about
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimagingClinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosisPresence of reactive microglia and neuroinflammatory mediators in a case of frontotemporal dementia with P301S mutation.Evidence for a Common Founder and Clinical Characteristics of Japanese Families with the MAPT R406W MutationPallidonigral TDP-43 pathology in Perry syndrome.Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration.Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America.
P2860
Q21203040-17B57EF0-15A2-416C-AF5F-5FBDA6508E28Q27020981-93716EB4-E70F-4F2C-9F66-32867AF12BF8Q30541723-F7C20895-A9C7-4C45-8BA4-7B526DEB07FCQ35546446-4C4FE2CF-E414-460E-ACAE-110D780A11F9Q35607649-C2591F5B-18ED-42CC-A31A-AF5E8F841979Q37221392-B29C997C-B183-47EA-B694-06B30A4ECC07Q37619559-151B747E-E051-41DC-B0A6-4E8BC144B855Q47952791-E10B2B70-F41A-4CF4-90B8-8C957938A162
P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Hereditary tauopathies and parkinsonism.
@ast
Hereditary tauopathies and parkinsonism.
@en
type
label
Hereditary tauopathies and parkinsonism.
@ast
Hereditary tauopathies and parkinsonism.
@en
prefLabel
Hereditary tauopathies and parkinsonism.
@ast
Hereditary tauopathies and parkinsonism.
@en
P2093
P1476
Hereditary tauopathies and parkinsonism.
@en
P2093
Mathew Farrer
Mike L Hutton
Yoshio Tsuboi
P304
P577
2003-01-01T00:00:00Z