Associated Papers
Clinical characteristics of semantic variant of primary progressive aphasia with TDP-43- and tau-related gene variants.
Ma Y et al.
Journal of Alzheimer's Disease : Jad, 2025
Genetics of Multiple System Atrophy and Progressive Supranuclear Palsy: A Systemized Review of the Literature.
Bougea A
International Journal of Molecular Sciences, 2023
Concurrent tau pathologies in frontotemporal lobar degeneration with TDP-43 pathology.
Koga S et al.
Neuropathology and Applied Neurobiology, 2022
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.
Moore KM et al.
The Lancet. Neurology, 2020
31810826 (PubMed )
Supplement: NIHMS1067362-supplement-Supplement.pdf
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases.
Ramos EM et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2020
Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN.
Whitwell JL et al.
Neurology, 2011
Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration.
Borroni B et al.
Neurobiology of Aging, 2011
GRN and MAPT Mutations in 2 Frontotemporal Dementia Research Centers in Brazil.
Takada LT et al.
Alzheimer Disease and Associated Disorders, 0
Recent advances in the molecular genetics of frontotemporal lobar degeneration.
Rainero I et al.
Functional Neurology, 0
Genetics of dementia: insights from Latin America.
Ramos C et al.
Dementia & Neuropsychologia, 0
Select a paper to view details