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Brain Research
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February 2, 2019
Impaired iPLA<sub>2</sub>β activity affects iron uptake and storage without iron accumulation: An in vitro study excluding decreased iPLA<sub>2</sub>β activity as the cause of iron deposition in PLAN
Yu-Pei Guo, Bei-Sha Tang, Hong-Li Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2005
Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration
Yu-hu Zhang, Bei-sha Tang, Ai-ling Zhao, et al.
Cerebellum (London, England)
|
July 2, 2013
Lithium chloride alleviates neurodegeneration partly by inhibiting activity of GSK3β in a SCA3 Drosophila model
Dan-Dan Jia, Li Zhang, Zhao Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 3, 2006
[Lecithin-cholesterol acyltransferase gene 608C/T polymorphism associated with atherosclerotic cerebral infarction]
Xiao-yan Zhu, Hong-wei Xu, Rong-yao Hou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 11, 2006
[Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L]
Ru-xu Zhang, Bei-sha Tang, Xiao-hong Zi, et al.
Neurology India
|
July 18, 2013
Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland China
Wen-Juan Guan, Xin-Jian Liu, Bei-Sha Tang, et al.
Frontiers in Neuroanatomy
|
November 23, 2017
Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients
Yan Tang, Xue Xiao, Hua Xie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2010
Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population
Qi-Ying Sun, Ji-Feng Guo, Lei Wang, et al.
Zhonghua Yi Xue Za Zhi
|
October 24, 2006
[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families]
Xing-Wang Song, Bei-sha Tang, Hong Jiang, et al.
Journal of Neurology
|
February 11, 2010
Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism
Ji-feng Guo, Xue-wei Zhang, Li-luo Nie, et al.
Page
of 24
Search research articles
Search
Showing results (81-90 of 236) with videos related to
Sort By:
Page
of 24
Brain Research
|
February 2, 2019
Impaired iPLA<sub>2</sub>β activity affects iron uptake and storage without iron accumulation: An in vitro study excluding decreased iPLA<sub>2</sub>β activity as the cause of iron deposition in PLAN
Yu-Pei Guo, Bei-Sha Tang, Hong-Li Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2005
Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration
Yu-hu Zhang, Bei-sha Tang, Ai-ling Zhao, et al.
Cerebellum (London, England)
|
July 2, 2013
Lithium chloride alleviates neurodegeneration partly by inhibiting activity of GSK3β in a SCA3 Drosophila model
Dan-Dan Jia, Li Zhang, Zhao Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 3, 2006
[Lecithin-cholesterol acyltransferase gene 608C/T polymorphism associated with atherosclerotic cerebral infarction]
Xiao-yan Zhu, Hong-wei Xu, Rong-yao Hou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 11, 2006
[Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L]
Ru-xu Zhang, Bei-sha Tang, Xiao-hong Zi, et al.
Neurology India
|
July 18, 2013
Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland China
Wen-Juan Guan, Xin-Jian Liu, Bei-Sha Tang, et al.
Frontiers in Neuroanatomy
|
November 23, 2017
Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients
Yan Tang, Xue Xiao, Hua Xie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2010
Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population
Qi-Ying Sun, Ji-Feng Guo, Lei Wang, et al.
Zhonghua Yi Xue Za Zhi
|
October 24, 2006
[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families]
Xing-Wang Song, Bei-sha Tang, Hong Jiang, et al.
Journal of Neurology
|
February 11, 2010
Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism
Ji-feng Guo, Xue-wei Zhang, Li-luo Nie, et al.
Page
of 24