Results 11 to 20 of about 3,002 (184)

Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review. [PDF]

Mol Genet Genomic Med
Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is a rare cause of nonimmune hydrops fetalis and most cases require fetal or neonatal transfusion. Although G6PD deficiency is an X‐linked recessive condition, female fetuses can be affected. Testing should be considered if parental history indicates.
Iyer NS, Mossayebi MH, Gao TJ, Haizler-Cohen L, Di Mascio D, McLaren RA, Al-Kouatly HB.   +6 more
europepmc   +2 more sources

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, Lagnel, J., Navajas, M., Pasteur, N., Tsagkarakou, A.   +4 more
core   +3 more sources

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, A.T. Whittington, Agar, Agar, Agar, Agar, Agar, Bethlenfalvay, Beutler, Bland, Board, C. Gallagher, Farber, G. Grigg, Godwin, Grigg, Grigg, Isaacks, Isaacks, Kim, Kim, L. Hinds, N.S. Agar, P. Kuchel, P.B.S. Spencer, Richardson   +25 more
core   +2 more sources

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

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

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, Brito, Marcelo, Franca, Gabriel Peixoto, Lacerda, Marcus Vinícius Guimarães de, Melo, Gisely Cardoso de, Monteiro, Wuelton Marcelo, Oliveira, Maria Regina Fernandes de, Peixoto, Henry Maia, Queiroz, Amanda de Lourdes Maciel, Romero, Gustavo Adolfo Sierra   +9 more
core   +2 more sources

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

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., BARRETTO, Orlando C. O., IGLESSIAS, Marli Auxiliadora C., MEDEIROS, Tereza Maria D., MOREIRA, Susiane S., SANTOS, Rosa Maria V., SILVA, Rosângela T.   +6 more
core   +1 more source

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

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

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

Cadernos 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, Sara T. O. Saad, Antonio Sérgio Ramalho   +2 more
doaj   +1 more source

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, Milankov Vesna R., Vujić Ante A.   +2 more
core   +1 more source