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Orphanet Journal of Rare Diseases|September 13, 2023
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort studyCheng-Hsuan Tsai, Chi-Chao Chao, Sung-Tsang Hsieh, et al.Acta Cardiologica Sinica|July 17, 2023
Efficacy of Tafamidis in Patients with Ala97Ser Hereditary Transthyretin Cardiac Amyloidosis: A Six-Month Follow-Up StudyCheng-Hsuan Tsai, An-Li Yu, Yuan-Kun Aden Wu, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|September 24, 2025
Perfusion defects on thallium-201 scintigraphy in cardiac amyloidosisYi-Hsin Hung, An-Li Yu, Chi-Lun Ko, et al.Therapeutic Advances in Chronic Disease|January 15, 2024
Tafamidis improves myocardial longitudinal strain in A97S transthyretin cardiac amyloidosisYuan-Kun Aden Wu, An-Li Yu, Mei-Fang Cheng, et al.Journal of the American Heart Association|January 12, 2024
Use of Technetium-99m-Pyrophosphate Single-Photon Emission Computed Tomography/Computed Tomography in Monitoring Therapeutic Changes of Eplontersen in Patients With Hereditary Transthyretin Amyloid CardiomyopathyAn-Li Yu, Yi-Chieh Chen, Cheng-Hsuan Tsai, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|October 10, 2024
Use of technetium-99m-pyrophosphate single-photon emission computed tomography/computed tomography in monitoring therapeutic changes of RNA interference therapeutics in patients with hereditary transthyretin amyloid cardiomyopathyYi-Hsin Hung, An-Li Yu, Yi-Chieh Chen, et al.Pageof 2