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Acta Neurologica|December 1, 1989
A double-blind, cross-over trial with madopar HBS in patients with Parkinson's diseaseG De Michele, A Mengano, A Filla, et al.Clinical Neurology and Neurosurgery|March 1, 1993
Heterogeneous findings in four cases of cerebellar ataxia associated with hypogonadism (Holmes' type ataxia)G De Michele, A Filla, S Striano, et al.European Journal of Neurology|October 2, 2019
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian familiesM Lieto, V Riso, D Galatolo, et al.Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.Journal of Neurology|April 14, 2009
Low-dose idebenone treatment in Friedreich's ataxia with and without cardiac hypertrophyC Rinaldi, T Tucci, S Maione, et al.Cardiology|January 1, 1988
Noninvasive assessment of systolic and diastolic function in 50 patients with Friedreich's ataxiaA Giunta, S Maione, R Biagini, et al.Journal of Neurology|June 1, 1991
Intrafamilial phenotype variation in Friedreich's disease: possible exceptions to diagnostic criteriaA Filla, G De Michele, F Cavalcanti, et al.European Neurology|July 15, 2000
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian familiesA Filla, C Mariotti, G Caruso, et al.Human Molecular Genetics|August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal allelesL Montermini, E Andermann, M Labuda, et al.Journal of Neurology|August 4, 1999
Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 familiesA Filla, G De Michele, L Santoro, et al.Pageof 21