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Emmanuel Broussolle

Showing results (81-90 of 117) with videos related to

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European Neurology|November 21, 2016
Liver Transplantation in Wilson's Disease with Neurological Impairment: Evaluation in 4 PatientsChloé Laurencin, Anne Sophie Brunet, Jérôme Dumortier, et al.
Archives of Neurology|May 21, 2003
Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography studyStéphane Thobois, Maria-Joao Ribeiro, Ebba Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2021
Serotonergic and Dopaminergic Lesions Underlying Parkinsonian Neuropsychiatric SignsAudrey Maillet, Elise Météreau, Léon Tremblay, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 11, 2009
Cerebrospinal fluid detection of enterovirus genome in ALS: a study of 242 patients and 354 controlsNadia Vandenberghe, Nicolas Leveque, Philippe Corcia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 20, 2012
Psychostimulant effect of levodopa: reversing sensitisation is possibleAnna Castrioto, Andrea Kistner, Hélène Klinger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2022
Limbic Serotonergic Plasticity Contributes to the Compensation of Apathy in Early Parkinson's DiseaseStéphane Prange, Elise Metereau, Audrey Maillet, et al.
Brain : a Journal of Neurology|February 16, 2013
C9orf72 repeat expansions are a rare genetic cause of parkinsonismSuzanne Lesage, Isabelle Le Ber, Christel Condroyer, et al.
Journal of Neurology|November 2, 2013
Heterogeneity and frequency of movement disorders in juvenile and adult-onset Niemann-Pick C diseaseMathieu Anheim, Ouhaïd Lagha-Boukbiza, Marie-Céline Fleury-Lesaunier, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 21, 2009
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutationsMaria-João Ribeiro, Stéphane Thobois, Ebba Lohmann, et al.
American Journal of Human Genetics|January 5, 2010
A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth diseasePhilippe Latour, Christel Thauvin-Robinet, Chantal Baudelet-Méry, et al.
Pageof 12

Showing results (81-90 of 117) with videos related to

Sort By:
Pageof 12
European Neurology|November 21, 2016
Liver Transplantation in Wilson's Disease with Neurological Impairment: Evaluation in 4 PatientsChloé Laurencin, Anne Sophie Brunet, Jérôme Dumortier, et al.
Archives of Neurology|May 21, 2003
Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography studyStéphane Thobois, Maria-Joao Ribeiro, Ebba Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2021
Serotonergic and Dopaminergic Lesions Underlying Parkinsonian Neuropsychiatric SignsAudrey Maillet, Elise Météreau, Léon Tremblay, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 11, 2009
Cerebrospinal fluid detection of enterovirus genome in ALS: a study of 242 patients and 354 controlsNadia Vandenberghe, Nicolas Leveque, Philippe Corcia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 20, 2012
Psychostimulant effect of levodopa: reversing sensitisation is possibleAnna Castrioto, Andrea Kistner, Hélène Klinger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2022
Limbic Serotonergic Plasticity Contributes to the Compensation of Apathy in Early Parkinson's DiseaseStéphane Prange, Elise Metereau, Audrey Maillet, et al.
Brain : a Journal of Neurology|February 16, 2013
C9orf72 repeat expansions are a rare genetic cause of parkinsonismSuzanne Lesage, Isabelle Le Ber, Christel Condroyer, et al.
Journal of Neurology|November 2, 2013
Heterogeneity and frequency of movement disorders in juvenile and adult-onset Niemann-Pick C diseaseMathieu Anheim, Ouhaïd Lagha-Boukbiza, Marie-Céline Fleury-Lesaunier, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 21, 2009
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutationsMaria-João Ribeiro, Stéphane Thobois, Ebba Lohmann, et al.
American Journal of Human Genetics|January 5, 2010
A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth diseasePhilippe Latour, Christel Thauvin-Robinet, Chantal Baudelet-Méry, et al.
Pageof 12