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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 cardiomyopathy.
J Formos Med Assoc. 2024 Oct 10:S0929-6646(24)00481-9. doi: 10.1016/j.jfma.2024.10.005. Online ahead of print.
J Formos Med Assoc. 2024.
PMID: 39389803
Free article.
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study.
Tsai CH, Chao CC, Hsieh ST, Yu AL, Wu YA, Cheng MF, Lee MJ, Chou CH, Shun CT, Hsueh HW, Jyh-Ming Juang J, Tseng PH, Su MY, Lin YH.
Tsai CH, et al. Among authors: jyh ming juang j.
Orphanet J Rare Dis. 2023 Sep 13;18(1):289. doi: 10.1186/s13023-023-02824-0.
Orphanet J Rare Dis. 2023.
PMID: 37705003
Free PMC article.
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2021 TSOC Expert Consensus on the Clinical Features, Diagnosis, and Clinical Management of Cardiac Manifestations of Fabry Disease.
Hung CL, Wu YW, Lin CC, Lai CH, Jyh-Ming Juang J, Chao TH, Kuo L, Sung KT, Wang CY, Wang CL, Chu CY, Yu WC, Hou CJ.
Hung CL, et al. Among authors: jyh ming juang j.
Acta Cardiol Sin. 2021 Jul;37(4):337-354. doi: 10.6515/ACS.202107_37(4).20210601A.
Acta Cardiol Sin. 2021.
PMID: 34257484
Free PMC article.
Review.
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