Quantitative muscle ultrasound as a disease biomarker in hereditary transthyretin amyloidosis with polyneuropathy
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10072-024-07340-y.pdf
Reference42 articles.
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2. Obi CA, Mostertz WC, Griffin JM, Judge DP (2022) ATTR epidemiology, genetics, and prognostic factors. Methodist Debakey Cardiovasc J 18(2):17–26
3. Luigetti M, Romano A, Di Paolantonio A, Bisogni G, Sabatelli M (2020) Diagnosis and treatment of hereditary transthyretin amyloidosis (hATTR) polyneuropathy: current perspectives on improving patient care. Ther Clin Risk Manag 16:109–123
4. Low SC, Md Sari NA, Tan CY et al (2021) Hereditary transthyretin amyloidosis in multi-ethnic Malaysians. Neuromuscul Disord 31(7):642–650
5. Adams D, Ando Y, Beirao JM et al (2021) Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy. J Neurol 268(6):2109–2122
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