61+ results for “G6PD”

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G6PD
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Gene · 107 articles

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G6PD “Hemoglobin SE (HbSE) disease is a rare hemoglobinopathy that may be associated with significant clinical complications despite its traditional characterization as a mild condition, and concomitant glucose-6-phosphate dehydrogenase (G6PD) deficiency can further complicate diagnosis and management.”
glucose-6-phosphate dehydrogenase deficiency “Pregnancy-Triggered Vaso-Occlusive Crises in Hemoglobin SE Disease Complicated by Glucose-6-Phosphate Dehydrogenase Deficiency: A Case Report.”
Matches:
G6PD “Neonatal Screening for Glucose-6-Phosphate Dehydrogenase (G6PD) Gene Variants and Their Association With Hyperbilirubinemia and Phototherapy Needs.”
glucose-6-phosphate dehydrogenase deficiency “METHODS: We conducted a retrospective cohort study of neonates diagnosed with G6PD deficiency between January 2021 and December 2023.”
Matches:
G6PD “Spectrum of glucose-6-phosphate dehydrogenase (G6PD) mutations and trends in hemoglobin levels among adult dengue patients in Thailand.”
glucose-6-phosphate dehydrogenase deficiency “G6PD deficiency was identified in 24 individuals (10.4%), while G6PD mutations were detected in 111 patients (48.1%).”
Matches:
G6PD “Glucose-6-phosphate dehydrogenase (G6PD) is an enzyme that protects red blood cells, and its deficiency can cause hemolytic anemia when triggered by certain factors.”
glucose-6-phosphate dehydrogenase deficiency “Glucose-6-Phosphate Dehydrogenase Deficiency Presenting as Atypical Hemolytic Uremic Syndrome: A Case Series and Literature Review.”
Matches:
G6PD “Functional assays, including cell proliferation, cell cycle analysis, ROS measurement, glycolysis assessment, and G6PD activity, were performed to evaluate the effects of KDM1A inhibition.”
KDM1A “KDM1A Facilitates Oncogenic Potential in Colorectal Cancer Progression Through the Activation of AXIN/GSK3β/β-Catenin Signaling Pathways: Evidence From Integrated Transcriptomics and In Vitro Studies.”
Matches:
G6PD “Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, predisposing individuals to acute hemolytic anemia upon oxidative stress.”
glucose-6-phosphate dehydrogenase deficiency “A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.”
Matches:
G6PD “Public Knowledge, Attitudes, and Preventive Practices Toward G6PD Deficiency in Al-Kharj, Saudi Arabia: A Community-Based Cross-Sectional Study.”
glucose-6-phosphate dehydrogenase deficiency “Public Knowledge, Attitudes, and Preventive Practices Toward G6PD Deficiency in Al-Kharj, Saudi Arabia: A Community-Based Cross-Sectional Study.”
Matches:
G6PD “BackgroundGlucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic enzymatic disorder that affects millions of people worldwide and characterized by hemolysis under oxidative stress.”
glucose-6-phosphate dehydrogenase deficiency “Heartmate 3 left ventricular assist device system in patients with glucose-6-phosphate dehydrogenase deficiency.”
Matches:
G6PD “OBJECTIVE: To characterise quantitative glucose-6-phosphate dehydrogenase (G6PD) activity in term and preterm neonates, compare activity by gestational age (GA) and sex and derive neonatal screening cut-offs using percentile and WHO methods.”
Saudi Arabia, Riyadh “Neonatal glucose-6-phosphate dehydrogenase activity by gestational age and sex: evidence-based cut-offs for newborn screening in Saudi Arabia. SETTING: King Abdulaziz Medical City, Riyadh, Saudi Arabia, January 2016 to May 2022. Using the neonatal cut-off, prevalence rose to 4.97% (2888/58 139), adding 1725 infants (+583 males, +1142 females) and reducing the male share to 52.8%.”
Matches:
G6PD “Genetic analysis and molecular basis of G6PD deficiency among malaria patients in Thailand: implications for safe use of 8-aminoquinolines.”
malaria “Genetic analysis and molecular basis of G6PD deficiency among malaria patients in Thailand: implications for safe use of 8-aminoquinolines.”

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