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Y Agid

Showing results (541-550 of 611) with videos related to

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Neurology|October 1, 1993
Gangliosides and parkinsonismM T Herrero, A Kastner, I Perez-Otaño, et al.
American Journal of Medical Genetics|February 16, 1996
Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative GroupM Martinez, D Campion, M C Babron, et al.
Histology and Histopathology|January 1, 1997
Apoptosis and autophagy in nigral neurons of patients with Parkinson's diseaseP Anglade, S Vyas, F Javoy-Agid, et al.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Human Genetics|May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 familiesA Lezin, G Cancel, G Stevanin, et al.
Advances in Neurology|January 1, 1982
Biochemical neuroanatomy of the human substantia nigra (pars compacta) in normal and Parkinsonian subjectsF Javoy-Agid, M Ruberg, H Taquet, et al.
Genomics|January 1, 1989
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked markerR Fujita, Y Agid, P Trouillas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 23, 2002
Behavioural disorders, Parkinson's disease and subthalamic stimulationJ L Houeto, V Mesnage, L Mallet, et al.
Archives of Neurology|June 17, 1998
Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer diseaseM Martinez, D Campion, A Brice, et al.
Human Mutation|January 1, 1997
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 familiesH Rouger, E LeGuern, N Birouk, et al.
Pageof 62

Showing results (541-550 of 611) with videos related to

Sort By:
Pageof 62
Neurology|October 1, 1993
Gangliosides and parkinsonismM T Herrero, A Kastner, I Perez-Otaño, et al.
American Journal of Medical Genetics|February 16, 1996
Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative GroupM Martinez, D Campion, M C Babron, et al.
Histology and Histopathology|January 1, 1997
Apoptosis and autophagy in nigral neurons of patients with Parkinson's diseaseP Anglade, S Vyas, F Javoy-Agid, et al.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Human Genetics|May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 familiesA Lezin, G Cancel, G Stevanin, et al.
Advances in Neurology|January 1, 1982
Biochemical neuroanatomy of the human substantia nigra (pars compacta) in normal and Parkinsonian subjectsF Javoy-Agid, M Ruberg, H Taquet, et al.
Genomics|January 1, 1989
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked markerR Fujita, Y Agid, P Trouillas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 23, 2002
Behavioural disorders, Parkinson's disease and subthalamic stimulationJ L Houeto, V Mesnage, L Mallet, et al.
Archives of Neurology|June 17, 1998
Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer diseaseM Martinez, D Campion, A Brice, et al.
Human Mutation|January 1, 1997
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 familiesH Rouger, E LeGuern, N Birouk, et al.
Pageof 62