Amyotrophic lateral sclerosis patients show executive impairments on standard neuropsychological measures and an ecologically valid motor-free test of executive functions

scientific article published on 24 June 2010

Amyotrophic lateral sclerosis patients show executive impairments on standard neuropsychological measures and an ecologically valid motor-free test of executive functions is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1080/13803391003749236
P698PubMed publication ID20582796

P50authorGrega RepovšQ24278978
P2093author name stringSimon Podnar
Janez Zidar
Vita Stukovnik
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Word retrieval in amyotrophic lateral sclerosis: a functional magnetic resonance imaging study.Q51940534
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Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis. A longitudinal study in 52 patients.Q51993902
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The assessment of executive functions: coming out of the officeQ35951044
Mild traumatic brain injury: neuroimaging of sports-related concussionQ36265381
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Only subtle cognitive deficits in non-bulbar amyotrophic lateral sclerosis patientsQ38411966
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P433issue10
P921main subjectneuropsychologyQ3872
amyotrophic lateral sclerosisQ206901
P6104maintained by WikiProjectWikiProject EcologyQ10818384
P304page(s)1095-1109
P577publication date2010-06-24
P1433published inNeuropsychology, Development and Cognition. Section A: Journal of Clinical and Experimental NeuropsychologyQ15762076
P1476titleAmyotrophic lateral sclerosis patients show executive impairments on standard neuropsychological measures and an ecologically valid motor-free test of executive functions
P478volume32

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Q57158112ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS
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Q47368817ECAS A-B-C: alternate forms of the Edinburgh Cognitive and Behavioural ALS Screen
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Q50754216Selective attention and the three-process memory model for the interpretation of verbal free recall in amyotrophic lateral sclerosis.
Q38778723The frontotemporal dementia-motor neuron disease continuum
Q53850980Trail Making Test error analysis in classic motor neuron disease.

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