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Journal Article
Journal Article
Journal Article
Journal Article
Journal of Molecular Neuroscience, ISSN 0895-8696, 11/2011, Volume 45, Issue 3, pp. 384 - 389
A clinically and pathologically heterogeneous type of frontotemporal lobar degeneration has abnormal tau pathology in neurons and glia (FTLD-tau). Familial... 
Neurochemistry | Neurology | Neurosciences | Biomedicine | Progressive supranuclear palsy | Proteomics | Corticobasal degeneration | Pick’s disease | Cell Biology | Corticobasal syndrome | Frontotemporal lobar degeneration-tau | Richardson syndrome | Pick's disease | GENE-MUTATIONS | PROTEIN-TAU | CYTOSKELETAL PATHOLOGY | ALZHEIMER-DISEASE | DEMENTIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | 4R TAUOPATHY | PICKS-DISEASE | NEUROSCIENCES | BASAL GANGLIONIC DEGENERATION | Pick Disease of the Brain - physiopathology | Frontotemporal Lobar Degeneration - pathology | Supranuclear Palsy, Progressive - pathology | Supranuclear Palsy, Progressive - physiopathology | Tauopathies - genetics | Humans | Tauopathies - pathology | tau Proteins - metabolism | Frontotemporal Lobar Degeneration - physiopathology | Pick Disease of the Brain - genetics | Pick Disease of the Brain - pathology | Tauopathies - metabolism | tau Proteins - genetics | Frontotemporal Lobar Degeneration - genetics | Supranuclear Palsy, Progressive - genetics | Nervous system | Development and progression | Degeneration | Research | Pathology, Molecular | Niemann-Pick disease | Alternative splicing | Brain | Brain architecture | Neurodegenerative diseases | Astrocytes | Neurons | Neuropathology | biomarkers | Amino acids | Anatomy | Tau protein | Microtubules | Mutation | Differentiation | Frontotemporal dementia | Plaques | progressive supranuclear palsy | frontotemporal lobar degeneration – tau | corticobasal degeneration | corticobasal syndrome
Journal Article
Journal Article