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Frontiers in Human Neuroscience
|
August 22, 2024
The characteristics and reproducibility of motor speech functional neuroimaging in healthy controls
Katherine H Kenyon, Frederique Boonstra, Gustavo Noffs, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2022
Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments
Lottie D Morison, Ruth O Braden, David J Amor, et al.
Developmental Medicine and Child Neurology
|
June 27, 2020
Speech in children with cerebral palsy
Cristina Mei, Sheena Reilly, Molly Bickerton, et al.
Developmental Medicine and Child Neurology
|
February 23, 2026
Developmental stuttering with common and complex phenotypes
Sarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.
European Journal of Human Genetics : EJHG
|
December 18, 2022
Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature
Miya St John, Olivia van Reyk, David A Koolen, et al.
Archives of Disease in Childhood
|
November 25, 2018
Language in 2-year-old children born preterm and term: a cohort study
Katherine Sanchez, Alicia J Spittle, Jeanie Ly Cheong, et al.
Disability and Rehabilitation
|
September 1, 2024
Neural mechanisms driving speech and language recovery following childhood stroke: a scoping review
Christine C Muscat, Sarah A McCabe, Angela T Morgan, et al.
American Journal of Speech-Language Pathology
|
April 14, 2021
A Modeling-Guided Case Study of Disordered Speech in Minimally Verbal Children With Autism Spectrum Disorder
Karen V Chenausky, Amanda Brignell, Angela T Morgan, et al.
Developmental Medicine and Child Neurology
|
December 2, 2025
High prevalence of developmental coordination disorder risk in childhood apraxia of speech
Şermin Tükel, Emma K Baker, G Yazgi Tütüncü, et al.
European Journal of Medical Genetics
|
February 12, 2024
Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorder
Lottie D Morison, Olivia Van Reyk, Emma Baker, et al.
Page
of 15
Search research articles
Search
Showing results (81-90 of 148) with videos related to
Sort By:
Page
of 15
Frontiers in Human Neuroscience
|
August 22, 2024
The characteristics and reproducibility of motor speech functional neuroimaging in healthy controls
Katherine H Kenyon, Frederique Boonstra, Gustavo Noffs, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2022
Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments
Lottie D Morison, Ruth O Braden, David J Amor, et al.
Developmental Medicine and Child Neurology
|
June 27, 2020
Speech in children with cerebral palsy
Cristina Mei, Sheena Reilly, Molly Bickerton, et al.
Developmental Medicine and Child Neurology
|
February 23, 2026
Developmental stuttering with common and complex phenotypes
Sarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.
European Journal of Human Genetics : EJHG
|
December 18, 2022
Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature
Miya St John, Olivia van Reyk, David A Koolen, et al.
Archives of Disease in Childhood
|
November 25, 2018
Language in 2-year-old children born preterm and term: a cohort study
Katherine Sanchez, Alicia J Spittle, Jeanie Ly Cheong, et al.
Disability and Rehabilitation
|
September 1, 2024
Neural mechanisms driving speech and language recovery following childhood stroke: a scoping review
Christine C Muscat, Sarah A McCabe, Angela T Morgan, et al.
American Journal of Speech-Language Pathology
|
April 14, 2021
A Modeling-Guided Case Study of Disordered Speech in Minimally Verbal Children With Autism Spectrum Disorder
Karen V Chenausky, Amanda Brignell, Angela T Morgan, et al.
Developmental Medicine and Child Neurology
|
December 2, 2025
High prevalence of developmental coordination disorder risk in childhood apraxia of speech
Şermin Tükel, Emma K Baker, G Yazgi Tütüncü, et al.
European Journal of Medical Genetics
|
February 12, 2024
Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorder
Lottie D Morison, Olivia Van Reyk, Emma Baker, et al.
Page
of 15