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Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons|August 9, 2011
A double-blind randomized crossover study to evaluate the timing of pregabalin for third molar surgery under local anesthesiaChi Wai Cheung, Wing Shan Choi, Yiu Yan Leung, et al.
International Journal of Clinical and Health Psychology : IJCHP|September 22, 2025
Unravelling symptom interplay of depression, anxiety, insomnia and suicidality in adolescents: A network analysisHao Fong Sit, Forrest Tin Wai Cheung, Xiao Li, et al.
The Clinical Journal of Pain|April 6, 2017
Effects of Single Nucleotide Polymorphisms on Surgical and Postsurgical Opioid Requirements: A Systematic Review and Meta-AnalysisSiu-Wai Choi, David M H Lam, Stanley S C Wong, et al.
Plos One|April 18, 2017
Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disabilityChristina Grau, Molly Starkovich, Mahshid S Azamian, et al.
The Chinese Journal of Physiology|January 3, 2022
Lipotoxicity in human lung alveolar type 2 A549 cells: Mechanisms and protection by tannic acidKun-Feng Tsai, Chen-Jung Shen, Chi-Wai Cheung, et al.
BMC Medical Genetics|May 1, 2015
Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature reviewAyman W El-Hattab, Christian P Schaaf, Ping Fang, et al.
European Journal of Human Genetics : EJHG|December 2, 2010
MECP2 duplications in six patients with complex sex chromosome rearrangementsAmy M Breman, Melissa B Ramocki, Sung-Hae L Kang, et al.
Scientific Reports|January 14, 2017
Increased Renal Clearance of Rocuronium Compensates for Chronic Loss of Bile Excretion, via upregulation of Oatp2Long Wang, Mai-Tao Zhou, Cai-Yang Chen, et al.
Clocks & Sleep|October 25, 2024
A Longitudinal Examination between Chronotype and Insomnia in Youths: A Cross-Lagged Panel AnalysisForrest Tin Wai Cheung, Hao Fong Sit, Xiao Li, et al.
European Journal of Human Genetics : EJHG|March 15, 2013
Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delayJens Witsch, Przemyslaw Szafranski, Chun-An Chen, et al.
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