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D Brassat

Showing results (11-20 of 41) with videos related to

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Archives of Neurology|March 14, 2000
Frequency of the DYT1 mutation in primary torsion dystonia without family historyD Brassat, A Camuzat, M Vidailhet, et al.
Revue Neurologique|April 2, 2014
Multiple sclerosis and pregnancyE Bodiguel, C Bensa, D Brassat, et al.
Neurology|January 26, 2005
The HLA locus and multiple sclerosis in SicilyD Brassat, G Salemi, L F Barcellos, et al.
Revue Neurologique|February 14, 2012
Recommendations for useful serum testing with suspected multiple sclerosisJ-C Ouallet, E Bodiguel, C Bensa, et al.
Revue Neurologique|May 5, 2012
Recommendations for the management of multiple sclerosis relapsesD Laplaud, E Bodiguel, C Bensa, et al.
Revue Neurologique|November 26, 2013
[Nosology and etiologies of acute longitudinally extensive transverse myelitis]N Collongues, C Papeix, H Zéphir, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 19, 2008
Unexpected multiple sclerosis: follow-up of 30 patients with magnetic resonance imaging and clinical conversion profileC Lebrun, C Bensa, M Debouverie, et al.
Revue Neurologique|March 9, 2012
Recommendations for a definition of multiple sclerosis in support of early treatmentH Zéphir, E Bodiguel, C Bensa, et al.
Revue Neurologique|June 5, 2012
Recommendations for the detection and therapeutic management of cognitive impairment in multiple sclerosisC Bensa, E Bodiguel, D Brassat, et al.
American Journal of Human Genetics|May 23, 2000
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardationA Herman-Bert, G Stevanin, J C Netter, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Archives of Neurology|March 14, 2000
Frequency of the DYT1 mutation in primary torsion dystonia without family historyD Brassat, A Camuzat, M Vidailhet, et al.
Revue Neurologique|April 2, 2014
Multiple sclerosis and pregnancyE Bodiguel, C Bensa, D Brassat, et al.
Neurology|January 26, 2005
The HLA locus and multiple sclerosis in SicilyD Brassat, G Salemi, L F Barcellos, et al.
Revue Neurologique|February 14, 2012
Recommendations for useful serum testing with suspected multiple sclerosisJ-C Ouallet, E Bodiguel, C Bensa, et al.
Revue Neurologique|May 5, 2012
Recommendations for the management of multiple sclerosis relapsesD Laplaud, E Bodiguel, C Bensa, et al.
Revue Neurologique|November 26, 2013
[Nosology and etiologies of acute longitudinally extensive transverse myelitis]N Collongues, C Papeix, H Zéphir, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 19, 2008
Unexpected multiple sclerosis: follow-up of 30 patients with magnetic resonance imaging and clinical conversion profileC Lebrun, C Bensa, M Debouverie, et al.
Revue Neurologique|March 9, 2012
Recommendations for a definition of multiple sclerosis in support of early treatmentH Zéphir, E Bodiguel, C Bensa, et al.
Revue Neurologique|June 5, 2012
Recommendations for the detection and therapeutic management of cognitive impairment in multiple sclerosisC Bensa, E Bodiguel, D Brassat, et al.
American Journal of Human Genetics|May 23, 2000
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardationA Herman-Bert, G Stevanin, J C Netter, et al.
Pageof 5