The status of "Pick's Disease" and other tauopathies within the frontotemporal dementias

Neurobiology of Aging

Volumn 22, Issue 1, 2001, Pages 109-111

  Manna, David M A ^a   Pickering Brown, Stuart ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID BETA PROTEIN; APOLIPOPROTEIN E; ISOPROTEIN; TAU PROTEIN;

ALZHEIMER DISEASE; BIOACCUMULATION; CELL INCLUSION; CHROMOSOME 17; DISEASE CLASSIFICATION; DNA MODIFICATION; FAMILY HISTORY; FRONTOTEMPORAL DEMENTIA; GENE FREQUENCY; GENE MUTATION; GENOTYPE; GLIA CELL; HISTOPATHOLOGY; HUMAN; IMMUNOREACTIVITY; NERVE CELL DEGENERATION; NEUROFIBRILLARY TANGLE; NEUROPATHOLOGY; NOTE; PHENOTYPE; PICK PRESENILE DEMENTIA; PRIORITY JOURNAL;

DEMENTIA; HUMANS; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION; PICK DISEASE OF THE BRAIN; TAU PROTEINS;

EID: 0035061081     PISSN: 01974580     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0197-4580(00)00205-0     Document Type: Note

References (13)

1. Familial non-specific dementia maps to chromosome 3
2. Neuropsychiatric studies in a family with presenile dementia different from Alzheimer and Pick disease
3. Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia
4. Coding and 5′ splice mutations in tau associated with inherited dementia (FTDP-17)
5. Frontotemporal degeneration, Pick disease and corticobasal degeneration: One entity or 3?
6. The topographic distribution of brain atrophy in frontal lobe dementia
7. Molecular classification of the dementias
8. Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits
9. Frontotemporal degeneration, Pick disease and corticobasal degeneration: One entity or 3?
10. Apolipoprotein E ε4 allele has no effect on age at onset or duration of disease in cases of frontotemporal dementia with Pick- or microvacuolar-type histology
11. Pick's disease is associated with mutations in the tau gene
12. Phenotypic correlations in FTDP-17
13. Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau