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C Tranchant

Showing results (121-130 of 197) with videos related to

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Parkinsonism & Related Disorders|May 28, 2017
Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's diseaseT Wirth, S Weibel, S Montaut, et al.
Revue Neurologique|December 3, 2010
[Inaugural audiovisual impairment disclosing specific neurological disorders]B Bourre, J Aupy, M Saleh, et al.
Revue Neurologique|January 1, 1991
[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease]C Tranchant, K Doh-Ura, G Steinmetz, et al.
Clinical Genetics|August 11, 2010
Unexpected combination of inherited chorea-acanthocytosis with MDR3 (ABCB4) defect mimicking Wilson's diseaseM Anheim, P Chamouard, G Rudolf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
Pallido-Luysio-Nigral atrophy revealed by rapidly progressive hemidystonia: a clinical, radiologic, functional, and neuropathologic studyL Vercueil, A Hammouti, M L Andriantseheno, et al.
Revue Neurologique|June 17, 2008
[American Academy of Neurology, Chicago, 12-18 April 2008]I Bonnaud, F Sellal, M Ceccaldi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2006
Myopathy with tubular aggregates and gyrate atrophy of the choroid and retina due to hyperornithinaemiaM Fleury, R Barbier, F Ziegler, et al.
Revue Neurologique|January 1, 1990
[Contribution of MRI to the topography of oculomotor disorders in multiple sclerosis]L Rumbach, A M Eber, J L Dietemann, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1996
[Abnormal central nervous conduction in long-term treatments with retinoids]C J Le Coz, P Wasser, C Tranchant, et al.
Neurology|October 1, 1990
Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndromeJ Tateishi, T Kitamoto, K Doh-ura, et al.
Pageof 20

Showing results (121-130 of 197) with videos related to

Sort By:
Pageof 20
Parkinsonism & Related Disorders|May 28, 2017
Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's diseaseT Wirth, S Weibel, S Montaut, et al.
Revue Neurologique|December 3, 2010
[Inaugural audiovisual impairment disclosing specific neurological disorders]B Bourre, J Aupy, M Saleh, et al.
Revue Neurologique|January 1, 1991
[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease]C Tranchant, K Doh-Ura, G Steinmetz, et al.
Clinical Genetics|August 11, 2010
Unexpected combination of inherited chorea-acanthocytosis with MDR3 (ABCB4) defect mimicking Wilson's diseaseM Anheim, P Chamouard, G Rudolf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
Pallido-Luysio-Nigral atrophy revealed by rapidly progressive hemidystonia: a clinical, radiologic, functional, and neuropathologic studyL Vercueil, A Hammouti, M L Andriantseheno, et al.
Revue Neurologique|June 17, 2008
[American Academy of Neurology, Chicago, 12-18 April 2008]I Bonnaud, F Sellal, M Ceccaldi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2006
Myopathy with tubular aggregates and gyrate atrophy of the choroid and retina due to hyperornithinaemiaM Fleury, R Barbier, F Ziegler, et al.
Revue Neurologique|January 1, 1990
[Contribution of MRI to the topography of oculomotor disorders in multiple sclerosis]L Rumbach, A M Eber, J L Dietemann, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1996
[Abnormal central nervous conduction in long-term treatments with retinoids]C J Le Coz, P Wasser, C Tranchant, et al.
Neurology|October 1, 1990
Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndromeJ Tateishi, T Kitamoto, K Doh-ura, et al.
Pageof 20