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Amyloid
The Journal of Protein Folding Disorders
Volume 26, 2019 - Issue 4
69
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Commentary

Response: Suhr OB: commentary to Isabel Conceição et al. early diagnosis through targeted follow-up of identified carriers of TTR gene mutations

Pages 248-249 | Received 21 May 2019, Accepted 08 Jul 2019, Published online: 31 Jul 2019

References

  • Suhr OB, Wixner J, Anan I, et al. Amyloid fibril composition within hereditary Val30Met (p. Val50Met) transthyretin amyloidosis families. PLoS One. 2019;14:e0211983.
  • Conceição I, Damy T, Romero M, et al. Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations. Amyloid. 2019;26:3–9.
  • Koike H, Misu K, Ikeda S, et al. Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form. Arch Neurol. 2002;59:1771–1776.
  • Koike H, Misu K, Sugiura M, et al. Pathology of early- vs late-onset TTR Met30 familial amyloid polyneuropathy. Neurology. 2004;63:129–138.
  • Ihse E, Ybo A, Suhr O, et al. Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis. J Pathol. 2008;216:253–261.
  • Pilebro B, Suhr OB, Näslund U, et al. (99m)Tc-DPD uptake reflects amyloid fibril composition in hereditary transthyretin amyloidosis. Ups J Med Sci. 2016;121:17–24.
  • Coutinho MCA, Cortez-Dias N, Gonçalves S, et al. How useful is 99mTc-DPD scintigraphy in diagnosis of cardiac amyloidosis in transthyretin V30M familial amyloid polyneuropathy? J Am Coll Cardiol. 2017;69:1423.

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