Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Glucose-6-phosphate dehydrogenase deficiency and hereditary hemolytic anemia].

Annali dell'Istituto superiore di sanita - 1 Jan 1999

Salvati A M, Maffi D, Caprari P, Pasquino M T, Caforio M P, Tarzia A

Abstract excerpt

G6PD deficiency is the most common enzymopathy in the world. The highest frequency values are found in tropical Africa, in the Middle East, in some areas of the Mediterranean, in tropical and sub-tropical Asia and in Oceania. This genetic defect shows sex linked inheritance and a marked heterogeneity. At least 400 abnormal variants with different biochemical characteristics and about 100 diverse mutations have...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anemia, Hemolytic, Congenital
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 10645652

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Glucose-6-phosphate dehydrogenase deficiency and hereditary hemolytic anemia].PMID 10645652Read ↗

Glucose-6-phosphate dehydrogenase deficiencySemantic proximity Read ↗

[Glucose 6-phosphate dehydrogenase deficiency: a protection against malaria and a risk for hemolytic accidents].Semantic proximity Read ↗

Glucose-6-Phosphate Dehydrogenase Deficiency.Semantic proximity Read ↗

[Glucose-6-phosphate dehydrogenase].Semantic proximity Read ↗

Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classificationSemantic proximity Read ↗

Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.Semantic proximity Read ↗

G6PD deficiency: the genotype-phenotype association.Semantic proximity Read ↗

[Hereditary enzyme defects of erythrocytes: glucose-6-phosphate dehydrogenase deficiency and pyruvate kinase deficiency].Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency: correlation between the genotype, biochemistry and phenotype.Semantic proximity Read ↗

Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: description of seven new G6PD mutants.Semantic proximity Read ↗

Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

G6PD deficiency: global distribution, genetic variants and primaquine therapy.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.