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Journal Abstract Search

202 related items for PubMed ID: 12480568

  • 1. Inherited disorders of bilirubin metabolism.
    Bosma PJ.
    J Hepatol; 2003 Jan; 38(1):107-17. PubMed ID: 12480568
    [No Abstract] [Full Text] [Related]

  • 2. [Crigler-Najjar syndrome].
    Torres M, Bruguera M.
    Gastroenterol Hepatol; 2005 Dec; 28(10):637-40. PubMed ID: 16373016
    [No Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus].
    Kraemer D, Scheurlen M.
    Med Klin (Munich); 2002 Sep 15; 97(9):528-32. PubMed ID: 12371080
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  • 7. 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 Sep 15; 24(3):273-7. PubMed ID: 24341141
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  • 8. Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome).
    Strassburg CP.
    Best Pract Res Clin Gastroenterol; 2010 Oct 15; 24(5):555-71. PubMed ID: 20955959
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  • 14. 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]

  • 15. 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]

  • 16. Genetic defects at the UGT1 locus associated with Crigler-Najjar type I disease, including a prenatal diagnosis.
    Ciotti M, Obaray R, Martín MG, Owens IS.
    Am J Med Genet; 1997 Jan 20; 68(2):173-8. PubMed ID: 9028453
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  • 17. Assessment of UGT polymorphisms and neonatal jaundice.
    Bartlett MG, Gourley GR.
    Semin Perinatol; 2011 Jun 20; 35(3):127-33. PubMed ID: 21641485
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  • 19. [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
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  • 20. Congenital nonhemolytic hyperbilirubinemias.
    Cichoz-Lach H, Celiński K, Słomka M.
    Ann Univ Mariae Curie Sklodowska Med; 2004 Aug 10; 59(1):449-52. PubMed ID: 16146029
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