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

Year Number of Results
1799 2
1800 1
1803 2
1828 1
1850 2
1852 1
1877 1
1883 4
1884 2
1886 3
1888 1
1889 1
1895 4
1896 3
1897 2
1898 1
1900 2
1901 2
1902 2
1904 3
1905 3
1908 1
1909 1
1911 1
1914 2
1915 1
1918 1
1920 1
1921 4
1922 1
1923 2
1924 1
1925 5
1926 4
1927 2
1928 3
1929 2
1930 2
1931 4
1932 5
1933 2
1934 7
1935 2
1936 3
1937 2
1938 1
1941 2
1942 2
1943 1
1944 1
1945 8
1946 37
1947 27
1948 36
1949 32
1950 53
1951 43
1952 43
1953 35
1954 39
1955 40
1956 65
1957 56
1958 66
1959 42
1960 70
1961 53
1962 58
1963 81
1964 84
1965 81
1966 102
1967 86
1968 90
1969 101
1970 141
1971 102
1972 120
1973 132
1974 158
1975 176
1976 192
1977 177
1978 211
1979 203
1980 220
1981 217
1982 196
1983 229
1984 263
1985 269
1986 257
1987 290
1988 281
1989 313
1990 308
1991 323
1992 338
1993 360
1994 389
1995 387
1996 389
1997 401
1998 444
1999 453
2000 556
2001 527
2002 510
2003 518
2004 579
2005 681
2006 711
2007 800
2008 838
2009 937
2010 979
2011 1082
2012 1187
2013 1170
2014 1247
2015 1394
2016 1355
2017 1350
2018 1404
2019 1403
2020 1583
2021 1702
2022 1111
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30,530 results
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Diagnostic criteria and contributors to Gilbert's syndrome.
Wagner KH, Shiels RG, Lang CA, Seyed Khoei N, Bulmer AC. Wagner KH, et al. Crit Rev Clin Lab Sci. 2018 Mar;55(2):129-139. doi: 10.1080/10408363.2018.1428526. Epub 2018 Feb 1. Crit Rev Clin Lab Sci. 2018. PMID: 29390925 Review.
Diagnoses can include conditions of disordered bilirubin metabolism (Gilbert's, Crigler-Najjar, Rotor, or Dubin-Johnson syndromes) or an acquired disease, including alcoholic/non-alcoholic fatty liver disease, hepatotropic hepatitis, cirrhosis, or hepato-biliary mal …
Diagnoses can include conditions of disordered bilirubin metabolism (Gilbert's, Crigler-Najjar, Rotor, or Dubin-Johnson syndro …
[Gilbert's syndrome: hyperbilirubinemia enemy or friend].
Xiang GQ, Sun FR, Wang BY. Xiang GQ, et al. Zhonghua Gan Zang Bing Za Zhi. 2021 Oct 20;29(10):1024-1027. doi: 10.3760/cma.j.cn501113-20200212-00041. Zhonghua Gan Zang Bing Za Zhi. 2021. PMID: 34814402 Chinese.
Gilbert's syndrome is a kind of benign inherited disease of bilirubin binding disorder, mainly due to the homozygous polymorphism A(TA)7TAA in the promoter of the gene for uridine diphosphate -glucuronosyltransferase 1A1 (UGT1A1), which is a TA insertion into the pr
Gilbert's syndrome is a kind of benign inherited disease of bilirubin binding disorder, mainly due to the homozygous polymorph
Gilbert's Syndrome With Diabetes Mellitus.
Haixia L, Li R. Haixia L, et al. Cureus. 2021 Jul 22;13(7):e16557. doi: 10.7759/cureus.16557. eCollection 2021 Jul. Cureus. 2021. PMID: 34322357 Free PMC article.
Gilbert's syndrome (GS) could lead to the high bilirubin, and gestational diabetes mellitus might reverse this index. ...This is the first report to confirm that pregnant women with Gilbert's syndrome and gestational diabetes could give birth normally
Gilbert's syndrome (GS) could lead to the high bilirubin, and gestational diabetes mellitus might reverse this index. ...This
Gilbert's syndrome.
Watson KJ, Gollan JL. Watson KJ, et al. Baillieres Clin Gastroenterol. 1989 Apr;3(2):337-55. doi: 10.1016/0950-3528(89)90004-3. Baillieres Clin Gastroenterol. 1989. PMID: 2655758 Review.
While Gilbert's syndrome is extremely common and benign, its pathogenesis may not be as straightforward as once believed. ...Whether one or more genes is consistently culpable remains open to speculation. Despite the complicated pathogenesis of Gilbert's
While Gilbert's syndrome is extremely common and benign, its pathogenesis may not be as straightforward as once believed. ...W …
GILBERT'S SYNDROME - A CONCEALED ADVERSITY FOR PHYSICIANS AND SURGEONS.
Rasool A, Sabir S, Ashlaq M, Farooq U, Khan MZ, Khan FY. Rasool A, et al. J Ayub Med Coll Abbottabad. 2015 Jul-Sep;27(3):707-10. J Ayub Med Coll Abbottabad. 2015. PMID: 26721045 Review.
Gilbert's syndrome (often abbreviated as GS) is most common hereditary cause of mild unconjugated (indirect) hyperbilirubinemia. ...A systematic study of the available literature was done. Key words of Gilbert's syndrome, hyperbilirubinemia and clinica
Gilbert's syndrome (often abbreviated as GS) is most common hereditary cause of mild unconjugated (indirect) hyperbilirubinemi
[Gilbert's syndrome--myths and reality].
Muchová L, Kráslová I, Lenícek M, Vítek L. Muchová L, et al. Cas Lek Cesk. 2004;143(6):375-80. Cas Lek Cesk. 2004. PMID: 15309863 Review. Czech.
Gilbert's syndrome is defined as a hereditary, mild, chronic, unconjugated hyperbilirubinemia occurring in the absence of overt hemolysis or any other evidence of liver disease. It is caused by a mutation of the specific UDP glucuronosyl transferase conjugating bili
Gilbert's syndrome is defined as a hereditary, mild, chronic, unconjugated hyperbilirubinemia occurring in the absence of over
Gilbert's Syndrome in Children with Unconjugated Hyperbilirubinemia - An Analysis of 170 Cases.
Sood V, Lal BB, Sharma S, Khanna R, Siloliya MK, Alam S. Sood V, et al. Indian J Pediatr. 2021 Feb;88(2):154-157. doi: 10.1007/s12098-020-03271-6. Epub 2020 Mar 27. Indian J Pediatr. 2021. PMID: 32221786
There is limited literature on Gilbert's syndrome (GS) in children with persistent unconjugated hyperbilirubinemia from Indian subcontinent. ...
There is limited literature on Gilbert's syndrome (GS) in children with persistent unconjugated hyperbilirubinemia from Indian …
Pharmacogenetics of Gilbert's syndrome.
Strassburg CP. Strassburg CP. Pharmacogenomics. 2008 Jun;9(6):703-15. doi: 10.2217/14622416.9.6.703. Pharmacogenomics. 2008. PMID: 18518849 Review.
Gilbert's syndrome is characterized by mild unconjugated nonhemolytic hyperbilirubinemia, which does not lead to hepatic inflammation, fibrosis, chronic liver disease or liver failure. ...The prediction of unwanted drug reactions associated with Gilbert's
Gilbert's syndrome is characterized by mild unconjugated nonhemolytic hyperbilirubinemia, which does not lead to hepatic infla
Gilbert's syndrome and drug metabolism.
Macklon AF, Savage RL, Rawlins MD. Macklon AF, et al. Clin Pharmacokinet. 1979 May-Jun;4(3):223-32. doi: 10.2165/00003088-197904030-00004. Clin Pharmacokinet. 1979. PMID: 383356 Review.
Gilbert's syndrome is an inherited disorder which is characterised by unconjugated hyperbilirubinaemia. ...In addition, there is evidence suggesting impaired hepatic uptake of bilirubin in Gilbert's syndrome. Glucuronidation of a number of substrates a
Gilbert's syndrome is an inherited disorder which is characterised by unconjugated hyperbilirubinaemia. ...In addition, there
Gilbert's Syndrome, Bilirubin Level and UGT1A1∗28 Genotype in Men of North-West Region of Russia.
Ivanov A, Semenova E. Ivanov A, et al. J Clin Exp Hepatol. 2021 Nov-Dec;11(6):691-699. doi: 10.1016/j.jceh.2021.01.006. Epub 2021 Feb 4. J Clin Exp Hepatol. 2021. PMID: 34866848
BACKGROUND/OBJECTIVES: Gilbert's syndrome (GS) is a hereditary pathology that affects approximately 10% of the world's population. ...
BACKGROUND/OBJECTIVES: Gilbert's syndrome (GS) is a hereditary pathology that affects approximately 10% of the world's
30,530 results
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