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Neurology. Genetics|September 3, 2025
Single Nucleotide SMN1 Variants in a Cohort of Individuals With Spinal Muscular AtrophyMartina Rimoldi, Francesca Magri, Megi Meneri, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.
Neurology|June 15, 2011
A multicenter assessment of cervical cord atrophy among MS clinical phenotypesM A Rocca, M A Horsfield, S Sala, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 21, 2010
Bimonthly assessment of magnetization transfer magnetic resonance imaging parameters in multiple sclerosis: a 14-month, multicentre, follow-up studyS Mesaros, Ma Rocca, Mp Sormani, et al.
BMC Neurology|April 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutationSimone Scarcella, Laura Dell'Arti, Delia Gagliardi, et al.
AJNR. American Journal of Neuroradiology|November 15, 2011
Overcoming the clinical-MR imaging paradox of multiple sclerosis: MR imaging data assessed with a random forest approachK Kacar, M A Rocca, M Copetti, et al.
Cerebral Cortex (New York, N.Y. : 1991)|October 13, 2011
White matter damage in frontotemporal lobar degeneration spectrumF Agosta, E Scola, E Canu, et al.
Neurobiology of Aging|January 27, 2012
Ventral and dorsal visual streams in posterior cortical atrophy: a DT MRI studyRaffaella Migliaccio, Federica Agosta, Elisa Scola, et al.
Human Molecular Genetics|August 1, 2000
Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiencyY Torrente, M G D'Angelo, Z Li, et al.
Multiple Sclerosis and Related Disorders|February 25, 2020
Platelet glutamate uptake and Th1 cells inversely correlate in relapsing/remitting and in progressive multiple sclerosisGironi M, Dalla-Costa G, Frigo M, et al.
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