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G Fabbrini

Showing results (101-110 of 115) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, C Colosimo, et al.
Neurology|January 15, 2000
Smoking habits in multiple system atrophy and progressive supranuclear palsy. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, G Fabbrini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, G Fabbrini, et al.
Neurology|October 26, 1999
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical ParkinsonismD J Nicholl, P Bennett, L Hiller, et al.
Neurology|July 22, 2011
Environmental risk factors and clinical phenotype in familial and sporadic primary blepharospasmG Defazio, G Abbruzzese, M S Aniello, et al.
European Journal of Neurology|September 22, 2009
Lower limb involvement in adult-onset primary dystonia: frequency and clinical featuresD Martino, A Macerollo, G Abbruzzese, et al.
Neurology|March 29, 2001
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish familyC Casali, V Bonifati, F M Santorelli, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, et al.
European Journal of Neurology|January 3, 2013
Summary of the recommendations of the EFNS/MDS-ES review on therapeutic management of Parkinson's diseaseJ J Ferreira, R Katzenschlager, B R Bloem, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, C Colosimo, et al.
Neurology|January 15, 2000
Smoking habits in multiple system atrophy and progressive supranuclear palsy. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, G Fabbrini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, G Fabbrini, et al.
Neurology|October 26, 1999
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical ParkinsonismD J Nicholl, P Bennett, L Hiller, et al.
Neurology|July 22, 2011
Environmental risk factors and clinical phenotype in familial and sporadic primary blepharospasmG Defazio, G Abbruzzese, M S Aniello, et al.
European Journal of Neurology|September 22, 2009
Lower limb involvement in adult-onset primary dystonia: frequency and clinical featuresD Martino, A Macerollo, G Abbruzzese, et al.
Neurology|March 29, 2001
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish familyC Casali, V Bonifati, F M Santorelli, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, et al.
European Journal of Neurology|January 3, 2013
Summary of the recommendations of the EFNS/MDS-ES review on therapeutic management of Parkinson's diseaseJ J Ferreira, R Katzenschlager, B R Bloem, et al.
Pageof 12