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Developmental impact of a familial GABAA receptor epilepsy mutation.
Chiu C, Reid CA, Tan HO, Davies PJ, Single FN, Koukoulas I, Berkovic SF, Tan SS, Sprengel R, Jones MV, Petrou S. Chiu C, et al. Among authors: petrou s. Ann Neurol. 2008 Sep;64(3):284-93. doi: 10.1002/ana.21440. Ann Neurol. 2008. PMID: 18825662 Free PMC article.
Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy.
Tan HO, Reid CA, Single FN, Davies PJ, Chiu C, Murphy S, Clarke AL, Dibbens L, Krestel H, Mulley JC, Jones MV, Seeburg PH, Sakmann B, Berkovic SF, Sprengel R, Petrou S. Tan HO, et al. Among authors: petrou s. Proc Natl Acad Sci U S A. 2007 Oct 30;104(44):17536-41. doi: 10.1073/pnas.0708440104. Epub 2007 Oct 18. Proc Natl Acad Sci U S A. 2007. PMID: 17947380 Free PMC article.
Mechanisms of human inherited epilepsies.
Reid CA, Berkovic SF, Petrou S. Reid CA, et al. Among authors: petrou s. Prog Neurobiol. 2009 Jan 12;87(1):41-57. doi: 10.1016/j.pneurobio.2008.09.016. Epub 2008 Oct 5. Prog Neurobiol. 2009. PMID: 18952142 Review.
Multiple molecular mechanisms for a single GABAA mutation in epilepsy.
Reid CA, Kim T, Phillips AM, Low J, Berkovic SF, Luscher B, Petrou S. Reid CA, et al. Among authors: petrou s. Neurology. 2013 Mar 12;80(11):1003-8. doi: 10.1212/WNL.0b013e3182872867. Epub 2013 Feb 13. Neurology. 2013. PMID: 23408872 Free PMC article.
KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine.
Milligan CJ, Li M, Gazina EV, Heron SE, Nair U, Trager C, Reid CA, Venkat A, Younkin DP, Dlugos DJ, Petrovski S, Goldstein DB, Dibbens LM, Scheffer IE, Berkovic SF, Petrou S. Milligan CJ, et al. Among authors: petrou s. Ann Neurol. 2014 Apr;75(4):581-90. doi: 10.1002/ana.24128. Epub 2014 Apr 14. Ann Neurol. 2014. PMID: 24591078 Free PMC article.
746 results