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Kathrin Grundmann

Showing results (11-20 of 40) with videos related to

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Neurobiology of Disease|March 5, 2024
Disturbed brain energy metabolism in a rodent model of DYT-TOR1A dystoniaSusanne Knorr, Lisa Rauschenberger, Muthuraman Muthuraman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystoniasKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Diagnostics (Basel, Switzerland)|February 12, 2021
Nerve Ultrasound as Helpful Tool in PolyneuropathiesMagdalena Kramer, Alexander Grimm, Natalie Winter, et al.
Journal of Neurology|October 27, 2004
Mutation at the SCA17 locus is not a common cause of primary dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Proteomics. Clinical Applications|December 8, 2010
Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinAKathrin Grundmann, Jeannette Hübener, Karina Häbig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in GermanyClaudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Neuroradiology|May 24, 2025
Measuring cerebrovascular reactivity with breath-hold fMRI in patients with Moyamoya angiopathy: MR perfusion based delay correction significantly improves agreement to [<sup>15</sup>O]water PETLeonie Zerweck, Uwe Klose, Constantin Roder, et al.
Journal of Molecular Neuroscience : MN|March 1, 2020
Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 DystoniaFubo Cheng, Michael Walter, Zinah Wassouf, et al.
Archives of Neurology|September 17, 2003
Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Ingrid Bauer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Prevalence of THAP1 sequence variants in German patients with primary dystoniaAnne S Söhn, Nicola Glöckle, Andrea Duarte Doetzer, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Neurobiology of Disease|March 5, 2024
Disturbed brain energy metabolism in a rodent model of DYT-TOR1A dystoniaSusanne Knorr, Lisa Rauschenberger, Muthuraman Muthuraman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystoniasKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Diagnostics (Basel, Switzerland)|February 12, 2021
Nerve Ultrasound as Helpful Tool in PolyneuropathiesMagdalena Kramer, Alexander Grimm, Natalie Winter, et al.
Journal of Neurology|October 27, 2004
Mutation at the SCA17 locus is not a common cause of primary dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Proteomics. Clinical Applications|December 8, 2010
Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinAKathrin Grundmann, Jeannette Hübener, Karina Häbig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in GermanyClaudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Neuroradiology|May 24, 2025
Measuring cerebrovascular reactivity with breath-hold fMRI in patients with Moyamoya angiopathy: MR perfusion based delay correction significantly improves agreement to [<sup>15</sup>O]water PETLeonie Zerweck, Uwe Klose, Constantin Roder, et al.
Journal of Molecular Neuroscience : MN|March 1, 2020
Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 DystoniaFubo Cheng, Michael Walter, Zinah Wassouf, et al.
Archives of Neurology|September 17, 2003
Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Ingrid Bauer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Prevalence of THAP1 sequence variants in German patients with primary dystoniaAnne S Söhn, Nicola Glöckle, Andrea Duarte Doetzer, et al.
Pageof 4