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Apraxia Impairs Intentional Retrieval of Incidentally Acquired Motor Knowledge

[HTML] from cjb.netA Dovern, GR Fink, J Saliger, H Karbe… - The Journal of …, 2011 - neuro.cjb.net
Apraxia caused by left hemispheric stroke typically impairs skilled sequential movements. After
stroke, apraxic patients need to reacquire motor skills by motor learning. The current study assessed
for the first time incidental motor sequence learning in apraxic patients. Forty-eight human ...
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How to diagnose and treat limb apraxia

A Dovern, GR Fink… - Fortschritte der Neurologie, Psychiatrie, 2011 - cat.inist.fr
Apraxia is a disorder of higher motor cognition. Deficits in imitating abstract and symbolic gestures
as well as deficits in appropriate tool use are common apraxic symptoms which, importantly,
cannot be explained by primary sensorimotor deficits alone. In spite of the relevance of ...
Cited by 1 - Related articles - All 2 versions

Constraint-Induced Language Therapy: Treatment Effects on Two Individuals with Moderate to Severe Aphasia and Apraxia of Speech

NA Silva, J Kurland, K Burke… - 2011 - aphasiology.pitt.edu
Constraint-induced language therapy (CILT) has proven to be an effective treatment for improving
naming in some individuals with chronic aphasia. Whether constraint to the speech modality
or treatment intensity is responsible for such gains is still under investigation. Two ...
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Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients

B Castellotti, C Mariotti, M Rimoldi, R Fancellu… - neurogenetics, 2011 - Springer
Abstract Ataxia with oculomotor apraxia type1 (AOA1, MIM 208920) is a rare autosomal recessive
disease caused by mutations in the APTX gene. We screened a cohort of 204 patients with cerebellar
ataxia and 52 patients with early-onset isolated chorea. APTX gene mutations were found ...
Cited by 2 - Related articles - All 2 versions

Prevalence and phenotype of Childhood Apraxia of Speech in youth with galactosemia

[PDF] from wisc.eduLD Shriberg, NL Potter… - Journal of Speech, …, 2011 - jslhr.highwire.org
Purpose: In this article, the authors address the hypothesis that the severe and persistent speech
disorder reported in persons with galactosemia meets contemporary diagnostic criteria for Childhood
Apraxia of Speech (CAS). A positive finding for CAS in this rare metabolic disorder has ...
Cited by 7 - Related articles - All 3 versions

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