Results 71 to 80 of about 126,210 (239)
No association between autistic traits and contextual influences on eye-movements during reading [PDF]
PeerJ, 2014 Individuals with autism spectrum disorders are claimed to show a local cognitive bias, termed “weak central coherence”, which manifests in a reduced influence of contextual information on linguistic processing.
Nathan Caruana, Jon Brock
doaj +2 more sources
Autism Children's App using PECS [PDF]
Annals of Emerging Technologies in Computing (AETiC) , 2018, 2018 Since autistic children suffers from learning disabilities and communication barriers, this research aim to design, develop and evaluate an Android based mobile application (app) providing better learning environment with inclusion of graphical representation in a cost effective manner.
arxiv
Core Challenges of Autism.Emotionality on spectrum [PDF]
Аутизм и нарушение развития, 2017 Bill Nason — an American clinical psychologist, «a humanistic behaviorist» as he calls himself — tells us about the emotional problems of people on the autistic spectrum. The chapter 13 of his Blue book «The Autism Discussion Page» is devoted to specific
Nason William
doaj +1 more source
A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Our study aimed to evaluate cognitive function in individuals with genetic skin disorders involving neuroectoderm (n = 8) compared to individuals with only ectoderm or mesoderm (n = 16) involvement. We hypothesized that neuroectodermal involvement would result in poorer neurocognitive performance.
Sneha A. Rangu +10 more
wiley +1 more source
Heliyon, 2023 Autism Spectrum Disorder (ASD) treatment requires accurate diagnosis and effective rehabilitation. Artificial intelligence (AI) techniques in medical diagnosis and rehabilitation can aid doctors in detecting a wide range of diseases more effectively ...
Abdulqader M. Almars +2 more
doaj
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT SATB2‐associated syndrome (SAS) is characterized by intellectual disability, neurodevelopmental disorders, cleft palate, and dental abnormalities. SAS is caused by variants in the special AT‐rich sequence‐binding protein 2 (SATB2), which encodes a transcription factor containing two CUT domains and a homeobox (HOX) domain.
Nao Ukita +5 more
wiley +1 more source
Eggly: Designing Mobile Augmented Reality Neurofeedback Training Games for Children with Autism Spectrum Disorder [PDF]
Proceedings of the ACM on Interactive, Mobile, Wearable and
Ubiquitous Technologies 2023Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder that affects how children communicate and relate to other people and the world around them. Emerging studies have shown that neurofeedback training (NFT) games are an effective and playful intervention to enhance social and attentional capabilities for autistic children.
arxiv +1 more source
Phenotypic Expansion of Knobloch Syndrome Type 2 in an Individual With a De Novo PAK2 Variant
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT P21‐activated kinase 2 (PAK2) is a serine/threonine kinase essential for a variety of cellular processes including signal transduction, cellular survival, proliferation, and migration. A recent report proposed monoallelic PAK2 variants cause Knobloch syndrome type 2 (KNO2)—a developmental disorder primarily characterized by ocular anomalies ...
Elizabeth A. Werren +10 more
wiley +1 more source
Using Applied Behavior Analysis in Software to help Tutor Individuals with Autism Spectrum Disorder [PDF]
arXiv, 2018 There are currently many tutoring software systems which have been designed for neurotypical children. These systems cover academic topics such as reading and math, and are made available through various technological mediums. The majority of these systems were not designed for use by children with special needs, in particular those who are diagnosed ...
arxiv
Natural History of NAA15‐Related Neurodevelopmental Disorder Through Adolescence
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The NatA N‐terminal acetyltransferase complex is composed of the NAA10 catalytic subunit and the auxiliary subunits NAA15 and HYPK. While those with variants in the enzymatic subunit develop Ogden Syndrome, individuals with variants in the NAA15 coding region develop NAA15‐related neurodevelopmental syndrome, which presents with a wide array ...
Rikhil Makwana +5 more
wiley +1 more source