Neurological Manifestations in ATTRv Amyloidosis
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-17759-0_2
Reference45 articles.
1. Benson MD, Buxbaum JN, Eisemberg DS, Mrlini G et al. Amyloid nomenclature 2018: Recommendations by the International Society of Amyloidosis (ISA) nomenclature committee. Amyloid. https://doi.org/10.1080/13506129.2018.1549825.
2. Benson MD, Waddington-Cruz M, Berk JL, et al. Inotersen treatment for patients with hereditary transthyretin amyloidosis. New Engl J Med. 2018;379:22–31.
3. Pinto MV, Pinto LF, Dias M, et al. Late-onset hereditary ATTR V30 M amyloidosis with polyneuropathy: characterization of Brazilian subjects from the THAOS registry. J Neurol Sci. 2019;403:1–6.
4. Pinto MV, Barreira AA, Bulle AS, de Freitas MRG, et al. Brazilian consensus for diagnosis, management and treatment of transthyretin familial amyloid polyneuropathy. Arq Neuropsiquiatr. 2018;76(9):609–21.
5. Holmgren G, Steen L, Ekstedt J, Groth C-G. Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30). Clin Gen. 1991;40:242–6.
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