Zobrazeno 1 - 10
of 57
pro vyhledávání: '"g6pd enzyme"'
Autor:
Haydeh Hafez-Quran, Bijan Keikhaei, Homayon Yousefi, Amal Saki-Malehi, Najmaldin Saki, Zohre Rezaei-Kookhdan
Publikováno v:
Journal of Biological Research (2024)
The present study aimed to evaluate the prevalence of alpha-thalassemia and glucose-6-phosphate dehydrogenase (G6PD) deficiency in sickle cell trait (SCT) patients to determine its effect on red blood cells (RBC) parameters. This cross-sectional stud
Externí odkaz:
https://doaj.org/article/0500737aa510445cb6c1cd9b13112092
Autor:
Kezban Kartlaşmış, Nurten Dikmen
Publikováno v:
Cukurova Medical Journal, Vol 47, Iss 1, Pp 143-151 (2022)
Purpose: The aim of this study was to investigate in vitro effect of glyphosate on Glucose 6-phosphate dehydrogenase (G6PD) enzyme activity. Materials and Methods: In terms of G6PD enzyme deficiency, samples taken from healthy and enzyme deficient ma
Externí odkaz:
https://doaj.org/article/e3439bfa35c94d1abe9e97e03993a44a
Autor:
Arieh Riskin, Yulia Bravdo, Clair Habib, Irit Maor, Julnar Mousa, Sizett Shahbarat, Elena Shahak, Adel Shalata
Publikováno v:
Children, Vol 10, Iss 7, p 1172 (2023)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency and polymorphism in uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1) were associated with significant neonatal hyperbilirubinemia (NHB) and increased risk for kernicterus. However, quantita
Externí odkaz:
https://doaj.org/article/c4950416b57743c9a754cfb870a6fd5f
Autor:
Usa Boonyuen, Duantida Songdej, Sasipa Tanyaratsrisakul, Suparat Phuanukoonnon, Kamonwan Chamchoy, Aun Praoparotai, Phonchanan Pakparnich, Sirapapha Sudsumrit, Thomas Edwards, Christopher T. Williams, Rachel L. Byrne, Emily R. Adams, Mallika Imwong
Publikováno v:
Malaria Journal, Vol 20, Iss 1, Pp 1-12 (2021)
Abstract Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency, the most common enzymopathy in humans, is prevalent in tropical and subtropical areas where malaria is endemic. Anti-malarial drugs, such as primaquine and tafenoquine, can caus
Externí odkaz:
https://doaj.org/article/4e20ca24d0a346cbb5a1fd1b9cd24206
Akademický článek
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Autor:
Shalata, Arieh Riskin, Yulia Bravdo, Clair Habib, Irit Maor, Julnar Mousa, Sizett Shahbarat, Elena Shahak, Adel
Publikováno v:
Children; Volume 10; Issue 7; Pages: 1172
Glucose-6-phosphate dehydrogenase (G6PD) deficiency and polymorphism in uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1) were associated with significant neonatal hyperbilirubinemia (NHB) and increased risk for kernicterus. However, quantita
Akademický článek
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Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 17, Iss 3, Pp 108-113 (2015)
Background and Objective: The national screening program for G6PD enzyme deficiency is not able to detect all affected neonates. This study was done to compare the fluorescent spot test (FST), decolorization test, and quantitative enzyme assay (QEA)
Externí odkaz:
https://doaj.org/article/731edfa433ff4645b03ef3cd31b2d3fc
Autor:
Rachel L Byrne, Duantida Songdej, Sirapapha Sudsumrit, Aun Praoparotai, Thomas Edwards, Christopher T Williams, Suparat Phuanukoonnon, Phonchanan Pakparnich, Kamonwan Chamchoy, Usa Boonyuen, Emily R. Adams, Sasipa Tanyaratsrisakul, Mallika Imwong
Publikováno v:
Malaria Journal, Vol 20, Iss 1, Pp 1-12 (2021)
Malaria Journal
Malaria Journal
Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency, the most common enzymopathy in humans, is prevalent in tropical and subtropical areas where malaria is endemic. Anti-malarial drugs, such as primaquine and tafenoquine, can cause haemoly
Akademický článek
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