Results 21 to 30 of about 1,401 (195)

Gilbert’s syndrome as a protection against the development of other diseases

Journal of Education, Health and Sport, 2023
Introduction and purpose Gilbert's syndrome is a condition caused by a mutation in the gene responsible for the enzyme UDP-glucuronosyltransferase 1A1, which conjugates bilirubin in hepatocytes.
Dominika Miazga, Alicja Maziarczyk, Laura Surdacka, Monika Blicharz, Diana Bartosik-Zielińska   +4 more
doaj   +1 more source

A Systematic Review of the Safety and Tolerability of Theta Burst Stimulation in Children and Adolescents

Neuromodulation: Technology at the Neural Interface, EarlyView., 2021
Abstract Objectives Theta burst stimulation (TBS) is often used in clinical practice and research protocols for adults with neuropsychiatric disorders. There are substantial knowledge gaps related to the application of TBS in children and adolescents.
Rana Elmaghraby, Qi Sun, Can Ozger, Julia Shekunov, Magdalena Romanowicz, Paul E. Croarkin   +5 more
wiley   +1 more source

Influence of Gilbert's syndrome on the formation of ethyl glucuronide. [PDF]

, 2015
A drinking experiment with participants suffering from Gilbert's syndrome was performed to study the possible influence of this glucuronidation disorder on the formation of ethyl glucuronide (EtG). Gilbert's syndrome is a rather common and, in most cases,
Weinmann, Wolfgang, Gunsilius, Leonie, Lardi, Christelle, Thierauf-Emberger, Annette, Huppertz, Laura M., Huppertz, Laura M   +5 more
core   +1 more source

Gilbert’s syndrome targeted therapy

Zdorovʹe Rebenka, 2017
The article presents the diagnostic criteria and clinical features of Gilbert’s syndrome. The results of clinical studies and observations on the use of ursodeoxycholic acid preparation for targeted therapy of children with Gilbert’s syndrome were ...
O.M. Вabadzhanian, O.V. Shutova, L.G. Voloshyna, O.B. Hanzii, Abbas Kaafarani, O.L. Slobodianiuk   +5 more
doaj   +1 more source

Gilbert’s syndrome in children: Our experience [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2007
Introduction: Gilbert’s syndrome represents the most frequent hereditary disorder of bilirubin metabolism. It occurs in 2-7% of subjects in general population, and is manifested by mild unconjugated hyperbilirubinaemia of benign nature. Objective.
Radlović Nedeljko, Leković Zoran, Mladenović Marija, Ristić Dragana, Radlović Vladimir, Lekić Vojislav, Vuletić Biljana, Đurđević Jelena, Gajić Milan   +8 more
doaj   +1 more source

GALLSTONE DISEASE WITH UNCONJUGATED HYPERBILIRUBINEMIA: CLINICAL APPROACH TO GILBERT’S SYNDROME

Journal of Surgical Sciences, 2019
Gallstones are the commonest ailment affecting the hepato-biliary system. Associated jaundice is usually direct, commonly due to biliary obstructive lesions. Unconjugated hyperbilirubinemia with cholelithiasis is commonly seen with hemolytic disease.
Suneed Kumar, Sneha Jha, Anshuman Pandey, Shibumon M Madhavan, Dinesh Kumar, Smita Chauhan, Shakeel Masood   +6 more
doaj   +1 more source

Association of hereditary elliptocytosis and Gilbert’s syndrome as the cause of biliary calculosis: Case report [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2011
Introduction. Biliary calculosis is rare in children. It occurs associated with different haemolytic and non-haemolytic disorders, which are sometimes also combined. Case Outline.
Radlović Nedeljko, Ristić Dragana, Brdar Radivoj, Janić Nenad, Leković Zoran, Janić Dragana, Smoljanić Željko, Dokmanović Lidija, Jovanović Miodrag   +8 more
doaj   +1 more source

Gilbert’s syndrome - bright and dark sides of the disease - literature review

Journal of Education, Health and Sport
Gilbert’s syndrome is the most common inherited jaundice worldwide. It affects 5-10% of the population. It is caused by a mutation of the UGT1A1 gene, which results in impaired bilirubin metabolism.
Katarzyna Beutler, Jędrzej Lewandowski
doaj   +1 more source

Anesthetic Management of a Patient with Gilbert's Syndrome for Spine Surgery: A Case Report

Journal of Neuroanaesthesiology and Critical Care, 2019
Gilbert's syndrome, a hereditary disorder characterized by mild unconjugated hyperbilirubinemia, poses multiple anesthetic challenges during major surgery.
Bhagya R. Jena, Ankur Khandelwal, Mihir P. Pandia, Gyaninder P. Singh   +3 more
doaj   +1 more source

A systemic review of association between UDP glucuronosyltransferase family 1 member A1 (UGT1A1) polymorphisms in Gilbert's syndrome in Sickle Cell Disease

Journal of Clinical and Scientific Research, 2022
Gilbert's syndrome (GS) is a benign hereditary disorder of bilirubin metabolism due to a mutation in the UDP glucuronosyltransferase family 1 member A1 (UGT1A1) gene which results in hyperbilirubinaemia and related complications mainly cholelithiasis. It
Sanya Sachdeva, Ragini Bodade, Anand Bodade   +2 more
doaj   +1 more source