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29. Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study. Fogelfeld L; Sarova-Pinchas I; Meytes D; Barash V; Brok-Simoni F; Feigl D Isr J Med Sci; 1990 Jun; 26(6):328-33. PubMed ID: 2380035 [TBL] [Abstract][Full Text] [Related]
30. Coexisting Gilbert's syndrome and sickle cell disease. Borker A; Udall J; Warrier R South Med J; 2002 Aug; 95(8):939-40. PubMed ID: 12190239 [TBL] [Abstract][Full Text] [Related]
31. [Erythrocyte survival in children with chronic intermittent nonconjugated hyperbilirubinemia (Gilbert syndrome)]. Hajnzić TF; Jurcić Z; Filjak K; Oberiter V; Rudar D Lijec Vjesn; 1987; 109(4-5):143-5. PubMed ID: 3613827 [No Abstract] [Full Text] [Related]
32. [Contribution on the differential diagnosis of hyperbilirubinemia with special reference to the functional diagnosis of Gilbert's syndrome]. Buljevac M; Kis S; Straus B Vojnosanit Pregl; 1983; 40(2):110-3. PubMed ID: 6880103 [No Abstract] [Full Text] [Related]
33. Gilbert syndrome and the development of antiretroviral therapy-associated hyperbilirubinemia. Rotger M; Taffe P; Bleiber G; Gunthard HF; Furrer H; Vernazza P; Drechsler H; Bernasconi E; Rickenbach M; Telenti A; J Infect Dis; 2005 Oct; 192(8):1381-6. PubMed ID: 16170755 [TBL] [Abstract][Full Text] [Related]
34. [Diagnosis of functional hyperbilirubinemia of the Gilbert type in children]. Syr'eva TN; Spasibko AM; Pisarev AG; Fedotov VV Vopr Okhr Materin Det; 1977; 22(2):17-20. PubMed ID: 841937 [No Abstract] [Full Text] [Related]