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

Matthis Synofzik

Showing results (361-370 of 511) with videos related to

Pageof 52
Sort By:
Neuroimage|February 5, 2019
The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprintEnrico Premi, Vince D Calhoun, Matteo Diano, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|November 22, 2020
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohortLucy L Russell, Caroline V Greaves, Martina Bocchetta, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
The CBI-R detects early behavioural impairment in genetic frontotemporal dementiaAnnabel Nelson, Lucy L Russell, Georgia Peakman, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 19, 2026
CSF protein biomarkers are associated with atrophy and symptom severity in genetic FTD: a GENFI studyAbbe Ullgren, Melissa Taheri Rydell, Sofia Bergström, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersMaurice Pasternak, Saira S Mirza, Andrew D Paterson, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Subjective cognition trajectories, Alzheimer biomarkers, and incident mild cognitive impairmentElizabeth Kuhn, Luca Kleinedam, Melina Stark, et al.
The New England Journal of Medicine|June 23, 2021
Developmental Consequences of Defective ATG7-Mediated Autophagy in HumansJack J Collier, Claire Guissart, Monika Oláhová, et al.
Brain : a Journal of Neurology|April 1, 2025
Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanismHolger Hengel, Shabab B Hannan, Selina Reich, et al.
Brain : a Journal of Neurology|November 2, 2013
SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndromeMichael Krieger, Andreas Roos, Claudia Stendel, et al.
Brain : a Journal of Neurology|February 21, 2022
Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementiaGolia Shafiei, Vincent Bazinet, Mahsa Dadar, et al.
Pageof 52

Showing results (361-370 of 511) with videos related to

Sort By:
Pageof 52
Neuroimage|February 5, 2019
The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprintEnrico Premi, Vince D Calhoun, Matteo Diano, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|November 22, 2020
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohortLucy L Russell, Caroline V Greaves, Martina Bocchetta, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
The CBI-R detects early behavioural impairment in genetic frontotemporal dementiaAnnabel Nelson, Lucy L Russell, Georgia Peakman, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 19, 2026
CSF protein biomarkers are associated with atrophy and symptom severity in genetic FTD: a GENFI studyAbbe Ullgren, Melissa Taheri Rydell, Sofia Bergström, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersMaurice Pasternak, Saira S Mirza, Andrew D Paterson, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Subjective cognition trajectories, Alzheimer biomarkers, and incident mild cognitive impairmentElizabeth Kuhn, Luca Kleinedam, Melina Stark, et al.
The New England Journal of Medicine|June 23, 2021
Developmental Consequences of Defective ATG7-Mediated Autophagy in HumansJack J Collier, Claire Guissart, Monika Oláhová, et al.
Brain : a Journal of Neurology|April 1, 2025
Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanismHolger Hengel, Shabab B Hannan, Selina Reich, et al.
Brain : a Journal of Neurology|November 2, 2013
SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndromeMichael Krieger, Andreas Roos, Claudia Stendel, et al.
Brain : a Journal of Neurology|February 21, 2022
Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementiaGolia Shafiei, Vincent Bazinet, Mahsa Dadar, et al.
Pageof 52