Article

Cardiovascular autonomic failure in hereditary transthyretin amyloidosis and TTR carriers is an early and progressive disease marker

2024-03-07

Abstract excerpt

<title>Abstract</title> <p><italic>Background</italic>. The cardiomyopathic and neuropathic phenotype of hereditary transthyretin amyloidosis are well recognized. Cardiovascular autonomic dysfunction is less systematically and objectively assessed. <italic>Methods</italic>. Autonomic and clinical features, quantitative cardiovascular autonomic function, and potential autonomic prognostic markers of disease progre...

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Literature Corpus work: 3205bde6-613f-5116-a28c-b3166b5cd464
DOI: 10.21203/rs.3.rs-4003951/v1

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