Zobrazeno 1 - 10
of 3 936
pro vyhledávání: '"Shen Min"'
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:
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
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-4 (2024)
Abstract Background Lower limb deep vein thrombosis (DVT) concurrent with pulmonary embolism (PE) is perilous, particularly in the elderly, exhibiting heterogeneity with thrombophilia mutations. Tailored treatment is essential, yet sudden deaths comp
Externí odkaz:
https://doaj.org/article/b5a895251dd5478a9c60a1925307a7b1
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
Publikováno v:
Fayixue Zazhi, Vol 39, Iss 2, Pp 151-160 (2023)
ObjectiveTo establish an LC-MS/MS method based on single hair micro-segmental technique, and verify the detection of 42 psychoactive substances in 0.4 mm hair segments.MethodsEach piece of single hair was cut into 0.4 mm segments and extracted by son
Externí odkaz:
https://doaj.org/article/0c66af6728f344f6a2bd009bcb976cf9
Publikováno v:
Shanghai yufang yixue, Vol 35, Iss 3, Pp 262-266 (2023)
ObjectiveTo analyze the occurrence of suspected adverse events following immunization （AEFI） after changing the priority vaccination sites of the adsorbed acellular diphtherior-pertussis-tetanus vaccine （hereinafter referred to as DPT vaccine
Externí odkaz:
https://doaj.org/article/53940c8832d14e23b5155f1c9a020662
Publikováno v:
Fayixue Zazhi, Vol 38, Iss 4, Pp 507-514 (2022)
At present, the death cases of simple asphyxiant gas acute poisoning are increasing sharply. Common asphyxiant gases in death cases include nitrogen, helium, carbon dioxide, methane, propane, laughing gas, etc. Simple asphyxiant gas has no affinity f
Externí odkaz:
https://doaj.org/article/468046fa194c4b0ebd6333443fee6eb6
Publikováno v:
Fayixue Zazhi, Vol 38, Iss 2, Pp 254-257 (2022)
ObjectiveTo study the distribution of total phosphine in phosphine poisoning victims and summarize the characteristics of phosphine poisoning cases.MethodsThe phosphine and its metabolites in the biological samples of 29 victims in 16 phosphine poiso
Externí odkaz:
https://doaj.org/article/1c1e32699d8c419aaed5d1588a5e1389
Autor:
HONG Yuehui, SHEN Min, WANG Tao, MA Mingsheng, ZHAO Sen, FENG Feng, ZHAO Dachun, ZHANG Wen, ZENG Xuejun, XUAN Lei, YAO Ming, ZHU Yicheng
Publikováno v:
罕见病研究, Vol 1, Iss 2, Pp 151-157 (2022)
We presented an adolescent with recurrent intracranial hemorrhage and skin lesion. The diagnosis was unclear and the treatment was difficult. Through a multidisciplinary effort type Ⅰ interferon disease was suspected and later, an interferon-stimul
Externí odkaz:
https://doaj.org/article/b51bc46dc3a0449eb0ece91d44b1ebbe