Transthyretin-related familial amyloidotic polyneuropathy—Progress in Kumamoto, Japan (1967–2010)—
Author:
Affiliation:
1. Kumamoto University
2. Department of Diagnostic Medicine, Graduate School of Medical Sciences, Kumamoto University
Publisher
Japan Academy
Subject
General Physics and Astronomy,General Agricultural and Biological Sciences,General Medicine
Link
https://www.jstage.jst.go.jp/article/pjab/86/7/86_7_694/_pdf
Reference69 articles.
1. 1) Araki, S. (1984) Type I familial amyloidotic polyneuropathy (Japanese type). Brain Dev. 6, 128–133.
2. 2) Benson, M.D. (1989) Familial amyloidotic polyneuropathy. Trends Neurosci. 12, 88–92.
3. 4) Ando, Y., Araki, S. and Ando, M. (1993) Transthyretin related amyloidosis. Intern. Med. 32, 920–922.
4. 5) Andrade, C. (1952) A peculiar form of peripheral neuropathy: Familial generalized amyloidosis with special involvement of the peripheral nerves. Brain 75, 408–427.
5. 6) Araki, S., Mawatari, S., Ohta, M., Nakajima, A. and Kuroiwa, Y. (1968) Polyneurotic amyloidosis in a Japanese family. Arch. Neurol. 18, 593–602.
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