References
- Nasr SH, Said SM, Valeri AM, et al. The diagnosis and characteristics of renal heavy-chain and heavy/light-chain amyloidosis and their comparison with renal light-chain amyloidosis. Kidney Int. 2013;83(3):463–470.
- Wechalekar AD, Gillmore JD, Hawkins PN. Systemic amyloidosis. The Lancet. 2016;387(10038):2641–2654.
- Minori K, Satoshi K, Kamijo Y, et al. Muscle training-induced bilateral brachial plexopathy in an adolescent with sporadic hereditary neuropathy with liability to pressure palsies. Brain Behav. 2017;7(9):e00783.
- Abe R, Katoh N, Takahashi Y, et al. Distribution of amyloidosis subtypes based on tissue biopsy site – consecutive analysis of 729 patients at a single amyloidosis center in Japan. Pathol Int. 2021;71(1):70–79.
- Kametani F, Haga S. Accumulation of carboxy-terminal fragments of APP increases phosphodiesterase 8B. Neurobiol Aging. 2015;36(2):634–637.