Showing results (11-20 of 31) with videos related to
Sort By:
Pageof 4
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 14, 2019
Gender differences in the acquisition of suturing skills with the da Vinci surgical systemHsin-Yi Chiu, Yi-No Kang, Wei-Lin Wang, et al.Scientific Reports|April 27, 2023
The impact of sarcopenia on overall survival in patients with pan-RAS wild-type colorectal liver metastasis receiving hepatectomyYao-Ren Yang, Chung-Sheng Shi, Sheng-Wei Chang, et al.Plos One|May 10, 2021
Masticatory muscle index for indicating skeletal muscle mass in patients with head and neck cancerSheng-Wei Chang, Yuan-Hsiung Tsai, Cheng-Ming Hsu, et al.Plos One|May 31, 2024
Correction: Masticatory muscle index for indicating skeletal muscle mass in patients with head and neck cancerSheng-Wei Chang, Yuan-Hsiung Tsai, Cheng-Ming Hsu, et al.Frontiers in Neurology|September 10, 2019
Automatic Machine-Learning-Based Outcome Prediction in Patients With Primary Intracerebral HemorrhageHsueh-Lin Wang, Wei-Yen Hsu, Ming-Hsueh Lee, et al.The Laryngoscope|January 12, 2021
Prognostic Value of Third Cervical Vertebra Skeletal Muscle Index in Oral Cavity Cancer: A Retrospective StudySheng-Wei Chang, Cheng-Ming Hsu, Yuan-Hsiung Tsai, et al.The International Journal of Medical Robotics + Computer Assisted Surgery : MRCAS|August 4, 2018
Robotic transanal minimally invasive surgery for rectal cancer after clinical complete response to neoadjuvant chemoradiationJames Chi-Yong Ngu, Li-Jen Kuo, Ching-Huei Kung, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 12, 2022
Targeting the EGFR-ERK axis using the compatible solute ectoine to stabilize CFTR mutant F508delJack Wellmerling, Rachael E Rayner, Sheng-Wei Chang, et al.Frontiers in Neurology|May 22, 2018
Association of Chronic Kidney Disease With Small Vessel Disease in Patients With Hypertensive Intracerebral HemorrhageYuan-Hsiung Tsai, Meng Lee, Leng-Chieh Lin, et al.Human Mutation|June 15, 2013
Genetic abnormalities in FOXP1 are associated with congenital heart defectsSheng-Wei Chang, Mona Mislankar, Chaitali Misra, et al.Pageof 4