-
1
-
-
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: 1817–22.
-
(1992)
Blood
, vol.79
, pp. 1817-1822
-
-
Kyle, R.A.1
Linos, A.2
Beard, C.M.3
-
2
-
-
84876789377
-
Systemic amyloidosis in England: an epidemiological study
-
Pinney JH, Smith CJ, Taube JB et al. Systemic amyloidosis in England: an epidemiological study. Br J Haematol 2013; 161: 525–32.
-
(2013)
Br J Haematol
, vol.161
, pp. 525-532
-
-
Pinney, J.H.1
Smith, C.J.2
Taube, J.B.3
-
3
-
-
0022495898
-
Primary systemic amyloidosis: multivariate analysis for prognostic factors in 168 cases
-
Kyle RA, Greipp PR, O'Fallon WM. Primary systemic amyloidosis: multivariate analysis for prognostic factors in 168 cases. Blood 1986; 68: 220–4.
-
(1986)
Blood
, vol.68
, pp. 220-224
-
-
Kyle, R.A.1
Greipp, P.R.2
O'Fallon, W.M.3
-
4
-
-
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: 141–57.
-
(1998)
QJM
, vol.91
, pp. 141-157
-
-
Dubrey, S.W.1
Cha, K.2
Anderson, J.3
-
5
-
-
78650037877
-
Serum immunoglobulin free light-chain measurement in primary amyloidosis: prognostic value and correlations with clinical features
-
Kumar S, Dispenzieri A, Katzmann JA et al. Serum immunoglobulin free light-chain measurement in primary amyloidosis: prognostic value and correlations with clinical features. Blood 2010; 116: 5126–9.
-
(2010)
Blood
, vol.116
, pp. 5126-5129
-
-
Kumar, S.1
Dispenzieri, A.2
Katzmann, J.A.3
-
6
-
-
84904345373
-
Transthyretin-derived amyloidosis: probably a common cause of lumbar spinal stenosis
-
Westermark P, Westermark GT, Suhr OB, Berg S. Transthyretin-derived amyloidosis: probably a common cause of lumbar spinal stenosis. Ups J Med Sci 2014; 119: 223–8.
-
(2014)
Ups J Med Sci
, vol.119
, pp. 223-228
-
-
Westermark, P.1
Westermark, G.T.2
Suhr, O.B.3
Berg, S.4
-
8
-
-
0020519870
-
Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlation
-
Cornwell GG 3rd, Murdoch WL, Kyle RA, Westermark P, Pitkanen P. Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlation. Am J Med 1983; 75: 618–23.
-
(1983)
Am J Med
, vol.75
, pp. 618-623
-
-
Cornwell, G.G.1
Murdoch, W.L.2
Kyle, R.A.3
Westermark, P.4
Pitkanen, P.5
-
9
-
-
84884376755
-
Senile systemic amyloidosis: clinical features at presentation and outcome
-
Pinney JH, Whelan CJ, Petrie A et al. Senile systemic amyloidosis: clinical features at presentation and outcome. J Am Heart Assoc 2013; 2: e000098.
-
(2013)
J Am Heart Assoc
, vol.2
, pp. e000098
-
-
Pinney, J.H.1
Whelan, C.J.2
Petrie, A.3
-
10
-
-
0029946836
-
Revised transthyretin Ile 122 allele frequency in African-Americans
-
Jacobson DR, Pastore R, Pool S et al. Revised transthyretin Ile 122 allele frequency in African-Americans. Hum Genet 1996; 98: 236–8.
-
(1996)
Hum Genet
, vol.98
, pp. 236-238
-
-
Jacobson, D.R.1
Pastore, R.2
Pool, S.3
-
11
-
-
84864674714
-
Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS)
-
e1.
-
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: 222–8.e1.
-
(2012)
Am Heart J
, vol.164
, pp. 222-228
-
-
Ruberg, F.L.1
Maurer, M.S.2
Judge, D.P.3
-
12
-
-
84860615776
-
Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant
-
Sattianayagam PT, Hahn AF, Whelan CJ et al. Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant. Eur Heart J 2012; 33: 1120–7.
-
(2012)
Eur Heart J
, vol.33
, pp. 1120-1127
-
-
Sattianayagam, P.T.1
Hahn, A.F.2
Whelan, C.J.3
-
13
-
-
0022472793
-
Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis
-
Wallace MR, Dwulet FE, Conneally PM, Benson MD. Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis. J Clin Invest 1986; 78: 6–12.
-
(1986)
J Clin Invest
, vol.78
, pp. 6-12
-
-
Wallace, M.R.1
Dwulet, F.E.2
Conneally, P.M.3
Benson, M.D.4
-
14
-
-
0023619641
-
Hereditary amyloid polyneuropathy in north west Ireland
-
Staunton H, Dervan P, Kale R, Linke RP, Kelly P. Hereditary amyloid polyneuropathy in north west Ireland. Brain 1987; 110(Pt 5): 1231–45.
-
(1987)
Brain
, vol.110
, pp. 1231-1245
-
-
Staunton, H.1
Dervan, P.2
Kale, R.3
Linke, R.P.4
Kelly, P.5
-
15
-
-
77957180065
-
A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves
-
Andrade C. A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain 1952; 75: 408–27.
-
(1952)
Brain
, vol.75
, pp. 408-427
-
-
Andrade, C.1
-
16
-
-
84878406657
-
Diagnostic and prognostic value of low QRS voltages in cardiac AL amyloidosis
-
Mussinelli R, Salinaro F, Alogna A et al. Diagnostic and prognostic value of low QRS voltages in cardiac AL amyloidosis. Ann Noninvasive Electrocardiol 2013; 18: 271–80.
-
(2013)
Ann Noninvasive Electrocardiol
, vol.18
, pp. 271-280
-
-
Mussinelli, R.1
Salinaro, F.2
Alogna, A.3
-
17
-
-
70349655715
-
Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types
-
Rapezzi C, Merlini G, Quarta CC et al. Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation 2009; 120: 1203–12.
-
(2009)
Circulation
, vol.120
, pp. 1203-1212
-
-
Rapezzi, C.1
Merlini, G.2
Quarta, C.C.3
-
18
-
-
84863638985
-
The electrocardiographic features associated with cardiac amyloidosis of variant transthyretin isoleucine 122 type in Afro-Caribbean patients
-
Dungu J, Sattianayagam PT, Whelan CJ et al. The electrocardiographic features associated with cardiac amyloidosis of variant transthyretin isoleucine 122 type in Afro-Caribbean patients. Am Heart J 2012; 164: 72–9.
-
(2012)
Am Heart J
, vol.164
, pp. 72-79
-
-
Dungu, J.1
Sattianayagam, P.T.2
Whelan, C.J.3
-
19
-
-
84973330655
-
Heterogeneity of Electrocardiographic Findings in Cardiac Transthyretin (ATTR) Amyloidosis and Impact on Survival AHA Scientific Sessions Chicago
-
USA
-
Patel KS, Fontana M, Sachchithanantham S, Sayed R et al. Heterogeneity of Electrocardiographic Findings in Cardiac Transthyretin (ATTR) Amyloidosis and Impact on Survival AHA Scientific Sessions Chicago, USA, 2014.
-
(2014)
-
-
Patel, K.S.1
Fontana, M.2
Sachchithanantham, S.3
Sayed, R.4
-
20
-
-
84880834855
-
Prevalence and prognostic value of conduction disturbances at the time of diagnosis of cardiac AL amyloidosis
-
Boldrini M, Salinaro F, Mussinelli R et al. Prevalence and prognostic value of conduction disturbances at the time of diagnosis of cardiac AL amyloidosis. Ann Noninvasive Electrocardiol 2013; 18: 327–35.
-
(2013)
Ann Noninvasive Electrocardiol
, vol.18
, pp. 327-335
-
-
Boldrini, M.1
Salinaro, F.2
Mussinelli, R.3
-
21
-
-
4644336052
-
Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: a staging system for primary systemic amyloidosis
-
Dispenzieri A, Gertz MA, Kyle RA et al. Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: a staging system for primary systemic amyloidosis. J Clin Oncol 2004; 22: 3751–7.
-
(2004)
J Clin Oncol
, vol.22
, pp. 3751-3757
-
-
Dispenzieri, A.1
Gertz, M.A.2
Kyle, R.A.3
-
22
-
-
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: 989–95.
-
(2012)
J Clin Oncol
, vol.30
, pp. 989-995
-
-
Kumar, S.1
Dispenzieri, A.2
Lacy, M.Q.3
-
23
-
-
84879458198
-
A European collaborative study of treatment outcomes in 346 patients with cardiac stage III AL amyloidosis
-
Wechalekar AD, Schonland SO, Kastritis E et al. A European collaborative study of treatment outcomes in 346 patients with cardiac stage III AL amyloidosis. Blood 2013; 121: 3420–7.
-
(2013)
Blood
, vol.121
, pp. 3420-3427
-
-
Wechalekar, A.D.1
Schonland, S.O.2
Kastritis, E.3
-
24
-
-
23244448608
-
Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22 April 2004
-
Gertz MA, Comenzo R, Falk RH et al. Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22 April 2004. Am J Hematol 2005; 79: 319–28.
-
(2005)
Am J Hematol
, vol.79
, pp. 319-328
-
-
Gertz, M.A.1
Comenzo, R.2
Falk, R.H.3
-
25
-
-
0037842018
-
Longitudinal myocardial function assessed by tissue velocity, strain, and strain rate tissue Doppler echocardiography in patients with AL (primary) cardiac amyloidosis
-
Koyama J, Ray-Sequin PA, Falk RH. Longitudinal myocardial function assessed by tissue velocity, strain, and strain rate tissue Doppler echocardiography in patients with AL (primary) cardiac amyloidosis. Circulation 2003; 107: 2446–52.
-
(2003)
Circulation
, vol.107
, pp. 2446-2452
-
-
Koyama, J.1
Ray-Sequin, P.A.2
Falk, R.H.3
-
26
-
-
84866078444
-
Longitudinal left ventricular function for prediction of survival in systemic light-chain amyloidosis: incremental value compared with clinical and biochemical markers
-
Buss SJ, Emami M, Mereles D et al. Longitudinal left ventricular function for prediction of survival in systemic light-chain amyloidosis: incremental value compared with clinical and biochemical markers. J Am Coll Cardiol 2012; 60: 1067–76.
-
(2012)
J Am Coll Cardiol
, vol.60
, pp. 1067-1076
-
-
Buss, S.J.1
Emami, M.2
Mereles, D.3
-
27
-
-
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: 1442–8.
-
(2012)
Heart
, vol.98
, pp. 1442-1448
-
-
Phelan, D.1
Collier, P.2
Thavendiranathan, P.3
-
28
-
-
0023926566
-
Diagnostic radionuclide imaging of amyloid: biological targeting by circulating human serum amyloid P component
-
Hawkins PN, Myers MJ, Lavender JP, Pepys MB. Diagnostic radionuclide imaging of amyloid: biological targeting by circulating human serum amyloid P component. Lancet 1988; 1: 1413–8.
-
(1988)
Lancet
, vol.1
, pp. 1413-1418
-
-
Hawkins, P.N.1
Myers, M.J.2
Lavender, J.P.3
Pepys, M.B.4
-
29
-
-
79953733503
-
Usefulness and limitations of 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in the aetiological diagnosis of amyloidotic cardiomyopathy
-
Rapezzi C, Quarta CC, Guidalotti PL et al. Usefulness and limitations of 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in the aetiological diagnosis of amyloidotic cardiomyopathy. Eur J Nucl Med Mol Imaging 2011; 38: 470–8.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, pp. 470-478
-
-
Rapezzi, C.1
Quarta, C.C.2
Guidalotti, P.L.3
-
30
-
-
84874126402
-
High 99mTc-DPD myocardial uptake in a patient with apolipoprotein AI-related amyloidotic cardiomyopathy
-
Quarta CC, Obici L, Guidalotti PL et al. High 99mTc-DPD myocardial uptake in a patient with apolipoprotein AI-related amyloidotic cardiomyopathy. Amyloid 2013; 20: 48–51.
-
(2013)
Amyloid
, vol.20
, pp. 48-51
-
-
Quarta, C.C.1
Obici, L.2
Guidalotti, P.L.3
-
31
-
-
84925458040
-
Utility and limitations of 3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in systemic amyloidosis
-
Hutt DF, Quigley AM, Page J et al. Utility and limitations of 3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in systemic amyloidosis. Eur Heart J Cardiovasc Imaging 2014; 15: 1289–98.
-
(2014)
Eur Heart J Cardiovasc Imaging
, vol.15
, pp. 1289-1298
-
-
Hutt, D.F.1
Quigley, A.M.2
Page, J.3
-
32
-
-
19944430773
-
Cardiovascular magnetic resonance in cardiac amyloidosis
-
Maceira AM, Joshi J, Prasad SK et al. Cardiovascular magnetic resonance in cardiac amyloidosis. Circulation 2005; 111: 186–93.
-
(2005)
Circulation
, vol.111
, pp. 186-193
-
-
Maceira, A.M.1
Joshi, J.2
Prasad, S.K.3
-
35
-
-
84866107331
-
Cardiovascular magnetic resonance measurement of myocardial extracellular volume in health and disease
-
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.
-
(2012)
Heart
, vol.98
, pp. 1436-1441
-
-
Sado, D.M.1
Flett, A.S.2
Banypersad, S.M.3
-
36
-
-
84874533688
-
Quantification of myocardial extracellular volume fraction in systemic AL amyloidosis: an equilibrium contrast cardiovascular magnetic resonance study
-
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.
-
(2013)
Circ Cardiovasc Imaging
, vol.6
, pp. 34-39
-
-
Banypersad, S.M.1
Sado, D.M.2
Flett, A.S.3
-
37
-
-
84883868280
-
T1 mapping for myocardial extracellular volume measurement by CMR: bolus only versus primed infusion technique
-
White SK, Sado DM, Fontana M et al. T1 mapping for myocardial extracellular volume measurement by CMR: bolus only versus primed infusion technique. JACC Cardiovasc Imaging 2013; 6: 955–62.
-
(2013)
JACC Cardiovasc Imaging
, vol.6
, pp. 955-962
-
-
White, S.K.1
Sado, D.M.2
Fontana, M.3
-
38
-
-
0035120590
-
Abdominal fat pad aspiration biopsy for tissue confirmation of systemic amyloidosis: specificity, positive predictive value, and diagnostic pitfalls
-
Guy CD, Jones CK. Abdominal fat pad aspiration biopsy for tissue confirmation of systemic amyloidosis: specificity, positive predictive value, and diagnostic pitfalls. Diagn Cytopathol 2001; 24: 181–5.
-
(2001)
Diagn Cytopathol
, vol.24
, pp. 181-185
-
-
Guy, C.D.1
Jones, C.K.2
-
39
-
-
84903649455
-
Clinical diagnosis and typing of systemic amyloidosis in subcutaneous fat aspirates by mass spectrometry-based proteomics
-
Vrana JA, Theis JD, Dasari S et al. Clinical diagnosis and typing of systemic amyloidosis in subcutaneous fat aspirates by mass spectrometry-based proteomics. Haematologica 2014; 99: 1239–47.
-
(2014)
Haematologica
, vol.99
, pp. 1239-1247
-
-
Vrana, J.A.1
Theis, J.D.2
Dasari, S.3
-
40
-
-
0037030659
-
Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis
-
Lachmann HJ, Booth DR, Booth SE et al. Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis. N Engl J Med 2002; 346: 1786–91.
-
(2002)
N Engl J Med
, vol.346
, pp. 1786-1791
-
-
Lachmann, H.J.1
Booth, D.R.2
Booth, S.E.3
-
41
-
-
0019519787
-
Digoxin sensitivity in amyloid cardiomyopathy
-
Rubinow A, Skinner M, Cohen AS. Digoxin sensitivity in amyloid cardiomyopathy. Circulation 1981; 63: 1285–8.
-
(1981)
Circulation
, vol.63
, pp. 1285-1288
-
-
Rubinow, A.1
Skinner, M.2
Cohen, A.S.3
-
42
-
-
0021873337
-
Selective binding of nifedipine to amyloid fibrils
-
Gertz MA, Skinner M, Connors LH, Falk RH, Cohen AS, Kyle RA. Selective binding of nifedipine to amyloid fibrils. Am J Cardiol 1985; 55: 1646.
-
(1985)
Am J Cardiol
, vol.55
, pp. 1646
-
-
Gertz, M.A.1
Skinner, M.2
Connors, L.H.3
Falk, R.H.4
Cohen, A.S.5
Kyle, R.A.6
-
43
-
-
0027213967
-
Left ventricular systolic dysfunction precipitated by verapamil in cardiac amyloidosis
-
Pollak A, Falk RH. Left ventricular systolic dysfunction precipitated by verapamil in cardiac amyloidosis. Chest 1993; 104: 618–20.
-
(1993)
Chest
, vol.104
, pp. 618-620
-
-
Pollak, A.1
Falk, R.H.2
-
44
-
-
36349011376
-
Intracardiac thrombosis and embolism in patients with cardiac amyloidosis
-
Feng D, Edwards WD, Oh JK et al. Intracardiac thrombosis and embolism in patients with cardiac amyloidosis. Circulation 2007; 116: 2420–6.
-
(2007)
Circulation
, vol.116
, pp. 2420-2426
-
-
Feng, D.1
Edwards, W.D.2
Oh, J.K.3
-
45
-
-
84860897399
-
Cyclophosphamide, bortezomib, and dexamethasone therapy in AL amyloidosis is associated with high clonal response rates and prolonged progression-free survival
-
Venner CP, Lane T, Foard D et al. Cyclophosphamide, bortezomib, and dexamethasone therapy in AL amyloidosis is associated with high clonal response rates and prolonged progression-free survival. Blood 2012; 119: 4387–90.
-
(2012)
Blood
, vol.119
, pp. 4387-4390
-
-
Venner, C.P.1
Lane, T.2
Foard, D.3
-
46
-
-
84860898706
-
Cyclophosphamide-bortezomib-dexamethasone (CyBorD) produces rapid and complete hematologic response in patients with AL amyloidosis
-
Mikhael JR, Schuster SR, Jimenez-Zepeda VH et al. Cyclophosphamide-bortezomib-dexamethasone (CyBorD) produces rapid and complete hematologic response in patients with AL amyloidosis. Blood 2012; 119: 4391–4.
-
(2012)
Blood
, vol.119
, pp. 4391-4394
-
-
Mikhael, J.R.1
Schuster, S.R.2
Jimenez-Zepeda, V.H.3
-
47
-
-
0027193135
-
High-dose therapy and autologous transplantation in amyloidosis-AL
-
Majolino I, Marceno R, Pecoraro G et al. High-dose therapy and autologous transplantation in amyloidosis-AL. Haematologica 1993; 78: 68–71.
-
(1993)
Haematologica
, vol.78
, pp. 68-71
-
-
Majolino, I.1
Marceno, R.2
Pecoraro, G.3
-
48
-
-
0032525180
-
Dose-intensive melphalan with blood stem-cell support for the treatment of AL (amyloid light-chain) amyloidosis: survival and responses in 25 patients
-
Comenzo RL, Vosburgh E, Falk RH et al. Dose-intensive melphalan with blood stem-cell support for the treatment of AL (amyloid light-chain) amyloidosis: survival and responses in 25 patients. Blood 1998; 91: 3662–70.
-
(1998)
Blood
, vol.91
, pp. 3662-3670
-
-
Comenzo, R.L.1
Vosburgh, E.2
Falk, R.H.3
-
49
-
-
84919362791
-
Stringent patient selection improves outcomes in AL amyloidosis after autologous stem cell transplantation in the upfront and relapsed setting
-
Venner CP, Gillmore JD, Sachchithanantham S et al. Stringent patient selection improves outcomes in AL amyloidosis after autologous stem cell transplantation in the upfront and relapsed setting. Haematologica 2014; 99: e260–3.
-
(2014)
Haematologica
, vol.99
, pp. e260-e263
-
-
Venner, C.P.1
Gillmore, J.D.2
Sachchithanantham, S.3
-
50
-
-
36348976450
-
Long-term outcome of patients with AL amyloidosis treated with high-dose melphalan and stem-cell transplantation
-
Sanchorawala V, Skinner M, Quillen K, Finn KT, Doros G, Seldin DC. Long-term outcome of patients with AL amyloidosis treated with high-dose melphalan and stem-cell transplantation. Blood 2007; 110: 3561–3.
-
(2007)
Blood
, vol.110
, pp. 3561-3563
-
-
Sanchorawala, V.1
Skinner, M.2
Quillen, K.3
Finn, K.T.4
Doros, G.5
Seldin, D.C.6
-
51
-
-
84890954073
-
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial
-
Berk JL, Suhr OB, Obici L et al. Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. JAMA 2013; 310: 2658–67.
-
(2013)
JAMA
, vol.310
, pp. 2658-2667
-
-
Berk, J.L.1
Suhr, O.B.2
Obici, L.3
-
52
-
-
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: 785–92.
-
(2012)
Neurology
, vol.79
, pp. 785-792
-
-
Coelho, T.1
Maia, L.F.2
Martins da Silva, A.3
-
53
-
-
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
-
54
-
-
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): 34–6.
-
(2012)
Amyloid
, vol.19
, pp. 34-36
-
-
Obici, L.1
Cortese, A.2
Lozza, A.3
-
55
-
-
84883118140
-
Safety and efficacy of RNAi therapy for transthyretin amyloidosis
-
Coelho T, Adams D, Silva A et al. Safety and efficacy of RNAi therapy for transthyretin amyloidosis. N Engl J Med 2013; 369: 819–29.
-
(2013)
N Engl J Med
, vol.369
, pp. 819-829
-
-
Coelho, T.1
Adams, D.2
Silva, A.3
-
56
-
-
0033810109
-
Antibody-mediated resolution of light chain-associated amyloid deposits
-
Hrncic R, Wall J, Wolfenbarger DA et al. Antibody-mediated resolution of light chain-associated amyloid deposits. Am J Pathol 2000; 157: 1239–46.
-
(2000)
Am J Pathol
, vol.157
, pp. 1239-1246
-
-
Hrncic, R.1
Wall, J.2
Wolfenbarger, D.A.3
-
57
-
-
0141791455
-
Therapeutic potential of chimeric amyloid-reactive monoclonal antibody 11-1F4
-
Solomon A, Weiss DT, Wall JS. Therapeutic potential of chimeric amyloid-reactive monoclonal antibody 11-1F4. Clin Cancer Res 2003; 9: 3831S–8S.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 3831S-8S
-
-
Solomon, A.1
Weiss, D.T.2
Wall, J.S.3
-
58
-
-
0037118028
-
Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis
-
Pepys MB, Herbert J, Hutchinson WL et al. Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis. Nature 2002; 417: 254–9.
-
(2002)
Nature
, vol.417
, pp. 254-259
-
-
Pepys, M.B.1
Herbert, J.2
Hutchinson, W.L.3
-
59
-
-
76449109014
-
Sustained pharmacological depletion of serum amyloid P component in patients with systemic amyloidosis
-
Gillmore JD, Tennent GA, Hutchinson WL et al. Sustained pharmacological depletion of serum amyloid P component in patients with systemic amyloidosis. Br J Haematol 2010; 148: 760–7.
-
(2010)
Br J Haematol
, vol.148
, pp. 760-767
-
-
Gillmore, J.D.1
Tennent, G.A.2
Hutchinson, W.L.3
-
60
-
-
78149282151
-
Antibodies to human serum amyloid P component eliminate visceral amyloid deposits
-
Bodin K, Ellmerich S, Kahan MC et al. Antibodies to human serum amyloid P component eliminate visceral amyloid deposits. Nature 2010; 468: 93–7.
-
(2010)
Nature
, vol.468
, pp. 93-97
-
-
Bodin, K.1
Ellmerich, S.2
Kahan, M.C.3
-
61
-
-
0017399803
-
The conduction system in cardiac amyloidosis. Clinical and pathologic features of 23 patients
-
Ridolfi RL, Bulkley BH, Hutchins GM. The conduction system in cardiac amyloidosis. Clinical and pathologic features of 23 patients. Am J Med 1977; 62: 677–86.
-
(1977)
Am J Med
, vol.62
, pp. 677-686
-
-
Ridolfi, R.L.1
Bulkley, B.H.2
Hutchins, G.M.3
-
62
-
-
84877284718
-
ACCF/HRS/AHA/ASE/HFSA/SCAI/SCCT/SCMR 2013 appropriate use criteria for implantable cardioverter-defibrillators and cardiac resynchronization therapy. A Report of the American College of Cardiology Foundation Appropriate Use Criteria Task Force, Heart Rhythm Society, American Heart Association, American Society of Echocardiography, Heart Failure Society of America, Society for Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, and Society for Cardiovascular Magnetic Resonance
-
Russo AM, Stainback RF, Bailey SR et al. ACCF/HRS/AHA/ASE/HFSA/SCAI/SCCT/SCMR 2013 appropriate use criteria for implantable cardioverter-defibrillators and cardiac resynchronization therapy. A Report of the American College of Cardiology Foundation Appropriate Use Criteria Task Force, Heart Rhythm Society, American Heart Association, American Society of Echocardiography, Heart Failure Society of America, Society for Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, and Society for Cardiovascular Magnetic Resonance. J Am Coll Cardiol 2013; 61: 1318–68.
-
(2013)
J Am Coll Cardiol
, vol.61
, pp. 1318-1368
-
-
Russo, A.M.1
Stainback, R.F.2
Bailey, S.R.3
-
63
-
-
78249290790
-
Cardiac transplantation followed by dose-intensive melphalan and autologous stem-cell transplantation for light chain amyloidosis and heart failure
-
Dey BR, Chung SS, Spitzer TR et al. Cardiac transplantation followed by dose-intensive melphalan and autologous stem-cell transplantation for light chain amyloidosis and heart failure. Transplantation 2010; 90: 905–11.
-
(2010)
Transplantation
, vol.90
, pp. 905-911
-
-
Dey, B.R.1
Chung, S.S.2
Spitzer, T.R.3
-
64
-
-
71049187207
-
Cardiac transplantation should be considered in selected patients with either AL or hereditary forms of amyloidosis: the UK National Amyloidosis Centre experience
-
; author reply 7-8.
-
Gibbs SD, Sattianayagam PT, Hawkins PN, Gillmore JD. Cardiac transplantation should be considered in selected patients with either AL or hereditary forms of amyloidosis: the UK National Amyloidosis Centre experience. Intern Med J 2009; 39: 786–7; author reply 7-8.
-
(2009)
Intern Med J
, vol.39
, pp. 786-787
-
-
Gibbs, S.D.1
Sattianayagam, P.T.2
Hawkins, P.N.3
Gillmore, J.D.4
-
65
-
-
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: 242–6.
-
(1991)
Clin Genet
, vol.40
, pp. 242-246
-
-
Holmgren, G.1
Steen, L.2
Ekstedt, J.3
-
66
-
-
0027312398
-
Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis
-
Holmgren G, Ericzon BG, Groth CG et al. Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis. Lancet 1993; 341: 1113–6.
-
(1993)
Lancet
, vol.341
, pp. 1113-1116
-
-
Holmgren, G.1
Ericzon, B.G.2
Groth, C.G.3
-
67
-
-
0032558120
-
Progressive cardiac amyloidosis following liver transplantation for familial amyloid polyneuropathy: implications for amyloid fibrillogenesis
-
Stangou AJ, Hawkins PN, Heaton ND et al. Progressive cardiac amyloidosis following liver transplantation for familial amyloid polyneuropathy: implications for amyloid fibrillogenesis. Transplantation 1998; 66: 229–33.
-
(1998)
Transplantation
, vol.66
, pp. 229-233
-
-
Stangou, A.J.1
Hawkins, P.N.2
Heaton, N.D.3
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