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Neurology. Genetics|July 20, 2019
Human GABRG2 generalized epilepsy: Increased somatosensory and striatothalamic connectivityMangor Pedersen, Magdalena Kowalczyk, Amir Omidvarnia, et al.Epilepsia|January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrumJohn A Damiano, Rosemary Burgess, Sara Kivity, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|November 20, 2008
Multifocal epilepsy: the role of palliative resection - intractable frontal and occipital lobe epilepsy secondary to radiotherapy for acute lymphoblastic leukaemiaAshalatha Radhakrishnan, Pasiri Sithinamsuwan, A Simon Harvey, et al.Epilepsia|July 12, 2012
Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrumKarl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.Epilepsia|April 14, 2010
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3Sarah E Heron, Ingrid E Scheffer, Bronwyn E Grinton, et al.Epilepsia|July 23, 2011
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypesJohn C Mulley, Ingrid E Scheffer, Tarishi Desai, et al.Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.Epilepsia|December 24, 2011
Long-term follow-up of febrile infection-related epilepsy syndromeKatherine B Howell, Kamornwan Katanyuwong, Mark T Mackay, et al.Pageof 73