321 related articles for article (PubMed ID: 28923092)
1. Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report.
Kularatnam GAM; Warawitage D; Vidanapathirana DM; Jayasena S; Jasinge E; de Silva N; Liyanarachchi KLAMS; Wickramasinghe P; Devgun MS; Barbu V; Lascols O
BMC Res Notes; 2017 Sep; 10(1):487. PubMed ID: 28923092
[TBL] [Abstract][Full Text] [Related]
2. Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan.
Togawa T; Mizuochi T; Sugiura T; Kusano H; Tanikawa K; Sasaki T; Ichinose F; Kagimoto S; Tainaka T; Uchida H; Saitoh S
J Pediatr; 2018 May; 196():161-167.e1. PubMed ID: 29499989
[TBL] [Abstract][Full Text] [Related]
3. Dual hereditary jaundice: simultaneous occurrence of mutations causing Gilbert's and Dubin-Johnson syndrome.
Cebecauerova D; Jirasek T; Budisova L; Mandys V; Volf V; Novotna Z; Subhanova I; Hrebicek M; Elleder M; Jirsa M
Gastroenterology; 2005 Jul; 129(1):315-20. PubMed ID: 16012956
[TBL] [Abstract][Full Text] [Related]
4. Dubin-Johnson syndrome.
Nisa AU; Ahmad Z
J Coll Physicians Surg Pak; 2008 Mar; 18(3):188-9. PubMed ID: 18460254
[TBL] [Abstract][Full Text] [Related]
5. Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders.
Corpechot C; Barbu V; Chazouillères O; Broué P; Girard M; Roquelaure B; Chrétien Y; Dong C; Lascols O; Housset C; Jéru I
Liver Int; 2020 Jan; 40(1):163-174. PubMed ID: 31544333
[TBL] [Abstract][Full Text] [Related]
6. Genotype-Phenotype Association in
Kim JH; Kang MW; Kim S; Han JW; Jang JW; Choi JY; Yoon SK; Sung PS
Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555809
[TBL] [Abstract][Full Text] [Related]
7. Novel compound heterozygous ABCC2 variants in patients with Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy.
Huynh MT; Chrétien Y; Grison S; Delaunay JL; Lascols O; Tran CT; Goria O; Ramond MJ; Barbu V
Clin Genet; 2018 Nov; 94(5):480-481. PubMed ID: 30092126
[No Abstract] [Full Text] [Related]
8. A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile Ducts.
Chan KL; Varughese N; Jones PM; Zwick DL; Rajaram V; Lee M; Ramirez CM
Pediatr Dev Pathol; 2021; 24(2):154-158. PubMed ID: 33470920
[TBL] [Abstract][Full Text] [Related]
9. [Liver disease associated with hereditary defects of hepatobiliary transporters].
Wendum D
Ann Pathol; 2010 Dec; 30(6):426-31. PubMed ID: 21167428
[TBL] [Abstract][Full Text] [Related]
10. Exon-intron organization of the human multidrug-resistance protein 2 (MRP2) gene mutated in Dubin-Johnson syndrome.
Tsujii H; König J; Rost D; Stöckel B; Leuschner U; Keppler D
Gastroenterology; 1999 Sep; 117(3):653-60. PubMed ID: 10464142
[TBL] [Abstract][Full Text] [Related]
11. Neonatal Dubin-Johnson syndrome: novel compound heterozygous mutation in the ABCC2 gene.
Okada H; Kusaka T; Fuke N; Kunikata J; Kondo S; Iwase T; Nan W; Hirota T; Ieiri I; Itoh S
Pediatr Int; 2014 Oct; 56(5):e62-4. PubMed ID: 25336012
[TBL] [Abstract][Full Text] [Related]
12. A new mutation of the ATP-binding cassette, sub-family C, member 2 (ABCC2) gene in a Japanese patient with Dubin-Johnson syndrome.
Tate G; Li M; Suzuki T; Mitsuya T
Genes Genet Syst; 2002 Apr; 77(2):117-21. PubMed ID: 12087194
[TBL] [Abstract][Full Text] [Related]
13. Severe jaundice due to coexistence of Dubin-Johnson syndrome and hereditary spherocytosis: a case report.
Korkmaz U; Duman AE; Oğütmen Koç D; Gürbüz Y; Dındar G; Ensaroğlu F; Sener SY; Sentürk O; Hülagü S
Turk J Gastroenterol; 2011 Aug; 22(4):422-5. PubMed ID: 21948575
[TBL] [Abstract][Full Text] [Related]
14. Novel mutations in the Dubin-Johnson syndrome gene ABCC2/MRP2 and associated biochemical changes.
Devgun MS; El-Nujumi AM; O'Dowd GJ; Barbu V; Poupon R
Ann Clin Biochem; 2012 Nov; 49(Pt 6):609-12. PubMed ID: 23065530
[TBL] [Abstract][Full Text] [Related]
15. Dubin-Johnson syndrome coinciding with colon cancer and atherosclerosis.
Sticova E; Elleder M; Hulkova H; Luksan O; Sauer M; Wunschova-Moudra I; Novotny J; Jirsa M
World J Gastroenterol; 2013 Feb; 19(6):946-50. PubMed ID: 23429660
[TBL] [Abstract][Full Text] [Related]
16. Genetic cholestasis: lessons from the molecular physiology of bile formation.
Jansen PL; Müller M
Can J Gastroenterol; 2000 Mar; 14(3):233-8. PubMed ID: 10758420
[TBL] [Abstract][Full Text] [Related]
17. Infantile hepatic cholestasis with maternal Dubin-Johnson syndrome.
Cotton DB
South Med J; 1984 Sep; 77(9):1213-4. PubMed ID: 6484704
[TBL] [Abstract][Full Text] [Related]
18. Neonatal Dubin-Johnson syndrome: biochemical parameters, characteristics, and genetic variants study.
Fu H; Zhao R; Jia X; Li X; Li G; Yin C
Pediatr Res; 2022 May; 91(6):1571-1578. PubMed ID: 34050268
[TBL] [Abstract][Full Text] [Related]
19. Neonatal Dubin-Johnson syndrome with severe cholestasis: effective phenobarbital therapy.
Kimura A; Ushijima K; Kage M; Mahara R; Tohma M; Inokuchi T; Shibao K; Tanaka N; Fujisawa T; Ono E
Acta Paediatr Scand; 1991 Mar; 80(3):381-5. PubMed ID: 2035335
[TBL] [Abstract][Full Text] [Related]
20. In silico screening and analysis of single-nucleotide polymorphic variants of the ABCC2 gene affecting Dubin-Johnson syndrome.
Sharma P; Sharma S
Arab J Gastroenterol; 2022 Aug; 23(3):172-187. PubMed ID: 35477852
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]