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M Zappia

Showing results (111-120 of 140) with videos related to

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Neurology|April 27, 2005
Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)P Valentino, F L Conforti, D Pirritano, et al.
Parkinsonism & Related Disorders|April 23, 2015
Prevalence and associated features of self-reported freezing of gait in Parkinson disease: The DEEP FOG studyM Amboni, F Stocchi, G Abbruzzese, et al.
Acta Neurologica Scandinavica|June 18, 2002
Anti-GM1 ganglioside antibodies in Parkinson's diseaseM Zappia, L Crescibene, D Bosco, et al.
Parkinsonism & Related Disorders|February 21, 2016
Tremor pattern differentiates drug-induced resting tremor from Parkinson diseaseR Nisticò, A Fratto, B Vescio, et al.
Journal of Neurology|October 17, 1998
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocityA Gambardella, G Annesi, F Bono, et al.
Annals of Neurology|November 18, 1998
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron geneA Gambardella, R Mazzei, A Toscano, et al.
Neurology|October 26, 1999
Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PDR L Oliveri, G Annesi, M Zappia, et al.
Neurology|March 13, 2002
Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's diseaseD Messina, G Annesi, P Serra, et al.
Acta Neurologica Scandinavica|January 7, 2004
Gene conversion events in adult-onset spinal muscular atrophyR Mazzei, A Gambardella, F L Conforti, et al.
Neurology|May 1, 1996
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large familyA Quattrone, A Gambardella, F Bono, et al.
Pageof 14

Showing results (111-120 of 140) with videos related to

Sort By:
Pageof 14
Neurology|April 27, 2005
Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)P Valentino, F L Conforti, D Pirritano, et al.
Parkinsonism & Related Disorders|April 23, 2015
Prevalence and associated features of self-reported freezing of gait in Parkinson disease: The DEEP FOG studyM Amboni, F Stocchi, G Abbruzzese, et al.
Acta Neurologica Scandinavica|June 18, 2002
Anti-GM1 ganglioside antibodies in Parkinson's diseaseM Zappia, L Crescibene, D Bosco, et al.
Parkinsonism & Related Disorders|February 21, 2016
Tremor pattern differentiates drug-induced resting tremor from Parkinson diseaseR Nisticò, A Fratto, B Vescio, et al.
Journal of Neurology|October 17, 1998
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocityA Gambardella, G Annesi, F Bono, et al.
Annals of Neurology|November 18, 1998
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron geneA Gambardella, R Mazzei, A Toscano, et al.
Neurology|October 26, 1999
Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PDR L Oliveri, G Annesi, M Zappia, et al.
Neurology|March 13, 2002
Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's diseaseD Messina, G Annesi, P Serra, et al.
Acta Neurologica Scandinavica|January 7, 2004
Gene conversion events in adult-onset spinal muscular atrophyR Mazzei, A Gambardella, F L Conforti, et al.
Neurology|May 1, 1996
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large familyA Quattrone, A Gambardella, F Bono, et al.
Pageof 14