Results 81 to 90 of about 98,574 (255)

ERP correlates of word onset priming in infants and young children

Developmental Cognitive Neuroscience, 2014
Using word onset priming with early learned words, we tracked access to phonological representations and predictive phonological processing at 6, 12, 18, and 24 months after birth.
Angelika B.C. Becker, Ulrike Schild, Claudia K. Friedrich   +2 more
doaj   +1 more source

Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos, Natasha Monte, Kaio Evandro Cardoso Aguiar, Rita de Cássia Calderaro, Aline Pasquini Santos, Juliana Carla Gomes Rodrigues, André Maurício Ribeiro‐Dos‐Santos, Sandro José De Souza, Ândrea Ribeiro‐Dos‐Santos, João Farias Guerreiro, Sidney Emanuel Batista Dos Santos, Ney Pereira Carneiro Dos Santos   +11 more
wiley   +1 more source

Smoking and alcohol drinking during pregnancy as the risk factors for poor child neurodevelopment – A review of epidemiological studies

, 2015
Maternal active and passive smoking and low or moderate alcohol drinking during pregnancy, taking into account the level of exposure and developmental or behavioral outcomes, are recognized as a significant issue from both a clinical and a public health ...
Joanna Jurewicz, Wojciech Hanke
core   +1 more source

Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert, Danielle M. Pascual, Laurie Anne Bailey, Loren D. M. Peña, Paul C. Marcogliese   +4 more
wiley   +1 more source

Identifying the mRNA Targets of the RNA-binding Protein TIA-1 in Human Neurodevelopment [PDF]

, 2020
TIA-1 is an RNA binding protein that is implicated in neurodevelopment. I conducted RIP-seq on lysates from three in vitro stages of neurodevelopment: human embryonic stem cells (hESCs), neural progenitor cells (NPCs), and cortical neurons, to identify ...
Byres, Loryn Patricia
core   +1 more source

Teachers in the Home: Strategies Children Use to Support School-readiness Skills in Their Younger Siblings in Kenya and Ethiopia

Gulf Education and Social Policy Review
When children transition from home to school settings and are ready to engage in school tasks, they are more likely to succeed, not only in school but also in their work and social life later on.
Patrick Njoroge, Henriette Zeidler, Laura Shapiro, Missaye Mulatie Mengstie, Jeofrey Mtemeri, Rebecca Clarke, Claire Farrow, Pamela Wadende   +7 more
doaj   +1 more source

Recurrent encephalopathy in milliary neurocysticercosis: An uncommon manifestation of a common infection

Journal of Infection and Public Health, 2018
Neurocysticercosis is a common parasitic infection in children in developing countries and neurological symptoms such as seizures are the most common manifestations. However, symptoms of encephalopathy are an unusual presentation in children.
Indar K. Sharawat, Hansashree Padmanabha, Renu Suthar, Sameer Vyas, Naveen Sankhyan   +4 more
doaj   +1 more source

Data and analytic code for Neighborhood conditions and neurodevelopment: A systematic review of brain structure in children and adolescents

This repository contains two key files. Lewis_Gresham et al._Neigh_Neurodevelopment_Review.csv contains reference information and extracted data from the 37 articles eligible for inclusion in the review.
Ip, Ka I, Riegelman, Amy, Lewis, Lydia, Gresham, Bria   +3 more
core   +1 more source

Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen, Li Gao, Xu Han, Yunyun Cao, Lanlan Zhang, Yi Wu, Xinrong Zhao, Wenjing Hu, Ruiyu Ma, Renyi Hua, Niu Li, Yanlin Wang, Jian Wang, Shuyuan Li   +13 more
wiley   +1 more source

The Effect of Music Therapy on Preterm Infants’ Neurodevelopment

, 2023
Preterm infants can suffer a decrease in neurodevelopment because of the lack of time they have in the womb to develop fully. A preterm infant is defined as any baby born before 37 weeks of gestation (World Health Organization, 2022).
Hynson, Kira, Bubb, Nicholas, Kemp, Phoebe   +2 more
core   +2 more sources