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Journal Abstract Search

148 related items for PubMed ID: 17937877

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  • 3. Assessment of UGT polymorphisms and neonatal jaundice.
    Bartlett MG, Gourley GR.
    Semin Perinatol; 2011 Jun; 35(3):127-33. PubMed ID: 21641485
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  • 5. Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome.
    Kaplan M, Hammerman C, Beutler E.
    Eur J Pediatr; 2001 Mar; 160(3):195. PubMed ID: 11277384
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  • 6. Prolonged neonatal jaundice: a manifestation of heterozygote state for Crigler--Najjar syndrome?
    Odièvre M, Luzeau R, Alagille D.
    J Pediatr Gastroenterol Nutr; 1982 Mar; 1(2):239-41. PubMed ID: 6821110
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  • 8. Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus.
    Kadakol A, Sappal BS, Ghosh SS, Lowenheim M, Chowdhury A, Chowdhury S, Santra A, Arias IM, Chowdhury JR, Chowdhury NR.
    J Med Genet; 2001 Apr; 38(4):244-9. PubMed ID: 11370628
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  • 9. Vigintiphobia revisited.
    Watchko JF.
    Pediatrics; 2005 Jun; 115(6):1747-53. PubMed ID: 15930239
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  • 10. Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
    Canu G, Minucci A, Zuppi C, Capoluongo E.
    Blood Cells Mol Dis; 2013 Apr; 50(4):273-80. PubMed ID: 23403257
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  • 11. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
    Kadakol A, Ghosh SS, Sappal BS, Sharma G, Chowdhury JR, Chowdhury NR.
    Hum Mutat; 2000 Oct; 16(4):297-306. PubMed ID: 11013440
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  • 12. [Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice].
    Seco ML, del Río E, Barceló MJ, Remacha A, Ginovart G, Moliner E, Baiget M.
    An Esp Pediatr; 2002 Feb; 56(2):139-43. PubMed ID: 11827650
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  • 13. Genetic factors in neonatal hyperbilirubinemia and kernicterus.
    Sarici SU, Saldir M.
    Turk J Pediatr; 2007 Feb; 49(3):245-9. PubMed ID: 17990575
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  • 15. 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 Feb; 36(1):91-7. PubMed ID: 16269258
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  • 16. Gilbert syndrome accelerates development of neonatal jaundice.
    Bancroft JD, Kreamer B, Gourley GR.
    J Pediatr; 1998 Apr; 132(4):656-60. PubMed ID: 9580766
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  • 17. Gilbert-Meulengracht's syndrome and pharmacogenetics: is jaundice just the tip of the iceberg?
    Strassburg CP.
    Drug Metab Rev; 2010 Feb; 42(1):168-81. PubMed ID: 20070246
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  • 18. [Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome].
    Costa E, Vieira E, Cleto E, Cabeda JM, Pinho L, Coimbra E, Dos Santos R, Barbot J.
    Acta Med Port; 2002 Feb; 15(6):409-12. PubMed ID: 12680285
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  • 20. Inherited disorders of bilirubin metabolism.
    Bosma PJ.
    J Hepatol; 2003 Jan; 38(1):107-17. PubMed ID: 12480568
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