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Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy.
Wolking S, Moreau C, McCormack M, Krause R, Krenn M; EpiPGx Consortium; Berkovic S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Lerche H, Marson AG, O'Brien TJ, Petrovski S, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Sisodiya SM, Girard SL, Cossette P. Wolking S, et al. Among authors: marson ag. Ann Clin Transl Neurol. 2021 Jul;8(7):1376-1387. doi: 10.1002/acn3.51374. Epub 2021 May 21. Ann Clin Transl Neurol. 2021. PMID: 34018700 Free PMC article.
Current drug treatment of epilepsy in adults.
McCorry D, Chadwick D, Marson A. McCorry D, et al. Lancet Neurol. 2004 Dec;3(12):729-35. doi: 10.1016/S1474-4422(04)00935-4. Lancet Neurol. 2004. PMID: 15556805 Review.
The association between polymorphisms in RLIP76 and drug response in epilepsy.
Leschziner GD, Jorgensen AL, Andrew T, Williamson PR, Marson AG, Coffey AJ, Middleditch C, Balding DJ, Rogers J, Bentley DR, Chadwick D, Johnson MR, Pirmohamed M. Leschziner GD, et al. Among authors: marson ag. Pharmacogenomics. 2007 Dec;8(12):1715-22. doi: 10.2217/14622416.8.12.1715. Pharmacogenomics. 2007. PMID: 18086001
Epilepsy.
Marson AG, Maguire M, Ramaratnam S. Marson AG, et al. BMJ Clin Evid. 2009 Jan 28;2009:1201. BMJ Clin Evid. 2009. PMID: 19445769 Review.
Sulthiame add-on therapy for epilepsy.
Milburn-McNulty P, Powell G, Sills GJ, Marson AG. Milburn-McNulty P, et al. Among authors: marson ag. Cochrane Database Syst Rev. 2013 Mar 28;(3):CD009472. doi: 10.1002/14651858.CD009472.pub2. Cochrane Database Syst Rev. 2013. PMID: 23543577 Updated. Review.
De novo mutations in epileptic encephalopathies.
Epi4K Consortium; Epilepsy Phenome/Genome Project; Allen AS, Berkovic SF, Cossette P, Delanty N, Dlugos D, Eichler EE, Epstein MP, Glauser T, Goldstein DB, Han Y, Heinzen EL, Hitomi Y, Howell KB, Johnson MR, Kuzniecky R, Lowenstein DH, Lu YF, Madou MR, Marson AG, Mefford HC, Esmaeeli Nieh S, O'Brien TJ, Ottman R, Petrovski S, Poduri A, Ruzzo EK, Scheffer IE, Sherr EH, Yuskaitis CJ, Abou-Khalil B, Alldredge BK, Bautista JF, Berkovic SF, Boro A, Cascino GD, Consalvo D, Crumrine P, Devinsky O, Dlugos D, Epstein MP, Fiol M, Fountain NB, French J, Friedman D, Geller EB, Glauser T, Glynn S, Haut SR, Hayward J, Helmers SL, Joshi S, Kanner A, Kirsch HE, Knowlton RC, Kossoff EH, Kuperman R, Kuzniecky R, Lowenstein DH, McGuire SM, Motika PV, Novotny EJ, Ottman R, Paolicchi JM, Parent JM, Park K, Poduri A, Scheffer IE, Shellhaas RA, Sherr EH, Shih JJ, Singh R, Sirven J, Smith MC, Sullivan J, Lin Thio L, Venkat A, Vining EP, Von Allmen GK, Weisenberg JL, Widdess-Walsh P, Winawer MR. Epi4K Consortium, et al. Among authors: marson ag. Nature. 2013 Sep 12;501(7466):217-21. doi: 10.1038/nature12439. Epub 2013 Aug 11. Nature. 2013. PMID: 23934111 Free PMC article.
A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.
Speed D, Hoggart C, Petrovski S, Tachmazidou I, Coffey A, Jorgensen A, Eleftherohorinou H, De Iorio M, Todaro M, De T, Smith D, Smith PE, Jackson M, Cooper P, Kellett M, Howell S, Newton M, Yerra R, Tan M, French C, Reuber M, Sills GE, Chadwick D, Pirmohamed M, Bentley D, Scheffer I, Berkovic S, Balding D, Palotie A, Marson A, O'Brien TJ, Johnson MR. Speed D, et al. Hum Mol Genet. 2014 Jan 1;23(1):247-58. doi: 10.1093/hmg/ddt403. Epub 2013 Aug 19. Hum Mol Genet. 2014. PMID: 23962720 Free PMC article.
373 results