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A Brice

Showing results (81-90 of 353) with videos related to

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Journal of Neurology|February 24, 2001
Lack of alpha-synuclein gene mutations in families with autosomal dominant Parkinson's disease in RussiaS N Illarioshkin, I A Ivanova-Smolenskaya, E D Markova, et al.
Journal of Medical Genetics|February 12, 2002
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's diseaseM L Jacquemont, D Campion, V Hahn, et al.
Neurology|July 4, 2007
Clinical and neuropathologic study of a French family with a mutation in the neuroserpin geneI Gourfinkel-An, C Duyckaerts, A Camuzat, et al.
Journal of Neuroscience Research|July 1, 1989
Complete sequence of a cDNA encoding an active rat choline acetyltransferase: a tool to investigate the plasticity of cholinergic phenotype expressionA Brice, S Berrard, B Raynaud, et al.
Neurology|October 15, 2008
Re: Alpha-synuclein gene duplication is present in sporadic Parkinson diseaseA R Troiano, C Cazeneuve, I Le Ber, et al.
Brain : a Journal of Neurology|March 2, 1999
DYT1 mutation in French families with idiopathic torsion dystoniaA S Lebre, A Durr, P Jedynak, et al.
Journal of Strength and Conditioning Research|November 17, 2005
Influence of contraction velocity in untrained individuals over the initial early phase of resistance trainingChristopher M Neils, Brian E Udermann, Glenn A Brice, et al.
Human Molecular Genetics|September 16, 1998
De novo expansion of intermediate alleles in spinocerebellar ataxia 7G Stevanin, P Giunti, G D Belal, et al.
Neurology|June 9, 2004
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson diseaseP Ibáñez, E Lohmann, P Pollak, et al.
Nature Genetics|October 1, 1995
Gender equality in Machado-Joseph diseaseA Dürr, G Stevanin, G Cancel, et al.
Pageof 36

Showing results (81-90 of 353) with videos related to

Sort By:
Pageof 36
Journal of Neurology|February 24, 2001
Lack of alpha-synuclein gene mutations in families with autosomal dominant Parkinson's disease in RussiaS N Illarioshkin, I A Ivanova-Smolenskaya, E D Markova, et al.
Journal of Medical Genetics|February 12, 2002
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's diseaseM L Jacquemont, D Campion, V Hahn, et al.
Neurology|July 4, 2007
Clinical and neuropathologic study of a French family with a mutation in the neuroserpin geneI Gourfinkel-An, C Duyckaerts, A Camuzat, et al.
Journal of Neuroscience Research|July 1, 1989
Complete sequence of a cDNA encoding an active rat choline acetyltransferase: a tool to investigate the plasticity of cholinergic phenotype expressionA Brice, S Berrard, B Raynaud, et al.
Neurology|October 15, 2008
Re: Alpha-synuclein gene duplication is present in sporadic Parkinson diseaseA R Troiano, C Cazeneuve, I Le Ber, et al.
Brain : a Journal of Neurology|March 2, 1999
DYT1 mutation in French families with idiopathic torsion dystoniaA S Lebre, A Durr, P Jedynak, et al.
Journal of Strength and Conditioning Research|November 17, 2005
Influence of contraction velocity in untrained individuals over the initial early phase of resistance trainingChristopher M Neils, Brian E Udermann, Glenn A Brice, et al.
Human Molecular Genetics|September 16, 1998
De novo expansion of intermediate alleles in spinocerebellar ataxia 7G Stevanin, P Giunti, G D Belal, et al.
Neurology|June 9, 2004
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson diseaseP Ibáñez, E Lohmann, P Pollak, et al.
Nature Genetics|October 1, 1995
Gender equality in Machado-Joseph diseaseA Dürr, G Stevanin, G Cancel, et al.
Pageof 36