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Matthis Synofzik

Showing results (61-70 of 511) with videos related to

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Journal of Neurology|December 12, 2024
Frequency and neuropathology of HTT repeat expansions in FTD/ALS: co-existence rather than causationMilan Zimmermann, David Mengel, Katrin Raupach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2024
Reduced Age-Dependent Penetrance of a Large FGF14 GAA Repeat Expansion in a 74-Year-Old Woman from a German Family with SCA27BDavid Pellerin, Jens Seemann, Andreas Traschütz, et al.
Cerebellum (London, England)|April 14, 2016
POLG-Associated Ataxia Presenting as a Fragile X Tremor/Ataxia Phenocopy SyndromeMartin Paucar, Martin Engvall, Lisa Gordon, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 24, 2010
The human G93A SOD1 phenotype closely resembles sporadic amyotrophic lateral sclerosisMatthis Synofzik, Rubén Fernández-Santiago, Walter Maetzler, et al.
Neurology|November 2, 2012
Video game-based coordinative training improves ataxia in children with degenerative ataxiaWinfried Ilg, Cornelia Schatton, Julia Schicks, et al.
Journal of Neurology|January 27, 2016
Atypical parkinsonism in C9orf72 expansions: a case report and systematic review of 45 cases from the literatureCarlo Wilke, Jörn K Pomper, Saskia Biskup, et al.
Parkinsonism & Related Disorders|October 10, 2018
TSFM mutations cause a complex hyperkinetic movement disorder with strong relief by cannabinoidsAndreas Traschütz, Stefanie N Hayer, Benjamin Bender, et al.
The American Journal of Psychiatry|November 7, 2012
Suicide attempt as the presenting symptom of C9orf72 dementiaMatthis Synofzik, Saskia Biskup, Thomas Leyhe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 26, 2010
Long-term effects of coordinative training in degenerative cerebellar diseaseWinfried Ilg, Doris Brötz, Susanne Burkard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 9, 2013
Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patientsJennifer Müller Vom Hagen, Matthis Synofzik, Julia Schicks, et al.
Pageof 52

Showing results (61-70 of 511) with videos related to

Sort By:
Pageof 52
Journal of Neurology|December 12, 2024
Frequency and neuropathology of HTT repeat expansions in FTD/ALS: co-existence rather than causationMilan Zimmermann, David Mengel, Katrin Raupach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2024
Reduced Age-Dependent Penetrance of a Large FGF14 GAA Repeat Expansion in a 74-Year-Old Woman from a German Family with SCA27BDavid Pellerin, Jens Seemann, Andreas Traschütz, et al.
Cerebellum (London, England)|April 14, 2016
POLG-Associated Ataxia Presenting as a Fragile X Tremor/Ataxia Phenocopy SyndromeMartin Paucar, Martin Engvall, Lisa Gordon, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 24, 2010
The human G93A SOD1 phenotype closely resembles sporadic amyotrophic lateral sclerosisMatthis Synofzik, Rubén Fernández-Santiago, Walter Maetzler, et al.
Neurology|November 2, 2012
Video game-based coordinative training improves ataxia in children with degenerative ataxiaWinfried Ilg, Cornelia Schatton, Julia Schicks, et al.
Journal of Neurology|January 27, 2016
Atypical parkinsonism in C9orf72 expansions: a case report and systematic review of 45 cases from the literatureCarlo Wilke, Jörn K Pomper, Saskia Biskup, et al.
Parkinsonism & Related Disorders|October 10, 2018
TSFM mutations cause a complex hyperkinetic movement disorder with strong relief by cannabinoidsAndreas Traschütz, Stefanie N Hayer, Benjamin Bender, et al.
The American Journal of Psychiatry|November 7, 2012
Suicide attempt as the presenting symptom of C9orf72 dementiaMatthis Synofzik, Saskia Biskup, Thomas Leyhe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 26, 2010
Long-term effects of coordinative training in degenerative cerebellar diseaseWinfried Ilg, Doris Brötz, Susanne Burkard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 9, 2013
Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patientsJennifer Müller Vom Hagen, Matthis Synofzik, Julia Schicks, et al.
Pageof 52