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Susanne A Schneider

Showing results (1-10 of 172) with videos related to

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Parkinsonism & Related Disorders|September 1, 2015
Neurodegenerations with Brain Iron AccumulationSusanne A Schneider
Current Neurology and Neuroscience Reports|January 8, 2016
Neurodegeneration with Brain Iron AccumulationSusanne A Schneider
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2019
Iron chelation in pantothenate kinase-associated neurodegeneration: A possible new avenue for slowing down disease progression in neurodegenerationJulius Huebl, Susanne A Schneider
Movement Disorders Clinical Practice|October 27, 2018
<i>XPR1</i> Mutations: Another Cause of Primary Familial Brain CalcificationRoberto Erro, Susanne A Schneider
Movement Disorders : Official Journal of the Movement Disorder Society|July 23, 2013
Neurodegenerative disorder with brain iron accumulation previously known as SENDA syndrome now genetically determinedPetr Dusek, Susanne A Schneider
Movement Disorders : Official Journal of the Movement Disorder Society|March 6, 2013
Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutationsAthanasia Alexoudi, Susanne A Schneider
Current Opinion in Neurology|July 2, 2013
Huntington's disease and Huntington's disease-like syndromes: an overviewFelix Gövert, Susanne A Schneider
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 22, 2013
The treatment of tremorSusanne A Schneider, Günther Deuschl
Current Neurology and Neuroscience Reports|April 6, 2011
What is the role of genetic testing in movement disorders practice?Susanne A Schneider, Christine Klein
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2015
Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like familyFranziska Hopfner, Susanne A Schneider
Pageof 18

Showing results (1-10 of 172) with videos related to

Sort By:
Pageof 18
Parkinsonism & Related Disorders|September 1, 2015
Neurodegenerations with Brain Iron AccumulationSusanne A Schneider
Current Neurology and Neuroscience Reports|January 8, 2016
Neurodegeneration with Brain Iron AccumulationSusanne A Schneider
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2019
Iron chelation in pantothenate kinase-associated neurodegeneration: A possible new avenue for slowing down disease progression in neurodegenerationJulius Huebl, Susanne A Schneider
Movement Disorders Clinical Practice|October 27, 2018
<i>XPR1</i> Mutations: Another Cause of Primary Familial Brain CalcificationRoberto Erro, Susanne A Schneider
Movement Disorders : Official Journal of the Movement Disorder Society|July 23, 2013
Neurodegenerative disorder with brain iron accumulation previously known as SENDA syndrome now genetically determinedPetr Dusek, Susanne A Schneider
Movement Disorders : Official Journal of the Movement Disorder Society|March 6, 2013
Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutationsAthanasia Alexoudi, Susanne A Schneider
Current Opinion in Neurology|July 2, 2013
Huntington's disease and Huntington's disease-like syndromes: an overviewFelix Gövert, Susanne A Schneider
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 22, 2013
The treatment of tremorSusanne A Schneider, Günther Deuschl
Current Neurology and Neuroscience Reports|April 6, 2011
What is the role of genetic testing in movement disorders practice?Susanne A Schneider, Christine Klein
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2015
Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like familyFranziska Hopfner, Susanne A Schneider
Pageof 18