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Oncology Drug Dosing in Gilbert Syndrome Associated with UGT1A1: A Summary of the Literature.
Ha VH, Jupp J, Tsang RY. Ha VH, et al. Pharmacotherapy. 2017 Aug;37(8):956-972. doi: 10.1002/phar.1946. Epub 2017 Jun 28. Pharmacotherapy. 2017. PMID: 28494109 Review.
Gilbert syndrome (GS) is a hereditary condition that affects ~10% of the population. It is characterized by intermittent, unconjugated hyperbilirubinemia in the absence of hepatocellular damage and hemolysis. ...
Gilbert syndrome (GS) is a hereditary condition that affects ~10% of the population. It is characterized by intermittent, unco
Associations between Gilbert's syndrome and personality characteristics.
Düzenli T, Maden Ö, Tanoğlu A, Kaplan M, Yazgan Y. Düzenli T, et al. Trends Psychiatry Psychother. 2021 Apr-Jun;43(2):151-158. doi: 10.47626/2237-6089-2020-0003. Epub 2021 Apr 2. Trends Psychiatry Psychother. 2021. PMID: 33844900 Free PMC article.
RESULTS: GS patients had higher scores than healthy controls for disorderliness (NS4) (p = 0.018), sentimentality (RD1) (p = 0.042), and fatigability (HA4) (p = 0.03). Moreover, Gilbert syndrome patients scored lower than controls for empathy (C2) (p = 0.041) and tr …
RESULTS: GS patients had higher scores than healthy controls for disorderliness (NS4) (p = 0.018), sentimentality (RD1) (p = 0.042), and fat …
Clinical and genetic definition of serum bilirubin levels for the diagnosis of Gilbert syndrome and hypobilirubinemia.
Poynard T, Deckmyn O, Peta V, Sakka M, Lebray P, Moussalli J, Pais R, Housset C, Ratziu V, Pasmant E, Thabut D; FibroFrance Group. Poynard T, et al. Hepatol Commun. 2023 Sep 22;7(10):e0245. doi: 10.1097/HC9.0000000000000245. eCollection 2023 Oct 1. Hepatol Commun. 2023. PMID: 37738404 Free PMC article.
BACKGROUND AND AIMS: Gilbert syndrome (GS) is genotypically predetermined by UGT1A1*28 homozygosity in Europeans and is phenotypically defined by hyperbilirubinemia using total bilirubin (TB) cutoff 1mg/dL (17 mumol/L). ...
BACKGROUND AND AIMS: Gilbert syndrome (GS) is genotypically predetermined by UGT1A1*28 homozygosity in Europeans and is phenot …
Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening.
Berrueco R, Alonso-Saladrigues A, Martorell-Sampol L, Català-Temprano A, Ruiz-Llobet A, Toll T, Torrebadell M, Naudó M, Camós M, Rives S. Berrueco R, et al. Pediatr Blood Cancer. 2015 Jul;62(7):1195-201. doi: 10.1002/pbc.25457. Epub 2015 Apr 8. Pediatr Blood Cancer. 2015. PMID: 25855413
Although intensive chemotherapy has improved survival in those patients, important side effects, including hyperbilirubinemia, are frequent. Gilbert syndrome (GS) is a frequent condition that causes a reduction in glucuronidation and intermittent hyperbilirubinemia …
Although intensive chemotherapy has improved survival in those patients, important side effects, including hyperbilirubinemia, are frequent. …
Endothelial Dysfunction and Endocan Levels in Patients with Gilbert Syndrome and Moderate Hyperbilirubinemia.
Zengin O, Sahiner ES, Inan O, Topcuoglu C, Turhan T, Altiparmak E, Yilmaz N, Ates I. Zengin O, et al. Angiology. 2022 Nov-Dec;73(10):920-926. doi: 10.1177/00033197211057692. Epub 2021 Dec 21. Angiology. 2022. PMID: 34933608
In this study, we aim to evaluate the presence of endothelial dysfunction in Gilbert syndrome patients with left ventricular mass index (LVMI) and endocan levels. The study included 60 patients who diagnosed with Gilbert syndrome and 60 healthy control …
In this study, we aim to evaluate the presence of endothelial dysfunction in Gilbert syndrome patients with left ventricular m …
Hereditary Spherocytosis Associated with Gilbert Syndrome Diagnosed with Liver Biopsy Examination and Exome Sequencing.
Zou W, Zhang Z, Tan Y, Zhang L. Zou W, et al. J Coll Physicians Surg Pak. 2020 Feb;30(2):213-215. doi: 10.29271/jcpsp.2020.02.213. J Coll Physicians Surg Pak. 2020. PMID: 32036834
With the help of liver pathological examination and exome sequencing, this patient was finally diagnosed as hereditary spherocytosis combined with Gilbert syndrome....
With the help of liver pathological examination and exome sequencing, this patient was finally diagnosed as hereditary spherocytosis combine …
Scoliosis in a Patient With Gilbert Syndrome: A Case Report and Review of the Literature.
Li Z, Shen J, Liang J. Li Z, et al. Medicine (Baltimore). 2015 Nov;94(47):e2147. doi: 10.1097/MD.0000000000002147. Medicine (Baltimore). 2015. PMID: 26632744 Free PMC article.
Gilbert syndrome (GS) is mainly characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular disease or hemolysis. ...
Gilbert syndrome (GS) is mainly characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular
44 results