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Search Results - Zhan, Feixia
Search Results - Zhan, Feixia
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Late-onset autoimmune polyendocrine syndrome type 1: a case report and literature review
by
Zhan, Feixia
,
Cao, Li
Published in
Immunologic research
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Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene
by
Wu, Jingying
,
Tian, Wotu
,
Zhan, Feixia
,
Luan, Xinghua
,
Cao, Li
Published in
Stem cell research
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Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome
by
Zhan, Feixia
,
Liu, Xiaoli
,
Ni, Ruilong
,
Liu, Taotao
,
Cao, Yuwen
,
Wu, Jingying
,
Tian, Wotu
,
Luan, Xinghua
,
Cao, Li
Published in
Metabolic brain disease
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Clinical heterogeneity in a family with flail arm syndrome and review of hnRNPA1‐related spectrum
by
Han, Xiaochen
,
Zhan, Feixia
,
Yao, Yuxin
,
Cao, Li
,
Liu, Jianguo
,
Yao, Sheng
Published in
Annals of clinical and translational neurology
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Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in HSPB1 Gene: A Case Series
by
Shen, Xiya
,
Zhang, Jiawei
,
Zhan, Feixia
,
Tian, Wotu
,
Jiang, Qingqing
,
Luan, Xinghua
,
Zhang, Xiaojie
,
Cao, Li
Published in
Biomolecules (Basel, Switzerland)
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Excessive Startle with Novel GLRA1 Mutations in 4 Chinese Patients and a Literature Review of GLRA1 -Related Hyperekplexia
by
Zhan, Feixia
,
Zhang, Chao
,
Wang, Shige
,
Zhu, Zeyu
,
Chen, Guang
,
Zhao, Mingliang
,
Cao, Li
Published in
Journal of clinical neurology (Seoul, Korea)
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Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia
by
Liu, Xiaoli
,
Ke, Huiyi
,
Qian, Xiaohang
,
Wang, Shige
,
Zhan, Feixia
,
Li, Ziyi
,
Tian, Wotu
,
Huang, Xiaojun
,
Zhang, Bin
,
Cao, Li
Published in
Journal of neurology
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The Phenotypic and Genotypic Spectrum of CSF1R‐Related Disorder in China
by
Wu, Jingying
,
Cheng, Xin
,
Ji, Duxin
,
Niu, Huiwen
,
Yao, Songquan
,
Lv, Xukun
,
Wang, Jianqiang
,
Li, Ziyi
,
Zheng, Haoran
,
Cao, Yuwen
,
Zhan, Feixia
,
Zhang, Mengyuan
,
Tian, Wotu
,
Huang, Xiaojun
,
Luan, Xinghua
,
Cao, Li
Published in
Movement disorders
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Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic Spectrum
by
Zhan, Feixia
,
Tian, Wotu
,
Cao, Yuwen
,
Wu, Jingying
,
Ni, Ruilong
,
Liu, Taotao
,
Yuan, Yun
,
Luan, Xinghua
,
Cao, Li
Published in
Journal of clinical neurology (Seoul, Korea)
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Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in IHSPB1/I Gene: A Case Series
by
Shen, Xiya
,
Zhang, Jiawei
,
Zhan, Feixia
,
Tian, Wotu
,
Jiang, Qingqing
,
Luan, Xinghua
,
Zhang, Xiaojie
,
Cao, Li
Published in
Biomolecules (Basel, Switzerland)
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Novel mutations in the SPAST gene cause hereditary spastic paraplegia
by
Zhu, Zeyu
,
Zhang, Chao
,
Zhao, Guohua
,
Liu, Qing
,
Zhong, Ping
,
Zhang, Mei
,
Tang, Weiguo
,
Zhan, Feixia
,
Tian, Wotu
,
Wang, Yan
,
Yin, Kaili
,
Huang, Xiaojun
,
Jiang, Jingwen
,
Liu, Xiaoli
,
Liu, Shihua
,
Zhou, Haiyan
,
Luan, Xinghua
,
Tang, Huidong
,
Wang, Ying
,
Chen, Shengdi
,
Cao, Li
Published in
Parkinsonism & related disorders
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