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Titlebook: Antituberculosis Drugs; Karl Bartmann Book 1988 Springer-Verlag Berlin Heidelberg 1988 breathing.chemotherapy.kinetics.pharmacokinetics.ph

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發(fā)表于 2025-3-21 19:37:28 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱Antituberculosis Drugs
影響因子2023Karl Bartmann
視頻videohttp://file.papertrans.cn/159/158695/158695.mp4
學(xué)科分類Handbook of Experimental Pharmacology
圖書封面Titlebook: Antituberculosis Drugs;  Karl Bartmann Book 1988 Springer-Verlag Berlin Heidelberg 1988 breathing.chemotherapy.kinetics.pharmacokinetics.ph
影響因子This volume deals specifically with those antituberculosis drugs which passed the preclinical phase and have been or are used in the treatment of tuberculosis and other mycobacterial diseases (except leprosy) in at least some parts of the world. Despite this restriction, there are 14 such drugs, and as a result this volume has reached rather large proportions. To prevent it from becoming even larger and more unwidely, most derivatives of antituberculotics have been omitted, especially where it is claimed that they provide only better bioavailibility or tolerability. Only in the chapter on the chemotherapy of diseases due to so-called atypical mycobacteria is the clinical use of the drugs described to a certain extent. In addition to antituberculotics, also discussed are antimicrobials which have been found to be effective against these mycobacteria. The sequence in which the drugs are described is historical, reflecting not the time of discovery but rather the first clinical application. This order was selected for reasons which are now no longer relevant. In this volume less emphasis is placed on detection, biological or synthetic production of antituberculotics, and structure-act
Pindex Book 1988
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發(fā)表于 2025-3-21 20:24:32 | 只看該作者
Experimental Evaluation of Chemoprophylaxis and Preventive Treatment in Animals,es where infection can be prevented. However, in tuberculosis control we use the term BCG prophylaxis, although the bacillus Calmette-Guerin cannot prevent the tubercle bacillus from settling in a non-infected host: it can only prevent the further spread of infection. The terms primary chemoprophyla
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發(fā)表于 2025-3-22 05:00:45 | 只看該作者
Experimental Pharmacology and Toxicology of Antituberculosis Drugs,e various organ systems. These range from the very early recognized ototoxicity and nephrotoxicity of the aminoglycosides, to the question of neurotoxicity, carcinogenicity and mutagenicity of INH, to the oculotoxicity of ethambutol and to effects on neuro-muscular transmission of the aminoglycoside
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發(fā)表于 2025-3-22 11:07:48 | 只看該作者
Mode of Action, Biotransformation and Pharmacokinetics of Antituberculosis Drugs in Animals and Manf antituberculotics on mycobacteria in a disease focus. Knowledge of the mode of action yields further therapeutically important information, such as whether intervention of the agent in the bacterial metabolism has any serious consequences or whether the damage is reversible within limits, dependin
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發(fā)表于 2025-3-22 13:44:23 | 只看該作者
Product Ontology and OWL Correspondence,roxyaminobenzoic acids did not have this inhibitory effect, and that the substance acts specifically only against . strains. Lehmann described not his fundamental microbiological metabolic experiments but also the animal-experimental and clinical studies he performed with PAS.
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發(fā)表于 2025-3-23 02:19:17 | 只看該作者
Experimental Evaluation of Chemoprophylaxis and Preventive Treatment in Animals,the spread of infection is practised widely. The terms chemoprevention, preventive therapy and chemoprotection are sometimes used instead of secondary prophylaxis. The U.S. Committee on Therapy used the term infection prophylaxis for primary prophylaxis, and disease prophylaxis for secondary prophylaxis.
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發(fā)表于 2025-3-23 09:11:14 | 只看該作者
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