Pick's disease in 2 brothers with S305N mutation: Note in supplement to an earlier communication [1]

Clinical Neuropathology

Volumn 21, Issue 4, 2002, Pages 191-193

  Kobayashi, K ^a   Hayashi, M ^a   Kidani, T ^a   Nakano, H ^a   Miyazu, K ^a   Ujike, H ^a   Kuroda, S ^a   Koshino, Y ^a  

^a KANAZAWA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; DEGENERATIVE DISEASE; GENE MUTATION; HUMAN; LETTER; MALE; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PICK PRESENILE DEMENTIA; PRIORITY JOURNAL; SIBLING; GENETICS; MIDDLE AGED; MUTATION; PATHOLOGY;

CASE REPORT; HUMAN; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGE; MUTATION; PICK DISEASE OF THE BRAIN; SIBLINGS; HUMANS; MIDDLE AGED;

EID: 0035990472     PISSN: 07225091     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (12)

1. Distinct isoforms of τ aggregated in neurons and glial cells in brains of patients with Pick's disease, corticobasal degeneration and progressive supranuclear palsy
2. Progress in hereditary tauopathies: A mutation in the τ gene (G389R) causes a Pick disease-like syndrome
3. A distinct familial presenile dementia with novel missense mutation in the τ gene
4. KP1 expression of ghost Pick bodies, amyloid P-positive astrocytes and selective nigral degeneration in early onset Pick's disease
5. Pick's disease
6. τ gene mutation G387R causes a tauopathy with abundant Pick body-like inclusions and axonal deposits
7. Pick's disease associated with the novel τ gene mutation K3691
8. Pick's disease is associated with mutations in the τ gene
9. Phenotypic correlations in FTDP-17
10. τ gene mutation K257T causes a tauopathy similar to Pick's disease
11. The extended haplotype of the microtubule associated protein τ gene is not associated with Pick's disease
12. Structure of τ exon 10 splicing regulatory element RNA and destabilization by mutation of fronto-temporal dementia and parkinsonism linked to chromosome 17