|1.||Kuca, Kamil: 9 articles (06/2009 - 11/2005)|
|2.||Kassa, Jiri: 7 articles (06/2009 - 09/2006)|
|3.||McDonough, John H: 4 articles (01/2011 - 04/2003)|
|4.||Shih, Tsung-Ming: 4 articles (01/2011 - 04/2003)|
|5.||Jun, Daniel: 4 articles (09/2008 - 11/2005)|
|6.||Kassa, Jirí: 3 articles (01/2012 - 01/2008)|
|7.||Musilek, Kamil: 3 articles (06/2009 - 01/2009)|
|8.||Bajgar, Jiri: 3 articles (03/2009 - 09/2008)|
|9.||Karasova, Jana: 3 articles (01/2009 - 11/2007)|
|10.||Karasova, Jana Zdarova: 2 articles (06/2009 - 03/2009)|
01/01/2012 - "The ability of oxime mixtures to increase the reactivating and therapeutic efficacy of antidotal treatment of cyclosarin poisoning in rats and mice."
01/01/2008 - "They are therefore not suitable replacements for antidotal treatment of acute poisonings with cyclosarin."
01/01/1995 - "Changes in serum biochemical and hematological parameters were studied in 20 male rhesus monkeys following acute poisoning by the organophosphate nerve agent cyclohexylmethylphosphonofluoridate (CMPF or GF). "
01/01/1992 - "Evaluation of the toxicity, pathology, and treatment of cyclohexylmethylphosphonofluoridate (CMPF) poisoning in rhesus monkeys."
01/01/1992 - "Efficacy of various oximes against GF (cyclohexyl methylphosphonofluoridate) poisoning in mice."
01/01/2011 - "Pro-2-PAM was able to reactivate blood, heart, and spinal cord ChE inhibited by cyclosarin, but was not effective against cyclosarin-induced seizures."
01/01/2011 - "Pro-2-PAM was able to block sarin- or VX-induced seizures (16-33%) over a dose range of 24-32 mg/kg, but was ineffective against cyclosarin-induced seizures. "
11/01/2010 - "Comparison of extracellular striatal acetylcholine and brain seizure activity following acute exposure to the nerve agents cyclosarin and tabun in freely moving guinea pigs."
01/01/2007 - "With the lower dose of atropine, seizure occurrence increased to virtually 100% for all agents; the time to seizure onset decreased for sarin, cyclosarin, and VX; the signs of nerve agent intoxication were more severe; and coma resulted frequently with cyclosarin. "
09/01/2015 - "The treatment was given 1 and 5min after exposure to a supralethal dose of nerve agents, and the results showed that the triple regimen successfully prevented or terminated seizures and preserved the lives of rats exposed to 5×LD50 of soman, sarin, cyclosarin, or VX, but solely 3×LD50 of tabun was managed by this regimen. "
|1.||HI 6 (H16)
|5.||Obidoxime Chloride (Obidoxime)
|8.||pralidoxime (Protopam Chloride)