Zobrazeno 1 - 10
of 1 462
pro vyhledávání: '"ZHANG Shuyang"'
Autor:
CHEN Miao, YANG Chen, LIU Ziwei, CAO Wei, ZHANG Bo, LIU Xin, LI Jingnan, LIU Wei, PAN Jie, WANG Jian, ZHENG Yuehong, CHEN Yuexin, LI Fangda, DU Shunda, NING Cong, CHEN Limeng, YUE Cai, NI Jun, PENG Min, GUO Xiaoxiao, WANG Tao, LI Hongjun, LI Rongrong, WU Tong, HAN Bing, ZHANG Shuyang, Multidiscipline Collaboration Group on Rare Disease at Peking Union Medical College Hospital
Publikováno v:
Xiehe Yixue Zazhi, Vol 15, Iss 5, Pp 1011-1028 (2024)
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematopoietic stem cell disease caused by abnormal expression of glycosylphosphatidylinositol (GPI) on the cell membrane due to mutations in the phosphatidylinositol glycan class A(PIGA)
Externí odkaz:
https://doaj.org/article/c7dcc3d643aa474eac91a43434975641
Publikováno v:
JPRAS Open, Vol 41, Iss , Pp 240-243 (2024)
Intravascular papillary endothelial hyperplasia (IPEH), also called masson tumor which is a benign vascular tumor named after Pierre Masson, the French pathologist who originally described it in 1923, terming it “hémangioendothéliome végétant i
Externí odkaz:
https://doaj.org/article/e62e6bc36614449ea8363cc7744d6566
Publikováno v:
Xiehe Yixue Zazhi, Vol 15, Iss 5, Pp 1224-1229 (2024)
The clinical medicine postdoctoral training program embodies a pioneering initiative in China's pursuit of excellence in medical education in the contemporary era. The establishment of the Department of Rare Diseases at Peking Union Medical College H
Externí odkaz:
https://doaj.org/article/30b07c3deb584e84b8c8f6d35efba8d9
Publikováno v:
罕见病研究, Vol 3, Iss 3, Pp 387-390 (2024)
The diagnosis and treatment of rare diseases have long been significant challenges in the medical practice. With the rapid development of genomics and genetics, medical genetics has been widely applied in the diagnosis and treatment of rare diseases.
Externí odkaz:
https://doaj.org/article/a0989878b8494fabbc1f19a6f0587d07
Autor:
TIAN Zhuang, ZHANG Shuyang
Publikováno v:
Xiehe Yixue Zazhi, Vol 15, Iss 4, Pp 801-806 (2024)
In the past few years, there have been many breakthroughs in the treatment of heart failure, especially in drug therapy. The classification of chronic heart failure and treatment methods for heart failure and its complications are also constantly upd
Externí odkaz:
https://doaj.org/article/dd335a6ee7e94617b605ed9e99ec9a4b
Publikováno v:
罕见病研究, Vol 3, Iss 2, Pp 195-201 (2024)
Objective This study aims to sort out the rare disease drugs in the China′s Second List of Rare Diseases, to provide reference for the management of rare disease drug treatment. Methods Up to December 31, 2023, based on the China′s Second List of
Externí odkaz:
https://doaj.org/article/3f6b28acba4e4edd8bdbf6441afa75d9
Publikováno v:
罕见病研究, Vol 3, Iss 2, Pp 155-163 (2024)
In the past few years, China has pushed forward the availability of diagnosis and treatment of rare diseases. However, only 5% of patients receive effective treatment in the world. In China, the difficulties in having access to drugs against rare dis
Externí odkaz:
https://doaj.org/article/a61ea65467054c1696c6b1a7c618bc47
Autor:
SHEN Min, ZHANG Shuyang
Publikováno v:
罕见病研究, Vol 3, Iss 2, Pp 164-167 (2024)
The establishment of the Department of Rare Diseases at Peking Union Medical College Hospital (PUMCH) is a landmark in the disciplinary development of the rare diseases. The establishment of the department will booster the prominence of the influence
Externí odkaz:
https://doaj.org/article/6c64442cd0324ddbb5ff18e0b65859de
Autor:
LI Kexin, CHEN Jingdan, ZHANG Dingding, GUO Wudong, ZHENG Jiayin, LI Linkang, ZHAO Kun, ZHANG Shuyang
Publikováno v:
罕见病研究, Vol 3, Iss 2, Pp 269-274 (2024)
This article combs and summarizes the entire process of rare disease selection and priority theme determination, including the application and preliminary review of rare diseases, standardization of disease theme information, the evaluation methods o
Externí odkaz:
https://doaj.org/article/2617784f0fa34258b12a50b76c05efec
Autor:
CHEN Rui, ZHANG Shuyang
Publikováno v:
罕见病研究, Vol 3, Iss 2, Pp 221-223 (2024)
Externí odkaz:
https://doaj.org/article/61fb7ed2b92a4c2b80e107cfff66f4a8