Results 101 to 110 of about 1,092 (179)

Prevalence of glucose-6-phosphate dehydrogenase deficiency (G6PDd), CareStart qualitative rapid diagnostic test performance, and genetic variants in two malaria-endemic areas in Sudan

open access: yesPLoS Neglected Tropical Diseases, 2021
Glucose-6-phosphate dehydrogenase deficiency (G6PDd) is the most common enzymopathy globally, and deficient individuals may experience severe hemolysis following treatment with 8-aminoquinolines.
Musab M. Ali Albsheer   +7 more
doaj  

Review: Improving the Therapeutic Index of 8-Aminoquinolines by the Use of Drug Combinations: Review of the Literature and Proposal for Future Investigations [PDF]

open access: yes, 2011
Because 8-aminoquinolines affect critical survival stages of Plasmodium parasites, treatment and control of malaria could be markedly improved by more widespread use of these drugs; however, hemolytic toxicity, which is widely prevalent in G6PD-deficient
Baird, J. Kevin   +6 more
core   +2 more sources

Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria

open access: yesMalaria Journal, 2019
Background Glucose-6-phosphate dehydrogenase deficiency (G6PDd), haemoglobin C (HbC) and S (HbS) are inherited blood disorders (IBD) common in populations in malaria endemic areas.
Lynn Grignard   +20 more
doaj   +1 more source

Chimiothérapie des theilérioses bovines par un anticoccidien, l'halofuginone : note préliminaire [PDF]

open access: yes, 1980
L'anticoccidien halofuginone est un schizonticide puissant contre Theileria parva, agent de la fièvre de la Côte Est et de la Corridor disease des bovins en Afrique.
Franssen, F.F.J.   +3 more
core  

Prevalence and distribution of glucose-6-phosphate dehydrogenase (G6PD) variants in Thai and Burmese populations in malaria endemic areas of Thailand

open access: yesMalaria Journal, 2011
Background G6PD deficiency is common in malaria endemic regions and is estimated to affect more than 400 million people worldwide. Treatment of malaria patients with the anti-malarial drug primaquine or other 8-aminoquinolines may be associated with ...
Phompradit Papichaya   +6 more
doaj   +1 more source

Genotypic and phenotypic characterization of G6PD deficiency in Bengali adults with severe and uncomplicated malaria

open access: yesMalaria Journal, 2017
Background Control of malaria increasingly involves administration of 8-aminoquinolines, with accompanying risk of haemolysis in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Katherine Plewes   +14 more
doaj   +1 more source

Structures, targets and recent approaches in anti-leishmanial drug discovery and development. [PDF]

open access: yes, 2011
Recent years have seen a significant improvement in available treatment options for leishmaniasis. Two new drugs, miltefosine and paromomycin, have been registered for the treatment of visceral leishmaniasis (VL) in India since 2002.
Seifert, Karin
core   +2 more sources

Pharmacology of 8-aminoquinolines.

open access: yesBulletin of the World Health Organization, 1982
The 8-aminoquinolines were the first group of compounds to be synthesized specifically for their antimalarial activity. A large-scale research programme in the United States of America in the 1940s produced three new antimalarial drugs-pentaquine, isopentaquine, and primaquine -of which primaquine was the most effective.
openaire   +1 more source

Recent Advances in the Treatment of Malaria

open access: yesPharmaceutics
Malaria is still one of the major global health challenges affecting millions annually, particularly in non-Mediterranean Africa and Southeast Asia. Over the past two decades, substantial progress has been made in reducing malaria-related morbidity and ...
Jawaher M. Alghamdi   +3 more
doaj   +1 more source

8-Aminoquinolines from Walter Reed Army Institute for Research for treatment and prophylaxis of Pneumocystis pneumonia in rat models. [PDF]

open access: yes, 1991
Three 8-aminoquinolines from the Walter Reed Army Institute for Research (WRAIR), WR6026, WR238605, and WR242511, strongly inhibited Pneumocystis carinii growth in vitro at 1 microgram/ml. This activity was similar to that of primaquine.
Bartlett, M. S.   +6 more
core   +2 more sources

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