Back to search

Article

Patient and family experience with Transthyretin Amyloid Cardiomyopathy (ATTR-CM) and Polyneuropathy (ATTR-PN) Amyloidosis: Results of two focus groups

2021-01-15

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Transthyretin amyloidosis, or ATTR, is a progressive and debilitating rare proteopathy generally manifested as either transthyretin amyloid polyneuropathy (ATTR-PN) or transthyretin amyloid cardiomyopathy (ATTR-CM). Irrespective of the clinical presentation, affected patients manage a chronic and life-threatening condition that severely impacts their quality of...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
9a879594-f2e2-5901-b5a8-9aeb57a6703f
DOI
10.21203/rs.3.rs-48013/v3
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Patient and family experience with Transthyretin Amyloid Cardiomyopathy (ATTR-CM) and Polyneuropathy (ATTR-PN) Amyloidosis: Results of two focus groupsDOI 10.21203/rs.3.rs-48013/v3
Select a neighboring publication to make it the new centre.