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1
Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia
In: F1000Res (2020)
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2
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech
In: Clinical linguistics & phonetics. - London : Informa Healthcare 27 (2013) 3, 163-191
OLC Linguistik
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3
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
In: Clinical linguistics & phonetics. - London : Informa Healthcare 27 (2013) 3, 192-212
OLC Linguistik
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4
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
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5
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech
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6
Oral and hand movement speeds are associated with expressive language ability in children with speech sound disorder
In: Journal of psycholinguistic research. - New York, NY ; London [u.a.] : Springer 41 (2012) 6, 455-474
BLLDB
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7
Oral and Hand Movement Speeds are Associated with Expressive Language Ability in Children with Speech Sound Disorder
Peter, Beate. - 2012
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8
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
Abstract: Two functionally related genes, FOXP2 and CNTNAP2, influence language abilities in families with rare syndromic and common nonsyndromic forms of impaired language, respectively. We investigated whether these genes are associated with component phenotypes of dyslexia and measures of sequential motor ability. Quantitative transmission disequilibrium testing (QTDT) and linear association modeling were used to evaluate associations with measures of phonological memory (nonword repetition, NWR), expressive language (sentence repetition), reading (real word reading efficiency, RWRE; word attack, WATT), and timed sequential motor activities (rapid alternating place of articulation, RAPA; finger succession in the dominant hand, FS-D) in 188 family trios with a child with dyslexia. Consistent with a prior study of language impairment, QTDT in dyslexia showed evidence of CNTNAP2 single nucleotide polymorphism (SNP) association with NWR. For FOXP2, we provide the first evidence for SNP association with component phenotypes of dyslexia, specifically NWR and RWRE but not WATT. In addition, FOXP2 SNP associations with both RAPA and FS-D were observed. Our results confirm the role of CNTNAP2 in NWR in a dyslexia sample and motivate new questions about the effects of FOXP2 in neurodevelopmental disorders.
Keyword: Article
URL: https://doi.org/10.1007/s11689-010-9065-0
http://www.ncbi.nlm.nih.gov/pubmed/21484596
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163991
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9
Octave-shifted pitch matching in nonword imitations: The effects of lexical stress and speech sound disorder1
Peter, Beate; Larkin, Tara; Stoel-Gammon, Carol. - : Acoustical Society of America, 2009
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10
Central timing deficits in subtypes of primary speech disorders
In: Clinical linguistics & phonetics. - London : Informa Healthcare 22 (2008) 3, 171-198
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11
Timing errors in two children with suspected childhood apraxia of speech (sCAS) during speech and music-related tasks
In: Clinical linguistics & phonetics. - London : Informa Healthcare 19 (2005) 2, 67-88
OLC Linguistik
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12
Timing errors in two children with suspected childhood apraxia of speech (sCAS) during speech and music-related tasks
In: Clinical linguistics & phonetics. - London : Informa Healthcare 19 (2005) 2, 67-87
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