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Amyloid
The Journal of Protein Folding Disorders
Volume 27, 2020 - Issue 2
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Letters to the Editor

Clinical manifestations in hereditary amyloidosis with the variant Glu54Gln transthyretin: a comment

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Page 144 | Received 23 Nov 2019, Accepted 26 Dec 2019, Published online: 06 Jan 2020

References

  • Jercan A, Badelita S, Draghici M, et al. Clinical manifestations in hereditary amyloidosis with the variant Glu54Gln transthyretin. Amyloid. 2019;26(1):31–32.
  • Torres-Courchoud I, Martínez-Gil R, Aibar-Arregui MA, et al. Cardiac involvement secondary to a familial form of transthyretin amyloidosis resulting from the Glu54Gln mutation. Rev Española Cardiol (Engl Ed). 2017;70(4):297–299.
  • Tantau A, Avram I, Cozma A, et al. Cardiac amyloidosis with gastrointestinal involvement: a case report. Med Ultrason. 2015;17(1):123–125.
  • Benson MD, Buxbaum JN, Eisenberg DS, et al. Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee. Amyloid. 2018;25(4):215–219.

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