Cargando…

Using the Model, Lead, and Test Technique and “GoTalk NOW” App to Teach Children With Intellectual and Developmental Delays to Correctly Request

Augmentative and alternative communication systems have been successfully used to help pupils with intellectual and developmental disabilities for functional communication skills. Whereas the effects of the GoTalk NOW application (app) available on the iPad have been investigated, no such study has...

Descripción completa

Detalles Bibliográficos
Autor principal:	Almalki, Nabil Sharaf
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Psychology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865384/ https://www.ncbi.nlm.nih.gov/pubmed/35222163 http://dx.doi.org/10.3389/fpsyg.2021.811510

Ejemplares similares

Editorial: Developmental delay and intellectual disability
por: Banerjee, Santasree, et al.
Publicado: (2022)

Genomic diagnosis for children with intellectual disability and/or developmental delay
por: Bowling, Kevin M., et al.
Publicado: (2017)

SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures
por: Khan, Amjad, et al.
Publicado: (2022)

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions
por: Fan, Yanjie, et al.
Publicado: (2018)

Evaluation of Individuals with Non-Syndromic Global Developmental Delay and Intellectual Disability
por: AlMutiri, Rowim, et al.
Publicado: (2023)

Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures
por: Van De Vondel, Liedewei, et al.
Publicado: (2022)

Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures
por: Beijer, Danique, et al.
Publicado: (2022)

Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability
por: Belligni, Elga F, et al.
Publicado: (2009)

Genetic testing in patients with global developmental delay / intellectual disabilities. A review
por: MICLEA, DIANA, et al.
Publicado: (2015)

Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability
por: Lee, Jin Sook, et al.
Publicado: (2018)

Deletion at 12q12 increases the risk of developmental delay and intellectual disability
por: Weng, Ying, et al.
Publicado: (2018)

Targeted Next-Generation Sequencing of Korean Patients With Developmental Delay and/or Intellectual Disability
por: Han, Ji Yoon, et al.
Publicado: (2018)

Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability
por: Han, Ji Yoon, et al.
Publicado: (2019)

YWHAZ variation causes intellectual disability and global developmental delay with brain malformation
por: Wan, Rui-Ping, et al.
Publicado: (2022)

What Do We Talk About Now When We Talk About Segmentectomy for GGO?
por: Li, Hanyue, et al.
Publicado: (2022)

What’s going on with Covid-19 right now?
por: Planas-Pascual, Bernat, et al.
Publicado: (2023)

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems
por: Chénier, Sébastien, et al.
Publicado: (2014)

The Prevalence of Chromosomal Deletions Relating to Developmental Delay and/or Intellectual Disability in Human Euploid Blastocysts
por: He, Wenyin, et al.
Publicado: (2014)

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability
por: Bartnik, Magdalena, et al.
Publicado: (2013)

Genetic Analysis of Children With Unexplained Developmental Delay and/or Intellectual Disability by Whole-Exome Sequencing
por: Xiang, Jingjing, et al.
Publicado: (2021)

Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability
por: Türkyılmaz, A, et al.
Publicado: (2022)

Now That Your Products Can Talk, What Will They Tell You?
por: Gandhi, Suketu
Publicado: (2016)

Develop Microsoft HoloLens apps now
por: Taylor, Allen G
Publicado: (2016)

Implication of the APP Gene in Intellectual Abilities
por: Myrum, Craig, et al.
Publicado: (2017)

Intellectual and Developmental Disabilities: Eugenics
por: Grenon, Ingrid, et al.
Publicado: (2014)

Intellectual disabilitiy in developmental age
por: Giuffrè, Mario, et al.
Publicado: (2015)

EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay
por: Umair, Muhammad, et al.
Publicado: (2020)

COVID-19 – Where should we go now?
por: Allen, Claire, et al.
Publicado: (2020)

Low Rates of Genetic Testing in Children With Developmental Delays, Intellectual Disability, and Autism Spectrum Disorders
por: Peabody, John, et al.
Publicado: (2015)

De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism
por: Tanaka, Akemi J., et al.
Publicado: (2017)

Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children
por: Chen, Baiyu, et al.
Publicado: (2021)

Developmental Delays in Socio-Emotional Brain Functions in Persons with an Intellectual Disability: Impact on Treatment and Support
por: Sappok, Tanja, et al.
Publicado: (2022)

Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability
por: Miclea, Diana, et al.
Publicado: (2022)

“What ELSE about this job?” Teaching Job Decision-Making to College Students With Intellectual and Developmental Disabilities
por: Torres, Ayse, et al.
Publicado: (2021)

Pattern Learning for Detecting Defect Reports and Improvement Requests in App Reviews
por: Mangnoesing, Gino V. H., et al.
Publicado: (2020)

“Can you hear me now?”: a qualitative exploration of communication quality in virtual primary care encounters for patients with intellectual and developmental disabilities
por: Selick, Avra, et al.
Publicado: (2023)

Prospective survey of serial Troponin T requesting in an acute teaching hospital
por: Loughrey, Brona V, et al.
Publicado: (2007)

Phenotypic Analysis of Korean Patients with Abnormal Chromosomal Microarray in Patients with Unexplained Developmental Delay/Intellectual Disability
por: Kim, Hyo Jeong, et al.
Publicado: (2018)

A Review of the Genomic Analysis of Children Presenting with Developmental Delay/Intellectual Disability and Associated Dysmorphic Features
por: Vickers, Ramiah R, et al.
Publicado: (2019)

Diagnosis of intellectual disability/global developmental delay via genetic analysis in a central region of China
por: Liao, Li-Hong, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_v75kae1me64l6sio65usgkvudc