Machine Learning-Based Evaluation on Craniodentofacial Morphological Harmony of Patients After Orthodontic Treatment

por Wang, Xin, Zhao, Xiaoke, Song, Guangying, Niu, Jianwei, Xu, Tianmin
Publicado 2022

Virtual Reality-Based Sensory Stimulation for Pediatric Disorders of Consciousness: A Pilot Study

por Liang, Piao, Xu, Hong, Li, Sinan, Ren, Lei, Zhao, Xiaoke
Publicado 2022

Lentiviral-mediated ephrin B2 gene modification of rat bone marrow mesenchymal stem cells

por Zhu, Min, Hua, Yu, Tang, Jian, Zhao, Xiaoke, Zhang, Ling, Zhang, Yue
Publicado 2019

New Approach to Intelligence Screening for Children With Global Development Delay Using Eye-Tracking Technology: A Pilot Study

por Xu, Hong, Xuan, Xiaoyan, Zhang, Li, Zhang, Wenxin, Zhu, Min, Zhao, Xiaoke
Publicado 2021

Number comparison under the Ebbinghaus illusion

por Liu, Wei, Wang, Chunhui, Zhao, Xiaoke, Deng, Shixin, Zhao, Yajun, Zhang, Zhijun
Publicado 2022

Neonatal repetitive pain in rats leads to impaired spatial learning and dysregulated hypothalamic-pituitary-adrenal axis function in later life

por Chen, Mengying, Xia, Dongqing, Min, Cuiting, Zhao, Xiaoke, Chen, Yinhua, Liu, Li, Li, Xiaonan
Publicado 2016

Case report: Novel compound heterozygous missense mutations in the DDHD2 gene in a Chinese patient associated with spastic paraplegia type 54

por Xu, Xin, Lu, Fen, Du, Senjie, Zhao, Xiaoke, Li, Hongying, Zhang, Li, Tang, Jian
Publicado 2022

Case report: Expansion of phenotypic and genotypic data in TENM3-related syndrome: Report of two cases

por Lu, Fen, Xu, Xin, Zheng, Bixia, Wang, Chunli, Zhou, Wei, Tang, Jian, Zhao, Xiaoke
Publicado 2023

Novel variants in the CLCN4 gene associated with syndromic X-linked intellectual disability

por Li, Sinan, Zhang, Wenxin, Liang, Piao, Zhu, Min, Zheng, Bixia, Zhou, Wei, Wang, Chunli, Zhao, Xiaoke
Publicado 2023

Changes of Structural Brain Network Following Repetitive Transcranial Magnetic Stimulation in Children With Bilateral Spastic Cerebral Palsy: A Diffusion Tensor Imaging Study

por Zhang, Wenxin, Zhang, Shang, Zhu, Min, Tang, Jian, Zhao, Xiaoke, Wang, Ying, Liu, Yuting, Zhang, Ling, Xu, Hong
Publicado 2021

A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report

por Fu, Dalin, Lin, Weisheng, Lu, Fen, Du, Senjie, Zhu, Min, Zhao, Xiaoke, Tang, Jian, Chen, Chuan, Chui, Xiaoli, Tang, Shanmei, Wang, Kai, Yang, Chuanchun, Han, Bei
Publicado 2021

Diagnostic yield and novel candidate genes for neurodevelopmental disorders by exome sequencing in an unselected cohort with microcephaly

por Wang, Chunli, Zhou, Wei, Zhang, Luyan, Fu, Luhan, Shi, Wei, Qing, Yan, Lu, Fen, Tang, Jian, Gao, Xiucheng, Zhang, Aihua, Jia, Zhanjun, Zhang, Yue, Zhao, Xiaoke, Zheng, Bixia
Publicado 2023