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The V122I mutation in hereditary transthyretin-mediated amyloidosis is significantly associated with an increased incidence of polyneuropathy

28 August 2020 (08:00 - 18:00)
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Congress Presentation Part of: Cardiovascular Disease in Special Populations ePosters Neurologic Disorders and Heart Disease ESC Premium Access ESC Congress 2020

About the speaker

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Doctor Margaret Parker

Cambridge (United States of America)

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Implementation study of CT calcium score in patients with atypical angina pectoris and non-specific thoracic complaints in primary care: rationale, objectives, and design of the CONCRETE study
Miss M. Koopman (Groningen, NL)
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Serum uric acid possibly associated with abnormal left ventricular diastolic function in healthy individuals
Doctor C. Liu (Taipei, TW)
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Characteristics and health status of patients with and without confirmed HFpEF
Professor C. Deaton (Cambridge, GB)
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Evaluating the diagnostic and prognostic value of cardiac biomarkers for heart disease and major adverse cardiac events in patients with muscular dystrophy
Mr A. Nikhanj (Edmonton, CA)
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Heart involvement in type 1 and type 2 myotonic dystrophy. Insights from a 10-year follow-up study.
Doctor F. Fioravanti (Milan, IT)
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Cardiovascular Disease in Special Populations ePosters

The Event

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ESC Congress 2020

28 August 2020 08:00 CET

ESC 365 is supported by

novartis Explore sponsored resources
novo-nordisk Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources
novo-nordisk Explore sponsored resources