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I Le Ber

Showing results (11-20 of 23) with videos related to

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Neurology|January 24, 2007
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1I Le Ber, O Dubourg, J-F Benoist, et al.
Revue Neurologique|April 1, 2005
[Mutation of the aprataxin gene presenting with Charcot-Marie-Tooth-like neuropathy and cerebellar ataxia]F Ochsner, I Le Ber, G Said, et al.
Neurology|June 23, 2006
Valosin-containing protein gene mutations: clinical and neuropathologic featuresL Guyant-Maréchal, A Laquerrière, C Duyckaerts, et al.
Neurology|June 15, 2007
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?P Charles, A Camuzat, N Benammar, et al.
Bulletin De L'Academie Nationale De Medecine|April 24, 2020
[Toward a preventive management Alzheimer's disease]B Dubois, S Bombois, N Villain, et al.
Neurology|November 30, 2006
Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystoniaI Le Ber, F Clot, L Vercueil, et al.
Molecular Psychiatry|November 23, 2024
Disruption of macroscale functional network organisation in patients with frontotemporal dementiaA Bouzigues, V Godefroy, V Le Du, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 24, 2007
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutationY Baba, M C Baker, I Le Ber, et al.
AJNR. American Journal of Neuroradiology|August 18, 2018
Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French CasesP Codjia, X Ayrignac, F Mochel, et al.
Neurology|May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseI Le Ber, A Camuzat, E Berger, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Neurology|January 24, 2007
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1I Le Ber, O Dubourg, J-F Benoist, et al.
Revue Neurologique|April 1, 2005
[Mutation of the aprataxin gene presenting with Charcot-Marie-Tooth-like neuropathy and cerebellar ataxia]F Ochsner, I Le Ber, G Said, et al.
Neurology|June 23, 2006
Valosin-containing protein gene mutations: clinical and neuropathologic featuresL Guyant-Maréchal, A Laquerrière, C Duyckaerts, et al.
Neurology|June 15, 2007
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?P Charles, A Camuzat, N Benammar, et al.
Bulletin De L'Academie Nationale De Medecine|April 24, 2020
[Toward a preventive management Alzheimer's disease]B Dubois, S Bombois, N Villain, et al.
Neurology|November 30, 2006
Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystoniaI Le Ber, F Clot, L Vercueil, et al.
Molecular Psychiatry|November 23, 2024
Disruption of macroscale functional network organisation in patients with frontotemporal dementiaA Bouzigues, V Godefroy, V Le Du, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 24, 2007
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutationY Baba, M C Baker, I Le Ber, et al.
AJNR. American Journal of Neuroradiology|August 18, 2018
Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French CasesP Codjia, X Ayrignac, F Mochel, et al.
Neurology|May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseI Le Ber, A Camuzat, E Berger, et al.
Pageof 3