about
Neuropsychological features of patients with spinocerebellar ataxia (SCA) types 1, 2, 3, and 6.Cognitive impairments in patients with spinocerebellar ataxia types 1, 2 and 3 are positively correlated to the clinical severity of ataxia symptoms.Change in the cortical complexity of spinocerebellar ataxia type 3 appears earlier than clinical symptomsToward understanding Machado-Joseph diseaseDepression and clinical progression in spinocerebellar ataxias.Machado-Joseph disease/spinocerebellar ataxia type 3.A longitudinal investigation into cognition and disease progression in spinocerebellar ataxia types 1, 2, 3, 6, and 7Caring for Machado-Joseph disease: current understanding and how to help patients.Nonmotor and extracerebellar features in Machado-Joseph disease: a review.Association between spinocerebellar ataxias caused by glutamine expansion and psychiatric and neuropsychological signals - a literature review.Widespread neuronal damage and cognitive dysfunction in spinocerebellar ataxia type 3.Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Cognitive Changes in the Spinocerebellar Ataxias Due to Expanded Polyglutamine Tracts: A Survey of the Literature.Mouse ataxin-3 functional knock-out model.Cognition in SCA21 reflects developmental and adult onset cerebellar cognitive affective syndrome.Cerebellar cognitive affective syndrome in Machado Joseph disease: core clinical features.Cognitive dysfunction in spinocerebellar ataxia type 3: variable topographies and patterns.Dysautonomia is frequent in Machado-Joseph disease: clinical and neurophysiological evaluation.Cerebral cortex involvement in Machado-Joseph disease.Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan.Cognitive dysfunction in spinocerebellar ataxias.Spinocerebellar ataxia: a critical review of cognitive and socio-cognitive deficits.Neurophysiological studies and non-motor symptoms prior to ataxia in a patient with machado-joseph disease: trying to understand the natural history of brain degeneration.Depression comorbidity in spinocerebellar ataxia.Sleep disorders in machado-joseph disease: frequency, discriminative thresholds, predictive values, and correlation with ataxia-related motor and non-motor features.Progressive cognitive dysfunction in spinocerebellar ataxia type 3.Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.Cognitive deficits in Machado-Joseph disease correlate with hypoperfusion of visual system areas.Neocortical atrophy in Machado-Joseph disease: a longitudinal neuroimaging study.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
name
Cognitive impairments in Machado-Joseph disease
@ast
Cognitive impairments in Machado-Joseph disease
@en
Cognitive impairments in Machado-Joseph disease
@nl
type
label
Cognitive impairments in Machado-Joseph disease
@ast
Cognitive impairments in Machado-Joseph disease
@en
Cognitive impairments in Machado-Joseph disease
@nl
prefLabel
Cognitive impairments in Machado-Joseph disease
@ast
Cognitive impairments in Machado-Joseph disease
@en
Cognitive impairments in Machado-Joseph disease
@nl
P2093
P3181
P1433
P1476
Cognitive impairments in Machado-Joseph disease
@en
P2093
Akinori Takeda
Fumiaki Tanaka
Yoshinari Kawai
Yukihiko Washimi
P304
P3181
P356
10.1001/ARCHNEUR.61.11.1757
P407
P50
P577
2004-11-01T00:00:00Z