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Frontiers in Psychiatry|March 6, 2023
Effort-based decision making in schizotypy and its relationship with amotivation and psychosocial functioningRyan Sai Ting Chu, Co Co Ho Yi Tong, Corine Sau Man Wong, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|July 19, 2024
Longitudinal Analyses of Circulating Tumor DNA for the Detection of EGFR Mutation-Positive Advanced NSCLC Progression During Treatment: Data From FLAURA and AURA3Jhanelle E Gray, Aleksandra Markovets, Thanyanan Reungwetwattana, et al.
BMC Psychiatry|September 18, 2023
Functional and clinical outcomes of delusional disorder and schizophrenia patients after first episode psychosis: a 4-year follow-up studyChristy Lai Ming Hui, Evie Wai Ting Chan, Priscilla Wing Man Hui, et al.
European Journal of Human Genetics : EJHG|December 25, 2008
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15Lance Doucette, Nancy D Merner, Sandra Cooke, et al.
European Archives of Psychiatry and Clinical Neuroscience|May 21, 2025
Reinforcement learning impairment in individuals with euthymic bipolar I disorder with a history of psychosisSandra Chi Yiu Wong, Heidi Ka Ying Lo, Anson Kai Chun Chau, et al.
Anticancer Research|April 16, 2010
Molecular characterization of invasive subpopulations from an esophageal squamous cell carcinoma cell lineYu-Kuei Chen, Wun-Shaing Wayne Chang, I-Chen Wu, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|December 5, 2017
National bundle care program implementation to reduce ventilator-associated pneumonia in intensive care units in TaiwanChin-Chuan Kao, Hsiu-Tzy Chiang, Chih-Yu Chen, et al.
Clinical Pharmacology and Therapeutics|January 16, 2022
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 UpdateCraig R Lee, Jasmine A Luzum, Katrin Sangkuhl, et al.
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