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Items: 1 to 20 of 111

1.

Dubin-Johnson syndrome.

Nisa AU, Ahmad Z.

J Coll Physicians Surg Pak. 2008 Mar;18(3):188-9. doi: 03.2008/JCPSP.188189.

PMID:
18460254
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.

PMID:
16012956
3.

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.

4.

A case of the Dubin-Johnson syndrome complicated by acute hepatitis.

Varma RR, Grainger JM, Scheuer PJ.

Gut. 1970 Oct;11(10):817-21.

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. German. No abstract available.

PMID:
5127652
6.

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 14;19(6):946-50. doi: 10.3748/wjg.v19.i6.946.

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;17(2):199, 216. No abstract available.

PMID:
18697280
8.

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.

PMID:
10464142
9.

Dubin-Johnson syndrome with multiple liver cavernous hemangiomas: report of a familial case.

Li P, Wang Y, Zhang J, Geng M, Li Z.

Int J Clin Exp Pathol. 2013 Oct 15;6(11):2636-9. eCollection 2013.

10.

Gene replacement therapy for genetic hepatocellular jaundice.

van Dijk R, Beuers U, Bosma PJ.

Clin Rev Allergy Immunol. 2015 Jun;48(2-3):243-53. doi: 10.1007/s12016-014-8454-7. Review.

PMID:
25315738
11.

Association of Dubin-Johnson syndrome and portal vein thrombosis.

Makharia GK, Garg PK, Gupta SD, Tandon RK.

Indian J Gastroenterol. 2002 May-Jun;21(3):118-9.

PMID:
12118928
12.

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. doi: 10.1258/acb.2012.011279. Epub 2012 Oct 12.

PMID:
23065530
13.
14.
15.

Dubin-Johnson-like black liver with normal bilirubin level.

Kobayashi Y, Ishihara T, Wada M, Kajihara S, Araki J, Mifuji R, Itani T, Kuroda M, Urawa F, Kaito M, Adachi Y.

J Gastroenterol. 2004 Sep;39(9):892-5.

PMID:
15565410
16.
17.

Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.

Slachtova L, Seda O, Behunova J, Mistrik M, Martasek P.

Eur J Hum Genet. 2016 May;24(5):704-9. doi: 10.1038/ejhg.2015.181. Epub 2015 Sep 9.

18.

Dubin-Johnson syndrome presenting with neonatal cholestasis.

Shieh CC, Chang MH, Chen CL.

Arch Dis Child. 1990 Aug;65(8):898-9.

19.

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;284(1):G165-74. Epub 2002 Oct 2.

20.

Inheritance of the Dubin-Johnson-Sprinz syndrome.

Edwards RH.

Gastroenterology. 1975 Apr;68(4 Pt 1):734-49. No abstract available.

PMID:
1123140

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