Biomedical subjects
J K BEVERLEY
Publications and source records attributed to J K BEVERLEY.
Experimental ocular toxoplasmosis.
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Congenital toxoplasma infections.
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Ovine abortion due to toxoplasmosis.
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Congenital transmission of toxoplasmosis through successive generations of mice.
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Glandular toxoplasmosis; a survey of 30 cases.
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Lymphadenopathy in toxoplasmosis.
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Glandular toxoplasmosis; a report of three cases.
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A rational approach to the treatment of toxoplasmic uveitis.
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The treatment of experimental toxoplasmosis in rabbits.
Sulphadimidine alone is of little value in treating experimental toxoplasmosis in rabbits, because most rabbits acetylate the drug very rapidly. Within a short time of dosing such animals, there is little or none of the uncombined drug in the blood. In rabbits which do not acetylate sulphadimidine rapidly, relatively high concentrations of the free sulphonamide can be attained in the blood: in such animals, toxoplasmosis responds to treatment with sulphadimidine. Sulphathiazole is not acetylated so rapidly and is effective even in rabbits which acetylate sulphadimidine quickly. Pyrimethamine, even in doses as high as 50 mg. three times daily, is ineffective; dapsone is effective.
Sulphadimidine, pyrimethamine and dapsone in the treatment of toxoplasmosis in mice.
Sulphadimidine, dapsone, and pyrimethamine have been tested alone and in various combinations for their therapeutic effect against toxoplasma infection in mice. In the treatment of active infection, sulphadimidine by itself was effective, but relapses were common. Pyrimethamine gave complete cures and prevented the carrier state when used in doses near to the toxic level. Dapsone alone was not as good as either of the other two drugs tested. The best combination was found to be sulphadimidine and pyrimethamine, which were synergic. In doses well below the toxic level, this combination not only controlled the acute infection but also prevented relapses and the development of the carrier state. Dapsone and pyrimethamine were also synergic, but were not as effective as the previous combination. No synergy was found between dapsone and sulphadimidine. The mechanism of relapse and the development of the carrier state and the modes of action of the drugs alone and in combination are discussed.
Congenital toxoplasmosis simulating haemolytic disease of the newborn.
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Acquired toxoplasmosis with a report of a case of laboratory infection.
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Acquired toxoplasmosis; with a report of two cases simulating glandular fever and one possible case resembling typhus.
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Experimental toxoplasmosis of the uveal tract.
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