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C Tranchant

Showing results (71-80 of 197) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|November 21, 2007
Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutationM Anheim, D Hannequin, C Boulay, et al.
Neurology|March 12, 2003
Phenotypic variability of aprataxin gene mutationsC Tranchant, M Fleury, M C Moreira, et al.
Revue Neurologique|November 27, 2002
[Primary Moyamoya disease]A Echaniz-Laguna, B Degos, M C Fleury, et al.
Journal of Neurology|February 24, 2001
The Miller Fisher syndrome: neurophysiological and MRI evidence of both peripheral and central origin in one caseA Echaniz-Laguna, F Battaglia, R Heymann, et al.
Revue Neurologique|November 17, 2005
[Vogt-Koyanagi-Harada syndrome]F Blanc, M Fleury, V Talmant, et al.
Revue Neurologique|January 1, 1993
[Cervical myelopathy disclosing dissection of the extracranial vertebral artery]P Labouret, C Tranchant, M Jesel, et al.
Genes and Immunity|June 18, 2004
Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked lociM Giraud, G Beaurain, B Eymard, et al.
Revue Neurologique|June 1, 2005
[A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy]A Echaniz-Laguna, E Rousso, M Anheim, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1997
Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutationC Tranchant, N Sergeant, A Wattez, et al.
Clinical and Experimental Pathology|September 3, 1999
Gerstmann-Sträussler-Scheinker disease and the French-Alsatian A117V variantM Mohr, C Tranchant, G Steinmetz, et al.
Pageof 20

Showing results (71-80 of 197) with videos related to

Sort By:
Pageof 20
Journal of Neurology, Neurosurgery, and Psychiatry|November 21, 2007
Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutationM Anheim, D Hannequin, C Boulay, et al.
Neurology|March 12, 2003
Phenotypic variability of aprataxin gene mutationsC Tranchant, M Fleury, M C Moreira, et al.
Revue Neurologique|November 27, 2002
[Primary Moyamoya disease]A Echaniz-Laguna, B Degos, M C Fleury, et al.
Journal of Neurology|February 24, 2001
The Miller Fisher syndrome: neurophysiological and MRI evidence of both peripheral and central origin in one caseA Echaniz-Laguna, F Battaglia, R Heymann, et al.
Revue Neurologique|November 17, 2005
[Vogt-Koyanagi-Harada syndrome]F Blanc, M Fleury, V Talmant, et al.
Revue Neurologique|January 1, 1993
[Cervical myelopathy disclosing dissection of the extracranial vertebral artery]P Labouret, C Tranchant, M Jesel, et al.
Genes and Immunity|June 18, 2004
Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked lociM Giraud, G Beaurain, B Eymard, et al.
Revue Neurologique|June 1, 2005
[A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy]A Echaniz-Laguna, E Rousso, M Anheim, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1997
Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutationC Tranchant, N Sergeant, A Wattez, et al.
Clinical and Experimental Pathology|September 3, 1999
Gerstmann-Sträussler-Scheinker disease and the French-Alsatian A117V variantM Mohr, C Tranchant, G Steinmetz, et al.
Pageof 20