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Mathieu Anheim

Showing results (101-110 of 189) with videos related to

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Brain : a Journal of Neurology|July 30, 2014
TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairmentJérôme Delplanque, David Devos, Vincent Huin, et al.
Neurology|June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European populationAurélie Méneret, David Grabli, Christel Depienne, et al.
Scientific Reports|December 1, 2023
Imbalanced motivated behaviors according to motor sign asymmetry in drug-naïve Parkinson's diseaseMatthieu Béreau, Anna Castrioto, Mathieu Servant, et al.
Brain : a Journal of Neurology|February 10, 2026
No role of intronic expansions in HSF1 for essential tremor in EuropeJean-Loup Méreaux, Thomas Wirth, Claire-Sophie Davoine, et al.
Neurology|February 17, 2017
Low cancer prevalence in polyglutamine expansion diseasesGiulia Coarelli, Alhassane Diallo, Morgane Sonia Thion, et al.
Orphanet Journal of Rare Diseases|October 5, 2018
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effectYann Nadjar, Ana Lucia Hütter-Moncada, Philippe Latour, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2011
Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxiasEllis Chan, Perrine Charles, Pascale Ribai, et al.
Neurology|August 15, 2014
The pleiotropic movement disorders phenotype of adult ataxia-telangiectasiaAurélie Méneret, Yara Ahmar-Beaugendre, Guillaume Rieunier, et al.
Brain : a Journal of Neurology|December 27, 2013
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardationMartial Mallaret, Matthis Synofzik, Jaeho Lee, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2024
A Double-Blind, Randomized, Placebo-Controlled Trial of Bumetanide in Parkinson's DiseasePhilippe Damier, Bertrand Degos, Giovanni Castelonovo, et al.
Pageof 19

Showing results (101-110 of 189) with videos related to

Sort By:
Pageof 19
Brain : a Journal of Neurology|July 30, 2014
TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairmentJérôme Delplanque, David Devos, Vincent Huin, et al.
Neurology|June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European populationAurélie Méneret, David Grabli, Christel Depienne, et al.
Scientific Reports|December 1, 2023
Imbalanced motivated behaviors according to motor sign asymmetry in drug-naïve Parkinson's diseaseMatthieu Béreau, Anna Castrioto, Mathieu Servant, et al.
Brain : a Journal of Neurology|February 10, 2026
No role of intronic expansions in HSF1 for essential tremor in EuropeJean-Loup Méreaux, Thomas Wirth, Claire-Sophie Davoine, et al.
Neurology|February 17, 2017
Low cancer prevalence in polyglutamine expansion diseasesGiulia Coarelli, Alhassane Diallo, Morgane Sonia Thion, et al.
Orphanet Journal of Rare Diseases|October 5, 2018
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effectYann Nadjar, Ana Lucia Hütter-Moncada, Philippe Latour, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2011
Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxiasEllis Chan, Perrine Charles, Pascale Ribai, et al.
Neurology|August 15, 2014
The pleiotropic movement disorders phenotype of adult ataxia-telangiectasiaAurélie Méneret, Yara Ahmar-Beaugendre, Guillaume Rieunier, et al.
Brain : a Journal of Neurology|December 27, 2013
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardationMartial Mallaret, Matthis Synofzik, Jaeho Lee, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2024
A Double-Blind, Randomized, Placebo-Controlled Trial of Bumetanide in Parkinson's DiseasePhilippe Damier, Bertrand Degos, Giovanni Castelonovo, et al.
Pageof 19