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Developmental Medicine and Child Neurology|February 23, 2026
Developmental stuttering with common and complex phenotypesSarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2020
Levetiracetam efficacy in PCDH19 Girls Clustering EpilepsyLynette G Sadleir, Kristy L Kolc, Chontelle King, et al.Epilepsia|August 27, 2016
Hippocampal malrotation is an anatomic variant and has no clinical significance in MRI-negative temporal lobe epilepsyMeng-Han Tsai, David N Vaughan, Yuliya Perchyonok, et al.Journal of Medical Genetics|March 8, 2013
Recent advances in the molecular genetics of epilepsyMichael S Hildebrand, Hans-Henrik M Dahl, John Anthony Damiano, et al.Developmental Medicine and Child Neurology|June 15, 2013
Head stereotypies in STXBP1 encephalopathyYoung Ok Kim, Christian M Korff, Mel Michel G Villaluz, et al.Developmental Medicine and Child Neurology|March 5, 2019
Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizuresRima Nabbout, Stephane Auvin, Catherine Chiron, et al.Epilepsy Research|April 19, 2017
Evaluation of GLUT1 variation in non-acquired focal epilepsyAlexander Peeraer, John A Damiano, Susannah T Bellows, et al.Epilepsia|May 1, 2022
International consensus on diagnosis and management of Dravet syndromeElaine C Wirrell, Veronica Hood, Kelly G Knupp, et al.Nature Communications|July 21, 2022
Heterogeneous nuclear ribonucleoprotein U (HNRNPU) safeguards the developing mouse cortexTamar Sapir, Aditya Kshirsagar, Anna Gorelik, et al.Neurology|June 11, 2013
Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomalyMeng-Han Tsai, Heath R Pardoe, Yuliya Perchyonok, et al.Pageof 57