Idiopathic Epilepsies with Seizures Precipitated by Fever and <i>SCN1A</i> Abnormalities

Carla Marini, Davide Mei, Teresa Temudo, +14

Epilepsia

Germline and mosaic mutations of <i>FLN1</i> in men with periventricular heterotopia

Renzo Guerrini, Davide Mei, S. M. Sisodiya, +10

Neurology

Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutations

Valentina Cetica, Sara Chiari, Davide Mei, +16

Neurology

Mosaic mutations of the <i>LIS1</i> gene cause subcortical band heterotopia

Federico Sicca, Arpad Kelemen, Pierre Genton, +5

Neurology

Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-function of the Inwardly-Rectifying K+ Channel Kir4.1

Federico Sicca, Paola Imbrici, Maria Cristina D’Adamo, +8

Neurobiology of Disease

Neurodevelopmental DisordersMolecular NeurosciencePossible Causative RoleNeurophysiologySyndromic Autism +10

Epilepsy and malformations of the cerebral cortex

Renzo Guerrini, Federico Sicca, Lucio Parmeggiani

Epileptic Disorders

Developmental Cognitive NeuroscienceNeurological DisorderCorticobasal DegenerationPathologyBrain Lesion +18

Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish

Brian P. Grone, Maria Marchese, Kyla R. Hamling, +6

PLoS ONE

Brain DevelopmentGeneticsSynaptic TransmissionCrispr/cas9 GeneNeurotransmission +16

Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations

Nicola Specchio, Carla Marini, Davide Mei, +9

Epilepsia

Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype

Elena Ambrosini, Federico Sicca, Maria Stefania Brignone, +19

Human Molecular Genetics

Focal seizures with affective symptoms are a major feature of <i>PCDH19</i> gene–related epilepsy

Carla Marini, Francesca Darra, Nicola Specchio, +21

Epilepsia