Results 111 to 120 of about 20,164 (174)

A pilot study on the prevalence and patterns of haemoglobinopathies in Datia District, Madhya Pradesh, India. [PDF]

Sci Rep
Rajasubramaniam S, Mishra N, Balakrishna SL, Kumawat A, Gaur R, Sharma A, Das A.   +6 more
europepmc   +1 more source

New WHO classification of genetic variants causing G6PD deficiency. [PDF]

Bull World Health Organ
Luzzatto L, Bancone G, Dugué PA, Jiang W, Minucci A, Nannelli C, Pfeffer D, Prchal J, Sirdah M, Sodeinde O, Vulliamy T, Wanachiwanawin W, Cunningham J, Bosman A.   +13 more
europepmc   +1 more source

Acceptability and feasibility of glucose-6-phosphate dehydrogenase (G6PD) testing using SD Biosensor by village malaria workers in Cambodia: a qualitative study. [PDF]

BMJ Glob Health
Cassidy-Seyoum SA, Adhikari B, Chheng K, Chanpheakdey P, Meershoek A, Hsiang MS, von Seidlein L, Tripura R, Ley B, Price RN, Dysoley L, Thriemer K, Engel N.   +12 more
europepmc   +1 more source

Diagnostic accuracy of the point-of-care standard G6PD test™ (SD Biosensor) for glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis. [PDF]

Malar J
Martínez JC, Vélez-Marín V, Lopez-Perez M, Patiño-Lugo DF, Florez ID.   +4 more
europepmc   +1 more source

Evaluation of Glucose 6-Phosphate Dehydrogenase, Pyruvate Kinase, and New Generation Inflammation Biomarkers in Prolonged Neonatal Jaundice. [PDF]

Medicina (Kaunas)
Okuyan O, Dumur S, Elgormus N, Uzun H.
europepmc   +1 more source

Prospective observational study to assess the feasibility and safety of appropriate <i>Plasmodium vivax</i> radical cure with tafenoquine or primaquine after quantitative G6PD testing during pilot implementation in Thailand. [PDF]

BMJ Glob Health
Sudathip P, Khantikul N, Saejeng A, Duparc S, Grewal Daumerie P, Lynch C, Jambert E, Viboonsanti S, Areechokchai D, Kanjanasuwan J, Thong-Ard T, Kowsurat P, Borghini-Fuhrer I, Padungtod C.   +13 more
europepmc   +1 more source

Serum microRNAs as new biomarkers for detecting subclinical hemolysis in the nonacute phase of G6PD deficiency. [PDF]

Sci Rep
Boonpeng K, Shibuta T, Hirooka Y, Kulkeaw K, Palasuwan D, Umemura T.   +5 more
europepmc   +1 more source

Fulminant hepatitis and multi-organ failure following varicella zoster virus infection in an adult with G6PD deficiency: a case report. [PDF]

Virol J
Nezhad NZ, Heidari B, Nezhad AM, Nakhaie M, Jahangiri S.   +4 more
europepmc   +1 more source

Combined Glucosephosphate Isomerase and Glucose‐6‐Phosphate Dehydrogenase Deficiency of the Erythrocytes: A New Haemolytic Syndrome

British Journal of Haematology, 1971
Summary. A new haemolytic syndrome associated with the combination of genetically determined glucosephosphate isomerase and glucose‐6‐phosphate dehydrogenase deficiency of the erythrocytes was demonstrated in a German family. The propositus (a male), homozygous for the glucosephosphate isomerase deficiency and hemizygous for the glucose‐6‐phosphate ...
W, Schröter, G, Brittinger, E, Zimmerschmitt, E, König, D, Schrader   +4 more
semanticscholar   +4 more sources

Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcome

Blood Cells, Molecules, and Diseases, 2003
Glucosephosphate isomerase (GPI) deficiency in humans is an autosomal recessive disorder, which results in nonspherocytic hemolytic anemia of variable clinical expression. A 4-year-old female with severe congenital hemolytic anemia had low red cell GPI activity of 15.5 IU/g Hb (50% of normal mean) indicating GPI deficiency.
Julia L, Clarke, Tom J, Vulliamy, David, Roper, Seyed A, Mesbah-Namin, Barbara J, Wild, James I, Walker, Andrew M, Will, Paula H, Bolton-Maggs, Philip J, Mason, D Mark, Layton   +9 more
semanticscholar   +4 more sources