Zobrazeno 1 - 10
of 158
pro vyhledávání: '"Pu, Ke"'
Autor:
Pu, Ke1 (AUTHOR), Gao, Jingyuan2 (AUTHOR), Feng, Yang3 (AUTHOR), Hu, Jian4 (AUTHOR), Tang, Shunli5 (AUTHOR), Yang, Guodong1 (AUTHOR) ygd_ld2006@163.com, Xu, Chuan6,7 (AUTHOR) xuchuan19860530@163.com
Publikováno v:
BMC Gastroenterology. 10/1/2024, Vol. 24 Issue 1, p1-20. 20p.
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 23, Iss 12, Pp 1134-1138 (2023)
Selective dorsal rhizotomy (SDR) is an effective method for the treatment of lower limb spasm, especially the advancement of intraoperative neurophysiological monitoring technology, which can make surgery more and more minimally invasive and accurate
Externí odkaz:
https://doaj.org/article/595037a6e0af4b27bd1e784f28a55b63
Publikováno v:
In Heliyon 30 July 2024 10(14)
Autor:
Han, Guoqing, Huang, Zhifa, Qiao, Huanhuan, Zhu, Wei, Yan, Xuejiang, Pu, Ke, Li, Qingguo, Tong, Xiaoguang
Publikováno v:
In Heliyon 29 February 2024 10(4)
Autor:
Zhao, Yifan1,2,3 (AUTHOR), Pu, Ke4 (AUTHOR), Zheng, Ya2,3 (AUTHOR), Wang, Yuping2,3 (AUTHOR), Wang, Jun2,3 (AUTHOR) zhouyn@lzu.edu.cn, Zhou, Yongning2,3 (AUTHOR) zhouyn@lzu.edu.cn
Publikováno v:
PLoS ONE. 4/1/2024, Vol. 19 Issue 4, p1-19. 19p.
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 23, Iss 5, Pp 425-432 (2023)
Objective To investigate the optimal clinical therapy effects and prognostic factors of cerebral arteriovenous malformation (CAVM) in children following different treatment methods. Methods The clinical data of 47 children (< 18 years old) with CAVM
Externí odkaz:
https://doaj.org/article/46bd8fe919cc4b41a92f3a5e1a87075a
Progress on clinical characteristics and pathogenesis of cerebral cavernous malformation in children
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 23, Iss 5, Pp 393-397 (2023)
Cerebral cavernous malformation is the second most common vascular malformation of the central nervous system. The main clinical manifestations in children include epileptic seizure, spontaneous cerebral hemorrhage, and focal neurological deficits. T
Externí odkaz:
https://doaj.org/article/6cd6b8b8345d40c1a4fcdc2ae888420f
Publikováno v:
Zhongguo quanke yixue, Vol 25, Iss 24, Pp 3065-3069 (2022)
Background Neutral lipid storage disease with myopathy (NLSDM) has obscure onset and nonspecific clinical symptoms. Due to different clinical manifestations, the patients with NLSDM may be seen in neurology, cardiovascular disease and other departmen
Externí odkaz:
https://doaj.org/article/23286c91e8b9431097073d73c63c1fa6
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