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Annals of Clinical and Translational Neurology|May 23, 2015
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5Thomas Scerri, Jessica R Riseley, Greta Gillies, et al.
Brain Pathology (Zurich, Switzerland)|August 28, 2020
Medullary tyrosine hydroxylase catecholaminergic neuronal populations in sudden unexpected death in epilepsySmriti Patodia, Ian Tan, Matthew Ellis, et al.
Autism Research : Official Journal of the International Society for Autism Research|October 1, 2019
Cognitive processes predicting advanced theory of mind in the broader autism phenotypeCherie C Green, Natasha J Brown, Valerie M Z Yap, et al.
Molecular Psychiatry|February 17, 2024
Genetic architecture of childhood speech disorder: a reviewAngela T Morgan, David J Amor, Miya D St John, et al.
Archives of Neurology|June 15, 2011
Mutation of SCARB2 in a patient with progressive myoclonus epilepsy and demyelinating peripheral neuropathyLeanne M Dibbens, Ioannis Karakis, Marta A Bayly, et al.
Annals of Neurology|February 27, 2010
Predicting seizure control: cortical excitability and antiepileptic medicationRadwa A B Badawy, Richard A L Macdonell, Samuel F Berkovic, et al.
Neurology|February 15, 2013
Multiple molecular mechanisms for a single GABAA mutation in epilepsyChristopher A Reid, Taehwan Kim, A Marie Phillips, et al.
Epilepsy Research|February 14, 2017
SCN1A clinical spectrum includes the self-limited focal epilepsies of childhoodSara Kivity, Karen L Oliver, Zaid Afawi, et al.
British Journal of Pharmacology|October 25, 2016
Synaptic Zn2+ and febrile seizure susceptibilityChristopher A Reid, Michael S Hildebrand, Saul A Mullen, et al.
Epilepsy Research|July 17, 2019
Deciphering the role of epigenetics in self-limited epilepsy with centrotemporal spikesNamitha Mohandas, Yuk Jing Loke, Lisa Mackenzie, et al.
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