Browsing by Author Hong, Daojun

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Issue Date Title Author(s)
2019 Adult-onset SMALED2 due to a novel BICD2 mutation presenting with asymmetrical lower limb involvement Wan, Chenyi;Wang, Yuyao;Zhou, Qian;Yu, Yanyan;Hong, Daojun;Zhu, Min
2011 Asian patients with limb girdle muscular dystrophy 21 (LGMD21) Hong, Daojun;Zhang, Wei;Wang, Wei;Wang, Zhaoxia;Yuan, Yun
2010 Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene Hong, Daojun;Luan, Xinghua;Chen, Bin;Zheng, Riliang;Zhang, Wei;Wang, Zhaoxia;Yuan, Yun
2013 Chronic progressive external ophthalmoplegia coexistent with motor neuron disease in a patient with a novel large-scale mitochondrial DNA deletion Zhao, Danhua;Wang, Zhaoxia;Hong, Daojun;Zhang, Wei;Yuan, Yun
Jun-2020 Clinical and pathological features in adult-onset NIID patients with cortical enhancement Liang, Huiting;Wang, Bo;Li, Qing;Deng, Jianwen;Wang, Lulu;Wang, Huan;Li, Xiaobin;Zhu, Min;Cai, Yu;Wang, Zhaoxia;Yuan, Yun;Fang, Pu;Hong, Daojun
2019 Clinical findings and autophagic pathology in neutral lipid storage disease with myopathy Hong, Daojun;Zheng, Junjun;Xin, Ling;Xiang, Yining;Luan, Xinghua;Cao, Li;Cong, Lu;Fang, Pu;Zhang, Jun
2010 CLINICAL PHENOTYPE OF AUTOSOMAL DOMINANT PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA IN A FAMILY WITH A NOVEL MUTATION IN THE C10orf2 GENE Hong, Daojun;Bi, Hongyan;Yao, Sheng;Wang, Zhaoxia;Yuan, Yun
2019 Clonazepam improves the symptoms of two siblings with novel variants in the SYNJ1 gene Hong, Daojun;Cong, Lu;Zhong, Shanshan;He, Yang;Xin, Ling;Gao, Xuguang;Zhang, Jun
2012 Danon disease caused by two novel mutations of the LAMP2 gene: implications for two ends of the clinical spectrum Hong, Daojun;Shi, Zhihong;Zhang, Wei;Wang, Zhaoxia;Yuan, Yun
Jan-2020 Diagnostic indicators for adult-onset neuronal intranuclear inclusion disease Wang, Yan;Wang, Bo;Wang, Lu;Yao, Sheng;Zhao, Jing;Zhong, Shanshan;Cong, Lu;Liu, Ling;Zhang, Jiewen;Zhang, Jun;Hong, Daojun
4-Jun-2020 Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy Deng, Jianwen;Yu, Jiaxi;Li, Pidong;Luan, Xinghua;Cao, Li;Zhao, Juan;Yu, Meng;Zhang, Wei;Lv, He;Xie, Zhiying;Meng, LingChao;Zheng, Yiming;Zhao, Yawen;Gang, Qiang;Wang, Qingqing;Liu, Jing;Zhu, Min;Guo, Xueyu;Su, Yanan;Liang, Yu;Liang, Fan;Hayashi, Tomohiro;Maeda, Meiko Hashimoto;Sato, Tatsuro;Ura, Shigehisa;Oya, Yasushi;Ogasawara, Masashi;Iida, Aritoshi;Nishino, Ichizo;Zhou, Chang;Yan, Chuanzhu;Yuan, Yun;Hong, Daojun;Wang, Zhaoxia
Mar-2021 Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease Deng, Jianwen;Zhou, Binbin;Yu, Jiaxi;Han, Xiaochen;Fu, Jianhui;Li, Xiaobin;Xie, Xufang;Zhu, Min;Zheng, Yilei;Guo, Xueyu;Li, Pidong;Wang, Qingqing;Liu, Jing;Zhang, Wei;Yuan, Yun;Yao, Sheng;Wang, Zhaoxia;Hong, Daojun
Mar-2022 Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy Wu, Chengsi;Xiang, Haijie;Chen, Ran;Zheng, Yilei;Zhu, Min;Chen, Shuyun;Yu, Yanyan;Peng, Yun;Yu, Yaqing;Deng, Jianwen;Zhou, Meihong;Hong, Daojun
7-Jul-2021 GGC Repeat Expansion in the NOTCH2NLC Gene Is Associated With a Phenotype of Predominant Motor-Sensory and Autonomic Neuropathy Wang, Hui;Yu, Jiaxi;Yu, Meng;Deng, Jianwen;Zhang, Wei;Lv, He;Liu, Jing;Shi, Xin;Liang, Wei;Jia, Zhirong;Hong, Daojun;Meng, Lingchao;Wang, Zhaoxia;Yuan, Yun
Jun-2021 GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy Yu, Jiaxi;Luan, Xing-hua;Yu, Meng;Zhang, Wei;Lv, He;Cao, Li;Meng, Lingchao;Zhu, Min;Zhou, Binbin;Wu, Xiao-rong;Li, Pidong;Gang, Qiang;Liu, Jing;Shi, Xin;Liang, Wei;Jia, Zhirong;Yao, Sheng;Yuan, Yun;Deng, Jianwen;Hong, Daojun;Wang, Zhaoxia
2017 Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy Lu, Yuanyuan;Zhao, Danhua;Yao, Sheng;Wu, Shiwen;Hong, Daojun;Wang, Qingqing;Liu, Jing;Smeitink, Jan A. M.;Yuan, Yun;Wang, Zhaoxia
2015 Mutational spectrum and clinical features in 35 unrelated mainland Chinese patients with GNE myopathy Zhao, Juan;Wang, Zhaoxia;Hong, Daojun;Lv, He;Zhang, Wei;Chen, Juanjuan;Yuan, Yun
2011 Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes Zhao, Danhua;Hong, Daojun;Zhang, Wei;Yao, Sheng;Qi, Xiaokun;Lv, He;Zheng, Riliang;Feng, Liqun;Huang, Yining;Yuan, Yun;Wang, Zhaoxia
2010 Myocardial fibrosis in desmin-related hypertrophic cardiomyopathy He, Yi;Zhang, Zhaoqi;Hong, Daojun;Dai, Qinyi;Jiang, Tengyong
2019 Neutral lipid storage disease with myopathy in China: a large multicentric cohort study Zhang, Wei;Wen, Bing;Lu, Jun;Zhao, Yawen;Hong, Daojun;Zhao, Zhe;Zhang, Cheng;Luo, Yuebei;Qi, Xueliang;Zhang, Yingshuang;Song, Xueqin;Zhao, Yuying;Zhao, Chongbo;Hu, Jing;Yang, Huan;Wang, Zhaoxia;Yan, Chuanzhu;Yuan, Yun
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