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Sub-Saharan red cell antigen phenotypes and glucose-6-phosphate dehydrogenase deficiency variants in French GuianaRapid screening for glucose-6-phosphate dehydrogenase deficiency and haemoglobin polymorphisms in Africa by a simple high-throughput SSOP-ELISA methodThe anaemia of Plasmodium vivax malariaInherited glutathione reductase deficiency and Plasmodium falciparum malaria--a case studyHeterogeneity of G6PD deficiency prevalence in Mozambique: a school-based cross-sectional survey in three different regionsRed blood cell dysfunction in septic glucose-6-phosphate dehydrogenase-deficient miceGlucose-6-phosphate dehydrogenase deficiency and risk of diabetes: a systematic review and meta-analysis.An unusual syncope cause in the ED: favism.The molecular basis of disorders of red cell enzymesUsing nitrofurantoin while breastfeeding a newborn.Performance of the CareStart glucose-6-phosphate dehydrogenase (G6PD) rapid diagnostic test in Gressier, Haiti.Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi Arabia.Performance of the CareStart™ G6PD deficiency screening test, a point-of-care diagnostic for primaquine therapy screeningEthical and legal implications of pharmacogenomics.The association between malaria parasitaemia, erythrocyte polymorphisms, malnutrition and anaemia in children less than 10 years in Senegal: a case control studyGenetic determinants of glucose-6-phosphate dehydrogenase activity in KenyaCase Report: Paroxysmal nocturnal hemoglobinuria in a woman heterozygous for G6PD A-.Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency at the China-Myanmar BorderPrevalence and distribution of glucose-6-phosphate dehydrogenase (G6PD) variants in Thai and Burmese populations in malaria endemic areas of Thailand.A novel cytofluorometric assay for the detection and quantification of glucose-6-phosphate dehydrogenase deficiency.Risks of Hemolysis in Glucose-6-Phosphate Dehydrogenase Deficient Infants Exposed to Chlorproguanil-Dapsone, Mefloquine and Sulfadoxine-Pyrimethamine as Part of Intermittent Presumptive Treatment of Malaria in InfantsGlucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario.G6PD Deficiency Does Not Enhance Susceptibility for Acquiring Helicobacter pylori Infection in Sardinian Patients.An optimised age-based dosing regimen for single low-dose primaquine for blocking malaria transmission in CambodiaMolecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Families from the Republic of Macedonia and Genotype-phenotype Correlation.Heterogeneous alleles comprising G6PD deficiency trait in West Africa exert contrasting effects on two major clinical presentations of severe malaria.A multiplex method for detection of glucose-6-phosphate dehydrogenase (G6PD) gene mutations.Glucose-6-phosphate dehydrogenase deficiency among Yemeni children residing in malaria-endemic areas of Hodeidah governorate and evaluation of a rapid diagnostic test for its detectionRed blood cell polymorphism and susceptibility to Plasmodium vivax.Pediatric Provider Insight Into Newborn Screening for Glucose-6-Phosphate Dehydrogenase DeficiencyPrevalence of G6PD deficiency and Plasmodium falciparum parasites in asymptomatic school children living in southern Ghana.Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.Humanized mouse model of glucose 6-phosphate dehydrogenase deficiency for in vivo assessment of hemolytic toxicitySpatial distribution of G6PD deficiency variants across malaria-endemic regions.Glucose-6-phosphate dehydrogenase deficiency and malaria: cytochemical detection of heterozygous G6PD deficiency in women.Comparison of molecular mutations of G6PD deficiency gene between icteric and nonicteric neonates.Next generation sequencing (NGS) in glucose-6-phosphate dehydrogenase (G6PD) deficiency studies.Hemolyzed specimens: a major challenge for emergency departments and clinical laboratories.Should we screen newborns for glucose-6-phosphate dehydrogenase deficiency in the United States?Subversion of Schwann Cell Glucose Metabolism by Mycobacterium leprae
P2860
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P2860
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
G6PD: population genetics and clinical manifestations.
@en
type
label
G6PD: population genetics and clinical manifestations.
@en
prefLabel
G6PD: population genetics and clinical manifestations.
@en
P1433
P1476
G6PD: population genetics and clinical manifestations.
@en
P2093
P356
10.1016/S0268-960X(96)90019-3
P577
1996-03-01T00:00:00Z