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Georg A. Petroianu

Faculty of Medicine and Health Sciences

United Arab Emirates University

Department of Pharmacology & Therapeutics

P.O. Box 17 666

Al Ain - UAE

[email]@uaeu.ac.ae

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Faculty of Medicine and Health Sciences, United Arab Emirates University, Department of Pharmacology & Therapeutics, P.O. Box 17 666, Al Ain - UAE. 2008
  • UAE University, Faculty of Medicine & Health Sciences, Al Ain - United Arab Emirates. 2003 - 2008
  • UAE University, Al Ain-UAE. 2005 - 2007
  • Department of Pharmacology and Therapeutics, FMHS, United Arab Emirates University, Al Ain, United Arab Emirates. 2001 - 2007
  • Institute of Pharmacology & Toxicology, University of Heidelberg at Mannheim, D-68169 Mannheim, Germany. 2004

References

  1. Pyridinium oxime reactivators of cholinesterase inhibited by diisopropyl-fluorophosphate (DFP): predictive value of in-vitro testing for in-vivo efficacy. Petroianu, G.A., Lorke, D.E. Mini. Rev. Med. Chem (2008) [Pubmed]
  2. The history of cholinesterase inhibitors: who was Moschnin(e)?. Petroianu, G.A. Pharmazie (2008) [Pubmed]
  3. Five oximes (K-27, K-48, obidoxime, HI-6 and trimedoxime) in comparison with pralidoxime: survival in rats exposed to methyl-paraoxon. Petroianu, G.A., Nurulain, S.M., Nagelkerke, N., Shafiullah, M., Kassa, J., Kuca, K. J. Appl. Toxicol (2007) [Pubmed]
  4. In vitro oxime reactivation of red blood cell acetylcholinesterase inhibited by methyl-paraoxon. Petroianu, G.A., Arafat, K., Nurulain, S.M., Kuca, K., Kassa, J. J. Appl. Toxicol (2007) [Pubmed]
  5. Paraoxon has only a minimal effect on pralidoxime brain concentration in rats. Petroianu, G.A., Lorke, D.E., Hasan, M.Y., Adem, A., Sheen, R., Nurulain, S.M., Kalasz, H. J. Appl. Toxicol (2007) [Pubmed]
  6. Comparison of two pre-exposure treatment regimens in acute organophosphate (paraoxon) poisoning in rats: tiapride vs. pyridostigmine. Petroianu, G.A., Hasan, M.Y., Nurulain, S.M., Arafat, K., Sheen, R., Nagelkerke, N. Toxicol. Appl. Pharmacol. (2007) [Pubmed]
  7. Five oximes (K-27, K-33, K-48, BI-6 and methoxime) in comparison with pralidoxime: in vitro reactivation of red blood cell acetylcholinesterase inhibited by paraoxon. Petroianu, G.A., Arafat, K., Kuca, K., Kassa, J. J. Appl. Toxicol (2006) [Pubmed]
  8. Tiapride pre-treatment in acute exposure to paraoxon: comparison of effects of administration at different points-in-time in rats. Petroianu, G.A., Hasan, M.Y., Nurulain, S.M., Arafat, K., Shafiullah, M., Sheen, R. Mol. Cell. Biochem. (2006) [Pubmed]
  9. Five oximes (K-27, K-33, K-48, BI-6 and methoxime) in comparison with pralidoxime: survival in rats exposed to the organophosphate paraoxon. Petroianu, G.A., Nurulain, S.M., Nagelkerke, N., Al-Sultan, M.A., Kuca, K., Kassa, J. J. Appl. Toxicol (2006) [Pubmed]
  10. Effect of pyridostigmine, pralidoxime and their combination on survival and cholinesterase activity in rats exposed to the organophosphate paraoxon. Petroianu, G.A., Nurulain, S.M., Arafat, K., Rajan, S., Hasan, M.Y. Arch. Toxicol. (2006) [Pubmed]
  11. Ranitidine in acute high-dose organophosphate exposure in rats: effect of the time-point of administration and comparison with pyridostigmine. Petroianu, G.A., Hasan, M.Y., Nurulain, S.M., Shafiullah, M., Sheen, R., Nagelkerke, N. Basic Clin. Pharmacol. Toxicol. (2006) [Pubmed]
  12. Weak inhibitors protect cholinesterases from strong inhibitors (paraoxon): in vitro effect of ranitidine. Petroianu, G.A., Arafat, K., Schmitt, A., Hasan, M.Y. J. Appl. Toxicol (2005) [Pubmed]
  13. Protective agents in acute high-dose organophosphate exposure: comparison of ranitidine with pralidoxime in rats. Petroianu, G.A., Hasan, M.Y., Nurulain, S.M., Arafat, K., Sha Ullah, M., Naseer, O. J. Appl. Toxicol (2005) [Pubmed]
  14. Protective drugs in acute large-dose exposure to organophosphates: a comparison of metoclopramide and tiapride with pralidoxime in rats. Petroianu, G.A., Hasan, M.Y., Nurulain, S.M., Arafat, K., Sheen, R., Saleh, A., Schmitt, A. Anesth. Analg. (2005) [Pubmed]
  15. Organophosphate poisoning: the lesser-known face of a toxidrome. Petroianu, G.A. Eur. J. Emerg. Med (2005) [Pubmed]
  16. Weak inhibitors protect cholinesterases from stronger inhibitors (dichlorvos): in vitro effect of tiapride. Petroianu, G.A., Schmitt, A., Arafat, K., Hasan, M.Y. Int. J. Toxicol. (2005) [Pubmed]
  17. Weak inhibitors protect cholinesterases from strong inhibitors (paraoxon): in vitro effect of tiapride. Petroianu, G.A., Hasan, M.Y., Arafat, K., Nurulain, S.M., Schmitt, A. J. Appl. Toxicol (2005) [Pubmed]
  18. In vitro protection of plasma cholinesterases by metoclopramide from inhibition by mipafox. Petroianu, G., Kühn, F., Arafat, K., Zuleger, K., Missler, A. J. Appl. Toxicol (2004) [Pubmed]
  19. Enzyme reactivator treatment in organophosphate exposure: clinical relevance of thiocholinesteratic activity of pralidoxime. Petroianu, G.A., Missler, A., Zuleger, K., Thyes, C., Ewald, V., Maleck, W.H. J. Appl. Toxicol (2004) [Pubmed]
  20. Intravenous pyruvic acid application in minipigs partially protects acetylcholine-esteratic but not butyrylcholine-esteratic activity in plasma from inhibition by paraoxon. Petroianu, G.A., Ewald, V., Thyes, C., Missler, A., Maleck, W.H. J. Appl. Toxicol (2003) [Pubmed]
  21. In vitro protection of plasma cholinesterases by metoclopramide from inhibition by paraoxon. Petroianu, G., Kühn, F., Thyes, C., Ewald, V., Missler, A. J. Appl. Toxicol (2003) [Pubmed]
  22. Effect of in vitro hemodilution with hydroxyethyl starch and dextran on the activity of plasma clotting factors. Petroianu, G.A., Maleck, W.H., Koetter, K.P., Liu, J., Schmitt, A. Crit. Care Med. (2003) [Pubmed]
  23. In vitro protection of red blood cell acetylcholinesterase by metoclopramide from inhibition by organophosphates (paraoxon and mipafox). Petroianu, G., Arafat, K., Kosanovic, M., Saleh, A., Camasamudram, V., Hasan, M.Y. J. Appl. Toxicol (2003) [Pubmed]
  24. Kinetics of intravenous L-lactic acid in anaesthetized minipigs under normoxic/normocapnic/normohydrogenaemic conditions. Petroianu, G., Kern, N., Kaercher, B., Rüfer, R. J. Appl. Toxicol (2001) [Pubmed]
 
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