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Chinese Medical Journal
|
July 26, 2006
Rapid genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography
Hai-yan Zhu, Ling-qian Wu, Qian Pan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
June 14, 2005
Research on screening and identification of proteins interacting with ataxin-3
Lu Shen, Jian-guang Tang, Bei-sha Tang, et al.
Neuroscience Letters
|
March 13, 2012
Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese population
Jin-yong Tian, Bei-sha Tang, Chang-he Shi, et al.
Neurobiology of Aging
|
January 7, 2015
Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China
Zhen-hua Liu, Ji-feng Guo, Ya-qin Wang, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition
|
April 20, 2011
[Metabolic pathways of OGCP and the influence of parkin protein on the metabolism of OGCP]
Chun-yu Wang, Li Cao, Bei-sha Tang, et al.
Parkinsonism & Related Disorders
|
June 5, 2012
Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants
Chaodong Wang, Yanning Cai, Zheng Zheng, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 8, 2010
Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism
Ji-feng Guo, Lei Wang, Dan He, et al.
Neuroscience Letters
|
September 19, 2012
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population
Yu-Tao Liu, Bei-Sha Tang, Jun-Ling Wang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
November 16, 2012
Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China
Qi-ying Sun, Ji-feng Guo, Wei-wei Han, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
February 15, 2011
Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese population
Lei Wang, Ji-feng Guo, Li-luo Nie, et al.
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of 24
Search research articles
Search
Showing results (111-120 of 236) with videos related to
Sort By:
Page
of 24
Chinese Medical Journal
|
July 26, 2006
Rapid genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography
Hai-yan Zhu, Ling-qian Wu, Qian Pan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
June 14, 2005
Research on screening and identification of proteins interacting with ataxin-3
Lu Shen, Jian-guang Tang, Bei-sha Tang, et al.
Neuroscience Letters
|
March 13, 2012
Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese population
Jin-yong Tian, Bei-sha Tang, Chang-he Shi, et al.
Neurobiology of Aging
|
January 7, 2015
Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China
Zhen-hua Liu, Ji-feng Guo, Ya-qin Wang, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition
|
April 20, 2011
[Metabolic pathways of OGCP and the influence of parkin protein on the metabolism of OGCP]
Chun-yu Wang, Li Cao, Bei-sha Tang, et al.
Parkinsonism & Related Disorders
|
June 5, 2012
Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants
Chaodong Wang, Yanning Cai, Zheng Zheng, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 8, 2010
Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism
Ji-feng Guo, Lei Wang, Dan He, et al.
Neuroscience Letters
|
September 19, 2012
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population
Yu-Tao Liu, Bei-Sha Tang, Jun-Ling Wang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
November 16, 2012
Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China
Qi-ying Sun, Ji-feng Guo, Wei-wei Han, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
February 15, 2011
Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese population
Lei Wang, Ji-feng Guo, Li-luo Nie, et al.
Page
of 24