资讯

Soleno Therapeutics, Inc. (Soleno) (NASDAQ: SLNO), a biopharmaceutical company developing novel therapeutics for the ...
Prader-Willi 综合征(Prader-Willi syndrome,PWS)是一种极为罕见的神经发育障碍疾病,由 15q11.2 - q13 区域印记基因缺失所致。这种基因异常使得 PWS 患者在接受减重手术时,麻醉管理面临诸多棘手难题。肥胖在 PWS 患者中极为常见,由于下丘脑功能障碍引发的多食 ...
Soleno Therapeutics, Inc. (Soleno) (NASDAQ: SLNO), a biopharmaceutical company developing novel therapeutics for the ...
13-year-old Mikhael Azman and his parents Azman Ahmad Bakri and Farahiah Ariffin, with Prader-Willi Syndrome Association of Malaysia president Azhar Talib (right). (Bernama pic) No parent is ever ...
Katie Price has shared a concerning update over her son Harvey’s weight issues and worries he’s now at risk of suffering a ...
Harvey is blind, autistic, has septo-optic dysplasia, and is one of the 2,000 people in the UK with Prader-Willi syndrome, a genetic disorder. A recognised symptom of his Prader-Willi syndrome is ...
This initiative aligns with Sandoz’s ongoing efforts to support Egypt’s Vision 2030 and local healthcare authorities’ ...
Announced U.S. Food and Drug Administration (FDA) approval of VYKAT XR (diazoxide choline) extended-release tablets, ...