Characterizing behavioral and cognitive dysexecutive changes in progressive supranuclear palsy.
about
Clinical diagnostic criteria and classification controversies in frontotemporal lobar degenerationSocial cognitive deficits and their neural correlates in progressive supranuclear palsy.Comprehension of insincere communication in neurodegenerative disease: lies, sarcasm, and theory of mind.The Addenbrooke's Cognitive Examination for the differential diagnosis and longitudinal assessment of patients with parkinsonian disorders.Executive resources.Characteristics of Nonmotor Symptoms in Progressive Supranuclear Palsy.Behavioral abnormalities in progressive supranuclear palsy.Theory of mind in Parkinson's disease and related basal ganglia disorders: a systematic review.MM2 subtype of sporadic Creutzfeldt-Jakob disease may underlie the clinical presentation of progressive supranuclear palsy.Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Managing cognition in progressive supranuclear palsy.Minimal clinically important worsening on the progressive supranuclear Palsy Rating Scale.Predicting disease progression in progressive supranuclear palsy in multicenter clinical trials.Neuropathologic features of suicide victims who presented with acute poststroke depression: significance of association with neurodegenerative disorders.Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series.Reorganisation of brain networks in frontotemporal dementia and progressive supranuclear palsy.Impaired awareness of deficits in Alzheimer's disease: the role of everyday executive dysfunction.Brain gray matter abnormalities in progressive supranuclear palsy revisited.Clinical, cognitive, and behavioural correlates of white matter damage in progressive supranuclear palsy.The relationship between clinical and pathological variables in Richardson's syndrome.Postural instability, frontotemporal dementia, and ophthalmoplegia: clinicopathological case.Mild Cognitive Impairment and Progression to Dementia in Progressive Supranuclear Palsy.Frontal deficits differentiate progressive supranuclear palsy from Parkinson's disease.Gray matter correlates of behavioral severity in progressive supranuclear palsy.Executive Functioning
P2860
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P2860
Characterizing behavioral and cognitive dysexecutive changes in progressive supranuclear palsy.
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
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
@zh-hant
name
Characterizing behavioral and ...... rogressive supranuclear palsy.
@en
Characterizing behavioral and ...... rogressive supranuclear palsy.
@nl
type
label
Characterizing behavioral and ...... rogressive supranuclear palsy.
@en
Characterizing behavioral and ...... rogressive supranuclear palsy.
@nl
prefLabel
Characterizing behavioral and ...... rogressive supranuclear palsy.
@en
Characterizing behavioral and ...... rogressive supranuclear palsy.
@nl
P2093
P2860
P356
P1433
P1476
Characterizing behavioral and ...... rogressive supranuclear palsy.
@en
P2093
Adam J Zermansky
David Millar
Philipa Griffiths
P2860
P304
P356
10.1002/MDS.20707
P407
P50
P577
2006-02-01T00:00:00Z