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Mathieu Anheim

Showing results (81-90 of 189) with videos related to

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Journal of Parkinson'S Disease|May 9, 2022
Early Parkinson's Disease Phenotypes Tailored by Personality, Behavior, and Motor SymptomsBruna Meira, Eugénie Lhommée, Emmanuelle Schmitt, et al.
Neurology. Genetics|February 12, 2020
Spastic paraplegia due to recessive or dominant mutations in <i>ERLIN2</i> can convert to ALSMaria-Del-Mar Amador, François Muratet, Elisa Teyssou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 21, 2020
Is Motor Side Onset of Parkinson's Disease a Risk Factor for Developing Impulsive-Compulsive Behavior? A Cross-Sectional StudyClélie Phillipps, Nadine Longato, Matthieu Béreau, et al.
Movement Disorders Clinical Practice|August 28, 2023
Night-Time Apomorphine Infusion: Who Are the Best Candidates?Valérie Cochen De Cock, Pauline Dodet, Smaranda Leu-Semenescu, et al.
Journal of Neurology|January 24, 2024
Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?Thomas Wirth, Céline Bonnet, Clarisse Delvallée, et al.
Human Molecular Genetics|June 19, 2015
Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage diseaseJennifer Hirst, James R Edgar, Typhaine Esteves, et al.
Journal of Clinical Immunology|February 8, 2023
Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2Gaofeng Zhu, Mihaly Badonyi, Lina Franklin, et al.
Frontiers in Neurology|August 15, 2020
Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's DiseaseSabine Prud'hon, Samir Bekadar, Agnès Rastetter, et al.
Annals of Neurology|October 24, 2020
Reply to "PPP2R5D Genetic Mutations and Early Onset Parkinsonism"Christine Y Kim, Thomas Wirth, Cécile Hubsch, et al.
Annals of Neurology|August 4, 2020
Early-Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K MutationChristine Y Kim, Thomas Wirth, Cécile Hubsch, et al.
Pageof 19

Showing results (81-90 of 189) with videos related to

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Pageof 19
Journal of Parkinson'S Disease|May 9, 2022
Early Parkinson's Disease Phenotypes Tailored by Personality, Behavior, and Motor SymptomsBruna Meira, Eugénie Lhommée, Emmanuelle Schmitt, et al.
Neurology. Genetics|February 12, 2020
Spastic paraplegia due to recessive or dominant mutations in <i>ERLIN2</i> can convert to ALSMaria-Del-Mar Amador, François Muratet, Elisa Teyssou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 21, 2020
Is Motor Side Onset of Parkinson's Disease a Risk Factor for Developing Impulsive-Compulsive Behavior? A Cross-Sectional StudyClélie Phillipps, Nadine Longato, Matthieu Béreau, et al.
Movement Disorders Clinical Practice|August 28, 2023
Night-Time Apomorphine Infusion: Who Are the Best Candidates?Valérie Cochen De Cock, Pauline Dodet, Smaranda Leu-Semenescu, et al.
Journal of Neurology|January 24, 2024
Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?Thomas Wirth, Céline Bonnet, Clarisse Delvallée, et al.
Human Molecular Genetics|June 19, 2015
Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage diseaseJennifer Hirst, James R Edgar, Typhaine Esteves, et al.
Journal of Clinical Immunology|February 8, 2023
Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2Gaofeng Zhu, Mihaly Badonyi, Lina Franklin, et al.
Frontiers in Neurology|August 15, 2020
Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's DiseaseSabine Prud'hon, Samir Bekadar, Agnès Rastetter, et al.
Annals of Neurology|October 24, 2020
Reply to "PPP2R5D Genetic Mutations and Early Onset Parkinsonism"Christine Y Kim, Thomas Wirth, Cécile Hubsch, et al.
Annals of Neurology|August 4, 2020
Early-Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K MutationChristine Y Kim, Thomas Wirth, Cécile Hubsch, et al.
Pageof 19