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

Year Number of Results
1904 1
1946 1
1948 1
1950 1
1954 2
1955 1
1956 1
1957 2
1958 1
1959 2
1961 1
1962 1
1963 4
1964 6
1965 5
1966 2
1967 3
1968 3
1969 3
1970 6
1971 5
1972 5
1973 6
1974 6
1975 14
1976 7
1977 12
1978 8
1979 9
1980 4
1981 10
1982 17
1983 8
1984 13
1985 16
1986 7
1987 7
1988 7
1989 11
1990 11
1991 8
1992 7
1993 5
1994 8
1995 15
1996 8
1997 11
1998 18
1999 26
2000 20
2001 24
2002 24
2003 22
2004 15
2005 16
2006 8
2007 11
2008 11
2009 7
2010 5
2011 18
2012 15
2013 17
2014 19
2015 15
2016 16
2017 18
2018 33
2019 42
2020 69
2021 36
Text availability
Article attribute
Article type
Publication date

Similar articles for PMID: 11061796

747 results
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Page 1
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
Molecular genetic basis of Gilbert's syndrome.
Burchell B, Hume R. Burchell B, et al. J Gastroenterol Hepatol. 1999 Oct;14(10):960-6. doi: 10.1046/j.1440-1746.1999.01984.x. J Gastroenterol Hepatol. 1999. PMID: 10530490 Review.
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: the common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.
Kanai M, Kijima K, Shirahata E, Sasaki A, Akaba K, Umetsu K, Tezuka N, Kurachi H, Aikawa S, Hayasaka K. Kanai M, et al. Pediatr Int. 2005 Apr;47(2):137-41. doi: 10.1111/j.1442-200x.2005.02030.x. Pediatr Int. 2005. PMID: 15771689
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