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4. 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]
5. UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis. Fretzayas A; Kitsiou S; Tsezou A; Alexaki A; Nicolaidou P Scand J Infect Dis; 2006; 38(6-7):537-40. PubMed ID: 16798708 [TBL] [Abstract][Full Text] [Related]
6. Gilbert's syndrome--clinical and pharmacological implications. Radu P; Atsmon J Isr Med Assoc J; 2001 Aug; 3(8):593-8. PubMed ID: 11519385 [No Abstract] [Full Text] [Related]
7. Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes. Costa E Blood Cells Mol Dis; 2006; 36(1):77-80. PubMed ID: 16386929 [TBL] [Abstract][Full Text] [Related]
8. Linkage between A(TA)7TAA and -3279T>G mutations in UGT1A1 is not essential for pathogenesis of Gilbert syndrome. Jirsa M; Petrasek J; Vitek L Liver Int; 2006 Dec; 26(10):1302-3. PubMed ID: 17105600 [No Abstract] [Full Text] [Related]
10. Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects. Te Morsche RH; Zusterzeel PL; Raijmakers MT; Roes EM; Steegers EA; Peters WH Hepatology; 2001 Mar; 33(3):765. PubMed ID: 11230763 [No Abstract] [Full Text] [Related]
11. Melting temperature assay for a UGT1A gene variant in Gilbert syndrome. Marziliano N; Pelo E; Minuti B; Passerini I; Torricelli F; Da Prato L Clin Chem; 2000 Mar; 46(3):423-5. PubMed ID: 10702534 [No Abstract] [Full Text] [Related]
13. Gilbert syndrome: the UGT1A1*28 promoter polymorphism as a biomarker of multifactorial diseases and drug metabolism. Gil J; Sąsiadek MM Biomark Med; 2012 Apr; 6(2):223-30. PubMed ID: 22448797 [TBL] [Abstract][Full Text] [Related]
14. Use of double gradient denaturing gradient gel electrophoresis to detect (AT)n polymorphisms in the UDP-glucuronosyltransferase 1 gene promoter associated with Gilbert's syndrome. Gürtler V; Parkin JD; Mayall BC Electrophoresis; 1999 Oct; 20(14):2841-3. PubMed ID: 10546817 [TBL] [Abstract][Full Text] [Related]
15. Frequency of Gilbert's syndrome associated with UGTA1 (TA)(7) polymorphism in Southern Italy. Iolascon A; Perrotta S; Coppola B; Carbone R; Miraglia Del Giudice E Haematologica; 2000 Mar; 85(3):335-6. PubMed ID: 10702836 [No Abstract] [Full Text] [Related]
16. Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler-Najjar syndromes. Costa E; Vieira E; Martins M; Saraiva J; Cancela E; Costa M; Bauerle R; Freitas T; Carvalho JR; Santos-Silva E; Barbot J; Dos Santos R Blood Cells Mol Dis; 2006; 36(1):91-7. PubMed ID: 16269258 [TBL] [Abstract][Full Text] [Related]
17. TATA-Box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with clinical diagnosis of Gilbert Syndrome. Costa E; Vieira E; Santos-Silva E; Barbot J; dos Santos R Haematologica; 2002 Apr; 87(4):ELT21. PubMed ID: 11940506 [No Abstract] [Full Text] [Related]
18. Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia. Aiso M; Yagi M; Tanaka A; Miura K; Miura R; Arizumi T; Takamori Y; Nakahara S; Maruo Y; Takikawa H Intern Med; 2017; 56(6):661-664. PubMed ID: 28321066 [TBL] [Abstract][Full Text] [Related]
19. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias. Khan S; Irfan M; Sher G; Zubaida B; Alvi MA; Yasinzai M; Naeem M Ann Hum Genet; 2013 Nov; 77(6):482-7. PubMed ID: 23992562 [TBL] [Abstract][Full Text] [Related]
20. Mixed Dubin-Gilbert Syndrome: A Compound Heterozygous Phenotype of Two Novel Variants in Jiang J; Wang HG; Wu WL; Peng XX Chin Med J (Engl); 2017 Apr; 130(8):1003-1005. PubMed ID: 28397734 [No Abstract] [Full Text] [Related] [Next] [New Search]