Results 11 to 20 of about 8,028 (167)

Integrity of cerebellar tracts associated with the risk of bipolar disorder

open access: yesTranslational Psychiatry, 2022
This study examined the structural brain differences across individuals of different BD stages and the risks of developing bipolar disorder (BD) associated with these brain differences.
Le Hou   +6 more
doaj   +1 more source

Neurodevelopmental Disorder

open access: yesПсихологічне консультування i психотерапія, 2020
An approach to define a neurodevelopment disorders, intellectual, neuromotor and autism spectrum disabilities, but also of that wide border area that falls within the current definition of Special Educational Needs (SEDs), through a comparison between ...
Dimitris Argiropoulos
doaj   +1 more source

Working memory functions in Autism Spectrum Disorder: A review [PDF]

open access: yesKlinik Psikoloji Dergisi, 2021
Autism spectrum disorder, one of the most common neurodevelopmental disorders, is a lifelong condition, especially with difficulties in social communication, limited interest, and repetitive behavior.
Elçin Çağlar, Hande Kaynak
doaj   +1 more source

The Influence of Self-Referential Processing on Attentional Orienting in Frontoparietal Networks

open access: yesFrontiers in Human Neuroscience, 2018
Self-referential processing refers to the processing of information relevant to oneself and plays an important role in cognition. Behavioral studies have shown that directional cue stimuli have a qualitatively different function during attentional ...
Shuo Zhao   +6 more
doaj   +1 more source

Structural Correlates of Reading the Mind in the Eyes in Autism Spectrum Disorder

open access: yesFrontiers in Human Neuroscience, 2017
Behavioral studies have shown that individuals with autism spectrum disorder (ASD) have impaired ability to read the mind in the eyes. Although this impairment is central to their social malfunctioning, its structural neural correlates remain unclear. To
Wataru Sato   +8 more
doaj   +1 more source

Neural Mechanisms Underlying Conscious and Unconscious Gaze-Triggered Attentional Orienting in Autism Spectrum Disorder

open access: yesFrontiers in Human Neuroscience, 2017
Impaired joint attention represents the core clinical feature of autism spectrum disorder (ASD). Behavioral studies have suggested that gaze-triggered attentional orienting is intact in response to supraliminally presented eyes but impaired in response ...
Wataru Sato   +5 more
doaj   +1 more source

Neurocognitive Mechanisms Underlying Social Atypicalities in Autism: Weak Amygdala’s Emotional Modulation Hypothesis

open access: yesFrontiers in Psychiatry, 2020
Autism spectrum disorder (ASD) is a neurodevelopmental condition associated with atypicalities in social interaction. Although psychological and neuroimaging studies have revealed divergent impairments in psychological processes (e.g., emotion and ...
Wataru Sato   +3 more
doaj   +1 more source

De novo variants in GATAD2A in individuals with a neurodevelopmental disorder: GATAD2A-related neurodevelopmental disorder

open access: yesHGG Advances, 2023
Summary: GATA zinc finger domain containing 2A (GATAD2A) is a subunit of the nucleosome remodeling and deacetylase (NuRD) complex. NuRD is known to regulate gene expression during neural development and other processes.
Elizabeth A. Werren   +18 more
doaj   +1 more source

Reduced Gray Matter Volume in the Social Brain Network in Adults with Autism Spectrum Disorder

open access: yesFrontiers in Human Neuroscience, 2017
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by behavioral impairment in social interactions. Although theoretical and empirical evidence suggests that impairment in the social brain network could be the neural ...
Wataru Sato   +8 more
doaj   +1 more source

Case Report: A de novo CTNNB1 Nonsense Mutation Associated With Neurodevelopmental Disorder, Retinal Detachment, Polydactyly

open access: yesFrontiers in Pediatrics, 2020
CTNNB1 gene mutation was firstly reported related to intellectual disability in 2012, to explore the clinical phenotype and genotype characteristics of CTNNB1 mutation, we collected and analyzed the clinical data of a child with a neurodevelopmental ...
Zhongling KE, Yanhui CHEN
doaj   +1 more source

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