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2. 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 [Abstract] [Full Text] [Related]
3. 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 18; 10(1):487. PubMed ID: 28923092 [Abstract] [Full Text] [Related]
4. 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 18; 22(4):422-5. PubMed ID: 21948575 [Abstract] [Full Text] [Related]
5. [Familial benign conjugated hyperbilirubinemia with pigment deposition in the liver (Dubin-Johnson syndrome). Report of 4 cases in siblings]. Sosovec V, Pesek J. Z Gesamte Inn Med; 1971 Sep 15; 26(18):596-9. PubMed ID: 5127652 [No Abstract] [Full Text] [Related]
6. A case of the Dubin-Johnson syndrome complicated by acute hepatitis. Varma RR, Grainger JM, Scheuer PJ. Gut; 1970 Oct 15; 11(10):817-21. PubMed ID: 5485831 [Abstract] [Full Text] [Related]
7. Quiz HQ 45. A rare case of conjugated hyperbilirubinemia. Dubin-Johnson syndrome. Petria A, Simionov I, Becheanu G, Gheorghe L. J Gastrointestin Liver Dis; 2008 Jun 15; 17(2):199, 216. PubMed ID: 18697280 [No Abstract] [Full Text] [Related]
8. 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 15; 196():161-167.e1. PubMed ID: 29499989 [Abstract] [Full Text] [Related]
9. 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 May 15; 24(2):154-158. PubMed ID: 33470920 [Abstract] [Full Text] [Related]
12. Conjugated hyperbilirubinemia after surgery. A diagnosis of Dubin-Johnson syndrome confirmed by genetic testing. Baranguán Castro ML, García Romero R, Miramar Gallart MD. Rev Esp Enferm Dig; 2017 Nov 15; 109(11):801-802. PubMed ID: 29032691 [Abstract] [Full Text] [Related]
13. 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 15; 117(3):653-60. PubMed ID: 10464142 [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 15; 49(Pt 6):609-12. PubMed ID: 23065530 [Abstract] [Full Text] [Related]
19. Impaired protein maturation of the conjugate export pump multidrug resistance protein 2 as a consequence of a deletion mutation in Dubin-Johnson syndrome. Keitel V, Kartenbeck J, Nies AT, Spring H, Brom M, Keppler D. Hepatology; 2000 Dec 15; 32(6):1317-28. PubMed ID: 11093739 [Abstract] [Full Text] [Related]
20. A common Dubin-Johnson syndrome mutation impairs protein maturation and transport activity of MRP2 (ABCC2). Keitel V, Nies AT, Brom M, Hummel-Eisenbeiss J, Spring H, Keppler D. Am J Physiol Gastrointest Liver Physiol; 2003 Jan 15; 284(1):G165-74. PubMed ID: 12388192 [Abstract] [Full Text] [Related] Page: [Next] [New Search]