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          2023-09-05 09:56
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          姓名:張煒   性別:男 政治面貌:中共黨員  

          學歷:研究生   學位:博士   職稱:副主任醫(yī)師

          博、碩導師:碩導 本崗位工作年數(shù):

          研究方向:運動神經元病,周圍神經病,神經-肌肉接頭疾病,肌肉病,神經遺傳病

          榮譽稱號:無

          學術任職:中華醫(yī)學會神經病學分會神經遺傳學組委員;山西省醫(yī)學會神經病學分會常委

          近五年承擔科研課題情況:

          山西省基礎研究計劃(自由探索類基礎研究) 項目名稱:視神經萎縮伴共濟失調家系中致病基因功能驗證與藥物篩選,項目編號:20210302123245

          代表性論著及近五年的代表性論文(限10項以內):

          1. Zhang W, Ma J, Shi J, Huang S, Zhao R, Pang X, Wang J, Guo J, Chang X: GGC repeat expansions in NOTCH2NLC causing a phenotype of lower motor neuron syndrome. J Neurol 2022, 269(8):4469-4477.

          2. Shi J, Qin X, Chang X, Wang H, Guo J, Zhang W: Neurofilament markers in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis. Journal of cellular and molecular medicine 2022, 26(2):583-587.

          3. Ma J, Pang X, Huang S, Zhang J, Wang J, Zhao R, Chang X, Guo J, Zhang W: Genetic analysis in Chinese patients with familial or young-onset amyotrophic lateral sclerosis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022, 43(4):2579-2587.

          4. Zhao F, Wang J, Zhang J, Pang X, Huang S, Chang X, Guo J, Zhang W: Pain in acute motor axonal neuropathy. Muscle & nerve 2021, 64(6):739-743.

          5. Zhang J, Wang H, Liu W, Wang J, Chang X, Huang S, Pang X, Guo J, Wang Q, Zhang W: A novel Q93H missense mutation in DCTN1 caused distal hereditary motor neuropathy type 7B and Perry syndrome from a Chinese family. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021.

          6. Wen Q, Ma J, Pang X, Huang S, Zhang J, Wang J, Chang X, Guo J, Zhang W: Diaphragm ultrasound in the diagnosis of respiratory dysfunction in patients with amyotrophic lateral sclerosis. Revue neurologique 2021, 177(6):639-646.

          7. Shi J, Zhao F, Pang X, Huang S, Wang J, Chang X, Zhang J, Liu Y, Guo J, Zhang W: Whole-exome sequencing identifies a heterozygous mutation in SLC12A6 associated with hereditary sensory and motor neuropathy. Neuromuscular disorders : NMD 2021, 31(2):149-157.

          8. Ma J, Wen Q, Pang X, Huang S, Zhang J, Wang J, Chang X, Guo J, Zhang W: Fasciculation score: a sensitive biomarker in amyotrophic lateral sclerosis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021.

          9. Juan W, Fang L, Qi W, Jing M, Shan H, Jing Z, Xueli C, Wei Z, Junhong G: Muscle ultrasonography in the diagnosis of amyotrophic lateral sclerosis. Neurological research 2020:1-5.

          10. Wei Z, Jiaying S, Junhong G: Bilateral facial paralysis as a rare neurological manifestation of primary Sjogren's syndrome: case-based review. Rheumatology international 2019, 39(9):1651-1654.

           

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