Zobrazeno 1 - 10
of 1 355
pro vyhledávání: '"Xu Kexin"'
Autor:
XU Kexin, LI Guozhuang, LI Qing, YIN Xiangjie, FANG Kun, WU Zhihong, ZHANG Jianguo, DISCO (Deciphering Disorders Involving Scoliosis ＆ COmorbidities) Study Group, WU Nan
Publikováno v:
罕见病研究, Vol 3, Iss 3, Pp 295-303 (2024)
The Ehlers-Danlos syndromes (EDS) are a group of rare hereditary connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. The clinical and genetic hetero- geneity of EDS frequently leads to unde
Externí odkaz:
https://doaj.org/article/db6025bccc7742379bb0fdaab73a2b71
Autor:
XU Kexin, LI Guozhuang, WU Zhihong, DISCO (Deciphering Disorders Involving Scoliosis & COmorbidities) Study Group, ZHANG Jianguo, WU Nan
Publikováno v:
罕见病研究, Vol 2, Iss 4, Pp 633-640 (2023)
Joint hypermobility (JH) refers to the ability of joints to move beyond the 'normal' limits, which can be either physiologic or pathologic. Hypermobility spectrum disorders (HSDs) are a group of joint hypermobility-related clinical conditions. HSDs p
Externí odkaz:
https://doaj.org/article/fd695b79149147a194738e68b9ba6273
Publikováno v:
罕见病研究, Vol 2, Iss 4, Pp 469-475 (2023)
Deep phenotyping is a precise and comprehensive approach used for the precise analysis and comprehensive assessment of multi-system phenotypes of the patients. The approach uses symptoms, signs, various medical examination and laboratory results, and
Externí odkaz:
https://doaj.org/article/8ca809fdfad04eef938397d23aab0e6d
Autor:
LI Guozhuang, XU Kexin, ZHAO Sen, ZHANG Jianguo, QIU Guixing, SUI Ruifang, WANG Tao, SHEN Min, ZENG Xuejun, WANG Wei, MA Mingsheng, WEI Min, LONG Xiao, LYU Ke, HUO Li, XUAN Lei, WU Nan
Publikováno v:
罕见病研究, Vol 2, Iss 4, Pp 547-553 (2023)
Blau syndrome is a rare genetic disorder characterized by the a mix of granulomatous arthritis, uveitis, and dermatitis. Patients typically manifest multisystem involvement, including ocular, skin, and skeletal abnormalities. Blau syndrome is extreme
Externí odkaz:
https://doaj.org/article/3649a4c3f98c4b3a9d93d2b6873ffd03
Autor:
Li, Guozhuang1,2,3 (AUTHOR), Xu, Kexin1,2,3 (AUTHOR), Yin, Xiangjie1,2,3 (AUTHOR), Yang, Jianle1,2,3 (AUTHOR), Cai, Jihao1,2,3 (AUTHOR), Yang, Xinyu1,2,3 (AUTHOR), Li, Qing1,2,3 (AUTHOR), Wang, Jie1,2,3 (AUTHOR), Zhao, Zhengye1,2,3 (AUTHOR), Mahesahti, Aoran1,2,3 (AUTHOR), Zhang, Ning1,2,3 (AUTHOR), Zhang, Terry Jianguo1,2,3,4 (AUTHOR) jgzhang_pumch@yahoo.com, Wu, Nan1,2,3,4 (AUTHOR) dr.wunan@pumch.cn
Publikováno v:
Orphanet Journal of Rare Diseases. 10/8/2024, Vol. 19 Issue 1, p1-7. 7p.
The tracks recorded by a gaseous detector provide a possibility for charged particle identification. For searching the neutrinoless double beta decay events of 136Xe in the PandaX-III experiment, we optimized the convolutional neural network based on
Externí odkaz:
http://arxiv.org/abs/2211.00237
Autor:
Zhang, Mengmeng, Shen, Junfeng, Li, Chenglu, Santosh, M., Xu, Bo, Alam, Masroor, Zhao, Gexue, Xu, Kexin, Liu, Jiajun
Publikováno v:
In Ore Geology Reviews November 2024 174
Publikováno v:
In Computers and Electronics in Agriculture November 2024 226
Autor:
Yang, Si, Li, Chenxi, Li, Xinyu, Jiang, Jingying, Zhao, Yansong, Wang, Xiaoli, Chen, Wenliang, Liu, Rong, Xu, Kexin
Publikováno v:
In Computers and Electronics in Agriculture October 2024 225
Publikováno v:
In Ocean Engineering 1 October 2024 309 Part 2