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European Journal of Neurology|December 4, 2008
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletionsC P Trevisan, E Pastorello, G Tomelleri, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 4, 2006
Friedreich's ataxia: clinical heterogeneity in two sistersM Armani, M Zortea, E Pastorello, et al.Clinical Genetics|March 27, 2009
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sampleM L Mostacciuolo, E Pastorello, G Vazza, et al.Journal of Medical Genetics|June 19, 2002
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1M Zortea, A Vettori, C P Trevisan, et al.Rivista Di Neurologia|November 1, 1986
[Therapeutic effects of trazodone in the treatment of tremor. Multicentric double-blind study]F Sanson, E Schergna, D Semenzato, et al.Brain & Development|March 15, 2001
Ataxia and congenital muscular dystrophy: the follow-up of a new specific phenotypeC P Trevisan, E Pastorello, S Tonello, et al.European Journal of Neurology|August 2, 2006
Exploring mental status in Friedreich's ataxia: a combined neuropsychological, behavioral and neuroimaging studyM C Mantovan, A Martinuzzi, F Squarzanti, et al.Journal of Medical Genetics|January 16, 1998
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutationsM Fanin, D J Duggan, M L Mostacciuolo, et al.Human Mutation|June 29, 2004
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?M Fanin, L Fulizio, A C Nascimbeni, et al.Neuroepidemiology|August 7, 2004
Prevalence of inherited ataxias in the province of Padua, ItalyM Zortea, M Armani, E Pastorello, et al.Pageof 4