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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1962 1
1964 1
1982 1
1993 1
1995 2
1997 3
1998 3
1999 4
2000 5
2001 3
2002 12
2003 2
2004 3
2005 8
2006 6
2007 7
2008 2
2010 6
2011 3
2012 2
2013 7
2014 2
2015 6
2016 2
2017 1
2018 1
2020 3
2021 3
2022 1
2023 1
2024 0

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Similar articles for PMID: 11370628

96 results

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Page 1
Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus.
Kadakol A, Sappal BS, Ghosh SS, Lowenheim M, Chowdhury A, Chowdhury S, Santra A, Arias IM, Chowdhury JR, Chowdhury NR. Kadakol A, et al. J Med Genet. 2001 Apr;38(4):244-9. doi: 10.1136/jmg.38.4.244. J Med Genet. 2001. PMID: 11370628 Free PMC article. No abstract available.
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. Takeuchi K, et al. J Gastroenterol Hepatol. 2004 Sep;19(9):1023-8. doi: 10.1111/j.1440-1746.2004.03370.x. J Gastroenterol Hepatol. 2004. PMID: 15304120
96 results