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	1.	[Efficacy and safety of cyclophosphamide as a sequential immunotherapy drug for anti-N-methyl-D-aspartate receptor encephalitis in children]. [electronic resource] by Zhu, Wei-Wen Liao, Wei-Ping Yi, Yong-Hong Song, Xing-Wang Producer: 20170831 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	2.	Comparison of serum apolipoprotein A-I between Chinese multiple sclerosis and other related autoimmune disease. [electronic resource] by Zhang, Bin Pu, ShuXiang Li, BinMei Ying, JianRui Song, Xing Wang Gao, Cong Producer: 20100820 In: Lipids in health and disease vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders. [electronic resource] by Zhang, Chao Zhan, Fei-Xia Tian, Wo-Tu Xu, Yang-Qi Zhu, Ze-Yu Wang, Yan Song, Xing-Wang Cao, Li Producer: 20200505 In: Clinical neurology and neurosurgery vol. 177 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China]. [electronic resource] by Song, Xing-wang Tang, Bei-sha Jiang, Hong Shen, Lu Yang, Qian Liao, Shu-sheng Li, Qing-hua Tang, Jian-guang Producer: 20070329 In: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	5.	[Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome]. [electronic resource] by Song, Xing-wang Wang, Yu-liang Shi, Yi-wu Deng, Wei-yi Chen, Sheng-qiang Lin, Han Yi, Yong-hong Liao, Wei-ping Producer: 20100427 In: Zhonghua yi xue za zhi vol. 89 Availability: No items available. Save to lists Add to cart (remove)
	6.	[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families]. [electronic resource] by Song, Xing-Wang Tang, Bei-sha Jiang, Hong Shen, Lu Yang, Qian Liao, Shu-sheng Li, Qing-hua Liang, Xiao-chun Tang, Jian-guang Producer: 20070717 In: Zhonghua yi xue za zhi vol. 86 Availability: No items available. Save to lists Add to cart (remove)
	7.	A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis. [electronic resource] by Wang, Yu-Liang Zeng, Zhi-Yong Song, Xing-Wang Hao, Zhuo-Fang Shi, Yi-Wu Tang, Bin Chen, Sheng-Qiang Gao, Mei-Mei Di, Wei Long, Yue-Sheng Yi, Yong-Hong Liao, Wei-Ping Producer: 20110506 In: Neurogenetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings. [electronic resource] by Wang, Jun-Ling Xiao, Bin Cui, Xiang-Xiang Guo, Ji-Feng Lei, Li-Fang Song, Xing-Wang Shen, Lu Jiang, Hong Yan, Xin-Xiang Pan, Qian Long, Zhi-Gao Xia, Kun Tang, Bei-Sha Producer: 20100111 In: Movement disorders : official journal of the Movement Disorder Society vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)