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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 1, 2020
MyomiRNAs and myostatin as physical rehabilitation biomarkers for myotonic dystrophyValentina Pegoraro, Paola Cudia, Alfonc Baba, et al.American Journal of Physical Medicine & Rehabilitation|April 19, 2016
Effects of Functional Electrical Stimulation Lower Extremity Training in Myotonic Dystrophy Type I: A Pilot Controlled StudyPaola Cudia, Luca Weis, Alfonc Baba, et al.Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|September 25, 2018
Neurophysiological Evidence of Motor Network Reorganization in Myotonic Dystrophy Type 1: A Pilot Magnetoencephalographic StudyEmanuela Formaggio, Alessandra Del Felice, Cristina Turco, et al.Biochimica Et Biophysica Acta|November 4, 2008
Identification of novel mutations in five patients with mitochondrial encephalomyopathyLucia Valente, Daniela Piga, Eleonora Lamantea, et al.Journal of Human Genetics|June 7, 2013
A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 geneRaffaella Brugnoni, Dimos Kapetis, Paola Imbrici, et al.Muscle & Nerve|June 15, 2010
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical scoreCostanza Lamperti, Greta Fabbri, Liliana Vercelli, et al.Pageof 1