Results 121 to 130 of about 114,486 (309)
Breastfeeding and Neurodevelopment in infants exposed to alcohol during pregnancy [PDF]
Few previous studies have evaluated the differential benefits of breastfeeding on infantneurodevelopment depending on the level of prenatal alcohol exposure (PAE).
Schaffer, Kristen Elizabeth
core
Data from: Maternal thyroid dysfunction and neurodevelopment in children.
Data from: Maternal thyroid dysfunction and neurodevelopment in ...
Jun Zhang (48506) +6 more
core +1 more source
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George +11 more
wiley +1 more source
ERP correlates of word onset priming in infants and young children
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 +2 more
doaj +1 more source
Acetylcholinesterase Activity and Neurodevelopment in Boys and Girls [PDF]
BackgroundOrganophosphate exposures can affect children's neurodevelopment, possibly due to neurotoxicity induced by acetylcholinesterase (AChE) inhibition, and may affect boys more than girls.
Jacobs, David R +4 more
core +1 more source
Distribution of chronic undernutrition status and neurodevelopment outcomes.
Distribution of chronic undernutrition status and neurodevelopment outcomes.
Edson Serván-Mori (5474423) +10 more
core +1 more source
ABSTRACT Arrhythmias affect approximately half of patients with Costello syndrome (CS, OMIM # 218040), with non‐reentrant atrial tachycardia being the most common. This case describes an infant with Costello syndrome carrying the pathogenic HRAS c.34G>A (p.G12S) variant who developed early‐onset, drug‐refractory multifocal atrial tachycardia (MAT ...
Vanina Taliercio +11 more
wiley +1 more source
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young +6 more
wiley +1 more source
Developmental Coordination Disorder Investigation and Neurodevelopment Study Group
Materials for Developmental Coordination Disorder Investigation and Neurodevelopment Study Group reading groups @ CRNL and DDL. The DCD-INSIGHTS group is a common space to discuss papers, get feedback, share ideas, invite guest speakers within the ...
ALESSANDRO FARNE +2 more
core +1 more source
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 +3 more
core +1 more source

