Results 191 to 200 of about 10,333 (209)
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Treatment perspectives for human African trypanosomiasis
Fundamental & Clinical Pharmacology, 2003AbstractHuman African trypanosomiasis (HAT), or sleeping sickness, is currently on the rise. HAT develops in two stages, the first involving the hemolymphatic system, and the second, the neurological system. Left untreated, HAT is invariably fatal. There have been no therapeutic advances in more than 40 years.
Sylvie Bisser+3 more
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Treatment and control of human African trypanosomiasis
Current Opinion in Infectious Diseases, 2004Access to treatment is a multi-step process and little progress has been made to improve treatments for sleeping sickness over the past 50 years. The current strategy is based on diagnostic tools developed in the 1960s while available drugs are still the same as those developed in the middle of the last century.
P Cattand, J Jannin
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Human African Trypanosomiasis (HAT)
2016Human African trypanosomiasis (HAT) found only in sub-Saharan Africa is caused by the parasite Trypanosoma brucei which is transmitted by tsetse flies. Only two subspecies of T.brucei are pathogenic for humans: T.b. gambiense and T.b. rhodesiense. HAT is endemic in 36 sub-Saharan countries, and 98 % of all reported HAT cases are due to T. b. gambiense.
Pascal Lutumba+2 more
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Eflornithine for the treatment of human African trypanosomiasis
Parasitology Research, 2003Eflornithine is the only new molecule registered for the treatment of human African trypanosomiasis over the last 50 years. It is the drug used mainly as a back-up for melarsoprol refractory Trypanosoma brucei gambiense cases. The most commonly used dosage regimen for the treatment of T. b.
Christian Burri, Reto Brun
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New developments in human African trypanosomiasis
Current Opinion in Infectious Diseases, 2006To review recent literature on human African trypanosomiasis, focussing on genome sequencing, diagnosis and drug discovery, and typing of trypanosomes.The most important recent development has been the completion of the Trypanosoma brucei genome which will greatly facilitate the discovery of new drug targets and genetic markers.
Brun, Reto, Balmer, Oliver
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Hormones in human African trypanosomiasis
1999Humans suffering from African trypanosomiasis or sleeping sickness demonstrate major disruptions in their circadian sleep-wake distribution, with the intensity of the sleep-wake disturbances increasing with the stage of advancement of the disease [1]. Buguet et al. [1] postulated that the disruptions in the circadian sleep-wake cycle in infected humans
G. Brandenberger, M. W. Radomski
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Problems for the chemotherapy of human African trypanosomiasis
Current Opinion in Infectious Diseases, 2000Problems associated with the current therapies of sleeping sickness include toxicity, resistance and a lack of a guaranteed supply. However, no new formulations are close to gaining a licence for clinical use and relatively few compounds have been shown to be effective in experimental systems.
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The nitroimidazoles and human African trypanosomiasis
1999The arsenal of compounds available for the chemotherapy of human African trypanosomiasis (HAT) [1,2] is essentially limited to suramin and pentamidine, which are active in the hematological stage of the disease, and melarsoprol and eflornithine (DFMO) which have efficacy in the terminal (meningoencephalitic) phase.
J. Périé, G. Chauvière
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The epidemiology and control of human African trypanosomiasis
2001Human African trypanosomiasis is caused by Trypanosoma brucei gambiense in West and Central Africa, and by Trypanosoma brucei rhodesiense in East and southern Africa. In recent years there has been a dramatic resurgence of Gambian trypanosomiasis in Central Africa, especially in the Democratic Republic of Congo, Angola and Sudan.
Jacques Pépin, Honore Meda
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Human African trypanosomiasis–neurological aspects
Journal of Neurology, 2006Human African Trypanosomiasis (HAT),which is also known as sleeping sickness, is a major cause of death and disability in 36 countries in sub-Saharan Africa. The disease is caused by the protozoan parasite of the Trypanosoma genus which is transmitted by the bite of the tsetse fly.
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