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Journal of Neurology, Neurosurgery, and Psychiatry|June 21, 2005
Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathyS Benedetti, E Bertini, S Iannaccone, et al.
Nucleic Acids Research|September 18, 2008
Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybridsPeter Seibel, Chiara Di Nunno, Christian Kukat, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 14, 2012
Cortical activation to voluntary movement in amyotrophic lateral sclerosis is related to corticospinal damage: electrophysiological evidenceN Riva, A Falini, A Inuggi, et al.
Pediatric Neurology|October 18, 2011
Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation siteMaria Grazia D'Angelo, Maria Luisa Lorusso, Federica Civati, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|April 18, 2014
Forceps minor damage and co-occurrence of depression and fatigue in multiple sclerosisC Gobbi, M A Rocca, E Pagani, et al.
Scientific Reports|February 17, 2016
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotypeM Nizzardo, C Simone, F Rizzo, et al.
Cell Death & Disease|August 3, 2012
MiR-30e and miR-181d control radial glia cell proliferation via HtrA1 modulationA Nigro, R Menon, A Bergamaschi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 13, 2026
Event-related potentials and behavioural correlates of cognitive functions in MS: An EEG study during symbol digit modalities testMarta Tacchini, Giulia Gamberini, Michelangelo Dini, et al.
Neuro-Degenerative Diseases|February 12, 2011
Genetic background predicts poor prognosis in frontotemporal lobar degenerationB Borroni, M Grassi, S Archetti, et al.
Epilepsia|January 24, 2007
Quantitative EEG asymmetry correlates with clinical severity in unilateral Sturge-Weber syndromeLaura A Hatfield, Nathan E Crone, Eric H Kossoff, et al.
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