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Brain Sciences|August 6, 2020
Diagnosis and Management of Type 1 Sialidosis: Clinical Insights from Long-Term Care of Four Unrelated PatientsAntonietta Coppola, Marta Ianniciello, Ebru N Vanli-Yavuz, et al.
Biochemical and Biophysical Research Communications|January 25, 2006
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancyElena Gennaro, Filippo M Santorelli, Enrico Bertini, et al.
Epilepsia|March 11, 2015
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsyLaura Mumoli, Patrizia Tarantino, Roberto Michelucci, et al.
Neurology|September 22, 2017
Variable course of Unverricht-Lundborg disease: Early prognostic factorsLaura Canafoglia, Edoardo Ferlazzo, Roberto Michelucci, et al.
Neurology. Genetics|February 3, 2026
Functional Characterization of a De Novo SCN2A Mixed Variant Linked to Early Infantile Developmental and Epileptic EncephalopathyAnna Corradi, Antonella Riva, Bruno Sterlini, et al.
International Journal of Molecular Sciences|April 30, 2021
Biallelic Variants in KIF17 Associated with Microphthalmia and Coloboma SpectrumAntonella Riva, Antonella Gambadauro, Valeria Dipasquale, et al.
Epilepsy & Behavior : E&B|February 1, 2017
The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutationsRoberto Michelucci, Patrizia Pulitano, Carlo Di Bonaventura, et al.
American Journal of Medical Genetics. Part A|August 15, 2006
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new casesPasquale Striano, Michela Malacarne, Simona Cavani, et al.
Seizure|October 15, 2021
Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-upVincenzo Belcastro, Susanna Casellato, Pasquale Striano, et al.
Neurology International|April 25, 2025
Neonatal Perforator Stroke: Timing, Risk Factors, and Neurological Outcome from a Single-Center ExperienceAndrea Calandrino, Gaia Cipresso, Marcella Battaglini, et al.
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