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Deficiency of glucose-6-phosphate dehydrogenase

Known as: Deficiency, G6PD, Deficiencies, GPD, Deficiency of Glucose 6 Phosphate Dehydrogenase 
An X-linked recessive inherited disorder caused by mutations in the G6PD gene. It is characterized by the absence or presence of very low levels of… 
National Institutes of Health

Related topics

Related topics

36 relations
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Broader (5)

AnemiaAnemia, HemolyticAnemia, Hemolytic, CongenitalInborn Errors of Metabolism

Narrower (1)

Glycogen Storage Disease Type I

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Redox reactions and microbial killing in the neutrophil phagosome.
SIGNIFICANCE When neutrophils kill microorganisms, they ingest them into phagosomes and bombard them with a burst of reactive… 
Review
2003
Review
2003
Micronutrient deficiencies and cognitive functioning.
The relationship between four micronutrient deficiencies (iodine, iron, zinc and vitamin B-12) and children's cognitive… 
Review
1998
Review
1998
Glucose-6-phosphate dehydrogenase deficiency and malaria
Abstract Glucose-6-phosphate dehydrogenase (G6PD) is a cytoplasmic enzyme that is essential for a cell’s capacity to withstand… 
Review
1998
Review
1998
Micronutrients prevent cancer and delay aging.
Highly Cited
1997
Highly Cited
1997
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
Severe jaundice leading to kernicterus or death in the newborn is the most devastating consequence of glucose-6-phosphate… 
Highly Cited
1989
Highly Cited
1989
SYSTEMIC GLUTATHIONE DEFICIENCY IN SYMPTOM-FREE HIV-SEROPOSITIVE INDIVIDUALS
Highly Cited
1985
Highly Cited
1985
The severe and moderate phenotypes of heritable Mac-1, LFA-1 deficiency: their quantitative definition and relation to leukocyte dysfunction and clinical features.
An inherited syndrome characterized by recurrent or progressive necrotic soft-tissue infections, diminished pus formation… 
Highly Cited
1980
Highly Cited
1980
Inherited structural polymorphism of the fourth component of human complement.
Human fourth component of complement (C4) was found to be highly polymorphic by agarose gel electrophoresis of neuraminidase… 
Highly Cited
1972
Highly Cited
1972
Complete deficiency of leukocyte glucose-6-phosphate dehydrogenase with defective bactericidal activity.
A 52 yr old Caucasian female (F. E.) had hemolytic anemia, a leukemoid reaction, and fatal sepsis due to Escherichia coli. Her… 
Review
1970
Review
1970
GLUCOSE‐6‐PHOSPHATE DEHYDROGENASE DEFICIENCY
In the past two decades studies on abnormal haemoglobins have made great strides possible in the understanding of human biology… 
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