The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein.
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Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotypeTherapeutic and diagnostic challenges for frontotemporal dementiaA 43-kDa TDP-43 species is present in aggregates associated with frontotemporal lobar degenerationPlasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration.Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationStructural brain changes in First Episode Schizophrenia compared with Fronto-Temporal Lobar Degeneration: a meta-analysisA Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease.Frontotemporal lobar degeneration: current concepts in the light of recent advances.Efficacy of memantine on neuropsychiatric symptoms associated with the severity of behavioral variant frontotemporal dementia: A six-month, open-label, self-controlled clinical trial.Novel progranulin mutation detected in 2 patients with FTLD.Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRNTau alternative splicing in familial and sporadic tauopathies.Immunotherapy for neurodegenerative diseases: focus on α-synucleinopathies.Propagation of tau pathology in Alzheimer's disease: identification of novel therapeutic targets.Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.Cellular tau pathology and immunohistochemical study of tau isoforms in sporadic tauopathies.Frequency of early and late-onset dementias in a Japanese memory disorders clinic.Progressive anomia revisited: focal degeneration associated with progranulin gene mutation.Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.Mixed tau, TDP-43 and p62 pathology in FTLD associated with a C9ORF72 repeat expansion and p.Ala239Thr MAPT (tau) variant.Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration.
P2860
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P2860
The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
The neuropathology of frontote ...... haracteristics of tau protein.
@en
type
label
The neuropathology of frontote ...... haracteristics of tau protein.
@en
prefLabel
The neuropathology of frontote ...... haracteristics of tau protein.
@en
P2093
P2860
P1476
The neuropathology of frontote ...... haracteristics of tau protein.
@en
P2093
P2860
P356
10.1046/J.0305-1846.2003.00481.X
P577
2004-02-01T00:00:00Z