-
1
-
-
0042709605
-
Molecular mechanisms of amyloidosis
-
Merlini G, Bellotti V. Molecular mechanisms of amyloidosis. N Engl J Med 2003; 349:583-596
-
(2003)
N Engl J Med
, vol.349
, pp. 583-596
-
-
Merlini, G.1
Bellotti, V.2
-
2
-
-
84942042128
-
Therapeutic clearance of amyloid by antibodies to serum amyloid P component
-
Richards DB, Cookson LM, Berges AC, et al. Therapeutic clearance of amyloid by antibodies to serum amyloid P component. N Engl J Med 2015; 373:1106-1114
-
(2015)
N Engl J Med
, vol.373
, pp. 1106-1114
-
-
Richards, D.B.1
Cookson, L.M.2
Berges, A.C.3
-
3
-
-
84908547666
-
Nomenclature 2014: amyloid fibril proteins and clinical classification of the amyloidosis
-
Sipe JD, Benson MD, Buxbaum JN, et al. Nomenclature 2014: amyloid fibril proteins and clinical classification of the amyloidosis. Amyloid 2014; 21:221-224
-
(2014)
Amyloid
, vol.21
, pp. 221-224
-
-
Sipe, J.D.1
Benson, M.D.2
Buxbaum, J.N.3
-
4
-
-
84946480373
-
Cardiac amyloidosis: pathology, nomenclature, and typing
-
Maleszewski JJ. Cardiac amyloidosis: pathology, nomenclature, and typing. Cardiovasc Pathol 2015; 24:343-350
-
(2015)
Cardiovasc Pathol
, vol.24
, pp. 343-350
-
-
Maleszewski, J.J.1
-
5
-
-
0026519157
-
Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989
-
Kyle RA, Linos A, Beard CM, et al. Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989. Blood 1992; 79:1817-1822
-
(1992)
Blood
, vol.79
, pp. 1817-1822
-
-
Kyle, R.A.1
Linos, A.2
Beard, C.M.3
-
6
-
-
84920639910
-
Light chain amyloidosis: Experience in a tertiary hospital: 2005-2013
-
Krsnik I, Cabero M, Morillo D, et al. Light chain amyloidosis: Experience in a tertiary hospital: 2005-2013. Rev Clin Esp 2015; 215:1-8
-
(2015)
Rev Clin Esp
, vol.215
, pp. 1-8
-
-
Krsnik, I.1
Cabero, M.2
Morillo, D.3
-
7
-
-
0031913337
-
The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement
-
Dubrey SW, Cha K, Anderson J, et al. The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement. QJM 1998; 91:141-157
-
(1998)
QJM
, vol.91
, pp. 141-157
-
-
Dubrey, S.W.1
Cha, K.2
Anderson, J.3
-
8
-
-
84994210566
-
Efficacy of chemotherapy for light-chain amyloidosis in patients presenting with symptomatic heart failure
-
Sperry BW, Ikram A, Hachamovitch R, et al. Efficacy of chemotherapy for light-chain amyloidosis in patients presenting with symptomatic heart failure. J Am Coll Cardiol 2016; 67:2941-2948
-
(2016)
J Am Coll Cardiol
, vol.67
, pp. 2941-2948
-
-
Sperry, B.W.1
Ikram, A.2
Hachamovitch, R.3
-
9
-
-
85052319616
-
A new staging system for cardiac transthyretin amyloidosis
-
Oct 18. [Epub ahead of print]
-
Gillmore JD, Damy T, Fontana M, et al. A new staging system for cardiac transthyretin amyloidosis. Eur Heart J 2017; Oct 18. [Epub ahead of print] doi:10.1093/eurheartj/ehx589
-
(2017)
Eur Heart J
-
-
Gillmore, J.D.1
Damy, T.2
Fontana, M.3
-
10
-
-
41649088603
-
Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study
-
Tanskanen M, Peuralinna T, Polvikoski T, et al. Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study. Ann Med 2008; 40:232-239
-
(2008)
Ann Med
, vol.40
, pp. 232-239
-
-
Tanskanen, M.1
Peuralinna, T.2
Polvikoski, T.3
-
11
-
-
84947715741
-
Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction
-
González-López E, Gallego-Delgado M, Guzzo-Merello G, et al. Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction. Eur Heart J 2015; 36:2585-2594
-
(2015)
Eur Heart J
, vol.36
, pp. 2585-2594
-
-
González-López, E.1
Gallego-Delgado, M.2
Guzzo-Merello, G.3
-
12
-
-
84960087272
-
Coexistence of degenerative aortic stenosis and wild-type transthyretin-related cardiac amyloidosis
-
Longhi S, Lorenzini M, Gagliardi C, et al. Coexistence of degenerative aortic stenosis and wild-type transthyretin-related cardiac amyloidosis. JACC Cardiovasc Imaging 2016;9:325-327
-
(2016)
JACC Cardiovasc Imaging
, vol.9
, pp. 325-327
-
-
Longhi, S.1
Lorenzini, M.2
Gagliardi, C.3
-
13
-
-
84994501751
-
Natural history of wild-type transthyretin cardiac amyloidosis and risk stratification using a novel staging system
-
Grogan M, Scott CG, Kyle RA, et al. Natural history of wild-type transthyretin cardiac amyloidosis and risk stratification using a novel staging system. J Am Coll Cardiol 2016; 68:1014-1020
-
(2016)
J Am Coll Cardiol
, vol.68
, pp. 1014-1020
-
-
Grogan, M.1
Scott, C.G.2
Kyle, R.A.3
-
14
-
-
84874184208
-
ATTR amyloid in the carpal tunnel ligament is frequently of wildtype transthyretin origin
-
Gioeva Z, Urban P, Meliss RR, et al. ATTR amyloid in the carpal tunnel ligament is frequently of wildtype transthyretin origin. Amyloid 2013; 20:1-6
-
(2013)
Amyloid
, vol.20
, pp. 1-6
-
-
Gioeva, Z.1
Urban, P.2
Meliss, R.R.3
-
15
-
-
84921944204
-
Amyloid deposits derived from transthyretin in the ligamentum flavum as related to lumbar spinal canal stenosis
-
Yanagisawa A, Ueda M, Sueyoshi T, et al. Amyloid deposits derived from transthyretin in the ligamentum flavum as related to lumbar spinal canal stenosis. Mod Pathol 2015; 28:201-207
-
(2015)
Mod Pathol
, vol.28
, pp. 201-207
-
-
Yanagisawa, A.1
Ueda, M.2
Sueyoshi, T.3
-
16
-
-
85025116505
-
Cardiac amyloidosis: an update on pathophysiology, diagnosis, and treatment
-
Jul 13 [Epub ahead of print] 10.1016/j.tcm.2017.07.004
-
Siddiqi OK, Ruberg FL. Cardiac amyloidosis: an update on pathophysiology, diagnosis, and treatment. Trends Cardiovasc Med 2017; Jul 13 [Epub ahead of print] doi:10.1016/j.tcm.2017.07.004
-
(2017)
Trends Cardiovasc Med
-
-
Siddiqi, O.K.1
Ruberg, F.L.2
-
17
-
-
84959213056
-
Carpal tunnel syndrome: A common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis
-
Nakagawa M, Sekijima Y, Yazaki M, et al. Carpal tunnel syndrome: A common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis. Amyloid 2016; 23:58-63
-
(2016)
Amyloid
, vol.23
, pp. 58-63
-
-
Nakagawa, M.1
Sekijima, Y.2
Yazaki, M.3
-
18
-
-
84874150891
-
Familial Transthyretin Amyloidosis
-
In: Adam MP, Ardinger HH, Pagon RA, et al, eds. Seattle, WA: University of Washington, Seattle; 1993-2017. Updated January 26, 2012. Accessed November 16, 2017
-
Sekijima Y, Yoshida K, Tokuda T, Ikeda S-I. Familial Transthyretin Amyloidosis. In: Adam MP, Ardinger HH, Pagon RA, et al, eds. Seattle, WA: University of Washington, Seattle; 1993-2017. Available at: https://www-ncbi-nlm-nih-gov.ccmain.ohionet.org/books/NBK1194/. Updated January 26, 2012. Accessed November 16, 2017
-
-
-
Sekijima, Y.1
Yoshida, K.2
Tokuda, T.3
Ikeda, S.-I.4
-
19
-
-
33646072452
-
Transthyretin V122I in African Americans with congestive heart failure
-
Buxbaum J, Jacobson DR, Tagoe C, et al. Transthyretin V122I in African Americans with congestive heart failure. J Am Coll Cardiol 2006; 47:1724-1725
-
(2006)
J Am Coll Cardiol
, vol.47
, pp. 1724-1725
-
-
Buxbaum, J.1
Jacobson, D.R.2
Tagoe, C.3
-
20
-
-
84864674714
-
Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: The Transthyretin Amyloidosis Cardiac Study (TRACS)
-
Ruberg FL, Maurer MS, Judge DP, et al. Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: The Transthyretin Amyloidosis Cardiac Study (TRACS). Am Heart J 2012; 164:222-228.e1
-
(2012)
Am Heart J
, vol.164
, pp. 222.e1-228.e1
-
-
Ruberg, F.L.1
Maurer, M.S.2
Judge, D.P.3
-
21
-
-
0016612761
-
Amyloid in the aged heart: frequency and clinical significance
-
Wright JR, Calkins E. Amyloid in the aged heart: frequency and clinical significance. J Am Geriatr Soc 1975; 23:97-103
-
(1975)
J Am Geriatr Soc
, vol.23
, pp. 97-103
-
-
Wright, J.R.1
Calkins, E.2
-
22
-
-
85018310768
-
Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy
-
Vermeer AMC, Janssen A, Boorsma PC, Mannens MMAM, Wilde AAM, Christiaans I. Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy. Amyloid 2017; 24:87-91
-
(2017)
Amyloid
, vol.24
, pp. 87-91
-
-
Vermeer, A.M.C.1
Janssen, A.2
Boorsma, P.C.3
Mannens, M.M.A.M.4
Wilde, A.A.M.5
Christiaans, I.6
-
23
-
-
65749114621
-
Syncope cardiomyopathy in a patient with primary AL-type amyloid heart disease
-
Velazquez-Ceceña JL, Lubell DL, Nagajothi N, Al-Masri H, Siddiqui M, Khosla S. Syncope cardiomyopathy in a patient with primary AL-type amyloid heart disease. Tex Heart Inst J 2009; 36:50-54
-
(2009)
Tex Heart Inst J
, vol.36
, pp. 50-54
-
-
Velazquez-Ceceña, J.L.1
Lubell, D.L.2
Nagajothi, N.3
Al-Masri, H.4
Siddiqui, M.5
Khosla, S.6
-
24
-
-
84906070146
-
Left ventricular hypertrophy in a runner: things are not always what they seem
-
Stegman BM, Kwon D, Rodriguez ER, Hanna M, Cho L. Left ventricular hypertrophy in a runner: things are not always what they seem. Circulation 2014; 130:590-592
-
(2014)
Circulation
, vol.130
, pp. 590-592
-
-
Stegman, B.M.1
Kwon, D.2
Rodriguez, E.R.3
Hanna, M.4
Cho, L.5
-
25
-
-
3042729932
-
Endomyocardial biopsy plays a role in diagnosing patients with unexplained cardiomyopathy
-
Ardehali H, Qasim A, Cappola T, et al. Endomyocardial biopsy plays a role in diagnosing patients with unexplained cardiomyopathy. Am Heart J 2004; 147:919-923
-
(2004)
Am Heart J
, vol.147
, pp. 919-923
-
-
Ardehali, H.1
Qasim, A.2
Cappola, T.3
-
26
-
-
0038443824
-
Endothelial dysfunction precedes C-fiber abnormalities in primary (AL) amyloidosis
-
Berghoff M, Kathpal M, Khan F, Skinner M, Falk R, Freeman R. Endothelial dysfunction precedes C-fiber abnormalities in primary (AL) amyloidosis. Ann Neurol 2003; 53:725-730
-
(2003)
Ann Neurol
, vol.53
, pp. 725-730
-
-
Berghoff, M.1
Kathpal, M.2
Khan, F.3
Skinner, M.4
Falk, R.5
Freeman, R.6
-
29
-
-
84940043917
-
Atrial fibrillation in amyloidotic cardiomyopathy: prevalence, incidence, risk factors and prognostic role
-
Longhi S, Quarta CC, Milandri A, et al. Atrial fibrillation in amyloidotic cardiomyopathy: prevalence, incidence, risk factors and prognostic role. Amyloid 2015; 22:147-155
-
(2015)
Amyloid
, vol.22
, pp. 147-155
-
-
Longhi, S.1
Quarta, C.C.2
Milandri, A.3
-
30
-
-
84966318554
-
Are classic predictors of voltage valid in cardiac amyloidosis? A contemporary analysis of electrocardiographic findings
-
Sperry BW, Vranian MN, Hachamovitch R, et al. Are classic predictors of voltage valid in cardiac amyloidosis? A contemporary analysis of electrocardiographic findings. Int J Cardiol 2016; 214:477-481
-
(2016)
Int J Cardiol
, vol.214
, pp. 477-481
-
-
Sperry, B.W.1
Vranian, M.N.2
Hachamovitch, R.3
-
31
-
-
25444434458
-
Diagnosis and management of the cardiac amyloidoses
-
Falk RH. Diagnosis and management of the cardiac amyloidoses. Circulation 2005; 112:2047-2060
-
(2005)
Circulation
, vol.112
, pp. 2047-2060
-
-
Falk, R.H.1
-
32
-
-
0141465219
-
Persistent pleural effusions in primary systemic amyloidosis: etiology and prognosis
-
Berk JL, Keane J, Seldin DC, et al. Persistent pleural effusions in primary systemic amyloidosis: etiology and prognosis. Chest 2003; 124:969-977
-
(2003)
Chest
, vol.124
, pp. 969-977
-
-
Berk, J.L.1
Keane, J.2
Seldin, D.C.3
-
33
-
-
0036703121
-
Amyloidosis of epicardial and intramural coronary arteries as an unusual cause of myocardial infarction and refractory angina pectoris
-
Miani D, Rocco M, Alberti E, Spedicato L, Fioretti PM. Amyloidosis of epicardial and intramural coronary arteries as an unusual cause of myocardial infarction and refractory angina pectoris. Ital Heart J 2002; 3:479-482
-
(2002)
Ital Heart J
, vol.3
, pp. 479-482
-
-
Miani, D.1
Rocco, M.2
Alberti, E.3
Spedicato, L.4
Fioretti, P.M.5
-
34
-
-
85032888606
-
Cardiac amyloidosis and its new clinical phenotype: heart failure with preserved ejection fraction
-
Mesquita ET, Jorge AJL, Souza CV Junior, Andrade TR. Cardiac amyloidosis and its new clinical phenotype: heart failure with preserved ejection fraction. Arg Bras Cardiol 2017; 109:71-80
-
(2017)
Arg Bras Cardiol
, vol.109
, pp. 71-80
-
-
Mesquita, E.T.1
Jorge, A.J.L.2
Souza, C.V.3
Andrade, T.R.4
-
35
-
-
0017379739
-
Systolic and diastolic ventricular function in cardiac amyloidosis: studies in six cases diagnosed with endomyocardial biopsy
-
Swanton RH, Brooksby IAB, Davies MJ, Coltart DJ, Jenkins BS, Webb-Peploe MM. Systolic and diastolic ventricular function in cardiac amyloidosis: studies in six cases diagnosed with endomyocardial biopsy. Am J Cardiol 1977; 39:658-664
-
(1977)
Am J Cardiol
, vol.39
, pp. 658-664
-
-
Swanton, R.H.1
Brooksby, I.A.B.2
Davies, M.J.3
Coltart, D.J.4
Jenkins, B.S.5
Webb-Peploe, M.M.6
-
36
-
-
0019469735
-
Left ventricular filling in differentiating restrictive amyloid cardiomyopathy and constrictive pericarditis
-
Tyberg TI, Goodyer AVN, Hurst VW 3rd, Alexander J, Langou RA. Left ventricular filling in differentiating restrictive amyloid cardiomyopathy and constrictive pericarditis. Am J Cardiol 1981; 47:791-796
-
(1981)
Am J Cardiol
, vol.47
, pp. 791-796
-
-
Tyberg, T.I.1
Goodyer, A.V.N.2
Hurst, V.W.3
Alexander, J.4
Langou, R.A.5
-
37
-
-
84963632056
-
Recognizing transthyretin cardiac amyloidosis in patients with aortic stenosis: impact on prognosis
-
Sperry BW, Jones BM, Vranian MN, Hanna M, Jaber WA. Recognizing transthyretin cardiac amyloidosis in patients with aortic stenosis: impact on prognosis. JACC Cardiovasc Imaging 2016; 9:904-906
-
(2016)
JACC Cardiovasc Imaging
, vol.9
, pp. 904-906
-
-
Sperry, B.W.1
Jones, B.M.2
Vranian, M.N.3
Hanna, M.4
Jaber, W.A.5
-
38
-
-
84909619368
-
Prevalence and prognostic significance of low QRS voltage among the three main types of cardiac amyloidosis
-
Cyrille NB, Goldsmith J, Alvarez J, Maurer MS. Prevalence and prognostic significance of low QRS voltage among the three main types of cardiac amyloidosis. Am J Cardiol 2014; 114:1089-1093
-
(2014)
Am J Cardiol
, vol.114
, pp. 1089-1093
-
-
Cyrille, N.B.1
Goldsmith, J.2
Alvarez, J.3
Maurer, M.S.4
-
39
-
-
0034177317
-
Comparison of electrocardiographic findings in patients with AL (primary) amyloidosis and in familial amyloid polyneuropathy and anginal pain and their relation to histopathologic findings
-
Hongo M, Yamamoto H, Kohda T, et al. Comparison of electrocardiographic findings in patients with AL (primary) amyloidosis and in familial amyloid polyneuropathy and anginal pain and their relation to histopathologic findings. Am J Cardiol 2000; 85:849-853
-
(2000)
Am J Cardiol
, vol.85
, pp. 849-853
-
-
Hongo, M.1
Yamamoto, H.2
Kohda, T.3
-
40
-
-
85017002282
-
Addressing common questions encountered in the diagnosis and management of cardiac amyloidosis
-
Maurer MS, Elliott P, Comenzo R, Semigran M, Rapezzi C. Addressing common questions encountered in the diagnosis and management of cardiac amyloidosis. Circulation 2017; 135:1357-1377
-
(2017)
Circulation
, vol.135
, pp. 1357-1377
-
-
Maurer, M.S.1
Elliott, P.2
Comenzo, R.3
Semigran, M.4
Rapezzi, C.5
-
41
-
-
0032415798
-
Duration of pulmonary venous atrial reversal flow velocity and mitral inflow a wave: new measure of severity of cardiac amyloidosis
-
Abdalla I, Murray RD, Lee JC, Stewart WJ, Tajik AJ, Klein AL. Duration of pulmonary venous atrial reversal flow velocity and mitral inflow a wave: new measure of severity of cardiac amyloidosis. J Am Soc Echocardiogr 1998; 11:1125-1133
-
(1998)
J Am Soc Echocardiogr
, vol.11
, pp. 1125-1133
-
-
Abdalla, I.1
Murray, R.D.2
Lee, J.C.3
Stewart, W.J.4
Tajik, A.J.5
Klein, A.L.6
-
42
-
-
84967240038
-
Nonbiopsy diagnosis of cardiac transthyretin amyloidosis
-
Gillmore JD, Maurer MS, Falk RH, et al. Nonbiopsy diagnosis of cardiac transthyretin amyloidosis. Circulation 2016; 133:2404-2412
-
(2016)
Circulation
, vol.133
, pp. 2404-2412
-
-
Gillmore, J.D.1
Maurer, M.S.2
Falk, R.H.3
-
43
-
-
84983086778
-
Immunoglobulin light chain amyloidosis: 2016 update on diagnosis, prognosis, and treatment
-
Gertz MA. Immunoglobulin light chain amyloidosis: 2016 update on diagnosis, prognosis, and treatment. Am J Hematol 2016; 91:947-956
-
(2016)
Am J Hematol
, vol.91
, pp. 947-956
-
-
Gertz, M.A.1
-
44
-
-
84930918406
-
Cardiac amyloidosis: where are we today?
-
Patel KS, Hawkins PN. Cardiac amyloidosis: where are we today? J Intern Med 2015; 278:126-144
-
(2015)
J Intern Med
, vol.278
, pp. 126-144
-
-
Patel, K.S.1
Hawkins, P.N.2
-
45
-
-
85014424348
-
Current concepts of cardiac amyloidosis: diagnosis, clinical management, and the need for collaboration
-
Ritts AJ, Cornell RF, Swiger K, Singh J, Goodman S, Lenihan DJ. Current concepts of cardiac amyloidosis: diagnosis, clinical management, and the need for collaboration. Heart Fail Clin 2017; 13:409-416
-
(2017)
Heart Fail Clin
, vol.13
, pp. 409-416
-
-
Ritts, A.J.1
Cornell, R.F.2
Swiger, K.3
Singh, J.4
Goodman, S.5
Lenihan, D.J.6
-
46
-
-
84998667464
-
Subtype-specific interactions and prognosis in cardiac amyloidosis
-
Sperry BW, Vranian MN, Hachamovitch R, et al. Subtype-specific interactions and prognosis in cardiac amyloidosis. J Am Heart Assoc 2016; 5:e002877
-
(2016)
J Am Heart Assoc
, vol.5
-
-
Sperry, B.W.1
Vranian, M.N.2
Hachamovitch, R.3
-
47
-
-
84860643971
-
Revised prognostic staging system for light chain amyloidosis incorporating cardiac biomarkers and serum free light chain measurements
-
Kumar S, Dispenzieri A, Lacy MQ, et al. Revised prognostic staging system for light chain amyloidosis incorporating cardiac biomarkers and serum free light chain measurements. J Clin Oncol 2012; 30:989-995
-
(2012)
J Clin Oncol
, vol.30
, pp. 989-995
-
-
Kumar, S.1
Dispenzieri, A.2
Lacy, M.Q.3
-
48
-
-
84866137457
-
Relative apical sparing of longitudinal strain using two-dimensional speckle-tracking echocardiography is both sensitive and specific for the diagnosis of cardiac amyloidosis
-
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; 98:1442-1448
-
(2012)
Heart
, vol.98
, pp. 1442-1448
-
-
Phelan, D.1
Collier, P.2
Thavendiranathan, P.3
-
49
-
-
85030834953
-
Role of cardiac magnetic resonance in the diagnosis and prognosis of nonischemic cardiomyopathy
-
Patel AR, Kramer CM. Role of cardiac magnetic resonance in the diagnosis and prognosis of nonischemic cardiomyopathy. JACC Cardiovasc Imaging 2017; 10(10 Pt A):1180-1193
-
(2017)
JACC Cardiovasc Imaging
, vol.10
, Issue.10
, pp. 1180-1193
-
-
Patel, A.R.1
Kramer, C.M.2
-
50
-
-
84893860072
-
CMR imaging with rapid visual T1 assessment predicts mortality in patients suspected of cardiac amyloidosis
-
White JA, Kim HW, Shah D, et al. CMR imaging with rapid visual T1 assessment predicts mortality in patients suspected of cardiac amyloidosis. JACC Cardiovasc Imaging 2014; 7:143-156
-
(2014)
JACC Cardiovasc Imaging
, vol.7
, pp. 143-156
-
-
White, J.A.1
Kim, H.W.2
Shah, D.3
-
51
-
-
0016276201
-
A new method for radionuclide imaging of acute myocardial infarction in humans
-
Parkey RW, Bonte FJ, Meyer SL, et al. A new method for radionuclide imaging of acute myocardial infarction in humans. Circulation 1974; 50:540-546
-
(1974)
Circulation
, vol.50
, pp. 540-546
-
-
Parkey, R.W.1
Bonte, F.J.2
Meyer, S.L.3
-
52
-
-
0020351110
-
Value of positive myocardial technetium-99m-pyrophosphate scintigraphy in the noninvasive diagnosis of cardiac amyloidosis
-
Wizenberg TA, Muz J, Sohn YH, Samlowski W, Weissler AM. Value of positive myocardial technetium-99m-pyrophosphate scintigraphy in the noninvasive diagnosis of cardiac amyloidosis. Am Heart J 1982; 103(4 Pt 1):468-473
-
(1982)
Am Heart J
, vol.103
, Issue.4
, pp. 468-473
-
-
Wizenberg, T.A.1
Muz, J.2
Sohn, Y.H.3
Samlowski, W.4
Weissler, A.M.5
-
53
-
-
84877325205
-
99mTc-Pyrophosphate scintigraphy for differentiating light-chain cardiac amyloidosis from the transthyretin-related familial and senile cardiac amyloidoses
-
Bokhari S, Castaño A, Pozniakoff T, Deslisle S, Latif F, Maurer MS. 99mTc-Pyrophosphate scintigraphy for differentiating light-chain cardiac amyloidosis from the transthyretin-related familial and senile cardiac amyloidoses. Circ Cardiovasc Imaging 2013; 6:195-201
-
(2013)
Circ Cardiovasc Imaging
, vol.6
, pp. 195-201
-
-
Bokhari, S.1
Castaño, A.2
Pozniakoff, T.3
Deslisle, S.4
Latif, F.5
Maurer, M.S.6
-
54
-
-
85008213275
-
Technetium pyrophosphate uptake in transthyretin cardiac amyloidosis: associations with echocardiographic disease severity and outcomes
-
Jan 3. [Epub ahead of print]
-
Vranian MN, Sperry BW, Hanna M, et al. Technetium pyrophosphate uptake in transthyretin cardiac amyloidosis: associations with echocardiographic disease severity and outcomes. J Nucl Cardiol 2017; Jan 3. [Epub ahead of print] doi: 10.1007/s12350-016-0768-9
-
(2017)
J Nucl Cardiol
-
-
Vranian, M.N.1
Sperry, B.W.2
Hanna, M.3
-
55
-
-
84884712541
-
Evaluation of the role of endomyocardial biopsy in 851 patients with unexplained heart failure from 2000-2009
-
Bennett MK, Gilotra NA, Harrington C, et al. Evaluation of the role of endomyocardial biopsy in 851 patients with unexplained heart failure from 2000-2009. Circ Heart Fail 2013; 6:676-684
-
(2013)
Circ Heart Fail
, vol.6
, pp. 676-684
-
-
Bennett, M.K.1
Gilotra, N.A.2
Harrington, C.3
-
56
-
-
85039986660
-
Abdominal fat pad excisional biopsy for the diagnosis and typing of systemic amyloidosis
-
Nov 10. [Epub ahead of print]
-
Garcia Y, Collins AB, Stone JR. Abdominal fat pad excisional biopsy for the diagnosis and typing of systemic amyloidosis. Hum Pathol 2017; Nov 10. [Epub ahead of print] doi:10.1016/j.humpath.2017.11.001
-
(2017)
Hum Pathol
-
-
Garcia, Y.1
Collins, A.B.2
Stone, J.R.3
-
57
-
-
85021310899
-
Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis
-
Quarta CC, Gonzalez-Lopez E, Gilbertson JA, et al. Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis. Eur Heart J 2017; 38:1905-1908
-
(2017)
Eur Heart J
, vol.38
, pp. 1905-1908
-
-
Quarta, C.C.1
Gonzalez-Lopez, E.2
Gilbertson, J.A.3
-
58
-
-
84899994980
-
Yield of noncardiac biopsy for the diagnosis of transthyretin cardiac amyloidosis
-
Fine NM, Arruda-Olson AM, Dispenzieri A, et al. Yield of noncardiac biopsy for the diagnosis of transthyretin cardiac amyloidosis. Am J Cardiol 2014; 113:1723-1727
-
(2014)
Am J Cardiol
, vol.113
, pp. 1723-1727
-
-
Fine, N.M.1
Arruda-Olson, A.M.2
Dispenzieri, A.3
-
59
-
-
17744370515
-
Diagnostic performance of quantitative kappa and lambda free light chain assays in clinical practice
-
Katzmann JA, Abraham RS, Dispenzieri A, Lust JA, Kyle RA. Diagnostic performance of quantitative kappa and lambda free light chain assays in clinical practice. Clin Chem 2005; 51:878-781
-
(2005)
Clin Chem
, vol.51
, pp. 781-878
-
-
Katzmann, J.A.1
Abraham, R.S.2
Dispenzieri, A.3
Lust, J.A.4
Kyle, R.A.5
-
60
-
-
84984856819
-
Loop diuretics in the treatment of hypertension
-
Malha L, Mann SJ. Loop diuretics in the treatment of hypertension. Curr Hypertens Rep 2016; 18:27
-
(2016)
Curr Hypertens Rep
, vol.18
, pp. 27
-
-
Malha, L.1
Mann, S.J.2
-
61
-
-
0019519787
-
Digoxin sensitivity in amyloid cardiomyopathy
-
Rubinow A, Skinner M, Cohen AS. Digoxin sensitivity in amyloid cardiomyopathy. Circulation 1981; 63:1285-1288
-
(1981)
Circulation
, vol.63
, pp. 1285-1288
-
-
Rubinow, A.1
Skinner, M.2
Cohen, A.S.3
-
62
-
-
66549102428
-
Intracardiac thrombosis and anticoagulation therapy in cardiac amyloidosis
-
Feng D, Syed IS, Martinez M, et al. Intracardiac thrombosis and anticoagulation therapy in cardiac amyloidosis. Circulation 2009; 119:2490-2497
-
(2009)
Circulation
, vol.119
, pp. 2490-2497
-
-
Feng, D.1
Syed, I.S.2
Martinez, M.3
-
63
-
-
84928418312
-
Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs
-
Castaño A, Drachman BM, Judge D, Maurer MS. Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs. Heart Fail Rev 2015; 20:163-178
-
(2015)
Heart Fail Rev
, vol.20
, pp. 163-178
-
-
Castaño, A.1
Drachman, B.M.2
Judge, D.3
Maurer, M.S.4
-
64
-
-
84982793864
-
Outcome and incidence of appropriate implantable cardioverter-defibrillator therapy in patients with cardiac amyloidosis
-
Hamon D, Algalarrondo V, Gandjbakhch E, et al. Outcome and incidence of appropriate implantable cardioverter-defibrillator therapy in patients with cardiac amyloidosis. Int J Cardiol 2016; 222:562-568
-
(2016)
Int J Cardiol
, vol.222
, pp. 562-568
-
-
Hamon, D.1
Algalarrondo, V.2
Gandjbakhch, E.3
-
65
-
-
84920767664
-
Life-saving implantable cardioverter defibrillator therapy in cardiac AL amyloidosis
-
Dec 22
-
Patel KS, Hawkins PN, Whelan CJ, Gillmore JD. Life-saving implantable cardioverter defibrillator therapy in cardiac AL amyloidosis. BMJ Case Rep 2014; Dec 22. doi:10.1136/bcr-2014-206600
-
(2014)
BMJ Case Rep
-
-
Patel, K.S.1
Hawkins, P.N.2
Whelan, C.J.3
Gillmore, J.D.4
-
66
-
-
38549110552
-
Troponin T level as an exclusion criterion for stem cell transplantation in light-chain amyloidosis
-
Gertz M, Lacy M, Dispenzieri A, et al. Troponin T level as an exclusion criterion for stem cell transplantation in light-chain amyloidosis. Leuk Lymphoma 2008; 49:36-41
-
(2008)
Leuk Lymphoma
, vol.49
, pp. 36-41
-
-
Gertz, M.1
Lacy, M.2
Dispenzieri, A.3
-
68
-
-
85024089048
-
Novel pharmacotherapies for cardiac amyloidosis
-
Alexander KM, Singh A, Falk RH. Novel pharmacotherapies for cardiac amyloidosis. Pharmacol Ther 2017; 180:129-138
-
(2017)
Pharmacol Ther
, vol.180
, pp. 129-138
-
-
Alexander, K.M.1
Singh, A.2
Falk, R.H.3
-
69
-
-
84991646684
-
First report of safety and efficacy of daratumumab in 2 cases of advanced immunoglobulin light chain amyloidosis
-
Sher T, Fenton B, Akhtar A, Gertz MA. First report of safety and efficacy of daratumumab in 2 cases of advanced immunoglobulin light chain amyloidosis. Blood 2016; 128:1987-1989
-
(2016)
Blood
, vol.128
, pp. 1987-1989
-
-
Sher, T.1
Fenton, B.2
Akhtar, A.3
Gertz, M.A.4
-
70
-
-
85026898715
-
A phase 1/2 study of the oral proteasome inhibitor ixazomib in relapsed or refractory AL amyloidosis
-
Sanchorawala V, Palladini G, Kukreti V, et al. A phase 1/2 study of the oral proteasome inhibitor ixazomib in relapsed or refractory AL amyloidosis. Blood 2017; 130:597-605
-
(2017)
Blood
, vol.130
, pp. 597-605
-
-
Sanchorawala, V.1
Palladini, G.2
Kukreti, V.3
-
72
-
-
77954673020
-
Prognostic significance of strain Doppler imaging in light-chain amyloidosis
-
Koyama J, Falk RH. Prognostic significance of strain Doppler imaging in light-chain amyloidosis. JACC Cardiovasc Imaging 2010; 3:333-342
-
(2010)
JACC Cardiovasc Imaging
, vol.3
, pp. 333-342
-
-
Koyama, J.1
Falk, R.H.2
-
73
-
-
84871772553
-
New criteria for response to treatment in immunoglobulin light chain amyloidosis based on free light chain measurement and cardiac biomarkers: impact on survival outcomes
-
Palladini G, Dispenzieri A, Gertz MA, et al. New criteria for response to treatment in immunoglobulin light chain amyloidosis based on free light chain measurement and cardiac biomarkers: impact on survival outcomes. J Clin Oncol 2012; 30:4541-4549
-
(2012)
J Clin Oncol
, vol.30
, pp. 4541-4549
-
-
Palladini, G.1
Dispenzieri, A.2
Gertz, M.A.3
-
75
-
-
84963532664
-
First-in-human phase I/II study of NEOD001 in patients with light chain amyloidosis and persistent organ dysfunction
-
Gertz MA, Landau H, Comenzo RL, et al. First-in-human phase I/II study of NEOD001 in patients with light chain amyloidosis and persistent organ dysfunction. J Clin Oncol 2016; 34:1097-1103
-
(2016)
J Clin Oncol
, vol.34
, pp. 1097-1103
-
-
Gertz, M.A.1
Landau, H.2
Comenzo, R.L.3
-
76
-
-
0025990675
-
Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30)
-
Holmgren G, Steen L, Ekstedt J, et al. Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30). Clin Genet 1991; 40:242-246
-
(1991)
Clin Genet
, vol.40
, pp. 242-246
-
-
Holmgren, G.1
Steen, L.2
Ekstedt, J.3
-
77
-
-
84896725893
-
Novel drugs targeting transthyretin amyloidosis
-
Hanna M. Novel drugs targeting transthyretin amyloidosis. Curr Heart Fail Rep 2014; 11:50-57
-
(2014)
Curr Heart Fail Rep
, vol.11
, pp. 50-57
-
-
Hanna, M.1
-
78
-
-
84890954073
-
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial
-
Berk JL, Suhr OB, Obici L, et al; Diflunisal Trial Consortium. Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. JAMA 2013; 310:2658-2667
-
(2013)
JAMA
, vol.310
, pp. 2658-2667
-
-
Berk, J.L.1
Suhr, O.B.2
Obici, L.3
-
79
-
-
84869881017
-
Diflunisal for ATTR cardiac amyloidosis
-
Castaño A, Helmke S, Alvarez J, Delisle S, Maurer MS. Diflunisal for ATTR cardiac amyloidosis. Congest Heart Fail 2012; 18:315-319
-
(2012)
Congest Heart Fail
, vol.18
, pp. 315-319
-
-
Castaño, A.1
Helmke, S.2
Alvarez, J.3
Delisle, S.4
Maurer, M.S.5
-
80
-
-
84934290247
-
Safety and effi-cacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis
-
Sekijima Y, Tojo K, Morita H, Koyama J, Ikeda S-I. Safety and effi-cacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis. Amyloid 2015; 22:79-83
-
(2015)
Amyloid
, vol.22
, pp. 79-83
-
-
Sekijima, Y.1
Tojo, K.2
Morita, H.3
Koyama, J.4
Ikeda, S.-I.5
-
81
-
-
84862222705
-
Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial
-
Coelho T, Maia LF, Martins da Silva A, et al. Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial. Neurology 2012; 79:785-792
-
(2012)
Neurology
, vol.79
, pp. 785-792
-
-
Coelho, T.1
Maia, L.F.2
Martins da Silva, A.3
-
82
-
-
84938525710
-
Tafamidis in transthyretin amyloid cardiomyopathy: effects on transthyretin stabilization and clinical outcomes
-
Maurer MS, Grogan DR, Judge DP, et al. Tafamidis in transthyretin amyloid cardiomyopathy: effects on transthyretin stabilization and clinical outcomes. Circ Heart Fail 2015; 8:519-526
-
(2015)
Circ Heart Fail
, vol.8
, pp. 519-526
-
-
Maurer, M.S.1
Grogan, D.R.2
Judge, D.P.3
-
83
-
-
77954988796
-
Synergy of combined doxycycline/TUDCA treatment in lowering transthyretin deposition and associated biomarkers: studies in FAP mouse models
-
Cardoso I, Martins D, Ribeiro T, Merlini G, Saraiva MJ. Synergy of combined doxycycline/TUDCA treatment in lowering transthyretin deposition and associated biomarkers: studies in FAP mouse models. J Transl Med 2010; 8:74
-
(2010)
J Transl Med
, vol.8
, pp. 74
-
-
Cardoso, I.1
Martins, D.2
Ribeiro, T.3
Merlini, G.4
Saraiva, M.J.5
-
84
-
-
84861423778
-
Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: A phase II study
-
Obici L, Cortese A, Lozza A, et al. Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: A phase II study. Amyloid 2012; 19(suppl 1):34-36
-
(2012)
Amyloid
, vol.19
, pp. 34-36
-
-
Obici, L.1
Cortese, A.2
Lozza, A.3
-
85
-
-
84869109959
-
Green tea halts progression of cardiac transthyretin amyloidosis: An observational report
-
Kristen AV, Lehrke S, Buss S, et al. Green tea halts progression of cardiac transthyretin amyloidosis: An observational report. Clin Res Cardiol 2012; 101:805-813
-
(2012)
Clin Res Cardiol
, vol.101
, pp. 805-813
-
-
Kristen, A.V.1
Lehrke, S.2
Buss, S.3
-
86
-
-
84961203344
-
Novel conformationspecifi c monoclonal antibodies against amyloidogenic forms of forms of transthyretin
-
Higaki JN, Chakrabartty A, Galant NJ, et al. Novel conformationspecifi c monoclonal antibodies against amyloidogenic forms of forms of transthyretin. Amyloid 2016; 23:86-97
-
(2016)
Amyloid
, vol.23
, pp. 86-97
-
-
Higaki, J.N.1
Chakrabartty, A.2
Galant, N.J.3
|