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Brain Communications
|
July 17, 2024
Impaired glymphatic system in genetic frontotemporal dementia: a GENFI study
Enrico 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 aphasia
Kiran 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 cohort
Martina 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 enrichment
Hannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
Brain : a Journal of Neurology
|
May 27, 2025
Anatomical progression of genetic frontotemporal lobar degeneration across the lifespan
Vincent 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 dementia
Arabella 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 disease
David Mengel, Ester Soter, Julia Maren Ott, et al.
Neuroimage. Clinical
|
December 15, 2019
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study
Carole H Sudre, Martina Bocchetta, Carolin Heller, et al.
American Journal of Human Genetics
|
June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
Mohammad 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 dementia
Kamen A Tsvetanov, Maura Malpetti, P Simon Jones, et al.
Page
of 52
Search research articles
Search
Showing results (431-440 of 511) with videos related to
Sort By:
Page
of 52
Brain Communications
|
July 17, 2024
Impaired glymphatic system in genetic frontotemporal dementia: a GENFI study
Enrico 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 aphasia
Kiran 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 cohort
Martina 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 enrichment
Hannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
Brain : a Journal of Neurology
|
May 27, 2025
Anatomical progression of genetic frontotemporal lobar degeneration across the lifespan
Vincent 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 dementia
Arabella 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 disease
David Mengel, Ester Soter, Julia Maren Ott, et al.
Neuroimage. Clinical
|
December 15, 2019
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study
Carole H Sudre, Martina Bocchetta, Carolin Heller, et al.
American Journal of Human Genetics
|
June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
Mohammad 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 dementia
Kamen A Tsvetanov, Maura Malpetti, P Simon Jones, et al.
Page
of 52