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Year Number of Results
2006 2
2008 3
2009 1
2010 1
2011 2
2013 1
2014 1
2017 1
2018 1
2019 3
2024 0

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15 results

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Page 1
Sleep and epilepsy.
Derry CP, Duncan S. Derry CP, et al. Epilepsy Behav. 2013 Mar;26(3):394-404. doi: 10.1016/j.yebeh.2012.10.033. Epilepsy Behav. 2013. PMID: 23465654 Review.
Autoimmune limbic encephalitis.
Derry CP, Wilkie MD, Al-Shahi Salman R, Davenport RJ. Derry CP, et al. Clin Med (Lond). 2011 Oct;11(5):476-8. doi: 10.7861/clinmedicine.11-5-476. Clin Med (Lond). 2011. PMID: 22034711 Free PMC article.
Hiding in Plain Sight: Functional Neurological Disorders in the News.
Popkirov S, Nicholson TR, Bloem BR, Cock HR, Derry CP, Duncan R, Dworetzky BA, Edwards MJ, Espay AJ, Hallett M, Lang AE, Leach JP, Lehn A, McGonigal A, Morgante F, Perez DL, Reuber M, Richardson MP, Smith P, Stamelou M, Tijssen MAJ, Tinazzi M, Carson AJ, Stone J. Popkirov S, et al. Among authors: derry cp. J Neuropsychiatry Clin Neurosci. 2019 Fall;31(4):361-367. doi: 10.1176/appi.neuropsych.19010025. Epub 2019 May 23. J Neuropsychiatry Clin Neurosci. 2019. PMID: 31117907 Free PMC article.
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
Dibbens LM, Tarpey PS, Hynes K, Bayly MA, Scheffer IE, Smith R, Bomar J, Sutton E, Vandeleur L, Shoubridge C, Edkins S, Turner SJ, Stevens C, O'Meara S, Tofts C, Barthorpe S, Buck G, Cole J, Halliday K, Jones D, Lee R, Madison M, Mironenko T, Varian J, West S, Widaa S, Wray P, Teague J, Dicks E, Butler A, Menzies A, Jenkinson A, Shepherd R, Gusella JF, Afawi Z, Mazarib A, Neufeld MY, Kivity S, Lev D, Lerman-Sagie T, Korczyn AD, Derry CP, Sutherland GR, Friend K, Shaw M, Corbett M, Kim HG, Geschwind DH, Thomas P, Haan E, Ryan S, McKee S, Berkovic SF, Futreal PA, Stratton MR, Mulley JC, Gécz J. Dibbens LM, et al. Among authors: derry cp. Nat Genet. 2008 Jun;40(6):776-81. doi: 10.1038/ng.149. Epub 2008 May 11. Nat Genet. 2008. PMID: 18469813 Free PMC article.
Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations.
Corbett MA, Turner SJ, Gardner A, Silver J, Stankovich J, Leventer RJ, Derry CP, Carroll R, Ha T, Scheffer IE, Bahlo M, Jackson GD, Mackey DA, Berkovic SF, Gecz J. Corbett MA, et al. Among authors: derry cp. Eur J Med Genet. 2017 Aug;60(8):437-443. doi: 10.1016/j.ejmg.2017.06.002. Epub 2017 Jun 8. Eur J Med Genet. 2017. PMID: 28602933
15 results