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Neurology
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January 15, 2000
Smoking habits in multiple system atrophy and progressive supranuclear palsy. European Study Group on Atypical Parkinsonisms
N 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 Parkinsonisms
N 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 Parkinsonism
D J Nicholl, P Bennett, L Hiller, 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.
Journal of Medical Genetics
|
January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations
M Sharma, J C Mueller, A Zimprich, et al.
Human Molecular Genetics
|
May 16, 1998
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)
J R Vaughan, M J Farrer, Z K Wszolek, 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.
American Journal of Human Genetics
|
July 20, 2001
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36
C M van Duijn, M C Dekker, V Bonifati, et al.
American Journal of Human Genetics
|
June 23, 1998
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease
J Tassin, A Dürr, T de Broucker, et al.
Journal of Medical Genetics
|
December 14, 2004
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease
M Martinez, A Brice, J R Vaughan, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 78) with videos related to
Sort By:
Page
of 8
Neurology
|
January 15, 2000
Smoking habits in multiple system atrophy and progressive supranuclear palsy. European Study Group on Atypical Parkinsonisms
N 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 Parkinsonisms
N 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 Parkinsonism
D J Nicholl, P Bennett, L Hiller, 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.
Journal of Medical Genetics
|
January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations
M Sharma, J C Mueller, A Zimprich, et al.
Human Molecular Genetics
|
May 16, 1998
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)
J R Vaughan, M J Farrer, Z K Wszolek, 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.
American Journal of Human Genetics
|
July 20, 2001
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36
C M van Duijn, M C Dekker, V Bonifati, et al.
American Journal of Human Genetics
|
June 23, 1998
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease
J Tassin, A Dürr, T de Broucker, et al.
Journal of Medical Genetics
|
December 14, 2004
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease
M Martinez, A Brice, J R Vaughan, et al.
Page
of 8