High-resolution ultrasound of peripheral nerves in late-onset hereditary transthyretin amyloidosis with polyneuropathy: similarities and differences with CIDP
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Clinical Neurology,Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-021-05749-3.pdf
Reference29 articles.
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2. Adams D, Koike H, Slama M, Coelho ET (2019) Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease. Nat Rev Neurol 15(7):387–404. https://doi.org/10.1038/s41582-019-0210-4
3. Koike H et al (2004) Pathology of early- vs late-onset TTR Met30 familial amyloid polyneuropathy. Neurology 63(1):129–138. https://doi.org/10.1212/01.WNL.0000132966.36437.12
4. Ando Y et al (2013) Guideline of transthyretin-related hereditary amyloidosis for clinicians. Orphanet J Rare Dis 8(1):31. https://doi.org/10.1186/1750-1172-8-31
5. Plante-Bordeneuve V (2007) Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP) 7
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