Hereditary systemic transthyretin amyloidosis: a clinical case and an opinion on the problem-Reference-Cited by-同舟云学术

Hereditary systemic transthyretin amyloidosis: a clinical case and an opinion on the problem

Published:2019-07-08 Issue:6 Volume: Page:136-142
ISSN:2618-7620
Container-title:Russian Journal of Cardiology
language:
Short-container-title:Russ J Cardiol

Author:

Draganova A. S.¹^ORCID,Soboleva A. V.¹^ORCID,Ertman A. E.¹^ORCID,Galanskaya T. A.²^ORCID,Nikolaychuk E. I.¹^ORCID,Ryzhkova D. V.²^ORCID,Polyakova E. A.¹^ORCID,Shlyakhto E. V.¹^ORCID

Affiliation:

1. I. P. Pavlov First State Medical University of St. Petersburg; V. A. Almazov National Medical Research Center

2. V. A. Almazov National Medical Research Center

Publisher

Silicea - Poligraf, LLC

Subject

Cardiology and Cardiovascular Medicine

Reference15 articles.

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2. White JA, Fine NM. Recent Advances in Cardiovascular Imaging Relevant to the Management of Patients with Suspected Cardiac Amyloidosis. Curr Cardiol Rep. 2016 Aug; 18 (8):77 doi:10.1007/s11886-016-0752-7.

3. Myasnikov RP, Andreenko EYu, Kushunina DV, et al. Amyloidosis of the heart: modern aspects of diagnosis and treatment (clinical observation). Clin. Experiment. Surg. Petrovsky J. 2014;4:72-82. (In Russ.)

4. Brunjes DL, Dunlop M, Wu C, et al. Analysis of Skeletal Muscle Torque Capacity and Circulating Ceramides in Patients with Advanced Heart Failure. J Card Fail. 2016 May; 22 (5):347-55. doi:10.1016/j.cardfail.2016.02.002.

5. Johnson SM, Connelly S, Fearns C, et al. The transthyretin amyloidoses: from delineating the molecular mechanism of aggregation linked to pathology to a regulatory-agency approved drug. J Molec Biol. 2012 Aug 10;421 (2-3):185-203. doi:101016/j.jmb.2011.12.060.

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