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Sleep Medicine|December 14, 2024
Actigraphy validation in behavioral variant frontotemporal dementiaLudovica Tamburrino, Benedetta Tafuri, Valentina Gnoni, et al.Brain and Behavior|October 28, 2017
Gender differences in safety issues during Fingolimod therapy: Evidence from a real-life Relapsing Multiple Sclerosis cohortAlessia Manni, Vita Direnzo, Antonio Iaffaldano, et al.Journal of Clinical Pharmacology|November 27, 2015
Long-Term Data of Efficacy, Safety, and Tolerability in a Real-Life Setting of THC/CBD Oromucosal Spray-Treated Multiple Sclerosis PatientsDamiano Paolicelli, Vita Direnzo, Alessia Manni, et al.Journal of Neurology|June 20, 2023
The impact of upper and lower motor neuron burden on diagnostic certainty, and clinical course of spinal-onset amyotrophic lateral sclerosis: a cluster-based approachGiammarco Milella, Stefano Zoccolella, Alessia Giugno, et al.Neuromuscular Disorders : NMD|May 12, 2009
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegiaRoberto Negro, Stefano Zoccolella, Rosa Dell'aglio, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 9, 2012
Mitochondrial genome aberrations in skeletal muscle of patients with motor neuron diseaseLucia Artuso, Stefano Zoccolella, Paola Favia, et al.Journal of Neurology|March 3, 2021
Magnetic resonance metrics to evaluate the effect of therapy in amyotrophic lateral sclerosis: the experience with edaravoneEugenio Distaso, Giammarco Milella, Domenico Maria Mezzapesa, et al.Journal of Alzheimer'S Disease : JAD|July 12, 2020
Telemedicine for Delivery of Care in Frontotemporal Lobar Degeneration During COVID-19 Pandemic: Results from Southern ItalyRosa Capozzo, Stefano Zoccolella, Maria Elisa Frisullo, et al.Journal of Neurology|April 14, 2007
ALS multidisciplinary clinic and survival. Results from a population-based study in Southern ItalyStefano Zoccolella, Ettore Beghi, Guerrino Palagano, et al.BMC Medical Genetics|July 29, 2018
Leber's hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G >A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene - case reportAngelica Bianco, Luigi Bisceglia, Maria Fara De Caro, et al.Pageof 7