Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
about
Neurogenomics of speech and language disorders: the road aheadLanguage deficits, localization, and grammar: evidence for a distributive model of language breakdown in aphasic patients and neurologically intact individualsExpression analysis of the speech-related genes FoxP1 and FoxP2 and their relation to singing behavior in two songbird speciesStriatal FoxP2 is actively regulated during songbird sensorimotor learning.Domain-specific regulation of foxP2 CNS expression by lef1Movement sequencing in normal aging: speech, oro-facial, and finger movements.Disruption of Broca's Area Alters Higher-order Chunking Processing during Perceptual Sequence Learning.Functional brain activation differences in school-age children with speech sound errors: speech and print processingGeneralized motor abilities and timing behavior in children with specific language impairment.An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorderFunctional genetic analysis of mutations implicated in a human speech and language disorder.Motor response selection in overt sentence production: a functional MRI study.Williams syndrome: a surprising deficit in oromotor praxis in a population with proficient language production.Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language DevelopmentReplication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.The development of sentence interpretation: effects of perceptual, attentional and semantic interference.Fractionating nonword repetition: The contributions of short-term memory and oromotor praxis are different.Modification of spectral features by nonhuman primatesFOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways.Phonological working memory and FOXP2.The Many Sides of Hemispheric Asymmetry: A Selective Review and Outlook.Right hand, left brain: genetic and evolutionary bases of cerebral asymmetries for language and manual action.Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthriaDissection of molecular mechanisms underlying speech and language disorders
P2860
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P2860
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
description
2000 nî lūn-bûn
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2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
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2000年の論文
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2000年論文
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2000年論文
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name
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
@ast
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
@en
type
label
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
@ast
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
@en
prefLabel
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
@ast
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
@en
P50
P356
P1433
P1476
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia
@en
P2093
Passingham RE
P356
10.1006/BRLN.2000.2322
P577
2000-10-01T00:00:00Z