Titlebook: New Neuromuscular Blocking Agents; Basic and Applied As Dimitry A. Kharkevich (Professor and Chairman of t Book 1986 Springer-Verlag Berlin

necrosis

書目名稱New Neuromuscular Blocking Agents影響因子(影響力)




書目名稱New Neuromuscular Blocking Agents影響因子(影響力)學(xué)科排名




書目名稱New Neuromuscular Blocking Agents網(wǎng)絡(luò)公開度




書目名稱New Neuromuscular Blocking Agents網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱New Neuromuscular Blocking Agents被引頻次




書目名稱New Neuromuscular Blocking Agents被引頻次學(xué)科排名




書目名稱New Neuromuscular Blocking Agents年度引用




書目名稱New Neuromuscular Blocking Agents年度引用學(xué)科排名




書目名稱New Neuromuscular Blocking Agents讀者反饋




書目名稱New Neuromuscular Blocking Agents讀者反饋學(xué)科排名

剝皮

分期付款

On the Principles of Postsynaptic Action of Neuromuscular Blocking Agentsrtainly be argued that the important facts about tubocurarine were all known long before the voltage clamp was invented, it could not be argued that the reasons for its behaviour were understood. The emphasis in this chapter will be on the fundamental molecular effects of the drugs, rather than on t

peritonitis

stroke

On the Comparative Sensitivity of Acetylcholine Receptors of Various Groups of Skeletal Muscles to Nes. Thus, for instance, tubocurarine causes relaxation, first, of the cervical and facial muscles, then, of the muscles of the torso and limbs, and last, of respiratory muscles (intercostal and diaphragm). Often, this is considered to be true of other neuromuscular blocking agents, although the data

門閂

CORD

The Interaction of Neuromuscular Blocking Agents With Human Cholinesterases and Their Binding to Plaof the ester type NMBA, e.g., succinylcholine chloride (suxamethonium; SCh), suxethonium bromide, are hydrolyzed by human plasma butyrylcholinesterase (EC 3.1.1.8; BuChE) (. and . 1953; . et al. 1956). Their hydrolysis rate in most other mammalian plasmas is much lower than in human plasma (. and .

極小

外觀

Biodegradation and Elimination of Neuromuscular Blocking Agentsns. Thus, although quaternary ammonium compounds can be degraded to tertiary amines, in general this requires treatment with caustic alkali, i.e. approximately pH 14, at temperatures of around 100 °C (. 1851). It is not surprising, therefore, that the tetraalkylammonium group is not normally subject

Conduit