Diagnosis of cardiac transthyretin amyloidosis based on multimodality imaging
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://link.springer.com/article/10.1007/s00392-017-1092-3/fulltext.html
Reference8 articles.
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2. Gertz MA, Benson MD, Dyck PJ, Grogan M, Coelho T, Cruz M, Berk JL, Plante-Bordeneuve V, Schmidt HH, Merlini G (2015) Diagnosis, prognosis, and therapy of transthyretin amyloidosis. J Am Coll Cardiol 66(21):2451–2466. doi: 10.1016/j.jacc.2015.09.075
3. Mohty D, Pradel S, Magne J, Fadel B, Boulogne C, Petitalot V, Raboukhi S, Darodes N, Damy T, Aboyans V, Jaccard A (2016) Prevalence and prognostic impact of left-sided valve thickening in systemic light-chain amyloidosis. Clin Res Cardiol. doi: 10.1007/s00392-016-1058-x
4. aus dem Siepen F, Buss SJ, Andre F, Seitz S, Giannitsis E, Steen H, Katus HA, Kristen AV (2015) Extracellular remodeling in patients with wild-type amyloidosis consuming epigallocatechin-3-gallate: preliminary results of T1 mapping by cardiac magnetic resonance imaging in a small single center study. Clin Res Cardiol 104(8):640–647. doi: 10.1007/s00392-015-0826-3
5. Kristen AV, Rinn J, Hegenbart U, Lindenmaier D, Merkle C, Rocken C, Hardt S, Giannitsis E, Katus HA (2015) Improvement of risk assessment in systemic light-chain amyloidosis using human placental growth factor. Clin Res Cardiol 104(3):250–257. doi: 10.1007/s00392-014-0779-y
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