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7. [Manifestations of genetically determined formerly latent enzymopathies as a result of drug therapy: Gilbert's disease and acute intermittent porphyrial]. Tünde H; Arpád G; Csaba R; Andrea L; Tibor J Orv Hetil; 1975 Mar; 116(9):489-93. PubMed ID: 1114008 [No Abstract] [Full Text] [Related]
8. Gilbert's syndrome in identical twins. Graham JR Med J Aust; 1987 Nov; 147(10):524. PubMed ID: 3683272 [No Abstract] [Full Text] [Related]
9. Hereditary hyperbilirubinemias. Odell GB; Childs B Prog Med Genet; 1980; 4():103-34. PubMed ID: 7003652 [No Abstract] [Full Text] [Related]
10. No association between Gilbert's syndrome, the ABO blood groups and the haptoglobin phenotypes. Platzer R; Bircher J Experientia; 1977 Sep; 33(9):1142-3. PubMed ID: 891855 [No Abstract] [Full Text] [Related]
17. [A case of Meuleugracht-Gilbert syndrome]. Pytloch W Pediatr Pol; 1970 Mar; 45(3):349-50. PubMed ID: 5441596 [No Abstract] [Full Text] [Related]
18. [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]
19. [Intermittent juvenile icterus - Gilbert-Meulengracht's disease. A review and 3 case reports]. Hansen JN Ugeskr Laeger; 1982 Apr; 144(17):1212-4. PubMed ID: 7112708 [No Abstract] [Full Text] [Related]
20. [Clinical and pathological features of 16 patients with Gilbert syndrome and 2 cases with genetic analysis]. Peng XX; Wang TL Zhonghua Gan Zang Bing Za Zhi; 2008 May; 16(5):372-4. PubMed ID: 18510852 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]