The molecular genetic analysis demonstrated the APTX mutation W279X at locus 9p13.3 (ataxia with oculomotor apraxia 1 disease), and psychologic studies showed mild cognitive impairment.
The Cognitive Group, part 1 ... Adam: extending the therapeutic milieu into the community in the rehabilitation of a client with severe aphasia and apraxia Jacqui Cooper and Andrew Bateman 20. Malcolm ...
[11] Neuropsychologic testing of six patients with a normal IQ score revealed cognitive deficits characteristic of subcortical syndrome. The diagnosis of ataxia with oculomotor apraxia is based on ...
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