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Jun Suk Kang

Showing results (1-10 of 33) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|October 16, 2008
Botulinum toxin treatment of epilepsia partialis continuaJun-Suk Kang, Karsten Krakow, Julia Roggendorf, et al.
Cerebral Cortex (New York, N.Y. : 1991)|October 27, 2010
Deficient homeostatic regulation of practice-dependent plasticity in writer's crampJun-Suk Kang, Carmen Terranova, Rüdiger Hilker, et al.
Brain Stimulation|November 1, 2011
The relationship between TMS measures of functional properties and DTI measures of microstructure of the corticospinal tractAnnemarie Hübers, Johannes C Klein, Jun-Suk Kang, et al.
Muscle & Nerve|March 5, 2013
Description of a novel c.374 G>A mutation in Becker diseaseFranziska Hoche, Mayyada Qirshi, Tonio Heidegger, et al.
Journal of Cellular and Molecular Medicine|August 24, 2024
A novel KCND3 variant in the N-terminus impairs the ionic current of Kv4.3 and is associated with SCA19/22Marlen Colleen Reis, Laura Mandler, Jun-Suk Kang, et al.
Journal of Neurology|May 26, 2021
Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxiaDagmar Nolte, Jun-Suk Kang, Amrei Hofmann, et al.
Journal of Molecular Neuroscience : MN|December 3, 2013
A novel missense mutation in AFG3L2 associated with late onset and slow progression of spinocerebellar ataxia type 28Anna Mareike Löbbe, Jun-Suk Kang, Rüdiger Hilker, et al.
Muscle & Nerve|June 13, 2014
Novel N-terminal truncating CLCN1 mutation in severe Becker diseaseFranziska Hoche, Kay Seidel, Eduardo Barbosa-Sicard, et al.
Fortschritte Der Neurologie-Psychiatrie|June 29, 2018
[Cervical Dystonia]Gerhard Reichel, Christoph Kamm, Jun Suk Kang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
Ultrasound-based motion analysis demonstrates bilateral arm hypokinesia during gait in heterozygous PINK1 mutation carriersLucas Nürnberger, Christine Klein, Simon Baudrexel, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Movement Disorders : Official Journal of the Movement Disorder Society|October 16, 2008
Botulinum toxin treatment of epilepsia partialis continuaJun-Suk Kang, Karsten Krakow, Julia Roggendorf, et al.
Cerebral Cortex (New York, N.Y. : 1991)|October 27, 2010
Deficient homeostatic regulation of practice-dependent plasticity in writer's crampJun-Suk Kang, Carmen Terranova, Rüdiger Hilker, et al.
Brain Stimulation|November 1, 2011
The relationship between TMS measures of functional properties and DTI measures of microstructure of the corticospinal tractAnnemarie Hübers, Johannes C Klein, Jun-Suk Kang, et al.
Muscle & Nerve|March 5, 2013
Description of a novel c.374 G>A mutation in Becker diseaseFranziska Hoche, Mayyada Qirshi, Tonio Heidegger, et al.
Journal of Cellular and Molecular Medicine|August 24, 2024
A novel KCND3 variant in the N-terminus impairs the ionic current of Kv4.3 and is associated with SCA19/22Marlen Colleen Reis, Laura Mandler, Jun-Suk Kang, et al.
Journal of Neurology|May 26, 2021
Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxiaDagmar Nolte, Jun-Suk Kang, Amrei Hofmann, et al.
Journal of Molecular Neuroscience : MN|December 3, 2013
A novel missense mutation in AFG3L2 associated with late onset and slow progression of spinocerebellar ataxia type 28Anna Mareike Löbbe, Jun-Suk Kang, Rüdiger Hilker, et al.
Muscle & Nerve|June 13, 2014
Novel N-terminal truncating CLCN1 mutation in severe Becker diseaseFranziska Hoche, Kay Seidel, Eduardo Barbosa-Sicard, et al.
Fortschritte Der Neurologie-Psychiatrie|June 29, 2018
[Cervical Dystonia]Gerhard Reichel, Christoph Kamm, Jun Suk Kang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
Ultrasound-based motion analysis demonstrates bilateral arm hypokinesia during gait in heterozygous PINK1 mutation carriersLucas Nürnberger, Christine Klein, Simon Baudrexel, et al.
Pageof 4