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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 1
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 3
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 85
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 400
1998 441
1999 453
2000 554
2001 527
2002 510
2003 516
2004 578
2005 681
2006 711
2007 800
2008 837
2009 937
2010 977
2011 1082
2012 1186
2013 1170
2014 1246
2015 1390
2016 1344
2017 1342
2018 1393
2019 1392
2020 1436
2021 4
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27,971 results
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Page 1
Overview of Gilbert's syndrome.
King D, Armstrong MJ. King D, et al. Drug Ther Bull. 2019 Feb;57(2):27-31. doi: 10.1136/dtb.2018.000028. Drug Ther Bull. 2019. PMID: 30709860 Review. No abstract available.
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.
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 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
Effect of UDP-glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome.
Huang MJ, Chen YC, Huang YY, Yang SS, Chen PL, Huang CS. Huang MJ, et al. Kaohsiung J Med Sci. 2019 Jul;35(7):432-439. doi: 10.1002/kjm2.12077. Epub 2019 Apr 24. Kaohsiung J Med Sci. 2019. PMID: 31017737 Free article.

Among the 178 patients of Gilbert's syndrome, serum bilirubin value was inversely correlated with UGT1A1 activity (r = -.306, P < .001). The sensitivity was 72.0% and the specificity was 90.5% by using UGT1A1 activity 40% of normal as the cut-off point to disting

Among the 178 patients of Gilbert's syndrome, serum bilirubin value was inversely correlated with UGT1A1 activity (r = -.306, …
Gilbert's syndrome in healthy blood donors what next??
Kulkarni RG, Lakshmidevi KB, Ronghe V, Dinesh US. Kulkarni RG, et al. Asian J Transfus Sci. 2016 Jan-Jun;10(1):63-6. doi: 10.4103/0973-6247.165835. Asian J Transfus Sci. 2016. PMID: 27011673 Free PMC article.
SETTINGS: This study was done in a tertiary care hospital having bed strength of more than 700 beds at SDM Medical College of Medical Sciences and Hospital, Dharwad, located in Northern Karnataka. AIM: The study was done to ascertain prevalence of Gilbert's syndrome …
SETTINGS: This study was done in a tertiary care hospital having bed strength of more than 700 beds at SDM Medical College of Medical Scienc …
Gilbert's syndrome: an overview for clinical biochemists.
Hirschfield GM, Alexander GJ. Hirschfield GM, et al. Ann Clin Biochem. 2006 Sep;43(Pt 5):340-3. doi: 10.1258/000456306778520034. Ann Clin Biochem. 2006. PMID: 17022875 Review.
Gilbert's syndrome (GS) is a benign and inherited state characterized by mild, lifelong, unconjugated hyperbilirubinaemia in the absence of haemolysis or evidence of liver disease. ...
Gilbert's syndrome (GS) is a benign and inherited state characterized by mild, lifelong, unconjugated hyperbilirubinaemia in t
Postoperative hyperbilirubinemia and Gilbert's syndrome in patients undergoing cardiac surgery.
Fernández AL, Baluja A, Al-Hamwy Z, Alvarez J. Fernández AL, et al. Ann Card Anaesth. 2019 Apr-Jun;22(2):207-209. doi: 10.4103/aca.ACA_48_18. Ann Card Anaesth. 2019. PMID: 30971605 Free PMC article.
We report a series of seven patients with Gilbert's syndrome undergoing cardiac surgery. Early and transient increase of total, direct, and indirect bilirubin without other complications was observed. ...
We report a series of seven patients with Gilbert's syndrome undergoing cardiac surgery. Early and transient increase of total …
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