Page 51 - Read Online
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Page 10 of 11                   Pica et al. Vessel Plus 2022;6:10  https://dx.doi.org/10.20517/2574-1209.2021.81

                   preserved ejection fraction. Eur Heart J 2015;36:2585-94.  DOI  PubMed
               5.       Bennani Smires Y, Victor G, Ribes D, et al. Pilot study for left ventricular imaging phenotype of patients over 65 years old with heart
                   failure and preserved ejection fraction: the high prevalence of amyloid cardiomyopathy. Int J Cardiovasc Imaging 2016;32:1403-13.
                   DOI  PubMed
               6.       Castaño A, Narotsky DL, Hamid N, et al. Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with
                   severe aortic stenosis undergoing transcatheter aortic valve replacement. Eur Heart J 2017;38:2879-87.  DOI  PubMed  PMC
               7.       Ruberg FL, Berk JL. Transthyretin (TTR) cardiac amyloidosis. Circulation 2012;126:1286-300.  DOI  PubMed  PMC
               8.       Sipe JD, Benson MD, Buxbaum JN, et al. Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification
                   International Society of Amyloidosis 2016 Nomenclature Guidelines. Amyloid 2016;23:209-13.  DOI  PubMed
               9.       Pellikka PA, Holmes DR Jr. , Edwards WD, et al. Endomyocardial biopsy in 30 patients with primary amyloidosis and suspected
                   cardiac involvement. Arch Intern Med 1988;148:662-6.  PubMed
               10.      Dorbala S, Ando Y, Bokhari S, et al. ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for
                   multimodality imaging in cardiac amyloidosis: part 2 of 2-diagnostic criteria and appropriate utilization. J Card Fail 2019;25:854-65.
                   DOI  PubMed
               11.      Gillmore JD, Maurer MS, Falk RH, et al. Nonbiopsy diagnosis of cardiac transthyretin amyloidosis. Circulation 2016;133:2404-12.
                   DOI  PubMed
               12.      Hamer JP, Janssen S, van Rijswijk MH, Lie KI. Amyloid cardiomyopathy in systemic non-hereditary amyloidosis. Clinical,
                   echocardiographic and electrocardiographic findings in 30 patients with AA and 24 patients with AL amyloidosis. Eur Heart J
                   1992;13:623-7.  DOI  PubMed
               13.      Quarta CC, Solomon SD, Uraizee I, et al. Left ventricular structure and function in transthyretin-related versus light-chain cardiac
                   amyloidosis. Circulation 2014;129:1840-9.  DOI  PubMed
               14.      Phelan D, Collier P, Thavendiranathan P, et al. Relative apical sparing of longitudinal strain using two-dimensional speckle-tracking
                   echocardiography is both sensitive and specific for the diagnosis of cardiac amyloidosis. Heart 2012;98:1442-8.  DOI  PubMed
               15.      Williams LK, Forero JF, Popovic ZB, et al. Patterns of CMR measured longitudinal strain and its association with late gadolinium
                   enhancement in patients with cardiac amyloidosis and its mimics. J Cardiovasc Magn Reson 2017;19:61.  DOI  PubMed  PMC
                                                                                             99m
               16.      Löfbacka V, Axelsson J, Pilebro B, Suhr OB, Lindqvist P, Sundström T. Cardiac transthyretin amyloidosis   Tc-DPD SPECT
                   correlates with strain echocardiography and biomarkers. Eur J Nucl Med Mol Imaging 2021;48:1822-32.  DOI  PubMed  PMC
               17.      Steen H, Giusca S, Montenbruck M, et al. Left and right ventricular strain using fast strain-encoded cardiovascular magnetic resonance
                   for the diagnostic classification of patients with chronic non-ischemic heart failure due to dilated, hypertrophic cardiomyopathy or
                   cardiac amyloidosis. J Cardiovasc Magn Reson 2021;23:45.  DOI  PubMed  PMC
               18.      Giusca S, Steen H, Montenbruck M, et al. Multi-parametric assessment of left ventricular hypertrophy using late gadolinium
                   enhancement, T1 mapping and strain-encoded cardiovascular magnetic resonance. J Cardiovasc Magn Reson 2021;23:92.  DOI
                   PubMed  PMC
               19.      Maceira AM, Joshi J, Prasad SK, et al. Cardiovascular magnetic resonance in cardiac amyloidosis. Circulation 2005;111:186-93.  DOI
                   PubMed
               20.      Duca F, Kammerlander AA, Panzenböck A, et al. Cardiac magnetic resonance T mapping in cardiac amyloidosis. JACC Cardiovasc
                                                                        1
                   Imaging 2018;11:1924-6.  DOI  PubMed
               21.      Burrage MK, Ferreira VM. Cardiovascular magnetic resonance for the differentiation of left ventricular hypertrophy. Curr Heart Fail
                   Rep 2020;17:192-204.  DOI  PubMed  PMC
               22.      Fontana M, Pica S, Reant P, et al. Prognostic value of late gadolinium enhancement cardiovascular magnetic resonance in cardiac
                   amyloidosis. Circulation 2015;132:1570-9.  DOI  PubMed  PMC
               23.      Zhao L, Tian Z, Fang Q. Diagnostic accuracy of cardiovascular magnetic resonance for patients with suspected cardiac amyloidosis: a
                   systematic review and meta-analysis. BMC Cardiovasc Disord 2016;16:129.  DOI  PubMed  PMC
               24.      Syed IS, Glockner JF, Feng D, et al. Role of cardiac magnetic resonance imaging in the detection of cardiac amyloidosis. JACC
                   Cardiovasc Imaging 2010;3:155-64.  DOI  PubMed
               25.      Martinez-Naharro A, Treibel TA, Abdel-Gadir A, et al. Magnetic resonance in transthyretin cardiac amyloidosis. J Am Coll Cardiol
                   2017;70:466-77.  DOI  PubMed
               26.      Sado DM, White SK, Piechnik SK, et al. Identification and assessment of Anderson-Fabry disease by cardiovascular magnetic
                   resonance noncontrast myocardial T1 mapping. Circ Cardiovasc Imaging 2013;6:392-8.  DOI  PubMed
               27.      Sado DM, Flett AS, Banypersad SM, et al. Cardiovascular magnetic resonance measurement of myocardial extracellular volume in
                   health and disease. Heart 2012;98:1436-41.  DOI  PubMed
               28.      Karamitsos TD, Piechnik SK, Banypersad SM, et al. Noncontrast T1 mapping for the diagnosis of cardiac amyloidosis. JACC
                   Cardiovasc Imaging 2013;6:488-97.  DOI  PubMed
               29.      Fontana M, Banypersad SM, Treibel TA, et al. Native T1 mapping in transthyretin amyloidosis. JACC Cardiovasc Imaging
                   2014;7:157-65.  DOI  PubMed
               30.      Baggiano A, Boldrini M, Martinez-Naharro A, et al. Noncontrast magnetic resonance for the diagnosis of cardiac amyloidosis. JACC
                   Cardiovasc Imaging 2020;13:69-80.  DOI  PubMed
               31.      Banypersad SM, Sado DM, Flett AS, et al. Quantification of myocardial extracellular volume fraction in systemic AL amyloidosis: an
                   equilibrium contrast cardiovascular magnetic resonance study. Circ Cardiovasc Imaging 2013;6:34-9.  DOI  PubMed
               32.      Martinez-Naharro A, Kotecha T, Norrington K, et al. Native T1 and extracellular volume in transthyretin amyloidosis. JACC
                   Cardiovasc Imaging 2019;12:810-9.  DOI  PubMed
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