Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
about
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.Tools for the assessment of childhood apraxia of speechNeurogenomics of speech and language disorders: the road aheadData-driven subclassification of speech sound disorders in preschool children.Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication study.Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridizationEncoding, memory, and transcoding deficits in Childhood Apraxia of Speech.The hypothesis of apraxia of speech in children with autism spectrum disorder.Voice disorders in children with classic galactosemia.A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype.Perceptual and acoustic reliability estimates for the Speech Disorders Classification System (SDCS).Extensions to the Speech Disorders Classification System (SDCS).From mind to mouth: event related potentials of sentence production in classic galactosemia.White matter microstructure pathology in classic galactosemia revealed by neurite orientation dispersion and density imaging.Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.The adult galactosemic phenotypeCryptic residual GALT activity is a potential modifier of scholastic outcome in school age children with classic galactosemiaMotor and speech disorders in classic galactosemia.Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech.Insights into the genetic foundations of human communication.The role of candidate-gene CNTNAP2 in childhood apraxia of speech and specific language impairment.Cognitive, Linguistic, and Motor Abilities in a Multigenerational Family with Childhood Apraxia of Speech.Appropriateness of newborn screening for classic galactosaemia: a systematic review.A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.Longitudinal observations of typical English voicing acquisition in a 2-year-old child: Stability of the contrast and considerations for clinical assessment.Exploration of the Brain in Rest: Resting-State Functional MRI Abnormalities in Patients with Classic Galactosemia.Neuroanatomical correlates of childhood apraxia of speech: A connectomic approach.Pre-linguistic communication skill development in an infant with a diagnosis of galactosaemia.An exploratory study of the influence of load and practice on segmental and articulatory variability in children with speech sound disorders.A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: II. Validity Studies of the Pause Marker.Childhood apraxia of speech: A survey of praxis and typical speech characteristics.Treatment intensity and childhood apraxia of speech.Motor speech treatment protocol for developmental motor speech disorders.Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays.Phenotype of FOXP2 haploinsufficiency in a mother and son.
P2860
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P2860
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
name
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
@ast
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
@en
type
label
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
@ast
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
@en
prefLabel
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
@ast
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
@en
P2860
P356
P1476
Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia
@en
P2093
Edythe A Strand
Lawrence D Shriberg
P2860
P304
P356
10.1044/1092-4388(2010/10-0068)
P577
2010-10-21T00:00:00Z