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Elife|May 4, 2021
DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formationLaura Morcom, Timothy J Edwards, Eric Rider, et al.
Annals of Neurology|December 10, 2013
Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathyGökce Orhan, Merle Bock, Dorien Schepers, et al.
Brain : a Journal of Neurology|April 21, 2010
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patientsRichard J Leventer, Anna Jansen, Daniela T Pilz, et al.
Neurology|August 11, 2017
Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotypeLynette G Sadleir, Emily I Mountier, Deepak Gill, et al.
Brain : a Journal of Neurology|February 24, 2019
Dorsal language stream anomalies in an inherited speech disorderFrédérique J Liégeois, Samantha J Turner, Angela Mayes, et al.
Epilepsia|November 25, 2017
Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45Gemma L Carvill, Aijie Liu, Simone Mandelstam, et al.
Annals of Neurology|March 4, 2014
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformationsIngrid E Scheffer, Sarah E Heron, Brigid M Regan, et al.
Neurology|August 21, 2015
SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizuresKatherine B Howell, Jacinta M McMahon, Gemma L Carvill, et al.
Neurology. Genetics|April 12, 2016
Epileptic spasms are a feature of DEPDC5 mTORopathyGemma L Carvill, Douglas E Crompton, Brigid M Regan, et al.
Circulation|November 24, 2020
Neurocognitive Dysfunction and Smaller Brain Volumes in Adolescents and Adults With a Fontan CirculationCharlotte E Verrall, Joseph Y M Yang, Jian Chen, et al.
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