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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Detalles Bibliográficos
Autores principales: Eddleston, M., Worek, F., Eyer, P., Thiermann, H., Von Meyer, L., Jeganathan, K., Sheriff, M. H. R., Dawson, A. H., Buckley, N. A.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Original papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2766103/
https://www.ncbi.nlm.nih.gov/pubmed/19737786
http://dx.doi.org/10.1093/qjmed/hcp119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2766103/
https://www.ncbi.nlm.nih.gov/pubmed/19737786
http://dx.doi.org/10.1093/qjmed/hcp119

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