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Judith van Gaalen

Showing results (21-30 of 42) with videos related to

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Cerebellum (London, England)|March 6, 2024
Correction: Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Research Square|November 28, 2023
Cerebellar volumetry in ataxias: Relation to ataxia severity and durationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Cerebellum (London, England)|February 16, 2024
Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Neurology|February 10, 2019
Biallelic variants in <i>LARS2</i> and <i>KARS</i> cause deafness and (ovario)leukodystrophyMarjo S van der Knaap, Marianna Bugiani, Marisa I Mendes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral BloodJeannette Hübener-Schmid, Kirsten Kuhlbrodt, Julien Peladan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2022
Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3Roderick P P W M Maas, Steven Teerenstra, Manuela Lima, et al.
Neurology|August 11, 2017
Clinical and genetic characteristics of sporadic adult-onset degenerative ataxiaIlaria Giordano, Florian Harmuth, Heike Jacobi, et al.
Acta Neuropathologica Communications|July 19, 2025
Influence of ATXN2 intermediate CAG repeats, 9bp duplication and alternative splicing on SCA3 pathogenesisMarilena Lauerer, Jennifer Faber, Nicolas Casadei, et al.
Journal of Neurology|December 12, 2024
Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3Tim Lukas Elter, Daniel Sturm, Magda M Santana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2021
Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3Jennifer Faber, Tamara Schaprian, Koyak Berkan, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Cerebellum (London, England)|March 6, 2024
Correction: Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Research Square|November 28, 2023
Cerebellar volumetry in ataxias: Relation to ataxia severity and durationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Cerebellum (London, England)|February 16, 2024
Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Neurology|February 10, 2019
Biallelic variants in <i>LARS2</i> and <i>KARS</i> cause deafness and (ovario)leukodystrophyMarjo S van der Knaap, Marianna Bugiani, Marisa I Mendes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral BloodJeannette Hübener-Schmid, Kirsten Kuhlbrodt, Julien Peladan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2022
Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3Roderick P P W M Maas, Steven Teerenstra, Manuela Lima, et al.
Neurology|August 11, 2017
Clinical and genetic characteristics of sporadic adult-onset degenerative ataxiaIlaria Giordano, Florian Harmuth, Heike Jacobi, et al.
Acta Neuropathologica Communications|July 19, 2025
Influence of ATXN2 intermediate CAG repeats, 9bp duplication and alternative splicing on SCA3 pathogenesisMarilena Lauerer, Jennifer Faber, Nicolas Casadei, et al.
Journal of Neurology|December 12, 2024
Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3Tim Lukas Elter, Daniel Sturm, Magda M Santana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2021
Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3Jennifer Faber, Tamara Schaprian, Koyak Berkan, et al.
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