Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients
Song, Danyu, Dai, Yi, Chen, Xiaoyu, Fu, Xiaona, Chang, Xingzhi, Wang, Ning, Zhang, Cheng, Yan, Chuanzhu, Zheng, Hong, Wu, Liwen, Jiang, Li, Hua, Ying, Yang, Haipo, Wang, Zhiqiang, Dai, Tingjun, Zhu, Wenhua, Han, Chunxi, Yuan, Yun, Kobayashi, Kazuhiro, Toda, Tatsushi, Xiong, Hui
Published in Clinical genetics (01.03.2021)
Published in Clinical genetics (01.03.2021)
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Journal Article
Integrated head and neck imaging of symptomatic patients with stroke using simultaneous non-contrast cardiovascular magnetic resonance angiography and intraplaque hemorrhage imaging as compared with digital subtraction angiography
Jia, Yuxi, Liu, Xiaoming, Zhang, Lan, Kong, Xiangchuang, Chen, Shuo, Zhang, Lei, Wang, Jiazheng, Shu, Shenglei, Liu, Jia, Fu, Xiaona, Liu, Dingxi, Wang, Jing, Shi, Heshui
Published in Journal of cardiovascular magnetic resonance (21.03.2022)
Published in Journal of cardiovascular magnetic resonance (21.03.2022)
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Journal Article
Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvement
Ge, Lin, Fu, Xiaona, Zhang, Wei, Wang, Dong, Wang, Zhaoxia, Yuan, Yun, Nonaka, Ikuya, Xiong, Hui
Published in Neuromuscular disorders : NMD (01.05.2019)
Published in Neuromuscular disorders : NMD (01.05.2019)
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Journal Article
Decreased GABA levels of the anterior and posterior cingulate cortex are associated with executive dysfunction in mild cognitive impairment
Fu, Xiaona, Qin, Mengting, Liu, Xiaoming, Cheng, Lan, Zhang, Lan, Zhang, Xinli, Lei, Yu, Zhou, Qidong, Sun, Peng, Lin, Liangjie, Su, Ying, Wang, Jing
Published in Frontiers in neuroscience (11.08.2023)
Published in Frontiers in neuroscience (11.08.2023)
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Journal Article
Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing
Fu, Xiaona, Yang, Haipo, Jiao, Hui, Wang, Shuo, Liu, Aijie, Li, Xiaoqing, Xiao, Jiangxi, Yang, Yanling, Wu, Xiru, Xiong, Hui
Published in Scientific reports (01.08.2017)
Published in Scientific reports (01.08.2017)
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Journal Article
Congenital muscular dystrophies in China
Ge, Lin, Zhang, Cheng, Wang, Zhaoxia, Chan, Sophelia H.S., Zhu, Wenhua, Han, Chunxi, Zhang, Xiaoli, Zheng, Hong, Wu, Liwen, Jin, Bo, Shan, Jingli, Mao, Bing, Zhong, Jianmin, Peng, Xiaoyin, Cheng, Yaying, Hu, Jun, Sun, Yan, Lu, Junlan, Hua, Ying, Zhu, Sainan, Wei, Cuijie, Wang, Shuo, Jiao, Hui, Yang, Haipo, Fu, Xiaona, Fan, Yanbin, Chang, Xingzhi, Wang, Shuang, Bao, Xinhua, Zhang, Yuehua, Wang, Jingmin, Wu, Ye, Jiang, Yuwu, Yuan, Yun, Rutkowski, Anne, Bönnemann, Carsten G., Wei, Wei, Wu, Xiru, Xiong, Hui
Published in Clinical genetics (01.09.2019)
Published in Clinical genetics (01.09.2019)
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Journal Article
A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients
Song, Danyu, Fu, Xiaona, Ge, Lin, Chang, Xingzhi, Wei, Cuijie, Liu, Jieyu, Yang, Haipo, Qu, Suqing, Bao, Xinhua, Toda, Tatsushi, Wu, Xiru, Xiong, Hui
Published in Clinical genetics (01.05.2020)
Published in Clinical genetics (01.05.2020)
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Journal Article
Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation
Yang, Haipo, Manya, Hiroshi, Kobayashi, Kazuhiro, Jiao, Hui, Fu, Xiaona, Xiao, Jiangxi, Li, Xiaoqing, Wang, Jingmin, Jiang, Yuwu, Toda, Tatsushi, Endo, Tamao, Wu, Xiru, Xiong, Hui
Published in Journal of human genetics (01.08.2016)
Published in Journal of human genetics (01.08.2016)
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Journal Article
FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies
Fu, Xiaona, Yang, Haipo, Wei, Cuijie, Jiao, Hui, Wang, Shuo, Yang, Yanling, Han, Chunxi, Wu, Xiru, Xiong, Hui
Published in Journal of human genetics (01.12.2016)
Published in Journal of human genetics (01.12.2016)
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Journal Article
A Compact Frequency Scanning Planar Array Using Characteristic Mode Analysis
Fu, Xiaona, Zhang, Zhan, Wang, Junhong
Published in IEEE antennas and wireless propagation letters (01.09.2021)
Published in IEEE antennas and wireless propagation letters (01.09.2021)
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Journal Article
Pattern-Reconfigurable Bidirectional Antenna Design Using the Characteristic Mode Analysis
Cao, Shengli, Zhang, Zhan, Fu, Xiaona, Wang, Junhong
Published in IEEE antennas and wireless propagation letters (01.01.2021)
Published in IEEE antennas and wireless propagation letters (01.01.2021)
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Journal Article
GABA in the anterior cingulate cortex mediates the association of white matter hyperintensities with executive function: a magnetic resonance spectroscopy study
Fu, Xiaona, Sun, Peng, Zhang, Xinli, Zhu, Dongyong, Qin, Qian, Lu, Jue, Wang, Jing
Published in Aging (Albany, NY.) (01.03.2024)
Published in Aging (Albany, NY.) (01.03.2024)
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Journal Article
Prenatal Diagnosis of Fukuyama Congenital Muscular Dystrophy by Optical Genomic Mapping in a Chinese Family
Zhou, Jia, Xiong, Hui, Yang, Jingmin, Fu, Xiaona, Sun, Luming
Published in Maternal-fetal medicine (Online) (01.07.2024)
Published in Maternal-fetal medicine (Online) (01.07.2024)
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Journal Article
HyperCKemia: An early sign of childhood-onset neutral lipid storage disease with myopathy
Fu, Xiaona, Yang, Xinying, Wang, Xiaofei, Jia, Bingbing, Ma, Wenna, Xiong, Hui, Fang, Fang, Ren, Xiaotun, Lv, Junlan
Published in Neuromuscular disorders : NMD (01.09.2023)
Published in Neuromuscular disorders : NMD (01.09.2023)
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Journal Article