Associated Papers
Glucose-6-phosphate Dehydrogenase Variants: Analysing in Indian Plasmodium vivax Patients.
Jakhan J et al.
Acta Parasitologica, 2024
Genetic analysis and molecular basis of G6PD deficiency among malaria patients in Thailand: implications for safe use of 8-aminoquinolines.
Boonyuen U et al.
Malaria Journal, 2024
Molecular epidemiological characteristics, variant spectrum and genotype-phenotype correlation of glucose-6-phosphate dehydrogenase deficiency in China: A population-based multicenter study using newborn screening.
Tan M et al.
Plos One, 2024
Molecular Characterization of Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency in Different Ethnic Groups of Blood Donors in Mauritania.
Taleb M et al.
Frontiers in Bioscience (scholar Edition), 2023
An Overall View of the Functional and Structural Characterization of Glucose-6-Phosphate Dehydrogenase Variants in the Mexican Population.
Hernández-Ochoa B et al.
International Journal of Molecular Sciences, 2023
Prevalence and molecular analysis of glucose-6-phosphate dehydrogenase deficiency in Chin State, Myanmar.
Aung JM et al.
Parasites, Hosts and Diseases, 2023
Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Portuguese Population.
Manco L et al.
Acta Medica Portuguesa, 2023
Cut-off values for diagnosis of G6PD deficiency by flow cytometry in Thai population.
Thedsawad A et al.
Annals of Hematology, 2022
Prevalence of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency among Malaria Patients in Southern Thailand: 8 Years Retrospective Study.
Khammanee T et al.
The Korean Journal of Parasitology, 2022
Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity.
Lee HY et al.
Frontiers in Pediatrics, 2022
Distribution of G6PD deficiency genotypes among Southeast Asian populations.
Tantular IS et al.
Tropical Medicine and Health, 2021
G6PD deficiency in blood donors of Manaus, Amazon Region, northern Brazil.
Ferreira NS et al.
International Journal of Laboratory Hematology, 2021
Molecular Epidemiology of G6PD Genotypes in Different Ethnic Groups Residing in Saharan and Sahelian Zones of Mauritania.
Djigo OKM et al.
Pathogens (basel, Switzerland), 2021
Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population.
Sanephonasa A et al.
Malaria Journal, 2021
Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation.
Alina MF et al.
Journal of Human Genetics, 2020
Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies.
Robinson KM et al.
The Pharmacogenomics Journal, 2019
Glucose-6-phosphate dehydrogenase (G6PD) deficiency in Ethiopia: absence of common African and Mediterranean allelic variants in a nationwide study.
Assefa A et al.
Malaria Journal, 2018
Prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency among malaria patients in Upper Myanmar.
Lee J et al.
Bmc Infectious Diseases, 2018
Glucose-6-phosphate dehydrogenase (G6PD)-deficient infants: Enzyme activity and gene variants as risk factors for phototherapy in the first week of life.
Wong FL et al.
Journal of Paediatrics and Child Health, 2017
G6PD deficiency alleles in a malaria-endemic region in the Western Brazilian Amazon.
Dombrowski JG et al.
Malaria Journal, 2017
Genetic Epidemiology of Glucose-6-Phosphate Dehydrogenase Deficiency in the Arab World.
Doss CG et al.
Scientific Reports, 2016
Analysis of protein-coding genetic variation in 60,706 humans.
Lek M et al.
Nature, 2016
Prevalence and molecular characterization of G6PD deficiency in two Plasmodium vivax endemic areas in Venezuela: predominance of the African A-(202A/376G) variant.
Vizzi E et al.
Malaria Journal, 2016
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome.
Minucci A et al.
Pediatric Blood & Cancer, 2015
G6PD deficiency in Latin America: systematic review on prevalence and variants.
Monteiro WM et al.
Memorias Do Instituto Oswaldo Cruz, 2014
Glucose-6-phosphate dehydrogenase deficiency in Italian blood donors: prevalence and molecular defect characterization.
Maffi D et al.
Vox Sanguinis, 2014
Study of a family in the province of Matera presenting with glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome.
Dell'edera D et al.
Molecular Medicine Reports, 2012
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi Arabia.
Al-Jaouni SK et al.
Bmc Research Notes, 2011
Modification to reporting of qualitative fluorescent spot test results improves detection of glucose-6-phosphate dehydrogenase (G6PD)-deficient heterozygote female newborns.
Nadarajan V et al.
International Journal of Laboratory Hematology, 2011
Incidence and mutation analysis of glucose-6-phosphate dehydrogenase deficiency in eastern Indonesian populations.
Tantular IS et al.
Acta Medica Okayama, 2010
Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern Iraq.
Al-Allawi N et al.
Bmc Blood Disorders, 2010
The need for neonatal glucose-6-phosphate dehydrogenase screening: a global perspective.
Kaplan M et al.
Journal of Perinatology : Official Journal of the California Perinatal Association, 2009
Glucose-6-phosphate dehydrogenase mutations in Mon and Burmese of southern Myanmar.
Nuchprayoon I et al.
Journal of Human Genetics, 2008
Glucose-6-phosphate dehydrogenase variants associated with favism in Thai children.
Laosombat V et al.
International Journal of Hematology, 2006
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Fars province of Iran.
Karimi M et al.
Haematologica, 2003
Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency.
Pietrapertosa A et al.
Haematologica, 2001
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency in south-east Sicily.
Cittadella R et al.
Annals of Human Genetics, 1997
Molecular characterization of G6PD deficiency in Cyprus.
Drousiotou A et al.
Blood Cells, Molecules & Diseases, 0
Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind).
Laosombat V et al.
Blood Cells, Molecules & Diseases, 0
Glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome: a gene interaction underlies severe jaundice without severe hemolysis.
Nicolaidou P et al.
Pediatric Hematology and Oncology, 0
Molecular and biochemical data on some glucose-6-phosphate dehydrogenase variants from southern Sardinia.
Frigerio R et al.
Haematologica, 0
Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy.
Martinez di Montemuros F et al.
Haematologica, 0