Results 41 to 50 of about 23,995 (263)

Plasmodium falciparum clearance with artemisinin-based combination therapy (ACT) in patients with glucose-6-phosphate dehydrogenase deficiency in Mali [PDF]

open access: yes, 2010
URL : http://www.malariajournal.com/content/9/1/332Background: Artemisinin-based combination therapy (ACT) is currently the most effective medicine for the treatment of uncomplicated malaria.
Abdoulaye K Kone   +9 more
core   +2 more sources

To determine the prevalence of glucose-6-phosphate dehydrogenase deficiency using a novel water-soluble tetrazolium-8 formazan method' for neonatal screening in region of Himachal Pradesh, India

open access: yesAdvances in Human Biology, 2019
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most significant enzyme defect in India with an incidence ranging from 2% to 27.9% in different communities.
Seema Sharma, Milap Sharma
doaj   +1 more source

Prospective evaluation of BDProbeTec strand displacement amplification (SDA) system for diagnosis of tuberculosis in non-respiratory and respiratory samples. [PDF]

open access: yes, 2004
Nucleic acid amplification techniques (NAATs) have been demonstrated to make significant improvements in the diagnosis of tuberculosis (TB), particularly in the time to diagnosis and the diagnosis of smear-negative TB. The BD ProbeTec strand displacement
Billington, OJ   +7 more
core   +2 more sources

Impact of the method of G6PD deficiency assessment on genetic association studies of malaria susceptibility. [PDF]

open access: yesPLoS ONE, 2009
BACKGROUND:Clinical association studies have yielded varied results regarding the impact of glucose-6-phosphate dehydrogenase (G6PD) deficiency upon susceptibility to malaria.
Marla K Johnson   +4 more
doaj   +1 more source

G6PD Deficiency

open access: yesQatar Medical Journal, 2004
G6PD deficiency is the most common enzyme deficiency disease worldwide, affecting 10% of the world's population. It is an X linked recessive disease therefore it affects males more than females (females are usually carriers of the disease).
A. Al Muzrakchi, A. A. Gehani
openaire   +1 more source

Glucose-6-phosphate dehydrogenase deficiency among neonates with jaundice in Africa; systematic review and meta-analysis

open access: yesHeliyon, 2023
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder caused by a structural abnormality in the enzyme. G6PD deficiency is most prevalent among African, Asian, and Mediterranean people.
Woldeteklehaymanot Kassahun   +3 more
doaj   +1 more source

G6PD deficiency does not enhance susceptibility for acquiring Helicobacter pylori infection in Sardinian patients [PDF]

open access: yes, 2016
Background: Subjects with glucose-6-phosphate dehydrogenase (G6PD) deficiency may be more susceptible to infections due to impaired leukocyte bactericidal activity. The disorder is common in the Mediterranean area.
Dore, Maria Pina   +4 more
core   +2 more sources

Human G6PD variant structural studies: Elucidating the molecular basis of human G6PD deficiency [PDF]

open access: yes, 2022
Glucose-6-phosphate dehydrogenase deficiency is by far the most prevalent human enzymopathy and is gener ated by a series of point mutations in the X-linked gene encoding G6PD.
Ab Latif, Nurriza   +7 more
core   +1 more source

Risk of pneumococcal bacteremia in Kenyan children with glucose-6-phosphate dehydrogenase deficiency

open access: yesBMC Medicine, 2020
Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency state in humans. The clinical phenotype is variable and includes asymptomatic individuals, episodic hemolysis induced by oxidative stress, and chronic ...
James J. Gilchrist   +10 more
doaj   +1 more source

Effect of neonatal reticulocytosis on glucose 6-phosphate dehydrogenase (G6PD) activity and G6PD deficiency detection: a cross-sectional study

open access: yesBMC Pediatrics, 2022
Background Screening for G6PD deficiency in newborns can help prevent severe hemolysis, hyperbilirubinemia, and bilirubin encephalopathy, as recommended by the World Health Organization (WHO).
Thanaporn Pimpakan   +9 more
doaj   +1 more source

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