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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 22, 2022
Oculopharyngodistal myopathy with CGG repeat expansions in GIPC1: the first report from southwestern ChinaRan An, Huijiao Chen, Weiyue Gu, et al.
Channels (Austin, Tex.)|July 15, 2016
Sequence CLCN1 and SCN4A in patients with Nondystrophic myotonias in Chinese populations: Genetic and pedigree analysis of 10 families and review of the literatureXinglong Yang, Hua Jia, Ran An, et al.
Frontiers in Neurology|June 26, 2023
Constipation in multiple system atrophy: a pilot study in Chinese patientsYalan Chen, Hongyan Huang, Peng Zhang, et al.
Multiple Sclerosis and Related Disorders|June 25, 2019
Association between suicide and multiple sclerosis: An updated meta-analysisQiuyan Shen, Haitao Lu, Dan Xie, et al.
Frontiers in Neurology|October 3, 2022
Abnormal decrement on high-frequency repetitive nerve stimulation in congenital myasthenic syndrome with GFPT1 mutations and review of literatureRan An, Huijiao Chen, Song Lei, et al.
Genetic Testing and Molecular Biomarkers|September 10, 2016
SNP rs1805874 of the Calbindin1 Gene Is Associated with Parkinson's Disease in Han ChineseXinglong Yang, Quanzhen Zhao, Ran An, et al.
NPJ Precision Oncology|August 13, 2025
PharmaFormer predicts clinical drug responses through transfer learning guided by patient derived organoidYuru Zhou, Quanhui Dai, Yanming Xu, et al.
Neuroimage. Clinical|November 30, 2025
Acute effects of a single session of multitarget continuous Theta-Burst stimulation for essential Tremor: A Randomized, Sham-Controlled trialAnling Luo, Hongyan Huang, Jiaming Feng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 4, 2002
[A new point mutation on exon 2 of parkin gene in Parkinson's disease]Yanming Xu, Zhuolin Liu, Yukai Wang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 23, 2015
Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literatureQuanZhen Zhao, Xinglong Yang, SiJia Tian, et al.
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