QQ客服 官方微博 反馈留言

浏览/检索结果: 共7条，第1-7条 帮助 限定条件 专题：山东大学    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Communication interventions for autism spectrum disorder in minimally verbal children 期刊论文 COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2018, 卷号: 2018, 期号: 11 作者:  Brignell, Amanda;  Chenausky, Karen V.;  Song, Huan;  Zhu, Jianwei;  Suo, Chen 收藏  |  浏览/下载：1/0  |  提交时间：2019/12/11 Arcuate Fasciculus in Autism Spectrum Disorder Toddlers with Language Regression 期刊论文 OPEN MEDICINE, 2018, 卷号: 13, 期号: 1, 页码: 90-95 作者:  Zhang, Lin;  Li, Kailong;  Zhang, Chengqi;  Qi, Xianlong;  Zheng, Ning 收藏  |  浏览/下载：11/0  |  提交时间：2019/12/11 autism spectrum disorder  diffusion tensor imaging  language regression  language-related white matter tract  toddler   Improving Sparsity and Modularity of High-Order Functional Connectivity Networks for MCI and ASD Identification 期刊论文 FRONTIERS IN NEUROSCIENCE, 2018, 卷号: 12 作者:  Zhou, Yueying;  Zhang, Limei;  Teng, Shenghua;  Qiao, Lishan;  Shen, Dinggang 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11 high-order correlation  functional connectivity network  dynamic  network  modularity  mild cognitive impairment  autism spectrum disorder   Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis 期刊论文 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2018, 卷号: 177, 期号: 1, 页码: 93-100 作者:  Zhang, Yanqing;  Liu, Yi;  Zarrei, Mehdi;  Tong, Winnie;  Dong, Rui 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11 autism spectrum disorder (ASD)  IMMP2L  meta-analysis   Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder 期刊论文 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2015, 卷号: 168, 期号: 4, 页码: 258-264 作者:  Liu, Yi;  Zhang, Yanqing;  Zhao, Dongmei;  Dong, Rui;  Yang, Xiaomeng 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/17 metabotropic glutamate receptor 7 gene (GRM7)  autism spectrum disorders  (ASDs)  neuropsychiatric disorders   De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review 期刊论文 American journal of medical genetics, Part A, 2015, 卷号: 167, 期号: 6, 页码: 1381-1385 作者:  Liu, Yi;  Zhao, Dongmei;  Dong, Rui;  Yang, Xiaomeng;  Zhang, Yanqing 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/17 autism susceptibility candidate 2  neurodevelopmental disorders  autism spectrum disorder  developmental delay   Whole-genome sequencing of quartet families with autism spectrum disorder 期刊论文 NATURE MEDICINE, 2015, 卷号: 21, 期号: 2, 页码: 185-191 作者:  Yuen, Ryan K. C.;  Thiruvahindrapuram, Bhooma;  Merico, Daniele;  Walker, Susan;  Tammimies, Kristiina 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/17