Results 111 to 120 of about 22,836 (233)
Journal of Infection in Developing Countries, 2015 Introduction: Glucose-6-phosphate dehydrogenase deficiency (G6PD) is an X-linked genetic disorder with a relatively high frequency in malaria-endemic regions.
Seyed Mehdi Tabatabaei +4 more
doaj +1 more source
Addressing the challenge of neonatal mortality.
, 2013 Reducing neonatal mortality remains a challenge with an estimated 3.0 million neonatal deaths in 2011, three-quarters of these in sub-Saharan Africa and Southern Asia.
Blencowe, H, Cousens, S
core +1 more source
Pyruvate kinase deficiency and G6PD deficiency
SEIBUTSU BUTSURI KAGAKU, 1978 G6PD deficiency was discovered in 1956. It causes drug-induced acute hemolysis and is inherited by a sex-linked recessive trait. While the disorder is frequently seen in Negroes and inhabitants around the Mediterranean basin, it is rare in Japanese, the frequency of which is about 0.1%.
openaire +2 more sources
Journal of Extracellular Vesicles, Volume 15, Issue 5, May 2026.ABSTRACT SARS‐CoV‐2 infection is linked to persistent neurological symptoms Post‐Acute Sequelae SARS‐CoV‐2 (neuro‐PASC) and elevated risk of neurodegenerative disease, but molecular events connecting acute viral injury to long‐term CNS dysfunction remain unclear.
Gunjan Bawne +4 more
wiley +1 more source
Prevalence and distribution of G6PD deficiency: implication for the use of primaquine in malaria treatment in Ethiopia. [PDF]
, 2019 BackgroundG6PD enzyme deficiency is a common enzymatic X-linked disorder. Deficiency of the G6PD enzyme can cause free radical-mediated oxidative damage to red blood cells, leading to premature haemolysis.
Koepfli, Cristian +7 more
core
, 2008 Buffet and colleagues have reviewed some of the potential benefits and drawbacks of intermittent preventive antimalarial treatment in children (IPTc).
Bojang, Kalifa +5 more
core +1 more source
Molecular Characterization of G6PD Deficiency: Report of Three Novel G6PD Variants
Indian Journal of Hematology and Blood Transfusion, 2019 G6PD deficiency is a monogenic, X-linked genetic defect with a worldwide prevalence of around 400 million people and an overall prevalence of 8.5% in India. Hemolytic anemia is encountered in only a small proportion of patients with G6PD variants and is usually triggered by some exogenous agent.
Arun Kumar, Arunachalam +6 more
openaire +3 more sources
PERCC1‐associated enteropathy: Diagnostic challenges and enteral autonomy achieved with teduglutide
JPGN Reports, Volume 7, Issue 2, Page 266-270, May 2026.Abstract Congenital diarrheas and enteropathies (CODE) are rare inherited disorders characterized by early‐onset intractable diarrhea. Though progress has been made in elucidating the genetic basis of CODE, much remains to be discovered. Another challenge is the lack of curative therapies—treatment is primarily supportive including enteral and ...
Angela Tran, Vivien Nguyen, Phuong Huynh
wiley +1 more source
Hemolysis and methemoglobinemia due to hepatitis E virus infection in patient with G6PD deficiency [PDF]
, 2011 published_or_final_versionSpringer Open Choice, 21 Feb ...
Wing Y. Au +4 more
core +1 more source
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India
Annals of Human Biology, 2019 Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human erythroenzymopathy affecting more than 400 million people worldwide. G6PD deficiency was reported in India more than 50 years ago and the prevalence rate varies from 5.7% to 27.9% in different caste and tribal groups.Aim: To study the prevalence of, and the ...
Rati Devendra +7 more
openaire +3 more sources