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

Heike Jacobi

Showing results (41-50 of 63) with videos related to

Pageof 7
Sort By:
Neurology|August 11, 2017
Clinical and genetic characteristics of sporadic adult-onset degenerative ataxiaIlaria Giordano, Florian Harmuth, Heike Jacobi, et al.
Journal of Neurology|November 18, 2023
Correction to: The frequency of non‑motor symptoms in SCA3 and their association with disease severity and lifestyle factorsHolger Hengel, Peter Martus, Jennifer Faber, et al.
Journal of Neurology|December 21, 2024
Subtypes of cognitive impairment in cerebellar disease identified by cross-diagnostic cluster-analysis: results from a German multicenter studyQi Liu, Kerstin Rubarth, Jennifer Faber, et al.
EMBO Molecular Medicine|June 9, 2020
Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and miceCarlo Wilke, Eva Haas, Kathrin Reetz, et al.
NPJ Parkinson'S Disease|August 15, 2024
Risk willingness in multiple system atrophy and Parkinson's disease understanding patient preferencesAlexander Maximilian Bernhardt, Marc Oeller, Isabel Friedrich, 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|June 1, 2024
SARA captures disparate progression and responsiveness in spinocerebellar ataxiasEmilien Petit, Tanja Schmitz-Hübsch, Giulia Coarelli, et al.
Neurology|January 26, 2021
Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 DiseaseAndreas Traschütz, Andrea Cortese, Selina Reich, et al.
The Lancet. Neurology|March 20, 2018
Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort studyAlhassane Diallo, Heike Jacobi, Arron Cook, 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.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Neurology|August 11, 2017
Clinical and genetic characteristics of sporadic adult-onset degenerative ataxiaIlaria Giordano, Florian Harmuth, Heike Jacobi, et al.
Journal of Neurology|November 18, 2023
Correction to: The frequency of non‑motor symptoms in SCA3 and their association with disease severity and lifestyle factorsHolger Hengel, Peter Martus, Jennifer Faber, et al.
Journal of Neurology|December 21, 2024
Subtypes of cognitive impairment in cerebellar disease identified by cross-diagnostic cluster-analysis: results from a German multicenter studyQi Liu, Kerstin Rubarth, Jennifer Faber, et al.
EMBO Molecular Medicine|June 9, 2020
Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and miceCarlo Wilke, Eva Haas, Kathrin Reetz, et al.
NPJ Parkinson'S Disease|August 15, 2024
Risk willingness in multiple system atrophy and Parkinson's disease understanding patient preferencesAlexander Maximilian Bernhardt, Marc Oeller, Isabel Friedrich, 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|June 1, 2024
SARA captures disparate progression and responsiveness in spinocerebellar ataxiasEmilien Petit, Tanja Schmitz-Hübsch, Giulia Coarelli, et al.
Neurology|January 26, 2021
Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 DiseaseAndreas Traschütz, Andrea Cortese, Selina Reich, et al.
The Lancet. Neurology|March 20, 2018
Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort studyAlhassane Diallo, Heike Jacobi, Arron Cook, 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.
Pageof 7