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Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Nature Communications|February 11, 2025
Burst-like swarms in the Campi Flegrei caldera accelerating unrest from 2021 to 2024Flora Giudicepietro, Rosario Avino, Eliana Bellucci Sessa, et al.
Epilepsy Research|August 26, 2019
An Italian multicentre study of perampanel in progressive myoclonus epilepsiesLaura Canafoglia, Giuseppina Barbella, Edoardo Ferlazzo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 6, 2019
Hypertension, seizures, and epilepsy: a review on pathophysiology and managementSara Gasparini, Edoardo Ferlazzo, Chiara Sueri, et al.
Frontiers in Molecular Neuroscience|March 18, 2024
Human mutations in SLITRK3 implicated in GABAergic synapse development in miceStephanie Efthymiou, Wenyan Han, Muhammad Ilyas, et al.
Expert Review of Neurotherapeutics|July 2, 2019
Microbiota-gut brain axis involvement in neuropsychiatric disordersLuigi Francesco Iannone, Alberto Preda, Hervé M Blottière, et al.
Epilepsia Open|March 15, 2019
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepineBianca Berghuis, Caragh Stapleton, Anja C M Sonsma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 30, 2023
Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalitiesMarcello Scala, Kamal Khan, Claire Beneteau, et al.
American Journal of Human Genetics|August 30, 2025
Pathogenic variants in TMEM184B cause a neurodevelopmental syndrome associated with alteration of metabolic signalingKimberly A Chapman, Farid Ullah, Zachary A Yahiku, et al.
Brain Communications|December 15, 2021
Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathyLaura C Bott, Mitra Forouhan, Maria Lieto, et al.
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