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N Vanacore

Showing results (81-90 of 91) 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|February 3, 2017
Adaptation and psychometric properties of the Italian version of the Non-Motor Symptoms Questionnaire for Parkinson's diseaseI Cova, M E Di Battista, N Vanacore, 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|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|August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseV Bonifati, G De Michele, C B Lücking, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 21, 2010
Three years of experience: the Italian registry and safety data updateG L Mancardi, G Tedeschi, M P Amato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 3, 2009
The pharmacovigilance program on natalizumab in Italy: 2 years of experienceG Tedeschi, M P Amato, R D'Alessandro, et al.
Journal of Medical Genetics|November 8, 2005
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestorS Goldwurm, A Di Fonzo, E J Simons, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 3, 2017
Adaptation and psychometric properties of the Italian version of the Non-Motor Symptoms Questionnaire for Parkinson's diseaseI Cova, M E Di Battista, N Vanacore, 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|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|August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseV Bonifati, G De Michele, C B Lücking, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 21, 2010
Three years of experience: the Italian registry and safety data updateG L Mancardi, G Tedeschi, M P Amato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 3, 2009
The pharmacovigilance program on natalizumab in Italy: 2 years of experienceG Tedeschi, M P Amato, R D'Alessandro, et al.
Journal of Medical Genetics|November 8, 2005
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestorS Goldwurm, A Di Fonzo, E J Simons, et al.
Pageof 10