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Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|March 27, 2016
A dosimetric comparison of real-time adaptive and non-adaptive radiotherapy: A multi-institutional study encompassing robotic, gimbaled, multileaf collimator and couch trackingEmma Colvill, Jeremy Booth, Simeon Nill, et al.International Journal of Radiation Oncology, Biology, Physics|April 3, 2020
Real-Time Image Guided Ablative Prostate Cancer Radiation Therapy: Results From the TROG 15.01 SPARK TrialPaul Keall, Doan Trang Nguyen, Ricky O'Brien, et al.International Journal of Radiation Oncology, Biology, Physics|October 23, 2023
Impact of Interfractional Bladder and Trigone Displacement and Deformation on Radiation Exposure and Subsequent Acute Genitourinary Toxicity: A Post Hoc Analysis of Patients Treated with Magnetic Resonance Imaging-Guided Prostate Stereotactic Body Radiation Therapy in a Phase 3 Randomized TrialBeth K Neilsen, Ting Martin Ma, Wisdom O Akingbemi, et al.Medical Physics|August 26, 2018
Machine learning and modeling: Data, validation, communication challengesIssam El Naqa, Dan Ruan, Gilmer Valdes, et al.Medical Physics|April 28, 2021
Prediction of soft tissue sarcoma response to radiotherapy using longitudinal diffusion MRI and a deep neural network with generative adversarial network-based data augmentationYu Gao, Vahid Ghodrati, Anusha Kalbasi, et al.Thrombosis Journal|January 9, 2023
Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiencyHan-Lu Wang, Dan-Dan Ruan, Min Wu, et al.Pediatric Rheumatology Online Journal|October 23, 2023
Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritisShi-Jie Li, Dan-Dan Ruan, Wei-Zhen Wu, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2024
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemiaKai-Ying He, Hong-Ping Yu, Jing Zou, et al.Annals of Hematology|March 21, 2024
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case reportJian-Hui Zhang, Hui Chen, Dan-Dan Ruan, et al.Journal of Medical Genetics|July 19, 2023
Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndromeHong-Hong Pan, Dan-Dan Ruan, Min Wu, et al.Pageof 38