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Article

Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GPI) deficiency

17 Nov 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9856489
DOI: 10.1007/s004390050849

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GPI) deficiencyPMID 9856489Read ↗

Glucose-6-phosphate isomerase deficiency.Semantic proximity Read ↗

Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular studySemantic proximity Read ↗

A Novel Mutation of Glucose Phosphate Isomerase (GPI) Causing Severe Neonatal Anemia Due to GPI DeficiencySemantic proximity Read ↗

Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological DysfunctionSemantic proximity Read ↗

Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.Semantic proximity Read ↗

Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcome.Semantic proximity Read ↗

Hematologically important mutations: molecular abnormalities of glucose phosphate isomerase deficiency.Semantic proximity Read ↗

Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle DynamicsSemantic proximity Read ↗

Hematologic and systemic metabolic alterations due to Mediterranean type II G6PD deficiency in miceSemantic proximity Read ↗

Glucose-6-phosphate dehydrogenase--from oxidative stress to cellular functions and degenerative diseases.Semantic proximity Read ↗

Gene symbol: G6PD. Disease: Glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

Glycosyl phosphatidylinositol (GPI)-anchored molecules and the pathogenesis of paroxysmal nocturnal hemoglobinuriaSemantic proximity Read ↗

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