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Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.
Internal and Emergency Medicine|February 10, 2021
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there?Anna M Pietroboni, Silvia Lanfranconi, Alessio Novella, et al.
The Lancet. Neurology|May 3, 2017
Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trialEnrico Bertini, Eric Dessaud, Eugenio Mercuri, et al.
Neurobiology of Aging|July 6, 2013
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosisDaniela Calini, Lucia Corrado, Roberto Del Bo, et al.
Neuromuscular Disorders : NMD|August 28, 2016
Histological effects of givinostat in boys with Duchenne muscular dystrophyPaolo Bettica, Stefania Petrini, Valentina D'Oria, et al.
JAMA Neurology|April 7, 2015
Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular AtrophyMichela Ripolone, Dario Ronchi, Raffaella Violano, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Human Mutation|June 24, 2018
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channelConcetta Altamura, Sabrina Lucchiari, Dalila Sahbani, et al.
Molecular Biology and Evolution|February 10, 2012
A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosisR Cagliani, F R Guerini, M Fumagalli, et al.
Frontiers in Neurology|April 18, 2018
The Length of <i>SNCA</i> Rep1 Microsatellite May Influence Cognitive Evolution in Parkinson's DiseaseLucia Corrado, Fabiola De Marchi, Sara Tunesi, et al.
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