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Poisoning with the S-Alkyl organophosphorus insecticides profenofos and prothiofos
Background: Many organophosphorus (OP) insecticides have either two O-methyl or two O-ethyl groups attached to the phosphorus atom. This chemical structure affects their responsiveness to oxime-induced acetylcholinesterase (AChE) reactivation after poisoning. However, several OP insecticides are aty...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2766103/ https://ncbi.nlm.nih.gov/pubmed/19737786 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/qjmed/hcp119 |
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