Atypical progressive supranuclear palsy with corticospinal tract degeneration.
about
Neuropathology of non-Alzheimer degenerative disordersClinical Approach to Progressive Supranuclear PalsyGenetics of Progressive Supranuclear PalsyExpanding the phenotypic associations of globular glial tau subtypes.Propagation of tau pathology: hypotheses, discoveries, and yet unresolved questions from experimental and human brain studies.FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases.A familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal study.Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant.Typical or atypical progressive supranuclear palsy: a comparative clinicopathologic study of three Chinese cases.Neuropathology of frontotemporal lobar degeneration-tau (FTLD-tau).Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease.Temporal Variant Frontotemporal Dementia is Associated with Globular Glial Tauopathy.Clinical correlates of white matter tract degeneration in progressive supranuclear palsy.Frontotemporal lobar degenerationA novel tau mutation, p.K317N, causes globular glial tauopathyEarly onset familial Alzheimer Disease with spastic paraparesis, dysarthria, and seizures and N135S mutation in PSEN1.Unusual phenotype of pathologically confirmed progressive supranuclear palsy with autonomic dysfunction and cerebellar ataxia: Case report.White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration.Globular glial tauopathies (GGT): consensus recommendations.Corticobasal degeneration: a pathologically distinct 4R tauopathy.Neuropathological background of phenotypical variability in frontotemporal dementia.Invited review: Neuropathology of tauopathies: principles and practice.Which ante mortem clinical features predict progressive supranuclear palsy pathology?Progressive supranuclear palsy (PSP): Richardson syndrome and other PSP variants.Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.Amyotrophic lateral sclerosis-plus syndrome with TAR DNA-binding protein-43 pathologyA case of globular glial tauopathy presenting clinically as alzheimer disease.Magnetic resonance imaging corticospinal tract hyperintensities in progressive supranuclear palsy.Globular Glial Mixed Four Repeat Tau and TDP-43 Proteinopathy with Motor Neuron Disease and Frontotemporal Dementia.Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology.Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies.FDG-PET in pathologically confirmed spontaneous 4R-tauopathy variants.Diffuse Lewy body disease manifesting as corticobasal syndrome: A rare form of Lewy body diseaseProgressive Supranuclear Palsy and Corticobasal Degeneration
P2860
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P2860
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
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2006年學術文章
@zh-hant
name
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
@en
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
@nl
type
label
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
@en
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
@nl
prefLabel
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
@en
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
@nl
P2093
P2860
P50
P1476
Atypical progressive supranuclear palsy with corticospinal tract degeneration.
@en
P2093
Bradley F Boeve
Keith A Josephs
Matthew C Baker
Michael L Hutton
Omi Katsuse
Wen-Lang Lin
Yasuhiro Fujino
P2860
P304
P356
10.1097/01.JNEN.0000218446.38158.61
P577
2006-04-01T00:00:00Z