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Mathieu Anheim

Showing results (91-100 of 189) with videos related to

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Journal of Parkinson'S Disease|March 7, 2022
Fatigue in de novo Parkinson's Disease: Expanding the Neuropsychiatric Triad?Matthieu Béreau, Anna Castrioto, Eugénie Lhommée, et al.
Archives of Neurology|April 12, 2012
Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegiaSophie Tezenas du Montcel, Perrine Charles, Cyril Goizet, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2024
Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic DyskinesiaThomas Wirth, Emmanuel Roze, Clarisse Delvallée, et al.
JAMA Neurology|August 5, 2014
Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation studyMathilde Renaud, Mathieu Anheim, Erik-Jan Kamsteeg, et al.
Annals of Neurology|June 15, 2022
Limbic Stimulation Drives Mania in STN-DBS in Parkinson Disease: A Prospective StudyStéphane Prange, Zhengyu Lin, Mikail Nourredine, et al.
Journal of Neurology|June 20, 2023
Efficacy and safety of clonidine for the treatment of impulse control disorder in Parkinson's disease: a multicenter, parallel, randomised, double-blind, Phase 2b Clinical trialChloé Laurencin, Noémie Timestit, Ana Marques, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 14, 2014
A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificityMaya Tchikviladzé, Mylène Gilleron, Thierry Maisonobe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 20, 2023
Natural History and Phenotypic Spectrum of GAA-FGF14 Sporadic Late-Onset Cerebellar Ataxia (SCA27B)Thomas Wirth, Guillemette Clément, Clarisse Delvallée, et al.
Neurology. Clinical Practice|February 13, 2018
Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An updateMarc C Patterson, Peter Clayton, Paul Gissen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2025
RRP12 Variants Are Associated With Autosomal Recessive Brain CalcificationsEdoardo Monfrini, Paola Rinchetti, Mathieu Anheim, et al.
Pageof 19

Showing results (91-100 of 189) with videos related to

Sort By:
Pageof 19
Journal of Parkinson'S Disease|March 7, 2022
Fatigue in de novo Parkinson's Disease: Expanding the Neuropsychiatric Triad?Matthieu Béreau, Anna Castrioto, Eugénie Lhommée, et al.
Archives of Neurology|April 12, 2012
Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegiaSophie Tezenas du Montcel, Perrine Charles, Cyril Goizet, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2024
Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic DyskinesiaThomas Wirth, Emmanuel Roze, Clarisse Delvallée, et al.
JAMA Neurology|August 5, 2014
Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation studyMathilde Renaud, Mathieu Anheim, Erik-Jan Kamsteeg, et al.
Annals of Neurology|June 15, 2022
Limbic Stimulation Drives Mania in STN-DBS in Parkinson Disease: A Prospective StudyStéphane Prange, Zhengyu Lin, Mikail Nourredine, et al.
Journal of Neurology|June 20, 2023
Efficacy and safety of clonidine for the treatment of impulse control disorder in Parkinson's disease: a multicenter, parallel, randomised, double-blind, Phase 2b Clinical trialChloé Laurencin, Noémie Timestit, Ana Marques, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 14, 2014
A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificityMaya Tchikviladzé, Mylène Gilleron, Thierry Maisonobe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 20, 2023
Natural History and Phenotypic Spectrum of GAA-FGF14 Sporadic Late-Onset Cerebellar Ataxia (SCA27B)Thomas Wirth, Guillemette Clément, Clarisse Delvallée, et al.
Neurology. Clinical Practice|February 13, 2018
Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An updateMarc C Patterson, Peter Clayton, Paul Gissen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2025
RRP12 Variants Are Associated With Autosomal Recessive Brain CalcificationsEdoardo Monfrini, Paola Rinchetti, Mathieu Anheim, et al.
Pageof 19