Inflammatory checkpoints in amyotrophic lateral sclerosis: From biomarkers to therapeutic targets

por Jiang, Zongzhi, Wang, Ziyi, Wei, Xiaojing, Yu, Xue-Fan
Publicado 2022

A case report: Becker muscular dystrophy presenting with epilepsy and dysgnosia induced by duplication mutation of Dystrophin gene

por Miao, Jing, Feng, Jia-chun, Zhu, Dan, Yu, Xue-fan
Publicado 2016

A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy

por Miao, Jing, Wei, Xiao-jing, Wang, Xu, Yin, Xiang, Yu, Xue-fan
Publicado 2020

Let-7a gene knockdown protects against cerebral ischemia/reperfusion injury

por Wang, Zhong-kun, Liu, Fang-fang, Wang, Yu, Jiang, Xin-mei, Yu, Xue-fan
Publicado 2016

Acute bilateral cerebral infarction in the presence of neuromyelitis optica spectrum disorder: A case report

por Wang, Zi-Yi, Wang, Meng, Guo, Jiao-Jiao, Gao, Yan-Lu, Yu, Xue-Fan
Publicado 2020

Neuronal intranuclear inclusion disease mimicking acute cerebellitis: A case report

por Guo, Jiao-Jiao, Wang, Zi-Yi, Wang, Meng, Jiang, Zong-Zhi, Yu, Xue-Fan
Publicado 2020

Myoclonic epilepsy with ragged-red fibers: A case report

por YU, XUE-FAN, MIAO, JING, LI, YAN, JIANG, XIN-MEI, MA, YU-GANG, MENG, HONG-MEI
Publicado 2015

A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family

por Miao, Jing, Su, Fei-fei, Liu, Xue-mei, Wei, Xiao-jing, Yuan, Yun, Yu, Xue-fan
Publicado 2018

A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401 + 1G > A) in CLCN1 gene of a Chinese Han patient

por Miao, Jing, Wei, Xiao-jing, Liu, Xue-mei, Kang, Zhi-xia, Gao, Yan-lu, Yu, Xue-fan
Publicado 2018

A novel homozygous exon2 deletion of TRIM32 gene in a Chinese patient with sarcotubular myopathy: A case report and literature review

por Wei, Xiao-Jing, Miao, Jing, Kang, Zhi-Xia, Gao, Yan-Lu, Wang, Zi-Yi, Yu, Xue-Fan
Publicado 2021

Next-Generation Sequencing Technologies and Neurogenetic Diseases

por Sun, Hui, Shen, Xiao-Rong, Fang, Zi-Bing, Jiang, Zong-Zhi, Wei, Xiao-Jing, Wang, Zi-Yi, Yu, Xue-Fan
Publicado 2021

Clinical-pathological features and muscle imaging findings in 36 Chinese patients with rimmed vacuolar myopathies: case series study and review of literature

por Wei, Xiao-jing, Sun, Hui, Miao, Jing, Qiu, Ru-qing, Jiang, Zong-zhi, Ma, Zhen-wei, Sun, Wei, Yu, Xue-fan
Publicado 2023