Chromosome 22q13 terminal deletion size is associated with relevant clinical features in a sample of 63 Italian patients with Phelan-McDermid syndrome [0.03%]
染色体22q13末端缺失长度与63名意大利Phelan-McDermid综合征患者的临床特征相关性研究
Laura Sandoni,Fethia Chehbani,Lisa Asta et al.
Laura Sandoni et al.
Background: Phelan-McDermid syndrome (PMS) is caused in the majority of cases by the loss or mutation of one allele of the SHANK3 gene, located in human chr 22q13.33. PMS displays large interindividual differences in clin...
Comparative language performance in children and adolescents with 22q11.2ds syndrome and down syndrome [0.03%]
22q11.2DS综合征和唐氏综合症儿童及青少年的语言能力比较研究
Esther Moraleda-Sepúlveda,Miguel Lázaro-López-Villaseñor,Noelia Pulido-García et al.
Esther Moraleda-Sepúlveda et al.
Genetically defined neurodevelopmental syndromes provide a framework for examining constraints on language development. This study compared language performance in children and adolescents with 22q11.2 deletion syndrome (22q11.2DS; n = 40) ...
Associations among maternal prenatal depression, maternal autism traits, and child autism traits in the Environmental Influences on Child Health Outcome (ECHO) program [0.03%]
环境因素对儿童健康结果的影响计划(ECHO)项目中孕妇产前抑郁、母亲自闭症特征和儿童自闭症特征之间的关系
Chaela Nutor,Anne L Dunlop,Patricia A Brennan
Chaela Nutor
Background: Maternal depression during pregnancy has been associated with increased risk of offspring autism spectrum disorder (ASD) - a highly heritable neurodevelopmental disorder. However, no study to date has taken in...
The relationship between language and executive functions in adolescents with Down syndrome and fragile X syndrome [0.03%]
唐氏综合症和脆性X综合症青少年的语言与执行功能的关系
Audra Sterling,Marianne Elmquist,Amy Banasik et al.
Audra Sterling et al.
Background: Individuals with fragile X syndrome (FXS) and Down syndrome (DS) have significant and pervasive challenges in language (and more specifically grammar) and executive functions (EFs). While these aspects of deve...
Decreased attention in 10- and 14-month-olds with neurofibromatosis type 1 and association with later ADHD traits [0.03%]
神经纤维瘤病Ⅰ型患儿的注意力缺陷及与之后多动症关联的研究
Tessel Bazelmans,Francesca Penza,Jannath Begum-Ali et al.
Tessel Bazelmans et al.
Background: Identifying precursors to ADHD, which affects up to 5% of children, is crucial for early identification and support. To this end, we used a prospective sample to investigate endogenous attention and activity l...
Gaboxadol increases resting theta and alpha power without affecting evoked responses in fragile X syndrome in a home-based setting [0.03%]
Gaboxadol增加静息态theta和alpha波段功率而不影响脆弱X染色体综合征在家中的诱发反应
Lisa A De Stefano,Hyeonseok Kim,Craig A Erickson et al.
Lisa A De Stefano et al.
Background: Fragile X syndrome (FXS) lacks FDA-approved treatments despite various small molecules contributing to phenotypic rescue in the FMR1 knockout (KO) mouse model. Translation from the mouse model has been hampere...
Emotion regulation and self-inhibition's association with mental health outcomes, caregiver strain, and well-being in parents of autistic children: a dyadic analysis [0.03%]
情绪调节和自我抑制与自闭症儿童父母的心理健康结局、照料者压力及幸福感的关系：二元分析
Leonardo Dominguez Ortega,Alexandra Sturm,Meghan M Krushena et al.
Leonardo Dominguez Ortega et al.
Background: Parents of autistic children report more depression, anxiety, and caregiver strain, and poorer well-being than parents of non-autistic children. Though more research has begun to investigate how parent-specifi...
Neural oscillatory dynamics reveal altered top-down and integrative mechanisms during face processing in autistic children and unaffected siblings of autistic children [0.03%]
神经振荡动态机制揭示了自闭症儿童和非自闭症同胞在面部处理过程中的上下级和整合机制发生了改变
Theo Vanneau,Chloe Brittenham,Megan Darrell et al.
Theo Vanneau et al.
Face processing is fundamental to social communication and has been a major focus of autism research. While event-related potential (ERPs) studies of face processing have produced mixed results, little work has examined neuro-oscillatory dy...
Prevalence and age of diagnosis of neurodevelopmental conditions among Asian populations in Aotearoa New Zealand [0.03%]
新西兰亚裔人群神经发育障碍的患病率及诊断年龄分布状况研究
Noriko K Panther,Nicholas Bowden,Joanna Chu et al.
Noriko K Panther et al.
Driver or passenger? A new assessment of genes in the schizophrenia-associated 3q29 deletion locus for contribution to neurodevelopmental disorders [0.03%]
驾驶员还是乘客？对3q29缺失位点基因在精神分裂症相关神经发育障碍中作用的重新评估
Allyson R Herriges,Ryan H Purcell
Allyson R Herriges