; Jimenez-Rivera C; Alam S; Cananzi M; Laverdure N; Ferreira CT; Guerrero FO; Wang H; Sency V; Kim KM; Chen HL; de Carvalho E; Fabre A; Bernabeu JQ; Zellos A; Alonso EM; Sokol RJ; Suchy FJ; Loomes KM; McKiernan PJ; Rosenthal P; Turmelle Y; Horslen S; Schwarz K; Bezerra JA; Wang K; Hansen BE; Verkade HJ;
JHEP Rep; 2023 Feb; 5(2):100626. PubMed ID: 36687469
[TBL] [Abstract][Full Text] [Related]
11. Maralixibat for the treatment of PFIC: Long-term, IBAT inhibition in an open-label, Phase 2 study.
Loomes KM; Squires RH; Kelly D; Rajwal S; Soufi N; Lachaux A; Jankowska I; Mack C; Setchell KDR; Karthikeyan P; Kennedy C; Dorenbaum A; Desai NK; Garner W; Jaecklin T; Vig P; Miethke A; Thompson RJ
Hepatol Commun; 2022 Sep; 6(9):2379-2390. PubMed ID: 35507739
[TBL] [Abstract][Full Text] [Related]
12. Partial external biliary diversion in bile salt export pump deficiency: Association between outcome and mutation.
Ellinger P; Stindt J; Dröge C; Sattler K; Stross C; Kluge S; Herebian D; Smits SHJ; Burdelski M; Schulz-Jürgensen S; Ballauff A; Schulte Am Esch J; Mayatepek E; Häussinger D; Kubitz R; Schmitt L
World J Gastroenterol; 2017 Aug; 23(29):5295-5303. PubMed ID: 28839429
[TBL] [Abstract][Full Text] [Related]
13. MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease.
Girard M; Lacaille F; Verkarre V; Mategot R; Feldmann G; Grodet A; Sauvat F; Irtan S; Davit-Spraul A; Jacquemin E; Ruemmele F; Rainteau D; Goulet O; Colomb V; Chardot C; Henrion-Caude A; Debray D
Hepatology; 2014 Jul; 60(1):301-10. PubMed ID: 24375397
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Long-term outcomes after cholecystocolostomy for progressive familial intrahepatic cholestasis.
Chen L; Xiao H; Ren XH; Li L
Hepatol Res; 2018 Dec; 48(13):1163-1171. PubMed ID: 29934967
[TBL] [Abstract][Full Text] [Related]
16. Progressive familial intrahepatic cholestasis.
Davit-Spraul A; Gonzales E; Baussan C; Jacquemin E
Orphanet J Rare Dis; 2009 Jan; 4():1. PubMed ID: 19133130
[TBL] [Abstract][Full Text] [Related]
17. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis.
Jansen PL; Strautnieks SS; Jacquemin E; Hadchouel M; Sokal EM; Hooiveld GJ; Koning JH; De Jager-Krikken A; Kuipers F; Stellaard F; Bijleveld CM; Gouw A; Van Goor H; Thompson RJ; Müller M
Gastroenterology; 1999 Dec; 117(6):1370-9. PubMed ID: 10579978
[TBL] [Abstract][Full Text] [Related]
18. Progressive Familial Intrahepatic Cholestasis (PFIC) in Indian Children: Clinical Spectrum and Outcome.
Agarwal S; Lal BB; Rawat D; Rastogi A; Bharathy KG; Alam S
J Clin Exp Hepatol; 2016 Sep; 6(3):203-208. PubMed ID: 27746616
[TBL] [Abstract][Full Text] [Related]
19. A novel mutation within a transmembrane helix of the bile salt export pump (BSEP, ABCB11) with delayed development of cirrhosis.
Stindt J; Ellinger P; Weissenberger K; Dröge C; Herebian D; Mayatepek E; Homey B; Braun S; Schulte am Esch J; Horacek M; Canbay A; Schmitt L; Häussinger D; Kubitz R
Liver Int; 2013 Nov; 33(10):1527-35. PubMed ID: 23758865
[TBL] [Abstract][Full Text] [Related]
20. Reduced hepatic expression of farnesoid X receptor in hereditary cholestasis associated to mutation in ATP8B1.
Alvarez L; Jara P; Sánchez-Sabaté E; Hierro L; Larrauri J; Díaz MC; Camarena C; De la Vega A; Frauca E; López-Collazo E; Lapunzina P
Hum Mol Genet; 2004 Oct; 13(20):2451-60. PubMed ID: 15317749
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
