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Susen Schaake

Showing results (21-30 of 36) with videos related to

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Annals of Clinical and Translational Neurology|February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural VariantsAndré Fienemann, Theresa Lüth, Susen Schaake, et al.
Brain : a Journal of Neurology|May 16, 2025
FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?Joshua Laß, Mirja Thomsen, Max Borsche, et al.
Genes|January 21, 2022
Elucidating Hexanucleotide Repeat Number and Methylation within the X-Linked Dystonia-Parkinsonism (XDP)-Related SVA Retrotransposon in <i>TAF1</i> with Nanopore SequencingTheresa Lüth, Joshua Laβ, Susen Schaake, et al.
Brain : a Journal of Neurology|April 28, 2022
Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onsetJoanne Trinh, Theresa Lüth, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2022
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year StudyAngela Rosenbohm, Hendrik Pott, Mirja Thomsen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic ReviewChristina Wittke, Sonja Petkovic, Valerija Dobricic, et al.
Journal of the Neurological Sciences|March 22, 2017
Caffeine, creatine, GRIN2A and Parkinson's disease progressionDavid K Simon, Cai Wu, Barbara C Tilley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 13, 2018
Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic ReviewMeike Kasten, Corinna Hartmann, Jennie Hampf, et al.
Genes|October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other DystoniasEva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
Movement Disorders Clinical Practice|February 24, 2026
MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel InsightsCe Kang, Rajasumi Rajalingam, Zachary Walls, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Annals of Clinical and Translational Neurology|February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural VariantsAndré Fienemann, Theresa Lüth, Susen Schaake, et al.
Brain : a Journal of Neurology|May 16, 2025
FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?Joshua Laß, Mirja Thomsen, Max Borsche, et al.
Genes|January 21, 2022
Elucidating Hexanucleotide Repeat Number and Methylation within the X-Linked Dystonia-Parkinsonism (XDP)-Related SVA Retrotransposon in <i>TAF1</i> with Nanopore SequencingTheresa Lüth, Joshua Laβ, Susen Schaake, et al.
Brain : a Journal of Neurology|April 28, 2022
Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onsetJoanne Trinh, Theresa Lüth, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2022
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year StudyAngela Rosenbohm, Hendrik Pott, Mirja Thomsen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic ReviewChristina Wittke, Sonja Petkovic, Valerija Dobricic, et al.
Journal of the Neurological Sciences|March 22, 2017
Caffeine, creatine, GRIN2A and Parkinson's disease progressionDavid K Simon, Cai Wu, Barbara C Tilley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 13, 2018
Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic ReviewMeike Kasten, Corinna Hartmann, Jennie Hampf, et al.
Genes|October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other DystoniasEva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
Movement Disorders Clinical Practice|February 24, 2026
MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel InsightsCe Kang, Rajasumi Rajalingam, Zachary Walls, et al.
Pageof 4