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Neurology. Genetics|May 27, 2016
White matter involvement in a family with a novel PDGFB mutationRoberta Biancheri, Mariasavina Severino, Angela Robbiano, et al.
Epilepsia|February 4, 2009
Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patientsEdoardo Ferlazzo, Constant K Adjien, Renzo Guerrini, et al.
Journal of Epilepsy Research|March 4, 2021
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language ImpairmentPiero Pavone, Xena Giada Pappalardo, Ugochi Ngaobiri Nelly Ohazuruike, et al.
Acta Bio-Medica : Atenei Parmensis|April 20, 2022
Therapeutic aspects of Sydenham's Chorea: an updateGreta Depietri, Niccolo Carli, Attilio Sica, et al.
Biochemical and Biophysical Research Communications|June 29, 2023
Exome sequencing data screening to identify undiagnosed Aromatic l-amino acid decarboxylase deficiency in neurodevelopmental disordersAntonella Riva, Michele Iacomino, Chiara Piccardo, et al.
Expert Review of Neurotherapeutics|May 17, 2021
Diagnostic and therapeutic approach to drug-resistant juvenile myoclonic epilepsyMichele Ascoli, Giovanni Mastroianni, Sara Gasparini, et al.
Seizure|September 16, 2011
The genetics of monogenic idiopathic epilepsies and epileptic encephalopathiesFrancesco Nicita, Paola De Liso, Federica Rachele Danti, et al.
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