日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Aberrant brain structural-functional coupling and structural/functional network topology explain developmental delays in pediatric Prader-Willi syndrome

异常的脑结构-功能耦合和结构/功能网络拓扑结构可以解释儿童普拉德-威利综合征的发育迟缓。

Huang, Zhongxin; Zheng, Helin; Wang, Longlun; Ding, Shuang; Li, Rong; Qing, Yong; Peng, Song; Zhu, Min; Cai, Jinhua

Alterations in the white matter fiber tracts of preschool-aged children with autism spectrum disorder: an automated fiber quantification study

自闭症谱系障碍学龄前儿童白质纤维束的改变:一项自动化纤维定量研究

Wang, Longlun; Ding, Shuang; Qin, Weixuan; Zhang, Yun; Qin, Bin; Huang, Kaiping; Zheng, Helin; Cai, Jinhua

Preoperative prediction of sonic hedgehog and group 4 molecular subtypes of pediatric medulloblastoma based on radiomics of multiparametric MRI combined with clinical parameters

基于多参数磁共振成像放射组学结合临床参数对儿童髓母细胞瘤的Sonic Hedgehog和4组分子亚型进行术前预测

Wang, Yuanlin; Wang, Longlun; Qin, Bin; Hu, Xihong; Xiao, Wenjiao; Tong, Zanyong; Li, Shuang; Jing, Yang; Li, Lusheng; Zhang, Yuting

Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL1 m.3243A>G point mutation: Neuroradiological features and their implications for underlying pathogenesis

伴有乳酸性酸中毒和卒中样发作的线粒体脑肌病,伴有MT-TL1 m.3243A>G点突变:神经放射学特征及其对潜在发病机制的意义

Zheng, Helin; Zhang, Xuemei; Tian, Lu; Liu, Bo; He, Xiaoya; Wang, Longlun; Ding, Shuang; Guo, Yi; Cai, Jinhua

Functional Brain Networks in Preschool Children With Autism Spectrum Disorders

自闭症谱系障碍学龄前儿童的功能性脑网络

Qin, Bin; Wang, Longlun; Cai, Jinhua; Li, Tingyu; Zhang, Yun

Sex differences of language abilities of preschool children with autism spectrum disorder and their anatomical correlation with Broca and Wernicke areas

自闭症谱系障碍学龄前儿童语言能力的性别差异及其与布罗卡区和韦尼克区的解剖学相关性

Zhang, Yun; Qin, Bin; Wang, Longlun; Chen, Jie; Cai, Jinhua; Li, Tingyu

Convolutional neural network-based artificial intelligence for the diagnosis of early esophageal cancer based on endoscopic images: A meta-analysis

基于卷积神经网络的人工智能在内镜图像早期食管癌诊断中的应用:一项荟萃分析

Ma, Hongbiao; Wang, Longlun; Chen, Yinlin; Tian, Lu

Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population

南方汉族人群猝死综合征中DSP基因罕见变异的鉴定

Zhao, Qianhao; Chen, Yili; Peng, Longlun; Gao, Rui; Liu, Nian; Jiang, Pingping; Liu, Chao; Tang, Shuangbo; Quan, Li; Makielski, Jonathan C; Cheng, Jianding

In Vivo magnetic resonance imaging of xenografted tumors using FTH1 reporter gene expression controlled by a tet-on switch

利用四环素开关控制的FTH1报告基因表达,对异种移植肿瘤进行体内磁共振成像

He, Xiaoya; Cai, Jinhua; Li, Hao; Liu, Bo; Qin, Yong; Zhong, Yi; Wang, Longlun; Liao, Yifan