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Matthis Synofzik

Showing results (71-80 of 511) with videos related to

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Parkinsonism & Related Disorders|April 3, 2017
Individualized exergame training improves postural control in advanced degenerative spinocerebellar ataxia: A rater-blinded, intra-individually controlled trialCornelia Schatton, Matthis Synofzik, Zofia Fleszar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 5, 2011
Atypical juvenile parkinsonism in a consanguineous SPG15 familyJulia Schicks, Matthis Synofzik, Hjörvar Pétursson, et al.
Archives of Physical Medicine and Rehabilitation|February 21, 2018
Validity and Reliability of Outcome Measures Assessing Dexterity, Coordination, and Upper Limb Strength in Autosomal Recessive Spastic Ataxia of Charlevoix-SaguenayCynthia Gagnon, Isabelle Lessard, Bernard Brais, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Complex hyperkinetic movement disorders associated with POLG mutationsMatthis Synofzik, Rebecca Schüle, Claudia Schulte, et al.
Journal of the Neurological Sciences|May 27, 2018
Assessing mobility and balance in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay population: Validity and reliability of four outcome measuresIsabelle Lessard, Bernard Brais, Isabelle Côté, et al.
Journal of Neurology|October 1, 2014
Comparing speech characteristics in spinocerebellar ataxias type 3 and type 6 with Friedreich ataxiaBettina Brendel, Matthis Synofzik, Hermann Ackermann, et al.
Cerebellum (London, England)|March 16, 2023
Scale for the Assessment and Rating of Ataxia (SARA): Development of a Training Tool and Certification ProgramMarcus Grobe-Einsler, Arian Taheri Amin, Jennifer Faber, et al.
The AAPS Journal|May 24, 2024
Correction: Prediction of Individual Disease Progression Including Parameter Uncertainty in Rare Neurodegenerative Diseases: The Example of Autosomal-Recessive Spastic Ataxia Charlevoix Saguenay (ARSACS)Niels Hendrickx, France Mentré, Andreas Traschütz, et al.
Journal of Neurology|May 15, 2012
POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening studyMatthis Synofzik, Julia Schicks, Karin Srulijes, et al.
Annals of Clinical and Translational Neurology|June 21, 2022
Home-based biofeedback speech treatment improves dysarthria in repeat-expansion SCAsAdam P Vogel, Lisa H Graf, Michelle Magee, et al.
Pageof 52

Showing results (71-80 of 511) with videos related to

Sort By:
Pageof 52
Parkinsonism & Related Disorders|April 3, 2017
Individualized exergame training improves postural control in advanced degenerative spinocerebellar ataxia: A rater-blinded, intra-individually controlled trialCornelia Schatton, Matthis Synofzik, Zofia Fleszar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 5, 2011
Atypical juvenile parkinsonism in a consanguineous SPG15 familyJulia Schicks, Matthis Synofzik, Hjörvar Pétursson, et al.
Archives of Physical Medicine and Rehabilitation|February 21, 2018
Validity and Reliability of Outcome Measures Assessing Dexterity, Coordination, and Upper Limb Strength in Autosomal Recessive Spastic Ataxia of Charlevoix-SaguenayCynthia Gagnon, Isabelle Lessard, Bernard Brais, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Complex hyperkinetic movement disorders associated with POLG mutationsMatthis Synofzik, Rebecca Schüle, Claudia Schulte, et al.
Journal of the Neurological Sciences|May 27, 2018
Assessing mobility and balance in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay population: Validity and reliability of four outcome measuresIsabelle Lessard, Bernard Brais, Isabelle Côté, et al.
Journal of Neurology|October 1, 2014
Comparing speech characteristics in spinocerebellar ataxias type 3 and type 6 with Friedreich ataxiaBettina Brendel, Matthis Synofzik, Hermann Ackermann, et al.
Cerebellum (London, England)|March 16, 2023
Scale for the Assessment and Rating of Ataxia (SARA): Development of a Training Tool and Certification ProgramMarcus Grobe-Einsler, Arian Taheri Amin, Jennifer Faber, et al.
The AAPS Journal|May 24, 2024
Correction: Prediction of Individual Disease Progression Including Parameter Uncertainty in Rare Neurodegenerative Diseases: The Example of Autosomal-Recessive Spastic Ataxia Charlevoix Saguenay (ARSACS)Niels Hendrickx, France Mentré, Andreas Traschütz, et al.
Journal of Neurology|May 15, 2012
POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening studyMatthis Synofzik, Julia Schicks, Karin Srulijes, et al.
Annals of Clinical and Translational Neurology|June 21, 2022
Home-based biofeedback speech treatment improves dysarthria in repeat-expansion SCAsAdam P Vogel, Lisa H Graf, Michelle Magee, et al.
Pageof 52