[Value of hyperbaric oxygenation in rheumatic diseases].
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Humans↗
Biomedical subjects
R Joly
Publications and source records attributed to R Joly.
[Hyperbaric oxygen in treatment and rehabilitation of various rheumatic disorders].
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Humans↗
[Ultrastructural signs of cyclic secretory activity in the cerebral glands of Lithobius forficatus during intermolt].
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Animals↗
[Determination of extracellular and intracellular liquid volumes of the human body by electric measurement].
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Body Fluids↗
[Slaves and physicians in ancient Greece].
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Greece, Ancient↗
[Eventual biological and physiopathological effects of UHF electromagnetic radiation from "aerial radar"].
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Animals↗
[Comparative study of the cephalic endocrine complex in chilopod myriopods].
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Animals↗
[Hyperbaric oxygen therapy in dermatology. Preliminary results].
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Adult↗
[Biological effects and possible hazard of very high frequency rays from aircraft-spotting radar apparatus].
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Animals↗
[Experimental study of the molting cycle and of its endocrine regulation in chilopodous myriapods].
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Animals↗
[Influence of electromagnetic radiation from a RADAR EMITTER ON THE PHAGOCYTIC FUNCTION OF CELLS OF THE RETICULOENDOTHELIAL SYSTEM IN CONTACT WITH THE BLOOD IN MICE].
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Animals↗
[Influence of walking on the serum oxaloacetic glutamic transaminase activity in rats].
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Animals↗
[The prevention of hyperbaric oxygen convulsive complications in mice with gamma-sodium hydroxybutyrate and the combination of insulin-glucose-potassium chloride].
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Animals↗
[Demonstration in the rat of the antagonistic action of carnitine on nitrogen catabolism stimulated by cortisone administered over a period of several days].
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Animals↗
[Problems raised in the area of biological research by the use of hyperbaric and hyperoxygenated atmospheres].
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Biology↗
[Contribution to the study of the molting cycle and its determination in chilopodous myriapods].
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Animals↗
Oxidation of tenoxicam by leukocyte peroxidases and H2O2 produces novel products.
A leukocyte extract, which had a high peroxidase activity (mostly myeloperoxidase), converted tenoxicam [4-hydroxy-N-(2'-pyridyl)-2-methyl-2H-thieno-(2,3e)-1,2-thiazine-3 - carboxamide-1,1-dioxide] a potent antiinflammatory drug, into four novel metabolites in the presence of H2O2: 4,5-dihydro-4-oxo-5-methyliminopyrido (1,2a) imidazole (metabolite I), 2-carboxyl-3-thiofenesulfinic acid (metabolite II), 2-carboxyl-3-thiofenesulfonic acid (metabolite III), and N-methyl-N'-(2-pyridyl)oxamide (metabolite IV). These metabolites were probably formed by a one-electron oxidation reaction at the center carbon atom of the beta-diketone moiety of tenoxicam. Tenoxicam is a cofactor for the reduction of peroxidases and this capability may explain at least a part of the antiinflammatory effect of tenoxicam.
Anti-Inflammatory Agents, Non-Steroidal↗