Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bronwyn Carrigg"'
Publikováno v:
Journal of Speech, Language, and Hearing Research. 64:4599-4613
Purpose: This study aimed to provide detailed descriptive information about the speech of a heterogeneous cohort of children with autism spectrum disorder (ASD) and to explore whether subgroups exist based on this detailed speech data. High rates of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d49b613e1212d2145aaf7ee28710c1c8
https://doi.org/10.1044/2021_jslhr-20-00651
https://doi.org/10.1044/2021_jslhr-20-00651
Publikováno v:
Journal of Autism and Developmental Disorders.
Subgroups of children with different speech profiles have been described however, little is known about the trajectories of speech development or stability of subgroups over time. This longitudinal study described both speech trajectories and subgrou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c13650e98871bf9c21f41e9ea4221c60
https://doi.org/10.1007/s10803-022-05561-8
https://doi.org/10.1007/s10803-022-05561-8
Autor:
Angela T Morgan, Alison Holm, David J. Amor, Amanda Brignell, Daisy A. Sheppard, Conway Gu, Bronwyn Carrigg
Publikováno v:
Eur J Hum Genet
Communication difficulties are a core feature of Phelan-McDermid syndrome (PMS). However, a specific speech and language phenotype has not been delineated, preventing prognostic counselling and development of targeted therapies. We examined speech, l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c8f33294e9501b8e148c14525120b27
https://acuresearchbank.acu.edu.au/item/8w9vw/speech-and-language-phenotype-in-phelan-mcdermid-22q13-3-syndrome
https://acuresearchbank.acu.edu.au/item/8w9vw/speech-and-language-phenotype-in-phelan-mcdermid-22q13-3-syndrome
Autor:
Bronwyn Carrigg, Angela T Morgan, Amanda Brignell, Daisy A. Sheppard, Conway Gu, David J. Amor, Alison Holm
Publikováno v:
Eur J Hum Genet
Communication difficulties are a core feature of Phelan-McDermid syndrome (PMS). However, a specific speech and language phenotype has not been delineated, preventing prognostic counselling and development of targeted therapies. We examined speech, l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e01e36cd829d5d777bd04612058ac1
https://doi.org/10.1038/s41431-021-00855-4
https://doi.org/10.1038/s41431-021-00855-4
Publikováno v:
Archives of Clinical Neuropsychology
Objective This study describes the phenotype in a large family with a strong, multigenerational history of severe speech sound disorder (SSD) persisting into adolescence and adulthood in approximately half the cases. Aims were to determine whether a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9783dd81bdfd50f5101661d4cc8cfc05
https://doi.org/10.1093/arclin/acw077
https://doi.org/10.1093/arclin/acw077
Publikováno v:
Perspectives on School-Based Issues. 16:37-49
Persistent Speech Disorder (PSD) is present when a speech impairment extends beyond 8–9 years of age. Persistent Speech Disorder can extend into adolescence and adulthood. While PSD can include individuals with residual speech errors, such as disto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433733f458c5a0b0fdee36f82bad9d63
https://doi.org/10.1044/sbi16.2.37
https://doi.org/10.1044/sbi16.2.37