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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
August 24, 2006
Predominance of the contralateral movement-related activity in the subthalamo-cortical loop
D Devos, W Szurhaj, N Reyns, et al.
Neuroscience
|
September 6, 2015
Brain metabolic abnormalities during gait with freezing in Parkinson's disease
C Tard, A Delval, D Devos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 5, 2000
Linkage exclusion in French families with probable Parkinson' s disease
M Farrer, T Destée, E Becquet, et al.
Clinical Endocrinology
|
May 26, 2007
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism
M C Vantyghem, F Faivre-Defrance, S Marcelli-Tourvieille, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 14, 2006
Improvement of gait by chronic, high doses of methylphenidate in patients with advanced Parkinson's disease
D Devos, P Krystkowiak, F Clement, et al.
Neuroreport
|
August 10, 2001
Intermuscular coherence in Parkinson's disease: relationship to bradykinesia
P Brown, J Marsden, L Defebvre, et al.
Journal of the Neurological Sciences
|
August 18, 2014
Post-mortem 7.0-tesla magnetic resonance study of cortical microinfarcts in neurodegenerative diseases and vascular dementia with neuropathological correlates
J De Reuck, V Deramecourt, F Auger, et al.
European Journal of Neurology
|
April 5, 2014
Iron deposits in post-mortem brains of patients with neurodegenerative and cerebrovascular diseases: a semi-quantitative 7.0 T magnetic resonance imaging study
J L De Reuck, V Deramecourt, F Auger, et al.
Neurobiology of Disease
|
April 13, 2001
Genetic analysis of synphilin-1 in familial Parkinson's disease
M Farrer, A Destée, C Levecque, et al.
Revue Neurologique
|
July 13, 2021
Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern France
J-B Davion, P Bocquillon, F Cassim, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 185) with videos related to
Sort By:
Page
of 19
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
August 24, 2006
Predominance of the contralateral movement-related activity in the subthalamo-cortical loop
D Devos, W Szurhaj, N Reyns, et al.
Neuroscience
|
September 6, 2015
Brain metabolic abnormalities during gait with freezing in Parkinson's disease
C Tard, A Delval, D Devos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 5, 2000
Linkage exclusion in French families with probable Parkinson' s disease
M Farrer, T Destée, E Becquet, et al.
Clinical Endocrinology
|
May 26, 2007
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism
M C Vantyghem, F Faivre-Defrance, S Marcelli-Tourvieille, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 14, 2006
Improvement of gait by chronic, high doses of methylphenidate in patients with advanced Parkinson's disease
D Devos, P Krystkowiak, F Clement, et al.
Neuroreport
|
August 10, 2001
Intermuscular coherence in Parkinson's disease: relationship to bradykinesia
P Brown, J Marsden, L Defebvre, et al.
Journal of the Neurological Sciences
|
August 18, 2014
Post-mortem 7.0-tesla magnetic resonance study of cortical microinfarcts in neurodegenerative diseases and vascular dementia with neuropathological correlates
J De Reuck, V Deramecourt, F Auger, et al.
European Journal of Neurology
|
April 5, 2014
Iron deposits in post-mortem brains of patients with neurodegenerative and cerebrovascular diseases: a semi-quantitative 7.0 T magnetic resonance imaging study
J L De Reuck, V Deramecourt, F Auger, et al.
Neurobiology of Disease
|
April 13, 2001
Genetic analysis of synphilin-1 in familial Parkinson's disease
M Farrer, A Destée, C Levecque, et al.
Revue Neurologique
|
July 13, 2021
Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern France
J-B Davion, P Bocquillon, F Cassim, et al.
Page
of 19