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Acceptability and feasibility of glucose-6-phosphate dehydrogenase (G6PD) testing using SD Biosensor by village malaria workers in Cambodia: a qualitative study. [PDF]
Cassidy-Seyoum SA +12 more
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Blood Cells, Molecules, and Diseases, 2003
Glucosephosphate isomerase (GPI) deficiency in humans is an autosomal recessive disorder, which results in nonspherocytic hemolytic anemia of variable clinical expression. A 4-year-old female with severe congenital hemolytic anemia had low red cell GPI activity of 15.5 IU/g Hb (50% of normal mean) indicating GPI deficiency.
Julia L, Clarke +9 more
openaire +2 more sources
Glucosephosphate isomerase (GPI) deficiency in humans is an autosomal recessive disorder, which results in nonspherocytic hemolytic anemia of variable clinical expression. A 4-year-old female with severe congenital hemolytic anemia had low red cell GPI activity of 15.5 IU/g Hb (50% of normal mean) indicating GPI deficiency.
Julia L, Clarke +9 more
openaire +2 more sources
Human Genetics, 1981
A severe hemolytic crisis was observed in a 5-year-old boy of Italian origin. Analysis of his hemolysate revealed a hemizygous deficiency of glucose-6-phosphate dehydrogenase (G6PD) and a heterozygous deficiency of glucosephosphate isomerase (GPI). According to the literature this is the fourth family with a combined deficiency of these two enzymes ...
H, Arnold +3 more
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A severe hemolytic crisis was observed in a 5-year-old boy of Italian origin. Analysis of his hemolysate revealed a hemizygous deficiency of glucose-6-phosphate dehydrogenase (G6PD) and a heterozygous deficiency of glucosephosphate isomerase (GPI). According to the literature this is the fourth family with a combined deficiency of these two enzymes ...
H, Arnold +3 more
openaire +2 more sources
British Journal of Haematology, 1971
Summary. A new haemolytic syndrome associated with the combination of genetically determined glucosephosphate isomerase and glucose‐6‐phosphate dehydrogenase deficiency of the erythrocytes was demonstrated in a German family. The propositus (a male), homozygous for the glucosephosphate isomerase deficiency and hemizygous for the glucose‐6‐phosphate ...
W, Schröter +4 more
openaire +2 more sources
Summary. A new haemolytic syndrome associated with the combination of genetically determined glucosephosphate isomerase and glucose‐6‐phosphate dehydrogenase deficiency of the erythrocytes was demonstrated in a German family. The propositus (a male), homozygous for the glucosephosphate isomerase deficiency and hemizygous for the glucose‐6‐phosphate ...
W, Schröter +4 more
openaire +2 more sources
Exhaustion-associated cholesterol deficiency dampens the cytotoxic arm of antitumor immunity
Cancer Cell, 2023Chenqi Xu
exaly
[Glucosephosphate dehydrogenase deficiency and hemotherapy in Brazil].
Revista paulista de medicina, 1985A S, Ramalho +2 more
openaire +1 more source
[Glucosephosphate dehydrogenase deficiency (G6-PD) in Brazilian blood donors].
AMB : revista da Associacao Medica Brasileira, 1978A S, Ramalho, B, Beiguelman
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[Glucosephosphate dehydrogenase deficiency among the population of Tadzhik S.S.R].
Problemy gematologii i perelivaniia krovi, 1982A A, Voronov, G A, Aksianova
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Human dendritic cell deficiency: the missing ID?
Nature Reviews Immunology, 2011Mathew Collin +2 more
exaly

