Fragile X syndrome: a pilot proton magnetic resonance spectroscopy study in premutation carriers [0.03%]
脆性X综合征前突变携带者的波谱研究
Brian P Hallahan,Eileen M Daly,Andrew Simmons et al.
Brian P Hallahan et al.
Purpose: There is increasing evidence that neurodevelopmental differences in people with Fragile X syndrome (FraX) may be explained by differences in glutamatergic metabolism. Premutation carriers of FraX were originally ...
Adolescents with prenatal cocaine exposure show subtle alterations in striatal surface morphology and frontal cortical volumes [0.03%]
产前接触可卡因青少年的纹状体表面形态和额叶皮层体积微妙变化
Florence Roussotte,Lindsay Soderberg,Tamara Warner et al.
Florence Roussotte et al.
Background: Published structural neuroimaging studies of prenatal cocaine exposure (PCE) in humans have yielded somewhat inconsistent results, with several studies reporting no significant differences in brain structure b...
Of mice and monkeys: using non-human primate models to bridge mouse- and human-based investigations of autism spectrum disorders [0.03%]
从鼠到猴自闭症谱系障碍的啮齿类与非人灵长类模型研究异同及其互补关系
Karli K Watson,Michael L Platt
Karli K Watson
The autism spectrum disorders (ASDs) arise from a diverse array of genetic and environmental origins that disrupt the typical developmental trajectory of neural connectivity and synaptogenesis. ASDs are marked by dysfunctional social behavi...
Gabriel Dichter,Ralph Adolphs
Gabriel Dichter
This thematic series presents theoretical and empirical papers focused on understanding autism from the perspective of reward processing deficits. Although the core symptoms of autism have not traditionally been conceptualized with respect ...
Hyperactivity, impulsivity, and inattention in boys with cleft lip and palate: relationship to ventromedial prefrontal cortex morphology [0.03%]
腭裂男童的多动、冲动和注意力不集中：与腹内侧前额叶皮层形态的关系
Peggy Nopoulos,Aaron D Boes,Althea Jabines et al.
Peggy Nopoulos et al.
The purpose of this study is to evaluate quantitative structural measures of the ventromedial prefrontal cortex (vmPFC) in boys with isolated clefts of the lip and/or palate (ICLP) relative to a comparison group and to associate measures of...
TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes [0.03%]
TPH2多态性和不同遗传亚型普拉德-威利综合征患者中的表达水平
Rebecca S Henkhaus,Douglas C Bittel,Merlin G Butler
Rebecca S Henkhaus
Prader-Willi syndrome (PWS) is a genetic imprinting disease that causes developmental and behavioral disturbances resulting from loss of expression of genes from the paternal chromosome 15q11-q13 region. In about 70% of subjects, this porti...
Using animal models of enriched environments to inform research on sensory integration intervention for the rehabilitation of neurodevelopmental disorders [0.03%]
利用感觉整合干预的丰富环境动物模型研究修复神经发育障碍
Stacey Reynolds,Shelly J Lane,Lorie Richards
Stacey Reynolds
The field of behavioral neuroscience has been successful in using an animal model of enriched environments for over five decades to measure the rehabilitative and preventative effects of sensory, cognitive and motor stimulation in animal mo...
Cover essay [0.03%]
封面论文
J Piven
J Piven
Erratum to: Cover essay [0.03%]
正文中表缺失的更正
Joseph Piven
Joseph Piven
Published Erratum
Journal of neurodevelopmental disorders. 2010 Jun;2(2):117. DOI:10.1007/s11689-010-9050-7 2010
White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents [0.03%]
染色体22q11缺失综合征的脑白质微结构研究：儿童及青少年中弥散张量成像和体素形态学测量技术的初步研究
Frederick Sundram,Linda E Campbell,Rayna Azuma et al.
Frederick Sundram et al.
Young people with 22q11 Deletion Syndrome (22q11DS) are at substantial risk for developing psychosis and have significant differences in white matter (WM) volume. However, there are few in vivo studies of both WM microstructural integrity (...