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Showing results (491-500 of 611) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2002
Concurrent excitatory and inhibitory effects of high frequency stimulation: an oculomotor studyB-P Bejjani, I Arnulf, J-L Houeto, et al.
Neurobiology of Disease|November 1, 1994
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14qG Stevanin, P S Sousa, G Cancel, et al.
Brain : a Journal of Neurology|May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 casesN Birouk, R Gouider, E Le Guern, et al.
Neurology|November 1, 1995
Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletionR Gouider, E LeGuern, M Gugenheim, et al.
Journal of Neurochemistry|October 1, 1982
Enkephalin dipeptidyl carboxypeptidase (enkephalinase) activity: selective radioassay, properties, and regional distribution in human brainC Llorens, B Malfroy, J C Schwartz, et al.
Developmental Neuroscience|January 1, 1993
Neuromelanin accumulation with age in catecholaminergic neurons from Macaca fascicularis brainstemM T Herrero, E C Hirsch, A Kastner, et al.
Archives of Neurology|August 17, 1999
Dopaminergic dysfunction in midbrain dystonia: anatomoclinical study using 3-dimensional magnetic resonance imaging and fluorodopa F 18 positron emission tomographyM Vidailhet, C Dupel, S Lehéricy, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.
Neurology|August 1, 1994
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaB Fontaine, C S Rime, J Hazan, et al.
Pageof 62

Showing results (491-500 of 611) with videos related to

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Pageof 62
Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2002
Concurrent excitatory and inhibitory effects of high frequency stimulation: an oculomotor studyB-P Bejjani, I Arnulf, J-L Houeto, et al.
Neurobiology of Disease|November 1, 1994
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14qG Stevanin, P S Sousa, G Cancel, et al.
Brain : a Journal of Neurology|May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 casesN Birouk, R Gouider, E Le Guern, et al.
Neurology|November 1, 1995
Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletionR Gouider, E LeGuern, M Gugenheim, et al.
Journal of Neurochemistry|October 1, 1982
Enkephalin dipeptidyl carboxypeptidase (enkephalinase) activity: selective radioassay, properties, and regional distribution in human brainC Llorens, B Malfroy, J C Schwartz, et al.
Developmental Neuroscience|January 1, 1993
Neuromelanin accumulation with age in catecholaminergic neurons from Macaca fascicularis brainstemM T Herrero, E C Hirsch, A Kastner, et al.
Archives of Neurology|August 17, 1999
Dopaminergic dysfunction in midbrain dystonia: anatomoclinical study using 3-dimensional magnetic resonance imaging and fluorodopa F 18 positron emission tomographyM Vidailhet, C Dupel, S Lehéricy, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.
Neurology|August 1, 1994
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaB Fontaine, C S Rime, J Hazan, et al.
Pageof 62