Results 41 to 50 of about 1,019,197 (220)
Glucose-6-phosphate dehydrogenase (G6PD) Deficiency [PDF]
Iranian Journal of Public Health, 2008 Glucose-6-phosphate dehydrogenase (G6PD) Deficiency is the most prevalent enzymopathy in mankind. It has sex-linked inheritance. This enzyme exists in all cells. G6PD deficiency increases the sensitivity of red blood cells to oxidative damage.
DD Farhud , L Yazdanpanah
doaj +1 more source
Impact of the method of G6PD deficiency assessment on genetic association studies of malaria susceptibility. [PDF]
PLoS ONE, 2009 BACKGROUND:Clinical association studies have yielded varied results regarding the impact of glucose-6-phosphate dehydrogenase (G6PD) deficiency upon susceptibility to malaria.
Marla K Johnson +4 more
doaj +1 more source
G6PD diaxBox: Digital image-based quantification of G6PD deficiency
Talanta, 2021 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy in humans. More than 400 million people worldwide are affected by this genetic condition. Testing for G6PD deficiency before drug administration is essential for patient safety. Rapidly ascertaining the G6PD status of a person is desirable for proper treatment.
Duangdao Palasuwan +5 more
openaire +2 more sources
Medical Journal of Australia, 2020 The cure of patients with Plasmodium vivax malaria requires killing both the asexual stages of the parasites in the blood as well as the dormant liver stages (hypnozoites) — together known as radical cure.
R. Commons, J. McCarthy, R. Price
semanticscholar +1 more source
Angewandte Chemie, EarlyView.An efficient radiosynthesis of fluorine‐18 labeled gluconic acid ([18F]FGA) was developed using two readily available materials, 2‐deoxy‐2‐[18F]fluoro‐D‐glucose ([18F]FDG) and glucose oxidase. [18F]FGA is highly specific for bacterial gluconate metabolism mediated by gluconate permease (GntP) and gluconate kinase (GntK), with rapid clearance, low off ...
Sang Hee Lee +7 more
wiley +2 more sources
Qatar Medical Journal, 2004 G6PD deficiency is the most common enzyme deficiency disease worldwide, affecting 10% of the world's population. It is an X linked recessive disease therefore it affects males more than females (females are usually carriers of the disease).
A. Al Muzrakchi, A. A. Gehani
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Heliyon, 2023 Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder caused by a structural abnormality in the enzyme. G6PD deficiency is most prevalent among African, Asian, and Mediterranean people.
Woldeteklehaymanot Kassahun +3 more
doaj +1 more source
G6PD deficiency triggers dopamine loss and the initiation of Parkinson's disease pathogenesis.
Cell ReportsLoss of dopaminergic neurons in Parkinson's disease (PD) is preceded by loss of synaptic dopamine (DA) and accumulation of proteinaceous aggregates. Linking these deficits is critical to restoring DA signaling in PD.
Morgan G. Stykel +17 more
semanticscholar +1 more source
Laboratory diagnosis of G6PD deficiency. A British Society for Haematology Guideline
British Journal of Haematology, 2020 In addition to the authors’ comprehensive databases, a specific literature review was conducted on 18th April 2017 on the following databases: MEDLINE (OVID), EMBASE (OVID), CENTRAL (The Cochrane library) and Web of Science (SCI-Expanded, CPCI-S) using ...
D. Roper +6 more
semanticscholar +1 more source
Liver Failure in Neonates With G6PD Deficiency
ACG Case Reports Journal, 2022 ABSTRACT Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a commonly inherited enzyme defect that can present with hemolysis, hyperbilirubinemia, and jaundice and may cause kidney and liver dysfunction. G6PD deficiency may serve as a cofactor for chronic liver disease; however, an association with liver failure is not well described. We
Milaan Shah, Vani Gopalareddy
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