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L Defebvre

Showing results (171-180 of 185) with videos related to

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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 loopD Devos, W Szurhaj, N Reyns, et al.
Neuroscience|September 6, 2015
Brain metabolic abnormalities during gait with freezing in Parkinson's diseaseC 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 diseaseM 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 hyperaldosteronismM 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 diseaseD Devos, P Krystkowiak, F Clement, et al.
Neuroreport|August 10, 2001
Intermuscular coherence in Parkinson's disease: relationship to bradykinesiaP 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 correlatesJ 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 studyJ L De Reuck, V Deramecourt, F Auger, et al.
Neurobiology of Disease|April 13, 2001
Genetic analysis of synphilin-1 in familial Parkinson's diseaseM 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 FranceJ-B Davion, P Bocquillon, F Cassim, et al.
Pageof 19

Showing results (171-180 of 185) with videos related to

Sort By:
Pageof 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 loopD Devos, W Szurhaj, N Reyns, et al.
Neuroscience|September 6, 2015
Brain metabolic abnormalities during gait with freezing in Parkinson's diseaseC 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 diseaseM 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 hyperaldosteronismM 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 diseaseD Devos, P Krystkowiak, F Clement, et al.
Neuroreport|August 10, 2001
Intermuscular coherence in Parkinson's disease: relationship to bradykinesiaP 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 correlatesJ 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 studyJ L De Reuck, V Deramecourt, F Auger, et al.
Neurobiology of Disease|April 13, 2001
Genetic analysis of synphilin-1 in familial Parkinson's diseaseM 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 FranceJ-B Davion, P Bocquillon, F Cassim, et al.
Pageof 19