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

Response: concerning “late early and late onset” ATTR Val30Met patients

Page 250 | Received 20 Jun 2019, Accepted 08 Jul 2019, Published online: 26 Sep 2019

References

  • Suhr OB. Commentary to Isabel Conceicao et al. early diagnosis through targeted follow-up of identified carriers of TTR gene mutations. Amyloid. 2019;26:1–2.
  • Conceicao 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, Nishi R, Ikeda S, et al. The morphology of amyloid fibrils and their impact on tissue damage in hereditary transthyretin amyloidosis: an ultrastructural study. J Neurol Sci. 2018;394:99–106.
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  • Suhr OB, Wixner J, Anan I, et al. Amyloid fibril composition within hereditary Val30Met (p. Val50Met) transthyretin amyloidosis families. PLoS One. 2019;14:e0211983.
  • Coutinho MCA, Cortez-Dias N, Goncalves 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.
  • Arvidsson S, Pilebro B, Westermark P, et al. Amyloid cardiomyopathy in hereditary transthyretin V30M amyloidosis—impact of sex and amyloid fibril composition. PLoS One. 2015;10:e0143456.

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