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

Year Number of Results
1972 2
1973 1
1975 2
1976 6
1977 1
1978 2
1979 3
1980 4
1982 1
1983 4
1984 5
1985 2
1986 4
1987 4
1988 3
1989 6
1990 6
1991 6
1992 9
1993 10
1994 8
1995 10
1996 14
1997 11
1998 15
1999 10
2000 16
2001 12
2002 24
2003 15
2004 20
2005 23
2006 24
2007 28
2008 31
2009 26
2010 19
2011 18
2012 30
2013 28
2014 39
2015 53
2016 42
2017 50
2018 43
2019 39
2020 42
2021 37
2022 32
2023 48
2024 20

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819 results

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Page 1
Gilbert's syndrome revisited.
Vítek L, Tiribelli C. Vítek L, et al. J Hepatol. 2023 Oct;79(4):1049-1055. doi: 10.1016/j.jhep.2023.06.004. Epub 2023 Jun 28. J Hepatol. 2023. PMID: 37390966 Review.
Gilbert's syndrome, also known as benign hyperbilirubinaemia, was described more than 100 years ago. It has usually been considered a physiological abnormality characterised by a mild elevation of the systemic level of unconjugated bilirubin, in the absence of any u
Gilbert's syndrome, also known as benign hyperbilirubinaemia, was described more than 100 years ago. It has usually been consi
Alagille Syndrome: A Focused Review on Clinical Features, Genetics, and Treatment.
Kohut TJ, Gilbert MA, Loomes KM. Kohut TJ, et al. Semin Liver Dis. 2021 Nov;41(4):525-537. doi: 10.1055/s-0041-1730951. Epub 2021 Jul 2. Semin Liver Dis. 2021. PMID: 34215014 Review.
Alagille syndrome (ALGS) is an autosomal dominant disorder caused by pathogenic variants in JAG1 or NOTCH2, which encode fundamental components of the Notch signaling pathway. ...Medical management is supportive, focusing on clinical manifestations of disease, with …
Alagille syndrome (ALGS) is an autosomal dominant disorder caused by pathogenic variants in JAG1 or NOTCH2, which encode fundamental …
Evaluation of Jaundice in Adults.
Fargo MV, Grogan SP, Saguil A. Fargo MV, et al. Am Fam Physician. 2017 Feb 1;95(3):164-168. Am Fam Physician. 2017. PMID: 28145671 Free article. Review.
Jaundice in adults can be an indicator of significant underlying disease. It is caused by elevated serum bilirubin levels in the unconjugated or conjugated form. ...Unconjugated hyperbilirubinemia occurs with increased bilirubin production caused by red blood cell destruct …
Jaundice in adults can be an indicator of significant underlying disease. It is caused by elevated serum bilirubin levels in the unco …
Gilbert syndrome.
Fretzayas A, Moustaki M, Liapi O, Karpathios T. Fretzayas A, et al. Eur J Pediatr. 2012 Jan;171(1):11-5. doi: 10.1007/s00431-011-1641-0. Epub 2011 Dec 9. Eur J Pediatr. 2012. PMID: 22160004 Review.
Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular disease or hemolysis. In patients with Gilbert syndrom
Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermitt
Current understanding of the human microbiome.
Gilbert JA, Blaser MJ, Caporaso JG, Jansson JK, Lynch SV, Knight R. Gilbert JA, et al. Nat Med. 2018 Apr 10;24(4):392-400. doi: 10.1038/nm.4517. Nat Med. 2018. PMID: 29634682 Free PMC article. Review.
Our understanding of the link between the human microbiome and disease, including obesity, inflammatory bowel disease, arthritis and autism, is rapidly expanding. ...
Our understanding of the link between the human microbiome and disease, including obesity, inflammatory bowel disease, arthrit …
Inherited disorders of bilirubin clearance.
Memon N, Weinberger BI, Hegyi T, Aleksunes LM. Memon N, et al. Pediatr Res. 2016 Mar;79(3):378-86. doi: 10.1038/pr.2015.247. Epub 2015 Nov 23. Pediatr Res. 2016. PMID: 26595536 Free PMC article. Review.
Reduced hepatic bilirubin clearance can be due to defective (i) unconjugated bilirubin uptake and intrahepatic storage, (ii) conjugation of glucuronic acid to bilirubin (e.g., Gilbert syndrome, Crigler-Najjar syndrome, Lucey-Driscoll syndrome, breast m …
Reduced hepatic bilirubin clearance can be due to defective (i) unconjugated bilirubin uptake and intrahepatic storage, (ii) conjugation of …
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-bili …
Diagnoses can include conditions of disordered bilirubin metabolism (Gilbert's, Crigler-Najjar, Rotor, or Dubin-Johnson syndromes) or …
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.
Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome).
Strassburg CP. Strassburg CP. Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):555-71. doi: 10.1016/j.bpg.2010.07.007. Best Pract Res Clin Gastroenterol. 2010. PMID: 20955959 Review.
Dubin-Johnson and Rotor syndromes are rare, exhibit mixed direct and indirect hyperbilirubinemia as well as typical profiles or urinary coproporphyrin excretion. Gilbert-Meulengracht disease leads to unconjugated hyperbilirubinemia because of impaired glucuronidatio …
Dubin-Johnson and Rotor syndromes are rare, exhibit mixed direct and indirect hyperbilirubinemia as well as typical profiles or urinary copr …
A new era in functional genomics screens.
Przybyla L, Gilbert LA. Przybyla L, et al. Nat Rev Genet. 2022 Feb;23(2):89-103. doi: 10.1038/s41576-021-00409-w. Epub 2021 Sep 20. Nat Rev Genet. 2022. PMID: 34545248 Review.
Despite this, the function of many genes and gene regulatory elements remains poorly characterized, which limits our ability to apply these insights to human disease. The advent of new CRISPR functional genomics tools allows for scalable and multiplexable characterization …
Despite this, the function of many genes and gene regulatory elements remains poorly characterized, which limits our ability to apply these …
819 results