Results 191 to 200 of about 7,778 (203)

Diet Challenge in G6PD Deficient Egyptian Children: A One- Year Prospective Single Center Study with Genotype - Phenotype Correlation

Blood, 2015
Abstract Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is prevalent and add a burden on families in Egypt and Middle East due to lifelong diet restriction. Non-fava beans diet is the main food for most families in the region and parents and doctors consider it as a prohibited food whatever the genetic or
Mohsen Saleh ElAlfy
exaly   +2 more sources

Rapid and simple identification of the commonest glucose-6-phosphate dehydrogenase (G6PD) Italian mutations: From DNA extraction to genotyping

Clinica Chimica Acta, 2012
No ...
Minucci, Angelo, Gentile, Luigia, Zuppi, Cecilia, Giardina, Bruno, Capoluongo, Ettore Domenico   +4 more
openaire   +3 more sources

Screening and the analysis of genotypic and phenotypic characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Fujian province, China

Frontiers in Genetics
IntroductionGlucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked hereditary disorder in southern China. However, the incidence rate of G6PD deficiency and the frequency of the most common G6PD gene variants vary widely. The purpose of this study was to investigate the prevalence, genotype, and phenotypic features of G6PD deficiency ...
Jinfu Zhou, Yinglin Zeng, Jianping Tang, Shihong Chen, Guilin Li, Xiaolong Qiu, Peiran Zhao, Ting Huang, Jinying Luo, Na Lin, Liangpu Xu   +10 more
exaly   +4 more sources

Co‐inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler–Najjar type II syndrome

Pediatric Blood & Cancer, 2015
NO ABSTRACT ...
Minucci, Angelo, Ruggiero, Antonio, Canu, Giulia, Maurizi, Palma, De Bonis, Maria, Concolino, Paola, De Luca, Daniele, Capoluongo, Ettore Domenico   +7 more
openaire   +2 more sources

Diagnosis of red cell G6PD deficiency in rural Burkina Faso. Comparison of a rapid fluorescent enzyme test on filter paper with polymerase chain reaction based genotyping

British Journal of Haematology, 2005
SummaryGlucose‐6‐phosphate dehydrogenase (G6PD) deficient individuals are at increased risk of developing haemolysis following treatment with various antimalarial drugs. Reliable field tests for G6PD deficiency are thus needed in chemotherapy studies and their validity has to be assessed.
Peter E, Meissner, Boubacar, Coulibaly, Germain, Mandi, Ulrich, Mansmann, Steffen, Witte, Wolfgang, Schiek, Olaf, Müller, R Heiner, Schirmer, Frank P, Mockenhaupt, Ulrich, Bienzle   +9 more
openaire   +2 more sources

Glucose-6-phosphate dehydrogenase (G6PD) deficiency phenotype and genotype profile in Kodi Sub-district, West Sumba, Indonesia

2017
Primaquine is the only drug licensed for prevention of relapse in vivax and ovale malarias. It causes mild to severe hemolysis when administered to patients with G6PD deficiency. Because current methods for identifying these patients are not well-suited to care in malaria endemic areas like those in Indonesia, most patients do not receive anti-relapse ...
openaire   +1 more source

Simultaneous detection of G6PD mutations using SNPscan in a multiethnic minority area of Southwestern China

Frontiers in Genetics, 2023
Min Lin
exaly  

Analysis of genotype distribution of thalassemia and G6PD deficiency among Hakka population in Meizhou city of Guangdong Province

Journal of Clinical Laboratory Analysis, 2020
Heming Wu, Hua Zhong
exaly  

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017

Human Mutation, 2020
Jingkun Miao, Xiaoli Shu, Lu Qing
exaly  

Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies

Pharmacogenomics Journal, 2018
Wenjian Yang, Cyrine E Haidar, Jane S Hankins   +2 more
exaly