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Showing results (431-440 of 511) with videos related to

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Brain Communications|July 17, 2024
Impaired glymphatic system in genetic frontotemporal dementia: a GENFI studyEnrico Premi, Matteo Diano, Irene Mattioli, et al.
Brain Communications|March 20, 2023
Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasiaKiran Samra, Amy M MacDougall, Arabella Bouzigues, et al.
Brain Communications|March 27, 2023
Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohortMartina Bocchetta, Emily G Todd, Arabella Bouzigues, 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.
Brain : a Journal of Neurology|May 27, 2025
Anatomical progression of genetic frontotemporal lobar degeneration across the lifespanVincent Planche, Boris Mansencal, Vladimir Fonov, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 17, 2025
Structural and functional connectivity in tau mutation carriers: from presymptomatic to symptomatic frontotemporal dementiaArabella Bouzigues, Vincent Le Du, Matthieu Joulot, et al.
Molecular Psychiatry|April 17, 2025
Blood biomarkers confirm subjective cognitive decline (SCD) as a distinct molecular and clinical stage within the NIA-AA framework of Alzheimer´s diseaseDavid Mengel, Ester Soter, Julia Maren Ott, et al.
Neuroimage. Clinical|December 15, 2019
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI studyCarole H Sudre, Martina Bocchetta, Carolin Heller, et al.
American Journal of Human Genetics|June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Brain : a Journal of Neurology|November 24, 2025
Cellular signatures underlying functional resilience in presymptomatic frontotemporal dementiaKamen A Tsvetanov, Maura Malpetti, P Simon Jones, et al.
Pageof 52

Showing results (431-440 of 511) with videos related to

Sort By:
Pageof 52
Brain Communications|July 17, 2024
Impaired glymphatic system in genetic frontotemporal dementia: a GENFI studyEnrico Premi, Matteo Diano, Irene Mattioli, et al.
Brain Communications|March 20, 2023
Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasiaKiran Samra, Amy M MacDougall, Arabella Bouzigues, et al.
Brain Communications|March 27, 2023
Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohortMartina Bocchetta, Emily G Todd, Arabella Bouzigues, 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.
Brain : a Journal of Neurology|May 27, 2025
Anatomical progression of genetic frontotemporal lobar degeneration across the lifespanVincent Planche, Boris Mansencal, Vladimir Fonov, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 17, 2025
Structural and functional connectivity in tau mutation carriers: from presymptomatic to symptomatic frontotemporal dementiaArabella Bouzigues, Vincent Le Du, Matthieu Joulot, et al.
Molecular Psychiatry|April 17, 2025
Blood biomarkers confirm subjective cognitive decline (SCD) as a distinct molecular and clinical stage within the NIA-AA framework of Alzheimer´s diseaseDavid Mengel, Ester Soter, Julia Maren Ott, et al.
Neuroimage. Clinical|December 15, 2019
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI studyCarole H Sudre, Martina Bocchetta, Carolin Heller, et al.
American Journal of Human Genetics|June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Brain : a Journal of Neurology|November 24, 2025
Cellular signatures underlying functional resilience in presymptomatic frontotemporal dementiaKamen A Tsvetanov, Maura Malpetti, P Simon Jones, et al.
Pageof 52