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	1.	Unusual brain images of a boy with adolescent cerebral X-linked adrenoleukodystrophy presenting with exhibitionism: A CARE-compliant case report. [electronic resource] by Zheng, Feixia Lin, Zhongdong Ye, Xiuyun Shi, Xulai Producer: 20180212 In: Medicine vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Management of Refractory Orofacial Dyskinesia Caused by Anti- [electronic resource] by Zheng, Feixia Ye, Xiuyun Shi, Xulai Poonit, Neha Devi Lin, Zhongdong Publication details: Frontiers in neurology 2018 In: Frontiers in neurology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing. [electronic resource] by Liu, Zhenwei Li, Zhongshan Zhi, Xiao Du, Yaoqiang Lin, Zhongdong Wu, Jinyu Producer: 20190523 In: Molecular neurobiology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Hyponatremia in Children With Bacterial Meningitis. [electronic resource] by Zheng, Feixia Ye, Xiuyun Shi, Xulai Lin, Zhongdong Yang, Zuqin Jiang, Longxiang Publication details: Frontiers in neurology 2019 In: Frontiers in neurology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	EpilepsyGene: a genetic resource for genes and mutations related to epilepsy. [electronic resource] by Ran, Xia Li, Jinchen Shao, Qianzhi Chen, Huiqian Lin, Zhongdong Sun, Zhong Sheng Wu, Jinyu Producer: 20150629 In: Nucleic acids research vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Different experiences of two PRRT2-associated self-limited familial infantile epilepsy. [electronic resource] by Zhao, Qianlei Liu, Zhenwei Hu, Ying Fang, Shiyu Zheng, Feixia Li, Xiucui Li, Feng Lin, Zhongdong Producer: 20210608 In: Acta neurologica Belgica vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration: A case report. [electronic resource] by Shi, Xulai Zheng, Feixia Ye, Xiuyun Li, Xiucui Zhao, Qianlei Lin, Zhongdong Hu, Ying Wang, Jiwen Producer: 20180423 In: Medicine vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies. [electronic resource] by Lin, Zhongdong Liu, Zhenwei Li, Xiucui Li, Feng Hu, Ying Chen, Bingyu Wang, Zhen Liu, Yong Producer: 20180828 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	None [electronic resource] by Wang, Qiongdan Liu, Zhenwei Lin, Zhongdong Zhang, Ru Lu, Yutian Su, Weijue Li, Feng Xu, Xi Tu, Mengyun Lou, Yongliang Zhao, Junzhao Zheng, Xiaoqun Publication details: Frontiers in genetics 2019 In: Frontiers in genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)