Neurological onset in patients with V122I hereditary transthyretin amyloidosis: a glitch in the paradigm
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-023-06977-5.pdf
Reference5 articles.
1. Nehashi T, Oikawa M, Amami K et al (2019) Sporadic cardiac amyloidosis by amyloidogenic transthyretin V122I variant. Int Heart J 60(6):1441–1443. https://doi.org/10.1536/ihj.19-134
2. Dharmarajan K, Maurer MS (2012) Transthyretin cardiac amyloidoses in older North Americans. J Am Geriatr Soc 60(4):765–774. https://doi.org/10.1111/j.1532-5415.2011.03868.x
3. Chandrashekar P, Alhuneafat L, Mannello M et al (2021) Prevalence and outcomes of p.Val142Ile TTR amyloidosis cardiomyopathy: a systematic review. Circ Genom Precis Med. 14(5):e003356 https://doi.org/10.1161/CIRCGEN.121.003356
4. Gentile L, Di Bella G, Minutoli F et al (2020) Description of a large cohort of Caucasian patients with V122I ATTRv amyloidosis: neurological and cardiological features. J Peripher Nerv Syst 25(3):273–278. https://doi.org/10.1111/jns.12385
5. Zampino S, Sheikh FH, Vaishnav J et al (2023) Phenotypes associated with the Val122Ile, Leu58His, and Late-Onset Val30Met variants in patients with hereditary transthyretin amyloidosis. Neurology 100(19):e2036–e2044. https://doi.org/10.1212/WNL.0000000000207158
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