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Journal of the Neurological Sciences|December 12, 1997
Tumor necrosis factor alpha and its receptors in relapsing-remitting multiple sclerosisG Martino, A Consiglio, D M Franciotta, et al.Neurogenetics|August 25, 2007
SPG11: a consistent clinical phenotype in a family with homozygous spatacsin truncating mutationRoberto Del Bo, Alessio Di Fonzo, Serena Ghezzi, et al.Brain Research|October 28, 2011
Compensatory movement-related recruitment in amyotrophic lateral sclerosis patients with dominant upper motor neuron signs: an EEG source analysis studyAlberto Inuggi, Nilo Riva, Javier J González-Rosa, et al.Applied and Environmental Microbiology|February 8, 2006
Matrix-assisted laser desorption ionization-time of flight mass spectrometry for the discrimination of food-borne microorganismsMaria Fiorella Mazzeo, Alida Sorrentino, Marcello Gaita, et al.Acta Diabetologica Latina|July 1, 1983
Ganglioside treatment in diabetic peripheral neuropathy: a multicenter trialG Crepaldi, D Fedele, A Tiengo, et al.Journal of the International AIDS Society|November 15, 2014
Factors associated with HPV-DNA clearance in a cohort of HIV-positive patients: role of cART and genderElisa Suardi, Francesca Bai, Laura Comi, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|January 19, 2019
Imaging correlates of hand motor performance in multiple sclerosis: A multiparametric structural and functional MRI studyClaudio Cordani, Alessandro Meani, Federica Esposito, et al.The Lancet. Neurology|December 18, 2018
Safety and efficacy of nabiximols on spasticity symptoms in patients with motor neuron disease (CANALS): a multicentre, double-blind, randomised, placebo-controlled, phase 2 trialNilo Riva, Gabriele Mora, Gianni Sorarù, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|November 8, 2006
The Italian Multiple Sclerosis Database Network (MSDN): the risk of worsening according to IFNbeta exposure in multiple sclerosisMaria Trojano, Pierluigi Russo, Aurora Fuiani, et al.Neuromuscular Disorders : NMD|July 27, 2007
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiencyOlimpia Musumeci, Mohammed Aguennouz, Giacomo Pietro Comi, et al.Pageof 253