Cargando…

The G6PD flow-cytometric assay is a reliable tool for diagnosis of G6PD deficiency in women and anaemic subjects

Glucose-6-phosphate dehydrogenase (G6PD) activity is essential for redox equilibrium of red blood cells (RBCs) and, when compromised, the RBCs are more susceptible to haemolysis. 8-aminoquinolines (primaquine and tafenoquine) are used for the radical curative treatment of Plasmodium vivax malaria an...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bancone, Germana, Kalnoky, Michael, Chu, Cindy S., Chowwiwat, Nongnud, Kahn, Maria, Malleret, Benoit, Wilaisrisak, Pornpimon, Rénia, Laurent, Domingo, Gonzalo J., Nosten, Francois
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2017
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575121/ https://www.ncbi.nlm.nih.gov/pubmed/28852037 http://dx.doi.org/10.1038/s41598-017-10045-2

Ejemplares similares

Cytochemical flow analysis of intracellular G6PD and aggregate analysis of mosaic G6PD expression
por: Kalnoky, Michael, et al.
Publicado: (2018)

Suitability of Capillary Blood for Quantitative Assessment of G6PD Activity and Performances of G6PD Point-of-Care Tests
por: Bancone, Germana, et al.
Publicado: (2015)

Asian G6PD-Mahidol Reticulocytes Sustain Normal Plasmodium Vivax Development
por: Bancone, Germana, et al.
Publicado: (2017)

Characterization of G6PD Genotypes and Phenotypes on the Northwestern Thailand-Myanmar Border
por: Bancone, Germana, et al.
Publicado: (2014)

Validation of G6PD Point-of-Care Tests among Healthy Volunteers in Yangon, Myanmar
por: Oo, Nwe Nwe, et al.
Publicado: (2016)

Development of a new software tool and analysis method to improve determination of G6PD status
por: Kalnoky, Michael, et al.
Publicado: (2014)

Haemolysis in G6PD Heterozygous Females Treated with Primaquine for Plasmodium vivax Malaria: A Nested Cohort in a Trial of Radical Curative Regimens
por: Chu, Cindy S., et al.
Publicado: (2017)

Primaquine-induced haemolysis in females heterozygous for G6PD deficiency
por: Chu, Cindy S., et al.
Publicado: (2018)

G6PD Variants and Haemolytic Sensitivity to Primaquine and Other Drugs
por: Bancone, Germana, et al.
Publicado: (2021)

Validation of the quantitative point-of-care CareStart biosensor for assessment of G6PD activity in venous blood
por: Bancone, Germana, et al.
Publicado: (2018)

Point-of-Care Testing for G6PD Deficiency: Opportunities for Screening
por: Anderle, Athena, et al.
Publicado: (2018)

Maintaining Specimen Integrity for G6PD Screening by Cytofluorometric Assays
por: Kahn, Maria, et al.
Publicado: (2015)

Single Low Dose Primaquine (0.25mg/kg) Does Not Cause Clinically Significant Haemolysis in G6PD Deficient Subjects
por: Bancone, Germana, et al.
Publicado: (2016)

Methods for the field evaluation of quantitative G6PD diagnostics: a review
por: Ley, Benedikt, et al.
Publicado: (2017)

G6PD testing in support of treatment and elimination of malaria: recommendations for evaluation of G6PD tests
por: Domingo, Gonzalo J, et al.
Publicado: (2013)

Hemolytic Potential of Tafenoquine in Female Volunteers Heterozygous for Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency (G6PD Mahidol Variant) versus G6PD-Normal Volunteers
por: Rueangweerayut, Ronnatrai, et al.
Publicado: (2017)

The impact of using primaquine without prior G6PD testing: a case series describing the obstacles to the medical management of haemolysis
por: Chu, Cindy S., et al.
Publicado: (2019)

No evidence that chloroquine or hydroxychloroquine induce hemolysis in G6PD deficiency()
por: Schilling, William H.K., et al.
Publicado: (2020)

The challenges of introducing routine G6PD testing into radical cure: a workshop report
por: Ley, Benedikt, et al.
Publicado: (2015)

Using G6PD tests to enable the safe treatment of Plasmodium vivax infections with primaquine on the Thailand-Myanmar border: A cost-effectiveness analysis
por: Devine, Angela, et al.
Publicado: (2017)

Establishing a unique specimen repository with characterized G6PD enzyme activity for the development of new G6PD point-of-care tests
por: Kahn, Maria, et al.
Publicado: (2014)

Molecular characterization and mapping of glucose-6-phosphate dehydrogenase (G6PD) mutations in the Greater Mekong Subregion
por: Bancone, Germana, et al.
Publicado: (2019)

Optimizing G6PD testing for Plasmodium vivax case management and beyond: why sex, counseling, and community engagement matter
por: Chu, Cindy S, et al.
Publicado: (2020)

Recombinant human G6PD for quality control and quality assurance of novel point-of-care diagnostics for G6PD deficiency
por: Kahn, Maria, et al.
Publicado: (2017)

Clinical performance validation of the STANDARD G6PD test: A multi-country pooled analysis
por: Adissu, Wondimagegn, et al.
Publicado: (2023)

Repeatability and reproducibility of a handheld quantitative G6PD diagnostic
por: Ley, Benedikt, et al.
Publicado: (2022)

G6PD deficiency in malaria endemic areas of Nepal
por: Marasini, Baburam, et al.
Publicado: (2020)

Diagnostic performances of the fluorescent spot test for G6PD deficiency in newborns along the Thailand-Myanmar border: A cohort study
por: Thielemans, Laurence, et al.
Publicado: (2018)

Evaluation of a Novel Quantitative Test for Glucose-6-Phosphate Dehydrogenase Deficiency: Bringing Quantitative Testing for Glucose-6-Phosphate Dehydrogenase Deficiency Closer to the Patient
por: Pal, Sampa, et al.
Publicado: (2019)

Prevalence of G6PD deficiency and G6PD variants amongst the southern Thai population
por: Nuinoon, Manit, et al.
Publicado: (2022)

High Risk of Severe Anaemia after Chlorproguanil-Dapsone+Artesunate Antimalarial Treatment in Patients with G6PD (A-) Deficiency
por: Fanello, Caterina I., et al.
Publicado: (2008)

Production and differential activity of recombinant human wild-type G6PD and G6PD(Viangchan)
por: Vengidasan, Lelamekala, et al.
Publicado: (2020)

Genotypic and phenotypic characterization of G6PD deficiency in Bengali adults with severe and uncomplicated malaria
por: Plewes, Katherine, et al.
Publicado: (2017)

Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency
por: Boonyawat, Boonchai, et al.
Publicado: (2021)

Prevalence of G6PD Deficiency in Iran
por: Shahjahani, Mohammad, et al.
Publicado: (2013)

Is Hypoglycemia Caused by G6PD Deficiency?
por: Agarwal, Shubham, et al.
Publicado: (2021)

Structural analysis of clinically relevant pathogenic G6PD variants reveals the importance of tetramerization for G6PD activity
por: Cunningham, Anna D, et al.
Publicado: (2017)

Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population
por: Sanephonasa, Amkha, et al.
Publicado: (2021)

Assessment of CareStart G6PD rapid diagnostic test and CareStart G6PD biosensor in Mauritania
por: Djigo, Oum Kelthoum Mamadou, et al.
Publicado: (2021)

Technical evaluation and usability of a quantitative G6PD POC test in cord blood: a mixed-methods study in a low-resource setting
por: Bancone, Germana, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_mddjb7kp2fje955811mpmml0jl