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Epileptic Disorders : International Epilepsy Journal with Videotape|February 29, 2024
Acute encephalopathy with biphasic seizures and late reduced diffusion with concurrent transverse myelitisAmanda Austin-Keiller, Christine Saint-Martin, Kenneth A MyersClinical EEG and Neuroscience|December 26, 2022
Response to Hydrocortisone in an Extremely Preterm Neonate With Late-Onset Sepsis, Meningoencephalitis, and Drug-Resistant SeizuresRalf Eberhard, Katryn Paquette, Jarred Garfinkle, et al.Pediatric Neurology|January 23, 2013
Infantile ictal apneas in a child with williams-beuren syndromeKenneth A Myers, D Ross McLeod, Luis Bello-EspinosaEuropean Journal of Medical Genetics|September 24, 2009
4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairmentAlison Yeung, Damien Bruno, Ingrid E Scheffer, et al.The Journal of Clinical Endocrinology and Metabolism|November 29, 2007
Association of a nicotinic receptor mutation with reduced height and blunted physostigmine-stimulated growth hormone releaseMarco Fedi, Leon A Bach, Samuel F Berkovic, et al.Epilepsia|February 22, 2023
Genes4Epilepsy: An epilepsy gene resourceKaren L Oliver, Ingrid E Scheffer, Mark F Bennett, et al.Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|July 23, 2019
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of SpeechSamantha J Turner, Adam P Vogel, Bronwyn Parry-Fielder, et al.Human Mutation|May 10, 2005
SCN1A mutations and epilepsyJohn C Mulley, Ingrid E Scheffer, Steven Petrou, et al.Epilepsia|July 12, 2008
Factors influencing clinical features of absence seizuresLynette G Sadleir, Ingrid E Scheffer, Sherry Smith, et al.Nature Reviews. Disease Primers|May 4, 2018
EpilepsyOrrin Devinsky, Annamaria Vezzani, Terence J O'Brien, et al.Pageof 67