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A Quattrone

Showing results (231-240 of 273) with videos related to

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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.
Genes, Brain, and Behavior|June 3, 2006
Investigating the role of brain-derived neurotrophic factor in relapsing-remitting multiple sclerosisM Liguori, F Fera, M C Gioia, et al.
Neurology|December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASILM Liguori, R Mazzei, C Ungaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL familiesM T Dotti, A Federico, R Mazzei, et al.
Neurology|October 13, 2004
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)F L Conforti, M Muglia, R Mazzei, 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.
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.
European Journal of Neurology|May 11, 2016
Novel outcome measures for Charcot-Marie-Tooth disease: validation and reliability of the 6-min walk test and StepWatch(™) Activity Monitor and identification of the walking features related to higher quality of lifeL Padua, C Pazzaglia, D Pareyson, et al.
Pageof 28

Showing results (231-240 of 273) with videos related to

Sort By:
Pageof 28
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.
Genes, Brain, and Behavior|June 3, 2006
Investigating the role of brain-derived neurotrophic factor in relapsing-remitting multiple sclerosisM Liguori, F Fera, M C Gioia, et al.
Neurology|December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASILM Liguori, R Mazzei, C Ungaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL familiesM T Dotti, A Federico, R Mazzei, et al.
Neurology|October 13, 2004
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)F L Conforti, M Muglia, R Mazzei, 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.
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.
European Journal of Neurology|May 11, 2016
Novel outcome measures for Charcot-Marie-Tooth disease: validation and reliability of the 6-min walk test and StepWatch(™) Activity Monitor and identification of the walking features related to higher quality of lifeL Padua, C Pazzaglia, D Pareyson, et al.
Pageof 28