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Neuromuscular Disorders : NMD|June 26, 2012
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiencyM Pane, S Messina, G Vasco, et al.
European Journal of Neurology|December 10, 2019
Subgroup comparison according to clinical phenotype and serostatus in autoimmune encephalitis: a multicenter retrospective studyM Gastaldi, S Mariotto, M P Giannoccaro, et al.
Epilepsy Research|August 30, 2016
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter studyP De Liso, F Vigevano, N Specchio, et al.
Neurology|November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyE Mercuri, E Bertini, S Messina, et al.
Annals of Neurology|September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nucleiJ M Wilmshurst, S Lillis, H Zhou, et al.
Neurology|January 28, 2004
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosumC Casali, E M Valente, E Bertini, et al.
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric studyE Mercuri, S Messina, R Battini, et al.
Forensic Science International. Genetics|May 22, 2016
Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™M Eduardoff, T E Gross, C Santos, et al.
Nature Structural & Molecular Biology|March 6, 2019
Structural basis of broad ebolavirus neutralization by a human survivor antibodyBrandyn R West, Anna Z Wec, Crystal L Moyer, et al.
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