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25. THE CONGENITAL HYPERBILIRUBINEMIAS: CRIGLER, JOHNSON, NAJJAR, ROTOR, DUBIN AND GILBERT. KAPLEW LS Va Med Mon (1918); 1964 May; 91():215-6. PubMed ID: 14144368 [No Abstract] [Full Text] [Related]
26. 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. PubMed ID: 25315738 [TBL] [Abstract][Full Text] [Related]
27. [Hyperbilirubinemia]. Leu AJ Schweiz Rundsch Med Prax; 1992 Feb; 81(8):230-3. PubMed ID: 1539119 [TBL] [Abstract][Full Text] [Related]
28. [Case of Gilbert's disease]. Jonek J; Biskupska-Karasińska M; Sawaryn T; Grzybek H; Panz B Wiad Lek; 1976 Apr; 29(8):739-43. PubMed ID: 1266255 [No Abstract] [Full Text] [Related]
29. Iron metabolism and storage in Gilbert's disease, and in Rotor's and Dubin-Johnson's syndromes. Burger T; Gógl A; Jávor T; Patakfalvi A Acta Med Acad Sci Hung; 1973; 29(3):331-8. PubMed ID: 4747525 [No Abstract] [Full Text] [Related]
30. Hepatic transport of serum bilirubin, bromsulfophthalein, and indocyanine green in patients with congenital non-hemolytic hyperbilirubinemia and patients with constitutional indocyanine green excretory defect. Nambu M; Namihisa T J Gastroenterol; 1996 Apr; 31(2):228-36. PubMed ID: 8680543 [TBL] [Abstract][Full Text] [Related]
31. Rotor's and Dubin-Johnson syndromes. Namihisa T; Nambu M N Engl J Med; 1977 Sep; 297(10):560. PubMed ID: 887111 [No Abstract] [Full Text] [Related]
32. Porphyrin metabolism in Gilbert's, Dubin-Johnson, and Rotor's syndromes. Mikulecký M Gut; 1987 Nov; 28(11):1548-9. PubMed ID: 3428681 [No Abstract] [Full Text] [Related]
33. Chronic idiopathic jaundice in Papua and New Guinea: a report on nine patients with Dubin-Johnson's or Rotor's syndrome. Vaughan JP; Marubbio AT; Maddocks I; Cooke RA Trans R Soc Trop Med Hyg; 1970; 64(2):287-92. PubMed ID: 5449055 [No Abstract] [Full Text] [Related]
34. Gilbert's syndrome phenotypically expressed as Crigler-Najjar syndrome type II. Seo YS; Keum B; Park S; Kim du R; Kwon YD; Kim YS; Jeen YT; Chun HJ; Um SH; Kim CD; Ryu HS Scand J Gastroenterol; 2007 Apr; 42(4):540-1. PubMed ID: 17454871 [No Abstract] [Full Text] [Related]
35. Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency. Kaplan M J Perinatol; 2001 Dec; 21 Suppl 1():S30-4; discussion S35-9. PubMed ID: 11803413 [TBL] [Abstract][Full Text] [Related]
36. Relevance of urinary coproporphyrin isomers in hereditary hyperbilirubinemias. Frank M; Doss MO Clin Biochem; 1989 Jun; 22(3):221-2. PubMed ID: 2736773 [TBL] [Abstract][Full Text] [Related]
37. Inherited disorders of bilirubin transport and conjugation: new insights into molecular mechanisms and consequences. Erlinger S; Arias IM; Dhumeaux D Gastroenterology; 2014 Jun; 146(7):1625-38. PubMed ID: 24704527 [TBL] [Abstract][Full Text] [Related]
38. [Constitutional hyperbilirubinemia and mixed bilirubin. Clinical and functional study]. Rapaccini GL; Anti M; Miggiano G; De Vitis I; De Simone F; Fedeli G Minerva Med; 1980 Nov; 71(44):3221-8. PubMed ID: 7454089 [TBL] [Abstract][Full Text] [Related]
39. Conjugated bilirubin measurements in Gilbert's syndrome: method dependence. Thurlow V; Bailey IR; Griffiths W Ann Clin Biochem; 2005 Jan; 42(Pt 1):67-9. PubMed ID: 15802037 [TBL] [Abstract][Full Text] [Related]
40. Unconjugated hyperbilirubinemia. Clinical, laboratory and metabolic aspects. Okolicsányi L; Nassuato G; Strazzabosco M; Toso T Z Gastroenterol; 1993 Feb; 31 Suppl 2():78-80. PubMed ID: 7483724 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]