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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 Parkinsonisms
N Vanacore, V Bonifati, C Colosimo, 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 Parkinsonisms
N Vanacore, V Bonifati, G Fabbrini, et al.
Neurology
|
March 29, 2001
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family
C 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 cases
V Bonifati, M Joosse, D J Nicholl, et al.
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of 4
Search research articles
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Showing results (31-40 of 34) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 34 results.
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 Parkinsonisms
N Vanacore, V Bonifati, C Colosimo, 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 Parkinsonisms
N Vanacore, V Bonifati, G Fabbrini, et al.
Neurology
|
March 29, 2001
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family
C 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 cases
V Bonifati, M Joosse, D J Nicholl, et al.
Page
of 4