Neurological onset in patients with V122I hereditary transthyretin amyloidosis: a glitch in the paradigm

被引:0
作者
Francesca Vitali
Maria A. Sciarrone
Angela Romano
Valeria Guglielmino
Marco Luigetti
机构
[1] Università Cattolica del Sacro Cuore,
[2] Dipartimento di Neuroscienze,undefined
[3] Fondazione Policlinico Universitario Agostino Gemelli IRCCS,undefined
[4] UOC Neurologia,undefined
来源
Neurological Sciences | 2023年 / 44卷
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页码:4569 / 4571
页数:2
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Nehashi T(2019)Sporadic cardiac amyloidosis by amyloidogenic transthyretin V122I variant Int Heart J 60 1441-1443
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Oikawa M(2012)Transthyretin cardiac amyloidoses in older North Americans J Am Geriatr Soc 60 765-774
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Amami K(2021)Prevalence and outcomes of p.Val142Ile TTR amyloidosis cardiomyopathy: a systematic review Circ Genom Precis Med. 14 e003356-278
[4]  
Dharmarajan K(2020)Description of a large cohort of Caucasian patients with V122I ATTRv amyloidosis: neurological and cardiological features J Peripher Nerv Syst 25 273-e2044
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Maurer MS(2023)Phenotypes associated with the Val122Ile, Leu58His, and Late-Onset Val30Met variants in patients with hereditary transthyretin amyloidosis Neurology 100 e2036-undefined
[6]  
Chandrashekar P(undefined)undefined undefined undefined undefined-undefined
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Alhuneafat L(undefined)undefined undefined undefined undefined-undefined
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Mannello M(undefined)undefined undefined undefined undefined-undefined
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