The tip of the iceberg in ATTRv: when to start carrier monitoring and when to initiate treatment?
Author:
Publisher
BMJ
Subject
Psychiatry and Mental health,Neurology (clinical),Surgery
Reference5 articles.
1. Beauvais D , Labeyrie C , Cauquil C , et al . Detailed clinical, physiological and pathological Phenotyping can impact access to disease-modifying treatments in ATTR carriers. J Neurol Neurosurg Psychiatry 2023. doi:10.1136/jnnp-2023-332180
2. Early diagnosis of ATTR Amyloidosis through targeted follow-up of identified carriers of TTR gene mutations;Conceição;Amyloid,2019
3. Recommendations for Presymptomatic genetic testing and management of individuals at risk for hereditary Transthyretin Amyloidosis;Obici;Curr Opin Neurol,2016
4. Romano A , Guglielmino V , Bisogni G , et al . Early detection of nerve involvement in Presymptomatic TTR Mutation carriers: exploring potential markers of disease onset. Neurol Sci November 8, 2023. doi:10.1007/s10072-023-07177-x
5. Romano A , Primiano G , Antonini G , et al . Serum Neurofilament light chain: a promising early diagnostic biomarker for hereditary Transthyretin Amyloidosis Eur J Neurol September 19, 2023. doi:10.1111/ene.16070
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