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Showing results (331-340 of 611) with videos related to

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Experimental Brain Research|June 18, 1998
Effects of anterior cingulate cortex lesions on ocular saccades in humansB Gaymard, S Rivaud, J F Cassarini, et al.
Clinical Neuropharmacology|May 14, 1998
Attentional deficits in Parkinson's disease: partial reversibility with naphtoxazine (SDZ NVI-085), a selective noradrenergic alpha 1 agonistM A Bédard, F el Massioui, C Malapani, 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.
Neuroreport|May 9, 1995
Congruent unilateral impairments for real and imagined hand movementsA Sirigu, L Cohen, J R Duhamel, et al.
Brain : a Journal of Neurology|December 1, 1993
Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneityA Dürr, H Chneiweiss, C Khati, et al.
Human Molecular Genetics|March 1, 1993
No mutation in codon 713 of the amyloid precursor gene in schizophrenic patientsD Carter, D Campion, T d'Amato, et al.
Archives of Neurology|March 1, 1996
Striatopallidal and thalamic dystonia. A magnetic resonance imaging anatomoclinical studyS Lehéricy, M Vidailhet, D Dormont, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosisE LeGuern, N Ravise, R Gouider, et al.
Neuroscience|May 1, 1996
Nitric oxide synthase and neuronal vulnerability in Parkinson's diseaseS Hunot, F Boissière, B Faucheux, et al.
Pageof 62

Showing results (331-340 of 611) with videos related to

Sort By:
Pageof 62
Experimental Brain Research|June 18, 1998
Effects of anterior cingulate cortex lesions on ocular saccades in humansB Gaymard, S Rivaud, J F Cassarini, et al.
Clinical Neuropharmacology|May 14, 1998
Attentional deficits in Parkinson's disease: partial reversibility with naphtoxazine (SDZ NVI-085), a selective noradrenergic alpha 1 agonistM A Bédard, F el Massioui, C Malapani, 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.
Neuroreport|May 9, 1995
Congruent unilateral impairments for real and imagined hand movementsA Sirigu, L Cohen, J R Duhamel, et al.
Brain : a Journal of Neurology|December 1, 1993
Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneityA Dürr, H Chneiweiss, C Khati, et al.
Human Molecular Genetics|March 1, 1993
No mutation in codon 713 of the amyloid precursor gene in schizophrenic patientsD Carter, D Campion, T d'Amato, et al.
Archives of Neurology|March 1, 1996
Striatopallidal and thalamic dystonia. A magnetic resonance imaging anatomoclinical studyS Lehéricy, M Vidailhet, D Dormont, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosisE LeGuern, N Ravise, R Gouider, et al.
Neuroscience|May 1, 1996
Nitric oxide synthase and neuronal vulnerability in Parkinson's diseaseS Hunot, F Boissière, B Faucheux, et al.
Pageof 62