Frontal-subcortical defects correlate with task switching deficits in Parkinson`s disease.

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Frontal-subcortical defects correlate with task switching deficits in Parkinson`s disease.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Frontal-subcortical defects co ...... ficits in Parkinson`s disease.

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Frontal-subcortical defects co ...... ficits in Parkinson`s disease.

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label

Frontal-subcortical defects co ...... ficits in Parkinson`s disease.

@en

Frontal-subcortical defects co ...... ficits in Parkinson`s disease.

@nl

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Frontal-subcortical defects co ...... ficits in Parkinson`s disease.

@en

Frontal-subcortical defects co ...... ficits in Parkinson`s disease.

@nl

P1476

Frontal-subcortical defects co ...... ficits in Parkinson`s disease.

@en

P2093

Amara Gul

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Hira Ahmad

http://www.w3.org/2001/XMLSchema#string

Javed Yousaf

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P2860

Neural bases of set-shifting deficits in Parkinson's disease.

Rule-based category learning in patients with Parkinson's disease.

The burden of white matter hyperintensities is a predictor of progressive mild cognitive impairment in patients with Parkinson's disease.

Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030.

Impaired cognitive performance in Parkinson's disease is related to caudate dopaminergic hypofunction and hippocampal atrophy.

Dissociating executive mechanisms of task control following frontal lobe damage and Parkinson's disease.

Task switching deficits associated with Parkinson's disease reflect depleted attentional resources.

Grey matter atrophy in cognitively impaired Parkinson's disease.

Parkinson's disease-cognitive rating scale: a new cognitive scale specific for Parkinson's disease.

Cognitive deficits in mild Parkinson's disease are associated with distinct areas of grey matter atrophy.

P304

224-227

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P31

scholarly article

P356

10.17712/NSJ.2017.3.20160572

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P433

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P478

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P577

2017-07-01T00:00:00Z

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P698

28678219

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P921

Parkinson's disease

P932

5946369

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