Cardiovascular autonomic failure in hereditary transthyretin amyloidosis and TTR carriers is an early and progressive disease marker-Reference-Cited by-同舟云学术

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

Published:2024-05-20 Issue:3 Volume:34 Page:341-352
ISSN:0959-9851
Container-title:Clinical Autonomic Research
language:en
Short-container-title:Clin Auton Res

Author:

Chiaro Giacomo,Stancanelli Claudia,Koay Shiwen,Vichayanrat Ekawat,Sander Laura,Ingle Gordon T.,McNamara Patricia,Carr Aisling S.,Wechalekar Ashutosh D.,Whelan Carol J.,Gillmore Julian D.,Hawkins Philip N.,Reilly Mary M.,Mathias Christopher J.,Iodice Valeria

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s10286-024-01038-z.pdf

Reference48 articles.

1. Koike H, Katsuno M (2020) Transthyretin amyloidosis: update on the clinical spectrum, pathogenesis, and disease-modifying therapies. Neurol Ther 9:317–333

2. Reilly MM, Staunton H, Harding AE (1995) Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological study. J Neurol Neurosurg Psychiatry 59:45–49

3. Carr AS, Pelayo-Negro AL, Evans MR et al (2016) A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK. J Neurol Neurosurg Psychiatry 87:620–627

4. Adams D, Sekijima Y, Conceicao I et al (2023) Hereditary transthyretin amyloid neuropathies: advances in pathophysiology, biomarkers, and treatment. Lancet Neurol 22:1061–1074

5. Carroll A, Dyck PJ, de Carvalho M et al (2022) Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis. J Neurol Neurosurg Psychiatry 93:668–678

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