Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Qiu, Zhengqing"'
This paper addresses the robust beamforming design for rate splitting multiple access (RSMA)-aided visible light communication (VLC) networks with imperfect channel state information at the transmitter (CSIT). In particular, we first derive the theor
Externí odkaz:
http://arxiv.org/abs/2411.17056
Publikováno v:
Jichu yixue yu linchuang, Vol 44, Iss 7, Pp 1008-1012 (2024)
Objective To investigate the clinical characteristics of the hepatolenticular degeneration in children, and to clarify the significance of gene diagnosis in children with hepatolenticular degeneration. Methods A total of 75 patients with hepatolentic
Externí odkaz:
https://doaj.org/article/774c2414579e4689bccb7970ee2c39dc
Autor:
FU Yining, ZHOU Jingmin, LI Feng, HUANG Shangzhi, WANG Yining, HONG Xia, LYU Ke, LIU Yaping, LENG Ling, ZHENG Wenjie, QIU Zhengqing, ZHU Yicheng, ZHENG Yuehong, CHEN Yuexin
Publikováno v:
罕见病研究, Vol 3, Iss 2, Pp 224-231 (2024)
The Ehlers-Danlos syndrome(EDS)is a rare inherent connective tissue disorder. The prevalence of EDS in the population is estimated at one out of ten thousand to one out of a hundred thousand. The vascular EDS(vEDS) are rare among the subtypes but are
Externí odkaz:
https://doaj.org/article/8939ad54fb1c4e8fb3d504d46637b607
Autor:
Yao, Fengxia, Hao, Na, Li, Danhua, Zhang, Weimin, Zhou, Jingwen, Qiu, Zhengqing, Mao, Aiping, Meng, Wanli, Liu, Juntao
Publikováno v:
Human Genomics; 11/28/2024, Vol. 18 Issue 1, p1-15, 15p
Autor:
Hou, Gongmingzhu, Ahmad, Sajjad, Li, Yanfang, Yan, Duo, Yang, Shuhan, Chen, Siqi, Qiu, Zhengqing, Yu, Xingyu, Li, Nana, Li, Yang, Liang, Yan, Leng, Qingwen, Qu, Yonggang
Publikováno v:
Animals (2076-2615); May2024, Vol. 14 Issue 10, p1433, 19p
Autor:
Zhong, Linqing, Wang, Wei, Tang, Xiaoyan, Zhang, Yu, Gou, Lijuan, Wang, Lin, Wang, Changyan, Jian, Shan, Quan, Meiying, Zhang, Zhenjie, Yu, Zhongxun, Qiu, Zhengqing, Wei, Min, Song, Hongmei
Publikováno v:
Clinical Rheumatology; Mar2024, Vol. 43 Issue 3, p1171-1181, 11p
Autor:
Hou, Bo, Cidanwangjiu, Zhang, Haiping, Wang, Fengdan, Qiu, Zhengqing, Zhang, Yan, Jin, Zhengyu
Publikováno v:
Journal of Computer Assisted Tomography; Jul/Aug2023, Vol. 47 Issue 4, p637-642, 6p
Autor:
Ma, Mingsheng, Zhang, Mengqi, Zhou, Yu, Yao, Fengxia, Wei, Min, Li, Zhenghong, Qiu, Zhengqing
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-4 (2021)
BMC Nephrology
BMC Nephrology
Background Transient antenatal Bartter’s syndrome caused by MAGED2 mutation is a rare X-linked recessive renal tubular disorder. Cases reported are mostly infants, and the long-term prognosis of the disease is still under investigation. Case presen
Autor:
Ma, Mingsheng, Zhang, Mengqi, Zhou, Yu, Yao, Fengxia, Wei, Min, Li, Zhenghong, Qiu, Zhengqing
Additional file 1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23fb268dc2287ea89b8c84d51cea6dd8
Autor:
Xu, Na, Han, Xinxin, Zhang, Yun, Huang, Xiaoming, Zhu, Weiguo, Shen, Min, Zhang, Wen, Jialin, Chen, Wei, Min, Qiu, Zhengqing, Zeng, Xuejun
Publikováno v:
Arthritis Research & Therapy; 2/26/2022, Vol. 24 Issue 1, p1-16, 16p