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Journal of the Neurological Sciences
|
September 1, 1988
D1 and D2-type dopamine receptors in patients with Parkinson's disease and progressive supranuclear palsy
L Pierot, C Desnos, J Blin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1989
Selective loss of cholinergic neurons in the ventral striatum of patients with Alzheimer disease
S Lehéricy, E C Hirsch, P Cervera, et al.
Neuroscience
|
January 1, 1990
Choline acetyltransferase activity and [3H]vesamicol binding in the temporal cortex of patients with Alzheimer's disease, Parkinson's disease, and rats with basal forebrain lesions
M Ruberg, W Mayo, A Brice, et al.
Brain Research
|
October 21, 1985
Monoclonal antibodies raised against Lewy bodies in brains from subjects with Parkinson's disease
E Hirsch, M Ruberg, M Dardenne, et al.
The Journal of Comparative Neurology
|
September 12, 2000
Mitochondrial free calcium levels (Rhod-2 fluorescence) and ultrastructural alterations in neuronally differentiated PC12 cells during ceramide-dependent cell death
M P Muriel, N Lambeng, F Darios, et al.
Neurology
|
January 1, 1995
Alterations of GABAergic neurons in the basal ganglia of patients with progressive supranuclear palsy: an in situ hybridization study of GAD67 messenger RNA
R Levy, M Ruberg, M T Herrero, et al.
Journal of Neurochemistry
|
July 1, 1999
Systemic administration of NMDA and AMPA receptor antagonists reverses the neurochemical changes induced by nigrostriatal denervation in basal ganglia
M Vila, C Marin, M Ruberg, et al.
Human Molecular Genetics
|
November 5, 1999
Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP
J Lopes, S Tardieu, K Silander, et al.
Neuromuscular Disorders : NMD
|
July 19, 2003
Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene
H Azzedine, M Ruberg, D Ente, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 15, 1997
Consequences of nigrostriatal denervation on the functioning of the basal ganglia in human and nonhuman primates: an in situ hybridization study of cytochrome oxidase subunit I mRNA
M Vila, R Levy, M T Herrero, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 85) with videos related to
Sort By:
Page
of 9
Journal of the Neurological Sciences
|
September 1, 1988
D1 and D2-type dopamine receptors in patients with Parkinson's disease and progressive supranuclear palsy
L Pierot, C Desnos, J Blin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1989
Selective loss of cholinergic neurons in the ventral striatum of patients with Alzheimer disease
S Lehéricy, E C Hirsch, P Cervera, et al.
Neuroscience
|
January 1, 1990
Choline acetyltransferase activity and [3H]vesamicol binding in the temporal cortex of patients with Alzheimer's disease, Parkinson's disease, and rats with basal forebrain lesions
M Ruberg, W Mayo, A Brice, et al.
Brain Research
|
October 21, 1985
Monoclonal antibodies raised against Lewy bodies in brains from subjects with Parkinson's disease
E Hirsch, M Ruberg, M Dardenne, et al.
The Journal of Comparative Neurology
|
September 12, 2000
Mitochondrial free calcium levels (Rhod-2 fluorescence) and ultrastructural alterations in neuronally differentiated PC12 cells during ceramide-dependent cell death
M P Muriel, N Lambeng, F Darios, et al.
Neurology
|
January 1, 1995
Alterations of GABAergic neurons in the basal ganglia of patients with progressive supranuclear palsy: an in situ hybridization study of GAD67 messenger RNA
R Levy, M Ruberg, M T Herrero, et al.
Journal of Neurochemistry
|
July 1, 1999
Systemic administration of NMDA and AMPA receptor antagonists reverses the neurochemical changes induced by nigrostriatal denervation in basal ganglia
M Vila, C Marin, M Ruberg, et al.
Human Molecular Genetics
|
November 5, 1999
Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP
J Lopes, S Tardieu, K Silander, et al.
Neuromuscular Disorders : NMD
|
July 19, 2003
Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene
H Azzedine, M Ruberg, D Ente, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 15, 1997
Consequences of nigrostriatal denervation on the functioning of the basal ganglia in human and nonhuman primates: an in situ hybridization study of cytochrome oxidase subunit I mRNA
M Vila, R Levy, M T Herrero, et al.
Page
of 9