Pathways to primary neurodegenerative disease

Annals of the New York Academy of Sciences

Volumn 924, Issue , 2000, Pages 29-34

  Hardy, John ^a  

^a MAYO CLINIC   (United States)

Author keywords

Amyloid; Dementia; Genetic mutation; Parkinsonism; Prion; Synucleinopathy; Tauopathy

Indexed keywords

AMYLOID BETA PROTEIN;

ALZHEIMER DISEASE; AUTOSOMAL DOMINANT INHERITANCE; CELL DEATH; CONFERENCE PAPER; DEMENTIA; GENE MUTATION; GENETIC ANALYSIS; HUMAN; LEWY BODY; MOLECULAR GENETICS; NERVE DEGENERATION; PARKINSONISM; PRION DISEASE;

EID: 0034515761     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2000.tb05556.x     Document Type: Conference Paper

References (19)

1. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
2. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
3. Candidate gene for the chromosome 1 familial Alzheimer's disease locus
4. Mutation in the α-synuclein gene identified in families with Parkinson's disease
5. Tau is a candidate gene for chromosome 17 frontotemporal dementia
6. Coding and 5′ splice site mutations in tau associated with inherited dementia (FTDP-17)
7. Insertion in prion protein gene in familial Creutzfeldt-Jakob disease
8. Secreted amyloid β-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
9. Visualization of Aβ42(43) and Aβ40 in senile plaques with end-specific Aβ monoclonals: Evidence that an initially deposited species is Aβ42(43)
10. Alpha-synuclein in Lewy bodies
11. Frontotemporal dementia and Parkinsonism linked to chromosome 17: A new group of tauopathies
12. Regional mapping of prion proteins in brain
13. Familial Alzheimer's disease with the amyloid precursor protein position 717 mutation and sporadic Alzheimer's disease have the same cytoskeletal pathology
14. Linkage of the Indiana kindred of Gerstmann-Straussler-Scheinker disease to the prion protein gene
15. α-Synuclein accumulation in Gerstmann-Straussler-Schenker disease (GSS) with prion protein gene (PRNP) F198S
16. Hereditary form of Parkinsonism dementia
17. A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
18. Gerstmann-Straussler-Scheinker disease and the Indiana kindred
19. Trinucleotide repeats in neurogenetic disorders