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Letters

Establishment of a diagnostic center for amyloidosis in Japan by Kumamoto University

, , , , , , & show all
Pages 169-170 | Received 24 Jan 2017, Accepted 13 Feb 2017, Published online: 22 Apr 2017

References

  • Okumura K, Yamashita T, Masuda T, Misumi Y, Ueda A, Ueda M, Obayashi K, et al. Long-term outcome of patients with hereditary transthyretin V30M amyloidosis with polyneuropathy after liver transplantation. Amyloid 2016;23:39–45
  • Obayashi K, Misumi Y, Watanabe T, Ando T, Akagami T, Tasaki M, Shinriki S, et al. Dominant cardiac type of familial amyloidotic polyneuropathy associated with a novel transthyretin variant Thr59Arg. Muscle Nerve 2013;48:839–41
  • Misumi Y, Doki T, Ueda M, Obayashi K, Tasaki M, Tamura A, Ando Y. Myopathic phenotype of familial amyloid polyneuropathy with a rare transthyretin variant: ATTR Ala45Asp. Amyloid 2014;21:216–7
  • Yamashita T, Ueda M, Saga N, Nanto K, Tasaki M, Masuda T, Misumi Y, et al. Hereditary amyloidosis with cardiomyopathy caused by the novel variant transthyretin A36D. Amyloid 2016;23:207–8

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