Results 31 to 40 of about 1,143,701 (190)

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

Gilbert’s syndrome diagnosis in a pregnant woman: a case report

Family Medicine & Primary Care Review
Gilbert’s syndrome is a hereditary disease with raised levels of unconjugated bilirubin. The disorder is generally asymptomatic and often misdiagnosed, which can lead to unnecessary anxiety in patients, particularly during pregnancy.
ELHAM VAFAEI
doaj   +1 more source

Molecular diagnosis of Gilbert's syndrome [PDF]

, 2015
Gilbertov sindrom je autosomno-recesivna bolest karakterizirana povećanim vrijednostima nekonjugiranog bilirubina i predstavlja najčešći nasljedni uzrok povišenog bilirubina.
Karaga, Ana
core   +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

Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler–Najjar syndrome type II [PDF]

, 1998
In our mutation analyses of bilirubin UDP glycosyltransferase (UGT1A1) gene, we encountered six patients with Crigler–Najjar syndrome type II who were double homozygotes for G71R and Y486D, a patient with Gilbert's syndrome who was a single homozygote ...
Yamamoto, Kazuo, Doida, Yukio, Bamba, Tadao, Sato, Hiroshi, Fujiyama, Yoshihide   +4 more
core   +1 more source

Toward Fit‐for‐Purpose Data for Drug Assessment in Non‐small Cell Lung Cancer: A Core Dataset

Clinical Pharmacology &Therapeutics, EarlyView.
Considering the high unmet medical need in people with non‐small cell lung cancer (NSCLC), the drug assessment for targeted therapies often rely on small populations and single‐arm trials, challenging the evaluation by regulatory authorities, health technology assessment bodies (HTAb), and clinicians.
Geeske F. Grit, Maaike van Dartel, Laura Rodwell, Hanneke van der Woude, Cornelis Boersma, Peter G. M. Mol, Doranne Hilarius   +6 more
wiley   +1 more source

The effects of Gilbert's syndrome on the mean platelet volume and other hematological parameters

, 2013
Cure, Medine Cumhur/0000-0001-9253-6459; cure, erkan/0000-0001-7807-135XThe protective effect of increased levels of indirect bilirubin on atherosclerotic heart disease in patients of Gilbert's syndrome is well known.
Cüre, Medine Cumhur, Çiçek, Aysegül Çopur, Kırbaş, Aynur, Yüce, Süleyman, Cüre, Erkan   +4 more
core   +1 more source

Modifiable Transdiagnostic Risk and Protective Factors as Potential CBT Augmentation Targets for Eating Disorders: An Updated Umbrella Review

International Journal of Eating Disorders, EarlyView.
ABSTRACT Objective A focus on transdiagnostic targets is one of the key strategies for developing effective, efficient, and scalable treatments for mental health conditions. We conducted an umbrella review of recent meta‐analyses (August 2022 to May 2026) to update our understanding of critical transdiagnostic intervention targets that could inform ...
Yuan Zhou, Marcela Radunz, Tracey D. Wade   +2 more
wiley   +1 more source

Intractable neonatal jaundice due to hereditary spherocytosis and Gilbert's syndrome

, 2011
In this article the authors present a case of pathological neonatal jaundice resistant to phototherapy in a baby with a family history of Gilbert's syndrome and hereditary spherocytosis.
A. Q. T. Ismail, A. Gandhi, N. El-Shimy, Gandhi, Anjum, Ismail, Abdul Qader Tahir, El-Shimy, Nagui   +5 more
core   +1 more source

Case of parvovirus B19 infection and immunodeficiency in the patient with Gilbert syndrome

Медицинская иммунология, 2021
A case of long-term persistence of parvovirus B19 is described for the first time in a patient with Gilbert's syndrome against the background of immunodeficiency with predominance of infectious symptoms (chronic herpesvirus infection).
A. Yu. Antipova, V. G. Drobyshevskaia, I. V. Khamitova   +2 more
doaj   +1 more source