Revista Brasileira de Hematologia e Hemoterapia, 2010 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy. It affects as many as 330 million individuals worldwide.
Ulysses Madureira Maia +3 more
doaj +1 more source
Comparative Erythrocyte Metabolism in Marsupials and Monotremes [PDF]
, 1995 Concentrations of ATP and DPG, activities of 10 enzymes and the glycolytic rates were measured in the erythrocytes of 11 species of marsupials and two species of monotremes.
A.L. Parkinson +25 more
core +2 more sources
Clinical complications of G6PD deficiency in Latin American and Caribbean populations : systematic review and implications for malaria elimination programmes [PDF]
, 2014 Background: Although G6PDd individuals are generally asymptomatic throughout their life, the clinical burden of this genetic condition includes a range of haematological conditions, including acute haemolytic anaemia (AHA), neonatal jaundice (NNJ) and ...
Bassat, Quique +9 more
core +2 more sources
Deficiência de glicose-6-fosfato desidrogenase eritrocitária em recém-nascidos do sexo masculino e sua relação com a icterícia neonatal [PDF]
, 2010 Glucose-6-phosphate dehydrogenase (G6PD) deficiency, the commonest red cell enzymopathy in humans, has an X-linked inheritance. The major clinical manifestations are drug induced hemolytic anemia, neonatal jaundice and chronic nonspherocytic hemolytic ...
AMORIM, Maria do Socorro T. +6 more
core +1 more source
Asian 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
Asian 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
Genetic variability in Tetranychus urticae (Acari : Tetranychidae) from Greece : insecticide resistance and isozymes [PDF]
, 1996 Etude de la résistance au méthyl-parathion, au méthidathion et au méthomyl chez une population de #Tetranychus urticae$ Koch originaire de Grèce. A la CL 50 le taux de résistance est hautement variable avec le méthidathion (5 à 63 fois) et avec le ...
Gutierrez, Jean +4 more
core +3 more sources
Linkage disequlibrium in populations of Merodon avidus A. (Diptera, Syrphidae) [PDF]
, 2004 Analysis of the genetic structure in the populations of Merodon avidus A originated from the Dubašnica Mountain, Serbia (AADUB), Pindos Mountain Greece (AAPIN) and Morinj, Montenegro (AAMOR) was done.
Ludoški Jasmina Lj +2 more
core +1 more source
Ampliando a participação dos genes responsivos a T3 e cAMP na regulação da termogênese gerada pelas vias de oxidação biológica [PDF]
, 2010 OBJECTIVE: We sought to identify glycolysis, glycogenolysis, lipolysis, Krebs cycle, respiratory chain, and oxidative phosphorylation enzymes simultaneously regulated by T3 and cAMP.
Dias-da-Silva, Magnus Régios +2 more
core +2 more sources
Revista 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