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

Matthias Amprosi

Showing results (1-10 of 24) with videos related to

Pageof 3
Sort By:
Orphanet Journal of Rare Diseases|February 17, 2022
Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clueElisabetta Indelicato, Michael Zech, Matthias Amprosi, et al.
Neurology. Genetics|January 13, 2023
Toward the Definition of Patient-Reported Outcome Measurements in Hereditary Spastic ParaplegiaMatthias Amprosi, Elisabetta Indelicato, Andreas Eigentler, et al.
Cerebellum (London, England)|November 15, 2025
Resting-State EEG Analysis Characterizes the Signature of CACNA1A-and GAA-FGF14-Related ChannelopathiesRaphael Angerbauer, Iris Unterberger, Wolfgang Nachbauer, et al.
Journal of Neurology|January 26, 2026
Natural history in hereditary spastic paraplegias: real-world data from an Austrian cohortMatthias Amprosi, Elisabetta Indelicato, Andreas Eigentler, et al.
Frontiers in Neuroscience|November 29, 2023
Skeletal muscle proteome analysis underpins multifaceted mitochondrial dysfunction in Friedreich's ataxiaElisabetta Indelicato, Klaus Faserl, Matthias Amprosi, et al.
Frontiers in Neurology|February 3, 2022
Mast Syndrome Outside the Amish Community: <i>SPG21</i> in EuropeMatthias Amprosi, Elisabetta Indelicato, Wolfgang Nachbauer, et al.
Journal of Neurology|November 10, 2021
Instrumented gait analysis defines the walking signature of CACNA1A disordersElisabetta Indelicato, Cecilia Raccagni, Sarah Runer, et al.
Journal of Neurology|January 2, 2020
Cardiovascular autonomic testing in the work-up of cerebellar ataxia: insight from an observational single center studyElisabetta Indelicato, Alessandra Fanciulli, Wolfgang Nachbauer, et al.
Neurogenetics|August 25, 2020
Familial writer's cramp: a clinical clue for inherited coenzyme Q<sub>10</sub> deficiencyMatthias Amprosi, Michael Zech, Ruth Steiger, et al.
Journal of Neurology|February 5, 2021
The electrophysiological footprint of CACNA1A disordersElisabetta Indelicato, Iris Unterberger, Wolfgang Nachbauer, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Orphanet Journal of Rare Diseases|February 17, 2022
Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clueElisabetta Indelicato, Michael Zech, Matthias Amprosi, et al.
Neurology. Genetics|January 13, 2023
Toward the Definition of Patient-Reported Outcome Measurements in Hereditary Spastic ParaplegiaMatthias Amprosi, Elisabetta Indelicato, Andreas Eigentler, et al.
Cerebellum (London, England)|November 15, 2025
Resting-State EEG Analysis Characterizes the Signature of CACNA1A-and GAA-FGF14-Related ChannelopathiesRaphael Angerbauer, Iris Unterberger, Wolfgang Nachbauer, et al.
Journal of Neurology|January 26, 2026
Natural history in hereditary spastic paraplegias: real-world data from an Austrian cohortMatthias Amprosi, Elisabetta Indelicato, Andreas Eigentler, et al.
Frontiers in Neuroscience|November 29, 2023
Skeletal muscle proteome analysis underpins multifaceted mitochondrial dysfunction in Friedreich's ataxiaElisabetta Indelicato, Klaus Faserl, Matthias Amprosi, et al.
Frontiers in Neurology|February 3, 2022
Mast Syndrome Outside the Amish Community: <i>SPG21</i> in EuropeMatthias Amprosi, Elisabetta Indelicato, Wolfgang Nachbauer, et al.
Journal of Neurology|November 10, 2021
Instrumented gait analysis defines the walking signature of CACNA1A disordersElisabetta Indelicato, Cecilia Raccagni, Sarah Runer, et al.
Journal of Neurology|January 2, 2020
Cardiovascular autonomic testing in the work-up of cerebellar ataxia: insight from an observational single center studyElisabetta Indelicato, Alessandra Fanciulli, Wolfgang Nachbauer, et al.
Neurogenetics|August 25, 2020
Familial writer's cramp: a clinical clue for inherited coenzyme Q<sub>10</sub> deficiencyMatthias Amprosi, Michael Zech, Ruth Steiger, et al.
Journal of Neurology|February 5, 2021
The electrophysiological footprint of CACNA1A disordersElisabetta Indelicato, Iris Unterberger, Wolfgang Nachbauer, et al.
Pageof 3