Vutrisiran: a new drug in the treatment landscape of hereditary transthyretin amyloid polyneuropathy
Author:
Affiliation:
1. Department of Neurology, Henri Mondor University Hospital, AP-HP, Créteil, France
2. Mondor Biomedical Research Institute – IMRB, INSERM, U955 Team 10 “Biology of the Neuromuscular System”, Créteil, France
Publisher
Informa UK Limited
Link
https://www.tandfonline.com/doi/pdf/10.1080/17460441.2024.2306843
Reference62 articles.
1. Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis
2. Transthyretin familial amyloid polyneuropathy: an update
3. A multicentric study of the disease risks and first manifestations in hereditary transthyretin amyloidosis (ATTRv): insights for an earlier diagnosis
4. Genotype–phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France
5. Transthyretin cardiac amyloidosis
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1. A mini review of Patisiran's efficacy in the management of transthyretin cardiac amyloidosis;Discover Medicine;2024-09-12
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