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

Dagmar Timmann

Showing results (251-260 of 269) with videos related to

Pageof 27
Sort By:
Annals of Neurology|November 14, 2023
Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3Jennifer Faber, Moritz Berger, Carlo Wilke, et al.
Ebiomedicine|December 24, 2025
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichmentHannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
Neurology. Genetics|February 12, 2020
Clinical spectrum of POLR3-related leukodystrophy caused by biallelic <i>POLR1C</i> pathogenic variantsLaurence Gauquelin, Ferdy K Cayami, László Sztriha, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 21, 2024
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia studyThiago Junqueira Ribeiro Rezende, Isaac Adanyaguh, Orlando G P Barsottini, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Stage-dependent biomarker changes in spinocerebellar ataxia type 3Jennifer Faber, Moritz Berger, Wilke Carlo, et al.
Radiology. Artificial Intelligence|August 6, 2025
Automated Deep Learning-based Segmentation of the Dentate Nucleus Using Quantitative Susceptibility Mapping MRIDiogo H Shiraishi, Susmita Saha, Isaac M Adanyeguh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2026
A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-AtaxiaJason W Robertson, Isaac Adanyeguh, David J Arpin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Radiology|March 10, 2026
Identification of Biological Subtypes of Friedreich Ataxia with Structural MRI-based Machine LearningGiuseppe Pontillo, Simone Penna, Filippo Arrigoni, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2024
RORA-neurodevelopmental disorder: A unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizuresMariagrazia Talarico, Julitta de Bellescize, Matthias De Wachter, et al.
Pageof 27

Showing results (251-260 of 269) with videos related to

Sort By:
Pageof 27
Annals of Neurology|November 14, 2023
Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3Jennifer Faber, Moritz Berger, Carlo Wilke, et al.
Ebiomedicine|December 24, 2025
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichmentHannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
Neurology. Genetics|February 12, 2020
Clinical spectrum of POLR3-related leukodystrophy caused by biallelic <i>POLR1C</i> pathogenic variantsLaurence Gauquelin, Ferdy K Cayami, László Sztriha, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 21, 2024
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia studyThiago Junqueira Ribeiro Rezende, Isaac Adanyaguh, Orlando G P Barsottini, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Stage-dependent biomarker changes in spinocerebellar ataxia type 3Jennifer Faber, Moritz Berger, Wilke Carlo, et al.
Radiology. Artificial Intelligence|August 6, 2025
Automated Deep Learning-based Segmentation of the Dentate Nucleus Using Quantitative Susceptibility Mapping MRIDiogo H Shiraishi, Susmita Saha, Isaac M Adanyeguh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2026
A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-AtaxiaJason W Robertson, Isaac Adanyeguh, David J Arpin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Radiology|March 10, 2026
Identification of Biological Subtypes of Friedreich Ataxia with Structural MRI-based Machine LearningGiuseppe Pontillo, Simone Penna, Filippo Arrigoni, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2024
RORA-neurodevelopmental disorder: A unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizuresMariagrazia Talarico, Julitta de Bellescize, Matthias De Wachter, et al.
Pageof 27