Results 21 to 30 of about 1,143,701 (190)

Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study

open access: yesHepatology, EarlyView., 2022
Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel   +93 more
wiley   +1 more source

JILBER’S SYNDROME: CLINICAL AND PHARMACOLOGICAL ASPECTS. Review

open access: yesМедична наука України, 2020
Relevance. At present, the metabolism of drugs in patients with Gilbert's syndrome will be actively studied, as it may be associated with both the risk of dose-dependent adverse reactions and treatment ineffectiveness.
M.V. Khaitovych, D.V. Turchak
doaj   +1 more source

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

open access: yesJournal 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   +4 more
doaj   +1 more source

Gilbert’s syndrome targeted therapy

open access: yesZdorovʹe 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   +5 more
doaj   +1 more source

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

open access: yesNeuromodulation: 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   +5 more
wiley   +1 more source

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

open access: yes, 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   +5 more
core   +2 more sources

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

open access: yesSrpski 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   +8 more
doaj   +1 more source

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

open access: yesJournal 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   +6 more
doaj   +1 more source

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

open access: yesSrpski 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   +8 more
doaj   +1 more source

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

open access: yesJournal 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

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