دورية أكاديمية
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study
| العنوان: | Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study |
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| المؤلفون: | Tsai, Cheng-HsuanAff1, Aff2, Chao, Chi-Chao, Hsieh, Sung-Tsang, Yu, An-LiAff4, Aff5, Wu, Yuan-Kun (Aden)Aff4, Aff5, Cheng, Mei-FangAff6, Aff7, Lee, Ming-Jen, Chou, Chia-Hung, Shun, Chia-TungAff9, Aff10, Hsueh, Hsueh-Wen, Jyh-Ming Juang, JimmyAff4, Aff5, Tseng, Ping-Huei, Su, Mao-YuanAff12, Aff13, IDs13023023028240_cor13, Lin, Yen-HungAff4, Aff5, IDs13023023028240_cor14 |
| المصدر: | Orphanet Journal of Rare Diseases. 18(1) |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 17501172 |
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| DOI: | 10.1186/s13023-023-02824-0 |