Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Bao-Lai Hua"'
Autor:
Yang Yu, Hao Wang, Jing-Jing Yang, Shu Fang, Ya-Nan Wen, Yi-Fan Jiao, Kun Qian, Ning Le, Ruo-Qi Shan, Wen-Jing Gao, Bao-Lai Hua, Fei Li
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundAcute myeloid leukemia (AML) is a heterogeneous hematopoietic malignancy. Patient prognosis cannot be accurately assessed in National Comprehensive Cancer Network (NCCN) risk stratification subgroups based on the current criteria. This stud
Externí odkaz:
https://doaj.org/article/53572a6b2d1f4a36bda88e6fa3ff6317
Autor:
Ye-Fan, Wang, Zhen-Yang, Lin, Fei-Xu, Zhang, Xin-Yue, Zhou, Xia, Wu, Xiao, Xiao, Jun-Jiang, Sun, Bao-Lai, Hua
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 30(5)
To explore the effect of lenalidomide on human fibroblast-like synovial cells (HFLS) and the therapeutic efficacy on hemophilic arthropathy in hemophilia A mice model.In vitro, to remodel the inflammatory environment of synovial tissue after hemorrha
Autor:
Jing Sun, Zhen-yu Yan, Bao-Lai Hua, Changcheng Zheng, Jun Peng, Yun-feng Cheng, Pei-yan Sun, Chun-sen Wang, Ze-Ping Zhou, Feng'e Yang, Luo-jia Hong, Renchi Yang, Tao Guo, Ke-sheng Dai, Tong-hua Yang, Jianming Feng, Hu Zhou, Cong-ming Wu, Fang-ping Chen, Wen-man Wu, Xiaomin Wang, Yu-ping Gong, Guang-sen Zhang, Xinguang Liu, Rui-bing Huang, Min Zhou, Tie-nan Zhu, Yu Hu, Xinhong Guo, Xu Ye, Mi-mi Shu, Hong-li Zhu, Ming Hou, Yan Li, Yue Han, L H Yang, Shu-jie Wang, Rongfu Zhou, Mei-Yun Fang, Yu-Qian Sun, Lei Zhang, Xiao-chuan Bai
Publikováno v:
International Journal of Hematology. 107:615-623
Primary immune thrombocytopenia (ITP) is a bleeding disorder commonly encountered in clinical practice. The International Working Group (IWG) on ITP has published several landmark papers on terminology, definitions, outcome criteria, bleeding assessm
Publikováno v:
The Journal of Dermatology. 44:76-79
Epidermolysis bullosa acquisita (EBA) is a rare chronic subepidermal bullous autoimmune disease. The occurrence of acquired hemophilia A (AHA) is low and so the coexistence of EBA and AHA is extremely rare. We herein described a case of EBA coexistin
Publikováno v:
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae. 37(4)
To investigate the benefit of low-dose tertiary prophylaxis in adults with severe haemophilia A(SHA).Twenty-two SHA patients aged 18 to 60 years from the Haemophilia Centre of Peking Union Medical College Hospital, Beijing, China, were retrospectivel
Autor:
Xiao, Han, Dao-Bin, Zhou, Ming-Hui, Duan, Bao-Lai, Hua, Xuan, Wang, Jie-Ping, Zhang, Yong-Qiang, Zhao, Ti, Shen, Yong-Ji, Wu
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 22(5)
This study was aimed to explore the possible mechanisms of hepcidin increase in multiple myeloma patients. The clinical information and peripheral venous blood of eligible patients with previously untreated multiple myeloma were collected. Serum conc
Autor:
Li-xia, Chen, Bao-lai, Hua, Ying, Liu, Lan, Luo, Jian-ping, Zhang, Han-ying, Zhang, Yong-qiang, Zhao
Publikováno v:
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 33(5)
To analyze the clinical characteristics and effects of rehabilitation treatment on hemophiliacs with iliopsoas hemorrage.The hemophilia patients with iliopsoas bleeding treated in Peking Union Medical College Hospital between January 2006 to December
Autor:
Tie-Nan, Zhu, Yong-Qiang, Zhao, Qiu-Lan, Ding, Xia, Bai, Xiao-Yan, Wang, Xue-Feng, Wang, Ren-Chi, Yang, Zhao-Yue, Wang, Bao-Lai, Hua, Xu-Qian, Wel, Chang-Geng, Ruan, Nicole, Schlegel
Publikováno v:
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 33(2)
To explore the distribution and influence factors of protein C (PC), protein S (PS) and antithrombin (AT) activities and to determine the prevalence of their deficiencies in the Chinese Han healthy population.Healthy volunteers including blood donors
Autor:
Jing, Yang, Yong-Qiang, Zhao, Wei, Wu, Bao-Lai, Hua, Zu-Yi, Zhu, Ren-Chi, Yang, Shu-Jie, Wang
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 18(2)
This study was to evaluate the role of reticulated platelets (RP) assay in the distinguishing the different causes of thrombocytopenia. The RP and immature platelet fraction (IPF) were stained by a nucleic acid-specific dye oxazine, and assayed by XE
Autor:
Bao-lai, Hua, Zhen-yu, Yan, Yan, Liang, Mei, Yan, Lian-kai, Fan, Kui-xing, Li, Bai, Xiao, Jing-zhong, Liu, Yong-qiang, Zhao
Publikováno v:
Chinese medical journal. 123(3)
Hemophilia A (HA) is an X-linked inherited bleeding disorder caused by decreased activity of factor VIII (FVIII) due to heterogenous mutations in the FVIII coding gene (F8). The type of mutation plays an important role in the FVIII inhibitor formatio