Neurological Manifestations in AL and Wild-Type ATTR Amyloidosis
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-17759-0_3
Reference14 articles.
1. Gertz MA, Dispenzieri A. Systemic amyloidosis recognition, prognosis, and therapy: a systematic review. JAMA. 2020;324(1):79–89. https://doi.org/10.1001/jama.2020.5493.
2. Kaku M, Berk JL. Neuropathy associated with systemic amyloidosis. Semin Neurol. 2019;39(5):578–88. https://doi.org/10.1055/s-0039-1688994. Epub 2019 Oct 22.
3. Zivkovic S, Soman P, Lacomis D. Late-onset peripheral neuropathy in patients with wild type transthyretin amyloidosis (wtATTR). Amyloid. 2020;27(2):142–3. https://doi.org/10.1080/13506129.2019.1697224. Epub 2019 Nov 29.
4. Kharoubi M, Roche F, Bézard M, Hupin D, Silva S, Oghina S, Chalard C, Zaroui A, Galat A, Guendouz S, Canoui-Poitrine F, Hittinger L, Teiger E, Lefaucheur JP, Damy T. Prevalence and prognostic value of autonomic neuropathy assessed by Sudoscan® in transthyretin wild-type cardiac amyloidosis. ESC Heart Fail. 2021;8(2):1656–65. https://doi.org/10.1002/ehf2.13131. Epub 2020 Dec 22.
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