Results 31 to 40 of about 128,968 (183)

Adolescent Neurodevelopment

open access: yesJournal of Adolescent Health, 2013
The purpose of this article is to outline notable alterations occurring in the adolescent brain, and to consider potential ramifications of these developmental transformations for public policy and programs involving adolescents.Developmental changes in the adolescent brain obtained from human imaging work are reviewed, along with results of basic ...
openaire   +2 more sources

Methamphetamine, Neurotransmitters and Neurodevelopment

open access: yesPhysiological Research, 2021
Methamphetamine (MA), as massively abused psychoactive stimulant, has been associated with many neurological diseases. It has various potent and neurotoxic properties. There are many mechanisms of action that contribute to its neurotoxic and degenerative effects, including excessive neurotransmitter (NEU) release, blockage of NEU uptake transporters ...
B, Čechová, R, Šlamberová
openaire   +2 more sources

VEGF189 binds NRP1 and is sufficient for VEGF/NRP1-dependent neuronal patterning in the developing brain [PDF]

open access: yes, 2015
© 2015. Published by The Company of Biologists Ltd. This research was funded by a Wellcome Trust PhD fellowship to M.T. [092839/Z/10/Z] and a BBSRC project grant to C.R. and L.E. [BB/J00930X/1].
Cariboni, Anna   +6 more
core   +2 more sources

Comparison of three bioinformatics tools in the detection of ASD candidate variants from whole exome sequencing data

open access: yesScientific Reports, 2023
Autism spectrum disorder (ASD) is a heterogenous multifactorial neurodevelopmental condition with a significant genetic susceptibility component. Thus, identifying genetic variations associated with ASD is a complex task.
Apurba Shil   +8 more
doaj   +1 more source

Neurodevelopment and Recovery From Wasting

open access: yesPediatrics, 2022
BACKGROUND AND OBJECTIVES Acute illness with malnutrition is a common indication for hospitalization among children in low- and middle-income countries. We investigated the association between wasting recovery trajectories and neurodevelopmental outcomes in young children 6 months after hospitalization for an acute ...
Harriet M. Babikako   +19 more
openaire   +4 more sources

Competition and boundary formation in heterogeneous media: Application to neuronal differentiation [PDF]

open access: yes, 2014
We analyze an inhomogeneous system of coupled reaction-diffusion equations representing the dynamics of gene expression during differentiation of nerve cells. The outcome of this developmental phase is the formation of distinct functional areas separated
Perthame, Benoit   +2 more
core   +6 more sources

Some Considerations about Pain in the Child that was Born Premature [PDF]

open access: yes, 2017
Every single child born before completing the 37 weeks of gestational age (GA) is considered by major organizations such as UNICEF [1] and OMS [2] as premature.
Gómez, María Celeste
core   +1 more source

Detection of a de novo heterozygous ANK2 variant in a child with autism spectrum disorder and epilepsy: a case report

open access: yesEgyptian Journal of Medical Human Genetics, 2023
Background The pathogenesis of autism spectrum disorder (ASD) is not fully clarified. Next-generation sequencing technologies have greatly enhanced the identification of new genes associated with ASD.
Catarina Granjo Morais   +5 more
doaj   +1 more source

A dataset of EEG recordings from 47 participants collected during a virtual reality working memory task where attention was cued by a social avatar and non-social stick cue

open access: yesData in Brief, 2022
This data article describes electroencephalography (EEG) and behavioral data from 47 participants. Data was collected using a 64 channel eego™ sports mobile EEG system during a visual working memory task presented in virtual reality (VR) using Unity with
Samantha E.A. Gregory   +2 more
doaj   +1 more source

Identification of long non-coding RNAs involved in neuronal development and intellectual disability [PDF]

open access: yes, 2016
Recently, exome sequencing led to the identification of causal mutations in 16–31% of patients with intellectual disability (ID), leaving the underlying cause for many patients unidentified. In this context, the noncoding part of the human genome remains
D'haene, Eva   +5 more
core   +1 more source

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