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Journal Abstract Search

415 related items for PubMed ID: 24341141

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  • 2. 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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  • 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. Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.
    Maruo Y, Poon KK, Ito M, Iwai M, Takahashi H, Mori A, Sato H, Takeuchi Y.
    Clin Genet; 2003 Nov; 64(5):420-3. PubMed ID: 14616765
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  • 6. 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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  • 8. 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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  • 9. [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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  • 10. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.
    Khan S, Irfan M, Sher G, Zubaida B, Alvi MA, Yasinzai M, Naeem M.
    Ann Hum Genet; 2013 Nov 10; 77(6):482-7. PubMed ID: 23992562
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  • 11. Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.
    Costa E.
    Blood Cells Mol Dis; 2006 Nov 10; 36(1):77-80. PubMed ID: 16386929
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  • 13. [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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  • 16. 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 15; 31(2):403-8. PubMed ID: 26250421
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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 15; 42(1):168-81. PubMed ID: 20070246
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