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Journal Abstract Search

112 related items for PubMed ID: 7630272

  • 1. Genetic inheritance of Gilbert's syndrome.
    Bosma P, Chowdhury JR, Jansen PH.
    Lancet; 1995 Jul 29; 346(8970):314-5. PubMed ID: 7630272
    [No Abstract] [Full Text] [Related]

  • 2. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.
    Aono S, Adachi Y, Uyama E, Yamada Y, Keino H, Nanno T, Koiwai O, Sato H.
    Lancet; 1995 Apr 15; 345(8955):958-9. PubMed ID: 7715297
    [Abstract] [Full Text] [Related]

  • 3. Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.
    Sampietro M, Iolascon A.
    Haematologica; 1999 Feb 15; 84(2):150-7. PubMed ID: 10091414
    [Abstract] [Full Text] [Related]

  • 4. The genetic basis of Gilbert's syndrome.
    Sato H, Adachi Y, Koiwai O.
    Lancet; 1996 Mar 02; 347(9001):557-8. PubMed ID: 8596313
    [No Abstract] [Full Text] [Related]

  • 5. [From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].
    Drenth JP, Peters WH, Jansen JB.
    Ned Tijdschr Geneeskd; 2002 Aug 10; 146(32):1488-90. PubMed ID: 12198827
    [Abstract] [Full Text] [Related]

  • 6. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.
    Yamamoto K, Sato H, Fujiyama Y, Doida Y, Bamba T.
    Biochim Biophys Acta; 1998 Apr 28; 1406(3):267-73. PubMed ID: 9630669
    [Abstract] [Full Text] [Related]

  • 7. 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 28; 42(4):540-1. PubMed ID: 17454871
    [No Abstract] [Full Text] [Related]

  • 8. Gilbert's syndrome--a legitimate genetic anomaly?
    Schmid R.
    N Engl J Med; 1995 Nov 02; 333(18):1217-8. PubMed ID: 7565981
    [No Abstract] [Full Text] [Related]

  • 9. Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect.
    Yildiz D, Alan S, Kilic A, Yaman A, Erdeve O, Kuloglu Z, Atasay B, Arsan S.
    Genet Couns; 2013 Nov 02; 24(3):273-7. PubMed ID: 24341141
    [Abstract] [Full Text] [Related]

  • 10. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
    Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP.
    N Engl J Med; 1995 Nov 02; 333(18):1171-5. PubMed ID: 7565971
    [Abstract] [Full Text] [Related]

  • 11. Gilbert-Meulengracht's syndrome and pharmacogenetics: is jaundice just the tip of the iceberg?
    Strassburg CP.
    Drug Metab Rev; 2010 Feb 02; 42(1):168-81. PubMed ID: 20070246
    [Abstract] [Full Text] [Related]

  • 12. Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
    Chalasani N, Chowdhury NR, Chowdhury JR, Boyer TD.
    Gastroenterology; 1997 Jun 02; 112(6):2099-103. PubMed ID: 9178703
    [Abstract] [Full Text] [Related]

  • 13. Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.
    Costa E.
    Blood Cells Mol Dis; 2006 Jun 02; 36(1):77-80. PubMed ID: 16386929
    [Abstract] [Full Text] [Related]

  • 14. Assessment of UGT polymorphisms and neonatal jaundice.
    Bartlett MG, Gourley GR.
    Semin Perinatol; 2011 Jun 02; 35(3):127-33. PubMed ID: 21641485
    [Abstract] [Full Text] [Related]

  • 15. Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
    Takeuchi K, Kobayashi Y, Tamaki S, Ishihara T, Maruo Y, Araki J, Mifuji R, Itani T, Kuroda M, Sato H, Kaito M, Adachi Y.
    J Gastroenterol Hepatol; 2004 Sep 02; 19(9):1023-8. PubMed ID: 15304120
    [Abstract] [Full Text] [Related]

  • 16. 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 02; 62(9):1680-1. PubMed ID: 25822733
    [No Abstract] [Full Text] [Related]

  • 17. Crigler-Najjar Syndrome Type II Diagnosed in a Patient with Jaundice Since Birth.
    Liaqat A, Shahid A, Attiq H, Ameer A, Imran M.
    J Coll Physicians Surg Pak; 2018 Oct 02; 28(10):806-808. PubMed ID: 30266131
    [Abstract] [Full Text] [Related]

  • 18. 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 Oct 02; 36(1):91-7. PubMed ID: 16269258
    [Abstract] [Full Text] [Related]

  • 19. Familial unconjugated hyperbilirubinemia syndromes.
    Reichen J.
    Semin Liver Dis; 1983 Feb 02; 3(1):24-35. PubMed ID: 6836332
    [Abstract] [Full Text] [Related]

  • 20. 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 02; 16(4):297-306. PubMed ID: 11013440
    [Abstract] [Full Text] [Related]

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