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Neurology|January 18, 2015
GRIN2A: an aptly named gene for speech dysfunctionSamantha J Turner, Angela K Mayes, Andrea Verhoeven, et al.
Neuroscience and Biobehavioral Reviews|October 17, 2025
Pharmacological and dietary treatments for developmental stuttering: A systematic reviewSarah E Horton, Elana J Forbes, Ingrid E Scheffer, et al.
Neurology|August 22, 2014
Rasmussen encephalitis and comorbid autoimmune diseases: A window into disease mechanism?Dina Amrom, Demet Kinay, Yvonne Hart, et al.
Brain : a Journal of Neurology|June 27, 2025
Twins with temporal lobe epilepsy: genetic contributions to hippocampal sclerosis and other subtypesYew Li Dang, Kate Esnault, Gregory Fitt, et al.
Human Molecular Genetics|July 1, 2015
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiencyChuan Tan, Chloe Shard, Enzo Ranieri, et al.
Orphanet Journal of Rare Diseases|April 22, 2021
Guidelines on the diagnosis, clinical assessments, treatment and management for CLN2 disease patientsSara E Mole, Angela Schulz, Eben Badoe, et al.
Brain Communications|November 21, 2025
Novel, complex configurations of the MARCHF6 repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsyMark F Bennett, Mark A Corbett, Thessa Kroes, et al.
Brain : a Journal of Neurology|June 25, 2004
Temporal lobectomy: long-term seizure outcome, late recurrence and risks for seizure recurrenceAnne M McIntosh, Renate M Kalnins, L Anne Mitchell, et al.
American Journal of Human Genetics|July 26, 2016
Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic EpilepsyMichael S Hildebrand, Nicole G Griffin, John A Damiano, et al.
Developmental Medicine and Child Neurology|February 12, 2009
Electroencephalographic abnormalities during sleep in children with developmental speech-language disorders: a case-control studyBronwyn Parry-Fielder, Kevin Collins, John Fisher, et al.
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