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Neurogenetics|July 14, 2009
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxinGiovanni Airoldi, Andrea Guidarelli, Orazio Cantoni, et al.European Journal of Neurology|February 6, 2023
Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysisGhil Schwarz, Sara Bonato, Silvia Lanfranconi, et al.Neuromuscular Disorders : NMD|June 30, 2012
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patientsFrancesca Magri, Roberto Del Bo, Maria Grazia D'Angelo, 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.Journal of Neurology|March 15, 2011
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-upFrancesca Magri, Alessandra Govoni, Maria Grazia D'Angelo, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 2, 2006
Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patientsTanja Schmitz-Hübsch, Sophie Tezenas du Montcel, Laszlo Baliko, et al.Archives of Neurology|May 10, 2006
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegiaFrancesca Crippa, Chris Panzeri, Andrea Martinuzzi, et al.Neurobiology of Aging|July 11, 2016
Mutational analysis of COQ2 in patients with MSA in ItalyDario Ronchi, Ernesto Di Biase, Giulia Franco, et al.Pageof 3