![趙國華[浙江大學醫學院附屬第四醫院神經內科主任]](/img/3/ded/nBnauM3X1gzM0AjNyITOzYTN1UTM1QDN5MjM5ADMwAjMwUzLykzLwMzLt92YucmbvRWdo5Cd0FmLxE2LvoDc0RHa.jpg "趙國華[浙江大學醫學院附屬第四醫院神經內科主任]")
個人簡介
2006年畢業於中南大學湘雅醫學院，獲神經病學專業博士學位。2012年-2014年美國國立衛生研究院博士後。從事神經系統疾病臨床工作17年，擅長神經變性疾病和神經遺傳病、神經系統急危重病人、腦血管病、中樞神經系統感染、肌肉疾病等的診治。
研究方向
主要致力於神經變性疾病和神經遺傳病致病基因定位、克隆和發病機制方面的研究。
發表論文
(1) Zhao G, Liu X*, Jiang P*. Identification of a novel SPG4 mutation in a Chinese hereditary spastic paraplegia family.Neurol Sci, 2017, 38(5):903-905.
(2) Zhao G, Zhu PP, Renvoisé B, et al. Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology.Exp Cell Res, 2016, 349(1): 32-44.
(3) Wang K, Zhao G*. Exon 8-17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: A case report and literature review.J Neurol Sci, 2015, 357(1-2): 282-4.
(4) Zhao G, Blackstone C* ER Morphology: Sculpting with XendoU.Curr Biol, 2014, 24(24): R1170-2.
(5) Wu JY, Zhang BR, Zhao GH*. Cerebral infarction and cranial venous sinus thrombosis caused by paragonimiasis.CNS Neurosci Ther, 2013, 19(9):734-6.
(6) Zhao GH, Yin XZ, Wu DW, et al. Clinical features and Cu/Zn superoxide dismutase gene mutations in two Mainland Chinese families with amyotrophic lateral sclerosis.International Journal of Neuroscience, 2011, 121(4): 191-195.
(7) Yin XZ, Liu JR, Zhang BR, Zhang L, Wang PZ, Zhou FY, Ding MP, Zhao GH*. Report of two Chinese families and a review of Chinese CADASIL patients.Journal of the Neurological Sciences, 2009, 279(1-2): 88-92.
(8) Zhao G, Ding M, Zhang B, et al. Clinical manifestations and management of acute thallium poisoning.European Neurology, 2008, 60(6): 292-297.
(9) Zhao G, Hu Z, Shen L, Jiang H, Ren ZJ, Liu XM, Xia K, Guo P, Pan Q, Tang BS*. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.Chinese Medical Journal, 2008, 121(5): 430-434.
(10) Tang B*, Zhao G, Luo W, et al. Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.Human Genetics, 2005, 116(3): 222-224.
(11) Tang B*, Zhao G, Xia K, et al. Three novel mutations of thespastin gene in Chinese patients with hereditary spastic paraplegia.Archives of Neurology, 2004, 61(1): 49-55.
獲獎情況
神經系統遺傳病基因診斷平台的建立，湖南省科技廳，湖南省科學技術進步獎，二等獎，2006. （第7名）
帕金森病及相關運動障礙疾病的發病機制和治療的基礎與臨床研究，浙江省科技廳，浙江省科學技術進步獎，三等獎，2012 （第2名）
