Early diagnosis in ATTRv amyloidosis, how early is enough? How early is possible?-Reference-Cited by-同舟云学术

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Early diagnosis in ATTRv amyloidosis, how early is enough? How early is possible?

Published:2024-06 Issue:12 Volume:162 Page:e70-e73
ISSN:2387-0206
Container-title:Medicina Clínica (English Edition)
language:en
Short-container-title:Medicina Clínica (English Edition)

Author:

Conceição Isabel

Publisher

Elsevier BV

Reference51 articles.

1. Red-flag symptom clusters in transthyretin familial amyloid polyneuropathy;Conceição;J Peripher Nerv Syst,2016

2. Evolving landscape in the management of transthyretin amyloidosis;Hawkins;Ann Med,2015

3. Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update;Dispenzieri;Orphanet J Rare Dis,2022

4. Estimating the global prevalence of transthyretin familial amyloid polyneuropathy;Schmidt;Muscle Nerve,2018

5. Epidemiology of transthyretin familial amyloid polyneuropathy in Portugal: a nationwide study;Inês;Neuroepidemiology,2018

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