Results 11 to 20 of about 2,533 (132)

Digital epidemiology and geographic mapping of G6PD deficiency: retrospective analytic of trends database existing on the surface web

open access: yesAsian Journal of Medical Sciences, 2018
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited X-linked recessive condition in which the body does not synthesise a sufficient quantity of the G6PD enzyme.
Ahmed Al-Imam
doaj   +1 more source

The enzymopathy of G6PD deficiency in Jordan: a demographic and biochemical analysis

open access: yesAsian Journal of Medical Sciences, 2018
Background: G6PD deficiency is an inherited X-linked recessive condition leading to insufficient levels of glucose-6-phosphate dehydrogenase, thus causing hemolytic anaemia under certain circumstances.
Ahmed Al-Imam
doaj   +1 more source

The severity of acute viral hepatitis in patients with glucose-6-phosphate dehydrogenase deficiency: a case-control study

open access: yesJournal of the Pakistan Medical Association
Objectives: To compare outcomes and severity parameters in patients with acute viral hepatitis and those with acute viral hepatitis and glucose-6-phosphate dehydrogenase deficiency.
Mahrukh Ali   +3 more
doaj   +1 more source

Icterícia neonatal e deficiência de glicose-6-fosfato desidrogenase Neonatal jaundice and glucose-6-phosphate dehydrogenase

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2010
A deficiência de glicose-6-fosfato desidrogenase em neonatos pode ser a responsável pela icterícia neonatal. Este comentário científico é decorrente do relato sobre o tema publicado neste fascículo e que preocupa diversos autores de outros países em ...
Amauri Antiquera Leite
doaj   +1 more source

Investigação genético-epidemiológica e molecular da deficiência de G-6-PD em uma comunidade brasileira G-6-PD deficiency in a Brazilian community: an investigation involving epidemiological genetics and molecular techniques

open access: yesCadernos de Saúde Pública, 2000
Este trabalho teve por objetivo estudar a deficiência de G-6-PD em uma comunidade do interior do Estado de São Paulo (Bragança Paulista). Durante 36 meses foram selecionados 4.621 doadores de sangue do sexo masculino, detectando-se 80 deficientes em G-6 ...
Mariane B. Compri   +2 more
doaj   +1 more source

Deficiência da glicose-6-fosfato desidrogenase com infecções de repetição: relato de caso Glucose-6-phosphate dehydrogenase deficiency with recurrent infections: case report

open access: yesJornal de Pediatria, 2001
OBJETIVO: relatar a ocorrência de uma deficiência funcional de neutrófilos rara, com quadro clínico e laboratorial semelhante ao da doença granulomatosa crônica.
Abertina Rosa-Borges   +9 more
doaj   +1 more source

PGD: Shared gene linking polycystic ovary syndrome and endometrial cancer, influencing proliferation and migration through glycometabolism

open access: yesCancer Science, Volume 115, Issue 9, Page 2908-2922, September 2024.
PGD is a differentially expressed gene shared between polycystic ovary syndrome and endometrial cancer that modulates endometrial cancer cell proliferation and migration through carbon metabolism. Abstract The relationship among polycystic ovary syndrome (PCOS), endometrial cancer (EC), and glycometabolism remains unclear.
Jia‐ming Chen   +9 more
wiley   +1 more source

Cytotoxicity and toxicoproteomics analysis of thiazolidinedione exposure in human‐derived cardiomyocytes

open access: yesJournal of Applied Toxicology, Volume 44, Issue 8, Page 1214-1235, August 2024.
Abstract Thiazolidinediones (TZDs) (e.g. pioglitazone and rosiglitazone), known insulin sensitiser agents for type II diabetes mellitus, exhibit controversial effects on cardiac tissue. Despite consensus on their association with increased heart failure risk, limiting TZD use in diabetes management, the underlying mechanisms remain uncharacterised ...
Abdullah Al Sultan   +2 more
wiley   +1 more source

Scrub Typhus Infection Precipitating Hemolysis in a Patient With G6PD Deficiency: A Case Report

open access: yesClinical Case Reports
Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is a well‐known red blood cell enzymopathy and a cause of intravascular hemolysis. This case report presents a child with underlying G6PD deficiency who experienced an acute episode of extensive ...
Ravi Shukla   +5 more
doaj   +1 more source

Bioinformatic analysis of G6PD variants with a focus on key Iranian mutations [PDF]

open access: yesJournal of Clinical and Basic Research
Background: Glucose-6-phosphate dehydrogenase deficiency, an enzyme disorder, can lead to red blood cell dysfunction and affect millions of individuals worldwide.
Romina Jafari Kalokan   +2 more
doaj  

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