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Letters

Epidemiological and clinical characteristics of persons with transthyretin hereditary amyloid polyneuropathy: a global synthesis of 532 cases

, , , , , , , & show all
Pages 109-110 | Received 15 Nov 2016, Accepted 06 Feb 2017, Published online: 22 Apr 2017

References

  • Andrade C. A peculiar form of peripheral neuropathy: familiar atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain. 1952;75:408–27
  • Saraiva MJ, Birken S, Costa PP, Goodman DS. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin). J Clin Invest. 1984;74:104–19
  • Misu KI, Hattori N, Nagamatsu M, Ikeda S, Ando Y, Nakazato M, Takei Y, et al. Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features. Brain. 1999;122:1951–62

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