Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Susen Schaake

Showing results (11-20 of 36) with videos related to

Pageof 4
Sort By:
Cerebellum (London, England)|April 21, 2023
POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the LiteratureMax Borsche, Marija Dulovic-Mahlow, Hauke Baumann, et al.
Parkinsonism & Related Disorders|June 29, 2017
Screening study of TUBB4A in isolated dystoniaFranca Vulinovic, Susen Schaake, Aloysius Domingo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2018
Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic reviewJoanne Trinh, Florentine M J Zeldenrust, Jana Huang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 25, 2021
Genotype-Phenotype Relations in Primary Familial Brain Calcification: Systematic MDSGene ReviewAlexander Balck, Susen Schaake, Neele Sophie Kuhnke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2025
Classification and Genotype-Phenotype Relationships of GBA1 Variants: MDSGene Systematic ReviewMalco Rossi, Susen Schaake, Tatiana Usnich, et al.
Annals of Neurology|March 28, 2024
α-Synuclein Pathology in PRKN-Linked Parkinson's Disease: New Insights from a Blood-Based Seed Amplification AssayAnnika Kluge, Max Borsche, Linn Streubel-Gallasch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 15, 2024
Stability of Mosaic Divergent Repeat Interruptions in X-Linked Dystonia-ParkinsonismJoshua Laß, Theresa Lüth, Kathleen Schlüter, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2021
Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic ReviewLara M Lange, Johanna Junker, Sebastian Loens, et al.
Neurology. Genetics|July 12, 2021
Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore SequencingCharles Jourdan Reyes, Björn-Hergen Laabs, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 11, 2020
DNA Methylation as a Potential Molecular Mechanism in X-linked Dystonia-ParkinsonismChristin Krause, Susen Schaake, Karen Grütz, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Cerebellum (London, England)|April 21, 2023
POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the LiteratureMax Borsche, Marija Dulovic-Mahlow, Hauke Baumann, et al.
Parkinsonism & Related Disorders|June 29, 2017
Screening study of TUBB4A in isolated dystoniaFranca Vulinovic, Susen Schaake, Aloysius Domingo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2018
Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic reviewJoanne Trinh, Florentine M J Zeldenrust, Jana Huang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 25, 2021
Genotype-Phenotype Relations in Primary Familial Brain Calcification: Systematic MDSGene ReviewAlexander Balck, Susen Schaake, Neele Sophie Kuhnke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2025
Classification and Genotype-Phenotype Relationships of GBA1 Variants: MDSGene Systematic ReviewMalco Rossi, Susen Schaake, Tatiana Usnich, et al.
Annals of Neurology|March 28, 2024
α-Synuclein Pathology in PRKN-Linked Parkinson's Disease: New Insights from a Blood-Based Seed Amplification AssayAnnika Kluge, Max Borsche, Linn Streubel-Gallasch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 15, 2024
Stability of Mosaic Divergent Repeat Interruptions in X-Linked Dystonia-ParkinsonismJoshua Laß, Theresa Lüth, Kathleen Schlüter, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2021
Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic ReviewLara M Lange, Johanna Junker, Sebastian Loens, et al.
Neurology. Genetics|July 12, 2021
Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore SequencingCharles Jourdan Reyes, Björn-Hergen Laabs, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 11, 2020
DNA Methylation as a Potential Molecular Mechanism in X-linked Dystonia-ParkinsonismChristin Krause, Susen Schaake, Karen Grütz, et al.
Pageof 4