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Journal Abstract Search

173 related items for PubMed ID: 12680285

  • 1. [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; 15(6):409-12. PubMed ID: 12680285
    [Abstract] [Full Text] [Related]

  • 2. Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.
    Huang CS, Chang PF, Huang MJ, Chen ES, Chen WC.
    Gastroenterology; 2002 Jul; 123(1):127-33. PubMed ID: 12105841
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  • 3. Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome.
    Minucci A, Ruggiero A, Canu G, Maurizi P, De Bonis M, Concolino P, De Luca D, Capoluongo E.
    Pediatr Blood Cancer; 2015 Sep; 62(9):1680-1. PubMed ID: 25822733
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  • 5. Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.
    Akaba K, Kimura T, Sasaki A, Tanabe S, Wakabayashi T, Hiroi M, Yasumura S, Maki K, Aikawa S, Hayasaka K.
    J Hum Genet; 1999 Sep; 44(1):22-5. PubMed ID: 9929972
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  • 6. Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.
    Galanello R, Cipollina MD, Carboni G, Perseu L, Barella S, Corrias A, Cao A.
    Eur J Pediatr; 1999 Nov; 158(11):914-6. PubMed ID: 10541948
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  • 7. Low glucose-6-phosphate dehydrogenase enzyme activity level at the time of hemolysis in a male neonate with the African type of deficiency.
    Herschel M, Beutler E.
    Blood Cells Mol Dis; 2001 Nov; 27(5):918-23. PubMed ID: 11783956
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  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. A prolonged neonatal jaundice associated with a rare G6PD mutation.
    Minucci A, Concolino P, De Luca D, Giardina B, Zuppi C, Capoluongo E.
    Pediatr Blood Cancer; 2009 Sep; 53(3):475-8. PubMed ID: 19422023
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  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
    Kaplan M, Renbaum P, Levy-Lahad E, Hammerman C, Lahad A, Beutler E.
    Proc Natl Acad Sci U S A; 1997 Oct 28; 94(22):12128-32. PubMed ID: 9342374
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  • 12. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
    Jablonska-Skwiecinska E, Lewandowska I, Plochocka D, Topczewski J, Zimowski JG, Klopocka J, Burzynska B.
    Hum Mutat; 1999 Oct 28; 14(6):477-84. PubMed ID: 10571945
    [Abstract] [Full Text] [Related]

  • 13. Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.
    Žaja O, Tiljak MK, Štefanović M, Tumbri J, Jurčić Z.
    J Matern Fetal Neonatal Med; 2014 May 28; 27(8):844-50. PubMed ID: 23981182
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  • 16. The frequency of UDP-glucuronosyltransferase 1A1 promoter region (TA)7 polymorphism in newborns and it's relation with jaundice.
    Muslu N, Turhan AB, Eskandari G, Atici A, Ozturk OG, Kul S, Atik U.
    J Trop Pediatr; 2007 Feb 28; 53(1):64-8. PubMed ID: 17166930
    [Abstract] [Full Text] [Related]

  • 17. [Relationship between bilirubin UDP-glucuronosyl transferase polymorphism and neonatal jaundice].
    Sha B.
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Oct 28; 9(5):510-3. PubMed ID: 17937877
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  • 20. [Genetic factors in the occurrence of neonatal unconjugated hyperbilirubinemia].
    Sun LL, Chen YS, Yu ZZ, Huang BX, Xu G, Ma DL, Li CG, Liu L, Liu XH.
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Apr 28; 14(4):256-9. PubMed ID: 22537951
    [Abstract] [Full Text] [Related]

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