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Journal Abstract Search

312 related items for PubMed ID: 30266131

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  • 2. Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity.
    Cozzi L, Nuti F, Degrassi I, Civeriati D, Paolella G, Nebbia G.
    Ital J Pediatr; 2022 Apr 18; 48(1):59. PubMed ID: 35436954
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  • 4. [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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  • 8. Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.
    Gailite L, Rots D, Pukite I, Cernevska G, Kreile M.
    BMC Pediatr; 2018 Oct 03; 18(1):317. PubMed ID: 30285761
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  • 10. 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 03; 112(6):2099-103. PubMed ID: 9178703
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  • 12. Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
    Maruo Y, Nishizawa K, Sato H, Sawa H, Shimada M.
    Pediatrics; 2000 Nov 03; 106(5):E59. PubMed ID: 11061796
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  • 13. Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.
    Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y.
    J Gastroenterol Hepatol; 2016 Feb 03; 31(2):403-8. PubMed ID: 26250421
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  • 14. Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.
    Costa E.
    Blood Cells Mol Dis; 2006 Feb 03; 36(1):77-80. PubMed ID: 16386929
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  • 16. 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
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  • 17. Familial unconjugated hyperbilirubinemia syndromes.
    Reichen J.
    Semin Liver Dis; 1983 Feb 02; 3(1):24-35. PubMed ID: 6836332
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  • 18. 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 02; 42(4):540-1. PubMed ID: 17454871
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