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  • 简要介绍:邬剑军, 男,复旦大学附属华山医院神经内科副主任医师,现任静安分院神经内科执行主任,中华医学会神经病学分会神经遗传学组委员,中国医师协会神经内科医师分会神经遗传专业委员会委员,中国老年学学会老年医学委员会老年神经病学专家委员会委员。1995年毕业于原上海医科大学,毕业后即在华山医院神经内科工作,期间攻读研究生,并获得博士学位。2009年至2010年至美国匹兹堡大学神经变性病研究所进行帕金森病发病机制的博士后研究工作。二十年来,一直从事运动障碍疾病的临床诊治,特别是帕金森病的诊断和治疗。近十年来主导运动障碍的脑深部电刺激治疗,明显改善病人生活质量。从医来发表论著20余篇,参与《实用内科学》、《神经病学》、《运动障碍疾病》等著作编写。参加或支持中美合作基金、国家科学基金、上海市自然科学基金、上海市卫计委和静安区基金。
  • 代表成果:


    1.Sun YM, Dong Y, Wang J, Lu JH, Chen Y, Wu JJ. A novel mutation of VAPB in one Chinese familial amyotrophic lateral sclerosis pedigree and its clinical characteristics. J Neurol. 2017; 264(12):2387-2393.

    2.Chen K, Yang YJ, Liu FT, Li DK, Bu LL, Yang K, Wang Y, Shen B, Guan RY, Song J, Wang J, Wu JJ. Evaluation of PDQ-8 and its relationship with PDQ-39 in China: a three-year longitudinal study. Health Qual Life Outcomes. 2017 Aug 24;15(1):170.

    3.Wang YX, Zhao J, Li DK, Peng F, Wang Y, Yang K, Liu ZY, Liu FT, Wu JJ, Wang J. Associations between cognitiveimpairment and motor dysfunction in Parkinson“s disease. Brain Behav. 2017;7(6):e00719.

    4.Wang Y, Wu JJ, Liu FT, Chen K, Chen C, Luo SS, Wang YX, Li DK, Guan RY, Yang YJ, An Y, Wang J, Sun YM. Olfaction in Parkin carriers in Chinese patients with Parkinson disease. Brain Behav. 2017;7(5):e00680.

    5.Peng F, Sun YM, Chen C, Luo SS, Li DK, Wang YX, Yang K, Liu FT, Zuo CT, Ding ZT, An Y, Wu JJ, Wang J, The heterozygous R1441C mutation of leucine-rich repeat kinase 2 gene in a Chinese patient with Parkinson disease: A five-year follow-up and literatures review, J Neurol Sci, 2017; 373: 23-26.

    6.Xiong WX, Sun YM, Guan RY, Luo SS, Chen C, An Y, Wang J, Wu JJ. The heterozygous A53T mutation in the alphasynuclein gene in a Chinese Han patient with Parkinson disease: case report and literature review. J Neurol. 2016;263(10):1984-1992.

    7.陈嬿,董漪,卢家红,刘丰韬,蒋雨平,邬剑军.中国华东地区家族性肌萎缩侧索硬化症患者SOD1基因突变检测及临床特点分析.中国临床神经科学. 2016, 24(2): 146-152.

    8.Liu SY, Wu JJ, Zhao J, Huang SF, Wang YX, Ge JJ, Wu P, Zuo CT, Ding ZT, Wang J. Onset-related subtypes of Parkinson“s disease differ in the patterns of striatal dopaminergic dysfunction: A positron emission tomography study. Parkinsonism Relat Disord. 2015, 21(12):1448-1453

    9.Liu FT, Chen Y, Yang YJ, Yang L, Yu M, Zhao J, Wu JJ, Huang F, Liu W, Ding ZT, Wang J. Involvement of mortalin/GRP75/mthsp70 in the mitochondrial impairments induced by A53T mutantα-synuclein. Brain Res. 2015, 1604: 52-61

    10.Dong Y, Wu JJ, Wu ZY. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12. Parkinsonism Relat Disord. 2015, 21(4):398-401