Results 11 to 20 of about 3,031 (182)

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

Jornal 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, Márcia G. Sampaio, Antônio Condino-Neto, Orlando C.O. Barreto, Victor Nudelman, Magda M.S. Carneiro-Sampaio, Susie A. Nogueira, Thalita F. de Abreu, Jussara Rehder, Beatriz T. Costa-Carvalho   +9 more
doaj   +4 more sources

Glucose-6-phosphate Dehydrogenase Deficiency: A Review

International Journal of Medical Students, 2020
Deficiency of glucose-6-phosphate dehydrogenase enzyme is a common X-linked disorder that affects humans globally. It was first identified in the 1950s as a disorder that primarily affects the red blood cells causing a myriad of symptoms including acute
Nidhruv Ravikumar, Graeme Greenfield
doaj   +1 more source

Neonatal indirect hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency [PDF]

Korean Journal of Pediatrics, 2017
PurposeThis study aimed to determine the prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency among infants with neonatal indirect hyperbilirubinemia (NIH); compare G6PD-deficient and G6PD-normal patients regarding hyperbilirubinemia and ...
Hasan M. Isa, Masooma S. Mohamed, Afaf M. Mohamed, Adel Abdulla, Fuad Abdulla   +4 more
doaj   +1 more source

Confounding factors in the diagnosis and clinical course of rare congenital hemolytic anemias

Orphanet Journal of Rare Diseases, 2021
Congenital hemolytic anemias (CHAs) comprise defects of the erythrocyte membrane proteins and of red blood cell enzymes metabolism, along with alterations of erythropoiesis.
Bruno Fattizzo, Juri Alessandro Giannotta, Nicola Cecchi, Wilma Barcellini   +3 more
doaj   +1 more source

[Glucosephosphate dehydrogenase activity and reduced glutathione level in the erythrocytes of children with lymphoblastic leukemia].

Acta haematologica Polonica, 1982
The activity of glucose-6-phosphate dehydrogenase and the level of reduced glutathione were determined in the erythrocytes of children with acute lymphoblastic leukaemia treated by intensive combined chemotherapy (according to the authors from Memphis). The determinations were done before, during and after completion of treatment lasting about 3 years.
T, Warchoł, U, Radwańska, H, Karoń
openaire   +2 more sources

Prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in southeast Iran: implications for malaria elimination

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, Alireza Salimi Khorashad, Mohammad Sakeni, Ahmad Raeisi, Zahra Metanat   +4 more
doaj   +1 more source

Prevalência da deficiência da glicose-6-fosfato desidrogenase em doadores de sangue de Mossoró, Rio Grande do Norte Prevalence of glucose-6-phosphate dehydrogenase deficiency in blood donors of Mossoró, Rio Grande do Norte

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, Danielle Cristiny de Azevedo Batista, Wogelsanger Oliveira Pereira, Thales Allyrio Araújo de Medeiros Fernandes   +3 more
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, Lagnel, J., Navajas, M., Pasteur, N., Tsagkarakou, A.   +4 more
core   +3 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

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