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Neuromuscular Disorders : NMD|November 1, 1995
Duplication of dystrophin gene and dissimilar clinical phenotype in the same familyA Toscano, L Vitiello, G P Comi, et al.Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.Acta Neuropathologica Communications|September 13, 2014
MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samplesMarco Savarese, Giuseppina Di Fruscio, Margherita Mutarelli, et al.AJNR. American Journal of Neuroradiology|July 19, 2014
Transorbital sonography in acute optic neuritis: a case-control studyP Lochner, R Cantello, F Brigo, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|January 6, 2018
Cognitive reserve, cognition, and regional brain damage in MS: A 2 -year longitudinal studyMaria Assunta Rocca, Gianna C Riccitelli, Alessandro Meani, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|January 19, 2021
CSF extracellular vesicles and risk of disease activity after a first demyelinating eventGloria Dalla Costa, Tommaso Croese, Marco Pisa, et al.Journal of Clinical Medicine|April 17, 2019
K Index is a Reliable Marker of Intrathecal Synthesis, and an Alternative to IgG Index in Multiple Sclerosis Diagnostic Work-UpIlaria Crespi, Domizia Vecchio, Roberto Serino, et al.Brain Stimulation|July 11, 2012
Mapping early changes of cortical motor output after subcortical stroke: a transcranial magnetic stimulation studyRaffaella Chieffo, Alberto Inuggi, Laura Straffi, et al.Journal of the Peripheral Nervous System : JPNS|May 22, 2014
Balance exercise in patients with chronic sensory ataxic neuropathy: a pilot studyNilo Riva, Simone Faccendini, Ignazio D Lopez, et al.Muscle & Nerve|June 18, 2003
Novel missense mutation and large deletion of GNE gene in autosomal-recessive inclusion-body myopathyRoberto Del Bo, Pierluigi Baron, Alessandro Prelle, et al.Pageof 253