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Showing results (191-200 of 197) with videos related to

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Neurology|August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1I Pénisson-Besnier, M Devillers, R Porcher, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Scientific Reports|November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoproteinL L Mariani, S Rivaud-Péchoux, P Charles, et al.
Journal of the Neurological Sciences|August 20, 2016
The wide POLG-related spectrum: An integrated viewM Béreau, M Anheim, A Echaniz-Laguna, et al.
Journal of Neurology|July 23, 2022
Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective studyT Bogdan, T Wirth, A Iosif, et al.
Brain : a Journal of Neurology|August 22, 2009
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patientsM Anheim, B Monga, M Fleury, et al.
Revue Neurologique|February 17, 2009
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?]V Meininger, J-C Antoine, M C Arne-Bes, et al.
Pageof 20

Showing results (191-200 of 197) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 197 results.
Neurology|August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1I Pénisson-Besnier, M Devillers, R Porcher, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Scientific Reports|November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoproteinL L Mariani, S Rivaud-Péchoux, P Charles, et al.
Journal of the Neurological Sciences|August 20, 2016
The wide POLG-related spectrum: An integrated viewM Béreau, M Anheim, A Echaniz-Laguna, et al.
Journal of Neurology|July 23, 2022
Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective studyT Bogdan, T Wirth, A Iosif, et al.
Brain : a Journal of Neurology|August 22, 2009
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patientsM Anheim, B Monga, M Fleury, et al.
Revue Neurologique|February 17, 2009
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?]V Meininger, J-C Antoine, M C Arne-Bes, et al.
Pageof 20