Results 21 to 30 of about 23,995 (263)

Social Media Content Analysis of Public and Private Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Facebook Groups. [PDF]

Acta Med Philipp
Maceda EBG, Abadingo ME, Asor BBN, Cases RKC, Supan RJG, Anarna KS, Libo-On PCA, Vesagas TDC, Tumulak MJR.   +8 more
europepmc   +3 more sources

Prevalence of and mothers’ knowledge, attitude and practice towards glucose-6-phosphate dehydrogenase deficiency among neonates with jaundice: a cross-sectional study

BMJ Open, 2020
BackgroundNeonatal jaundice (NNJ) is a frequent complication of glucose-6-phosphate dehydrogenase (G6PD) deficiency.ObjectivesTo estimate the prevalence of G6PD deficiency among neonates with jaundice and to assess mothers’ perception towards G6PD and ...
Zeinab A Kasemy, Wael A Bahbah, Sally M El Hefnawy, Safa H Alkalash   +3 more
doaj   +1 more source

Fine mapping of Glucose 6 Phosphate Dehydrogenase (G6PD) deficiency in rural area of South West Odisha using the clinical, hematological and molecular approach

Mediterranean Journal of Hematology and Infectious Diseases, 2020
Introduction: The aim of the study was to enumerate the clinical, hematological and molecular spectrum of G6PD deficiency in malaria endemic regions of south west Odisha.
Ravindra Kumar, MPSS Singh, Soumendu Mahapatra, Sonam Chourasia, Malay Kumar Tripathi, John Oommen, Praveen Kumar Bharti, Rajasubramaniam Shanmugam   +7 more
doaj   +1 more source

Correlation Between Glucose – 6 – Phosphate Dehydrogenase Deficiency Level and Some Haematological Parameters on Newborn Blood in Al-Anbar Governorate-Ramadi [PDF]

مجلة جامعة الانبار للعلوم الصرفة, 2012
This study aimed to determine the prevalence of Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Al-Anbar Governorate-Ramadi and to study the different relationships between these cases and different haematological parameters values. In addition to
Sabri M. Hussain, Mohammed Q.Al-Ani, Khalid F.Al-Rawi, Mahmood. M.Atia   +3 more
doaj   +1 more source

Combined effects of double mutations on catalytic activity and structural stability contribute to clinical manifestations of glucose-6-phosphate dehydrogenase deficiency

Scientific Reports, 2021
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy in humans, affecting ~ 500 million worldwide. A detailed study of the structural stability and catalytic activity of G6PD variants is required to understand how different ...
Phonchanan Pakparnich, Sirapapha Sudsumrit, Mallika Imwong, Teeraporn Suteewong, Kamonwan Chamchoy, Danaya Pakotiprapha, Ubolsree Leartsakulpanich, Usa Boonyuen   +7 more
doaj   +1 more source

Molecular characterization of G6PD mutations identifies new mutations and a high frequency of intronic variants in Thai females.

PLoS ONE, 2023
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked enzymopathy caused by mutations in the G6PD gene. A medical concern associated with G6PD deficiency is acute hemolytic anemia induced by certain foods, drugs, and infections.
Kamonwan Chamchoy, Sirapapha Sudsumrit, Jutamas Wongwigkan, Songsak Petmitr, Duantida Songdej, Emily R Adams, Thomas Edwards, Ubolsree Leartsakulpanich, Usa Boonyuen   +8 more
doaj   +1 more source

Clinical spectrum and severity of hemolytic anemia in glucose 6-phosphate dehydrogenase-deficient children receiving dapsone [PDF]

, 2012
Drug-induced acute hemolytic anemia led to the discovery of G6PD deficiency. However, most clinical data are from isolated case reports. In 2 clinical trials of antimalarial preparations containing dapsone (4,4′-diaminodiphenylsulfone; 2.5 mg/kg once ...
Carter, Nick, Duparc, Stephan, Luzzatto, Lucio, Pamba, Allan, Premji, Zul, Richardson, Naomi D., Tiono, Alfred B.   +6 more
core   +5 more sources

Glucose-6-phosphate dehydrogenase deficiency in Nigerian children. [PDF]

PLoS ONE, 2013
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy and in Sub-Saharan Africa, is a significant cause of infection- and drug-induced hemolysis and neonatal jaundice.
Olatundun Williams, Daniel Gbadero, Grace Edowhorhu, Ann Brearley, Tina Slusher, Troy C Lund   +5 more
doaj   +1 more source

Glucose-6-phosphate dehydrogenase (G6PD) mutations and haemoglobinuria syndrome in the Vietnamese population [PDF]

, 2009
BACKGROUND: In Vietnam the blackwater fever syndrome (BWF) has been associated with malaria infection, quinine ingestion and G6PD deficiency. The G6PD variants within the Vietnamese Kinh contributing to the disease risk in this population, and more ...
Charlieu, JP, Chau, TT, Day, N, Dunstan, Sarah, Farrar, JJ, Hien, Tran, Hue, NT   +6 more
core   +4 more sources

The First Case of a Class I Glucose-6-phosphate Dehydrogenase Deficiency, G6PD Santiago de Cuba (1339 GA), in a Chinese Population as Found in a Survey for G6PD Deficiency in Northeastern and Central China [PDF]

, 2010
In Liaoning Province in northeastern China, we found a G6PD-deficient patient at the age of 3. By the classification of the World Health Organization, this patient was categorized as class I (very severe G6PD deficiency).
Hirai, Makoto, Luo, Enjie, Matsuoka, Hiroyuki, Mu, Ling, Wang, Jichun, Yang, Liandi   +5 more
core   +1 more source