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Neurogenetics|June 28, 2018
Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genesZied Landoulsi, Fatma Laatar, Eric Noé, et al.La Tunisie Medicale|March 12, 2024
Psychiatric disturbances in idiopathic epilepsySaloua Mrabet, Syrine Belguith, Imen Kacem, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|August 2, 2019
Juvenile myoclonic epilepsy phenotype in a family with Unverricht-Lundborg diseaseAmina Gargouri Berrechid, Mouna Bendjebara, Delphine Bouteiller, et al.Journal of Movement Disorders|April 22, 2024
The Impact of LRRK2 G2019S on Parkinson's Disease: Clinical Phenotype and Treatment in Tunisian PatientsGuedi Ali Barreh, Ikram Sghaier, Youssef Abida, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 17, 2020
Characteristics, onset, and evolution of neurological symptoms in patients with COVID-19Imen Kacem, Alya Gharbi, Chahida Harizi, et al.Journal of Neurology|February 3, 2026
Effect of late-onset on multiple sclerosis phenotype and outcome: evidence from a multi-national registryAmira Souissi, Francesco Patti, Tim Spelman, et al.Pageof 5