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- W2912158095 endingPage "61" @default.
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- W2912158095 abstract "Transthyretin (TTR) related cardiomyopathy is an underdiagnosed cause of heart failure but is increasingly recognized in various settings – from patients admitted with heart failure to symptomatic aortic stenosis – and is rapidly becoming the most frequent form of systemic amyloidosis. Following the recent publication of the landmark ATTR-ACT trial that showed tafamidis to be the first treatment to improve survival in patients with TTR-related cardiac amyloidosis and heart failure, we reviewed the drug's rationale, characteristics and evidence supporting its use in TTR amyloidosis." @default.
- W2912158095 created "2019-02-21" @default.
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- W2912158095 date "2019-03-01" @default.
- W2912158095 modified "2023-09-29" @default.
- W2912158095 title "Tafamidis for the treatment of transthyretin amyloidosis" @default.
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- W2912158095 doi "https://doi.org/10.2217/fca-2018-0078" @default.
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