-
1
-
-
84994890824
-
AL (light-chain) cardiac amyloidosis: a review of diagnosis and therapy
-
PID: 27634125
-
Falk RH, Alexander KM, Liao R, Dorbala S (2016) AL (light-chain) cardiac amyloidosis: a review of diagnosis and therapy. J Am Coll Cardiol 68:1323–1341
-
(2016)
J Am Coll Cardiol
, vol.68
, pp. 1323-1341
-
-
Falk, R.H.1
Alexander, K.M.2
Liao, R.3
Dorbala, S.4
-
2
-
-
84883118140
-
Safety and efficacy of RNAi therapy for transthyretin amyloidosis
-
COI: 1:CAS:528:DC%2BC3sXhtlyis7fK, PID: 23984729
-
Coelho T, Adams D, Silva A et al (2013) Safety and efficacy of RNAi therapy for transthyretin amyloidosis. N Engl J Med 369:819–829
-
(2013)
N Engl J Med
, vol.369
, pp. 819-829
-
-
Coelho, T.1
Adams, D.2
Silva, A.3
-
3
-
-
0042709605
-
Molecular mechanisms of amyloidosis
-
COI: 1:CAS:528:DC%2BD3sXmtFCmsbk%3D, PID: 12904524
-
Merlini G, Bellotti V (2003) Molecular mechanisms of amyloidosis. N Engl J Med 349:583–596
-
(2003)
N Engl J Med
, vol.349
, pp. 583-596
-
-
Merlini, G.1
Bellotti, V.2
-
4
-
-
0001629134
-
Heavy chain disease—a new disorder of serum gamma-globulins: report of the first case
-
COI: 1:STN:280:DyaF2M%2FhtlKksQ%3D%3D, PID: 14209281
-
Franklin EC, Lowenstein J, Bigelow B, Meltzer M (1964) Heavy chain disease—a new disorder of serum gamma-globulins: report of the first case. Am J Med 37:332–350
-
(1964)
Am J Med
, vol.37
, pp. 332-350
-
-
Franklin, E.C.1
Lowenstein, J.2
Bigelow, B.3
Meltzer, M.4
-
5
-
-
84882528609
-
Stanniocalcin1 is a key mediator of amyloidogenic light chain induced cardiotoxicity
-
PID: 23982491
-
Guan J, Mishra S, Shi J et al (2013) Stanniocalcin1 is a key mediator of amyloidogenic light chain induced cardiotoxicity. Basic Res Cardiol 108:378
-
(2013)
Basic Res Cardiol
, vol.108
, pp. 378
-
-
Guan, J.1
Mishra, S.2
Shi, J.3
-
7
-
-
35348906661
-
Hypertrophic spinal pachymeningitis associated with heavy-chain disease. Case report
-
PID: 17933324
-
Yunokawa K, Hagiyama Y, Mochizuki Y, Tanaka N, Ochi M (2007) Hypertrophic spinal pachymeningitis associated with heavy-chain disease. Case report. Journal of neurosurgery Spine 7:459–462
-
(2007)
Journal of neurosurgery Spine
, vol.7
, pp. 459-462
-
-
Yunokawa, K.1
Hagiyama, Y.2
Mochizuki, Y.3
Tanaka, N.4
Ochi, M.5
-
9
-
-
42149146250
-
Gamma heavy chain disease in a patient with diabetes and chronic renal insufficiency: diagnostic assessment of the heavy chain fragment
-
COI: 1:CAS:528:DC%2BD1cXmtFymtrY%3D, PID: 18348312
-
Lee MT, Parwani A, Humphrey R, Hamilton RG, Myers DI, Detrick B (2008) Gamma heavy chain disease in a patient with diabetes and chronic renal insufficiency: diagnostic assessment of the heavy chain fragment. J Clin Lab Anal 22:146–150
-
(2008)
J Clin Lab Anal
, vol.22
, pp. 146-150
-
-
Lee, M.T.1
Parwani, A.2
Humphrey, R.3
Hamilton, R.G.4
Myers, D.I.5
Detrick, B.6
-
10
-
-
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
-
PID: 16044444
-
Gertz MA, Comenzo R, Falk RH et al (2005) 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 79:319–328
-
(2005)
Am J Hematol
, vol.79
, pp. 319-328
-
-
Gertz, M.A.1
Comenzo, R.2
Falk, R.H.3
-
11
-
-
84930918406
-
Cardiac amyloidosis: where are we today?
-
COI: 1:CAS:528:DC%2BC2MXht1Sgs7rL, PID: 26077367
-
Patel KS, Hawkins PN (2015) Cardiac amyloidosis: where are we today? J Intern Med 278:126–144
-
(2015)
J Intern Med
, vol.278
, pp. 126-144
-
-
Patel, K.S.1
Hawkins, P.N.2
-
12
-
-
33845401240
-
A case report: isolated a heavy chain monoclonal gammopathy in a patient with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin change syndrome
-
Kim SK, Park IK, Park BH et al (2005) A case report: isolated a heavy chain monoclonal gammopathy in a patient with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin change syndrome. International journal of clinical practice Supplement 26-30
-
(2005)
International journal of clinical practice Supplement
, pp. 26-30
-
-
Kim, S.K.1
Park, I.K.2
Park, B.H.3
-
13
-
-
84884940241
-
Light chain amyloidosis: the heart of the problem
-
COI: 1:CAS:528:DC%2BC2cXit1SgsA%3D%3D, PID: 24091927
-
Merlini G, Palladini G (2013) Light chain amyloidosis: the heart of the problem. Haematologica 98:1492–1495
-
(2013)
Haematologica
, vol.98
, pp. 1492-1495
-
-
Merlini, G.1
Palladini, G.2
-
14
-
-
73949091104
-
Classification of amyloidosis by laser microdissection and mass spectrometry-based proteomic analysis in clinical biopsy specimens
-
COI: 1:CAS:528:DC%2BD1MXhsF2gsb7J, PID: 19797517
-
Vrana JA, Gamez JD, Madden BJ, Theis JD, Bergen HR 3rd, Dogan A (2009) Classification of amyloidosis by laser microdissection and mass spectrometry-based proteomic analysis in clinical biopsy specimens. Blood 114:4957–4959
-
(2009)
Blood
, vol.114
, pp. 4957-4959
-
-
Vrana, J.A.1
Gamez, J.D.2
Madden, B.J.3
Theis, J.D.4
Bergen, H.R.5
Dogan, A.6
-
15
-
-
84855822559
-
Reliable typing of systemic amyloidoses through proteomic analysis of subcutaneous adipose tissue
-
COI: 1:CAS:528:DC%2BC38XjsV2mu7c%3D, PID: 21917755
-
Brambilla F, Lavatelli F, Di Silvestre D et al (2012) Reliable typing of systemic amyloidoses through proteomic analysis of subcutaneous adipose tissue. Blood 119:1844–1847
-
(2012)
Blood
, vol.119
, pp. 1844-1847
-
-
Brambilla, F.1
Lavatelli, F.2
Di Silvestre, D.3
-
16
-
-
0019925256
-
The histopathology of gamma heavy-chain disease
-
COI: 1:STN:280:DyaL3s%2FksFGisg%3D%3D, PID: 6814232
-
Wester SM, Banks PM, Li CY (1982) The histopathology of gamma heavy-chain disease. Am J Clin Pathol 78:427–436
-
(1982)
Am J Clin Pathol
, vol.78
, pp. 427-436
-
-
Wester, S.M.1
Banks, P.M.2
Li, C.Y.3
-
17
-
-
84879458198
-
A European collaborative study of treatment outcomes in 346 patients with cardiac stage III AL amyloidosis
-
COI: 1:CAS:528:DC%2BC3sXntFWls7o%3D, PID: 23479568
-
Wechalekar AD, Schonland SO, Kastritis E et al (2013) A European collaborative study of treatment outcomes in 346 patients with cardiac stage III AL amyloidosis. Blood 121:3420–3427
-
(2013)
Blood
, vol.121
, pp. 3420-3427
-
-
Wechalekar, A.D.1
Schonland, S.O.2
Kastritis, E.3
-
18
-
-
79951934818
-
Changes in serum-free light chain rather than intact monoclonal immunoglobulin levels predicts outcome following therapy in primary amyloidosis
-
COI: 1:CAS:528:DC%2BC3MXks1Kgtb8%3D, PID: 21328431
-
Kumar SK, Dispenzieri A, Lacy MQ et al (2011) Changes in serum-free light chain rather than intact monoclonal immunoglobulin levels predicts outcome following therapy in primary amyloidosis. Am J Hematol 86:251–255
-
(2011)
Am J Hematol
, vol.86
, pp. 251-255
-
-
Kumar, S.K.1
Dispenzieri, A.2
Lacy, M.Q.3
-
19
-
-
2342591289
-
Superior survival in primary systemic amyloidosis patients undergoing peripheral blood stem cell transplantation: a case-control study
-
COI: 1:CAS:528:DC%2BD2cXjvF2hsrc%3D, PID: 14739213
-
Dispenzieri A, Kyle RA, Lacy MQ et al (2004) Superior survival in primary systemic amyloidosis patients undergoing peripheral blood stem cell transplantation: a case-control study. Blood 103:3960–3963
-
(2004)
Blood
, vol.103
, pp. 3960-3963
-
-
Dispenzieri, A.1
Kyle, R.A.2
Lacy, M.Q.3
-
20
-
-
0031913337
-
The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement
-
COI: 1:STN:280:DyaK1c3ktVSntg%3D%3D, PID: 9578896
-
Dubrey SW, Cha K, Anderson J et al (1998) The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement. QJM: monthly journal of the Association of Physicians 91:141–157
-
(1998)
QJM: monthly journal of the Association of Physicians
, vol.91
, pp. 141-157
-
-
Dubrey, S.W.1
Cha, K.2
Anderson, J.3
-
22
-
-
84994210566
-
Efficacy of chemotherapy for light-chain amyloidosis in patients presenting with symptomatic heart failure
-
COI: 1:CAS:528:DC%2BC28XhtVyhs7vI, PID: 27339491
-
Sperry BW, Ikram A, Hachamovitch R et al (2016) Efficacy of chemotherapy for light-chain amyloidosis in patients presenting with symptomatic heart failure. J Am Coll Cardiol 67:2941–2948
-
(2016)
J Am Coll Cardiol
, vol.67
, pp. 2941-2948
-
-
Sperry, B.W.1
Ikram, A.2
Hachamovitch, R.3
-
24
-
-
84870699271
-
Ten-year survival after autologous stem cell transplantation for immunoglobulin light chain amyloidosis
-
COI: 1:CAS:528:DC%2BC38XhslKrur7N, PID: 22707405
-
Cordes S, Dispenzieri A, Lacy MQ et al (2012) Ten-year survival after autologous stem cell transplantation for immunoglobulin light chain amyloidosis. Cancer 118:6105–6109
-
(2012)
Cancer
, vol.118
, pp. 6105-6109
-
-
Cordes, S.1
Dispenzieri, A.2
Lacy, M.Q.3
-
25
-
-
0036853299
-
Stem cell transplantation for the management of primary systemic amyloidosis
-
COI: 1:CAS:528:DC%2BD38XovFGqurw%3D, PID: 12459400
-
Gertz MA, Lacy MQ, Dispenzieri A et al (2002) Stem cell transplantation for the management of primary systemic amyloidosis. Am J Med 113:549–555
-
(2002)
Am J Med
, vol.113
, pp. 549-555
-
-
Gertz, M.A.1
Lacy, M.Q.2
Dispenzieri, A.3
-
26
-
-
84873684800
-
Role of high-dose melphalan and autologous peripheral blood stem cell transplantation in AL amyloidosis
-
COI: 1:CAS:528:DC%2BC38XhvVarsbY%3D, PID: 22432083
-
Sanchorawala V (2012) Role of high-dose melphalan and autologous peripheral blood stem cell transplantation in AL amyloidosis. American journal of blood research 2:9–17
-
(2012)
American journal of blood research
, vol.2
, pp. 9-17
-
-
Sanchorawala, V.1
-
27
-
-
84875027394
-
Heart transplantation and end-stage cardiac amyloidosis: a review and approach to evaluation and management
-
PID: 23227279
-
Estep JD, Bhimaraj A, Cordero-Reyes AM, Bruckner B, Loebe M, Torre-Amione G (2012) Heart transplantation and end-stage cardiac amyloidosis: a review and approach to evaluation and management. Methodist DeBakey cardiovascular journal 8:8–16
-
(2012)
Methodist DeBakey cardiovascular journal
, vol.8
, pp. 8-16
-
-
Estep, J.D.1
Bhimaraj, A.2
Cordero-Reyes, A.M.3
Bruckner, B.4
Loebe, M.5
Torre-Amione, G.6
-
28
-
-
84857062463
-
Cardiac amyloidosis: what are the indications for transplant?
-
PID: 22314298
-
Bradshaw SH, Veinot JP (2012) Cardiac amyloidosis: what are the indications for transplant? Curr Opin Cardiol 27:143–147
-
(2012)
Curr Opin Cardiol
, vol.27
, pp. 143-147
-
-
Bradshaw, S.H.1
Veinot, J.P.2
-
29
-
-
84990189506
-
Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey)
-
COI: 1:CAS:528:DC%2BC28XhtFanurzF, PID: 27386769
-
Maurer MS, Hanna M, Grogan M et al (2016) Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey). J Am Coll Cardiol 68:161–172
-
(2016)
J Am Coll Cardiol
, vol.68
, pp. 161-172
-
-
Maurer, M.S.1
Hanna, M.2
Grogan, M.3
-
31
-
-
84873979913
-
Guideline of transthyretin-related hereditary amyloidosis for clinicians
-
PID: 23425518
-
Ando Y, Coelho T, Berk JL et al (2013) Guideline of transthyretin-related hereditary amyloidosis for clinicians. Orphanet journal of rare diseases 8:31
-
(2013)
Orphanet journal of rare diseases
, vol.8
, pp. 31
-
-
Ando, Y.1
Coelho, T.2
Berk, J.L.3
-
33
-
-
77951551396
-
Significance of the amyloidogenic transthyretin Val 122 Ile allele in African Americans in the Arteriosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies
-
COI: 1:CAS:528:DC%2BC3cXlsVOhu7o%3D, PID: 20435197
-
Buxbaum J, Alexander A, Koziol J, Tagoe C, Fox E, Kitzman D (2010) Significance of the amyloidogenic transthyretin Val 122 Ile allele in African Americans in the Arteriosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies. Am Heart J 159:864–870
-
(2010)
Am Heart J
, vol.159
, pp. 864-870
-
-
Buxbaum, J.1
Alexander, A.2
Koziol, J.3
Tagoe, C.4
Fox, E.5
Kitzman, D.6
-
34
-
-
77954177629
-
Transthyretin-related amyloidoses and the heart: a clinical overview
-
COI: 1:CAS:528:DC%2BC3cXnvFylurc%3D, PID: 20479782
-
Rapezzi C, Quarta CC, Riva L et al (2010) Transthyretin-related amyloidoses and the heart: a clinical overview. Nat Rev Cardiol 7:398–408
-
(2010)
Nat Rev Cardiol
, vol.7
, pp. 398-408
-
-
Rapezzi, C.1
Quarta, C.C.2
Riva, L.3
-
35
-
-
84957433830
-
Survival after transplantation in patients with mutations other than Val30Met: extracts from the FAP world transplant registry
-
COI: 1:CAS:528:DC%2BC28XhvFOmtrc%3D, PID: 26656838
-
Suhr OB, Larsson M, Ericzon BG, Wilczek HE (2016) Survival after transplantation in patients with mutations other than Val30Met: extracts from the FAP world transplant registry. Transplantation 100:373–381
-
(2016)
Transplantation
, vol.100
, pp. 373-381
-
-
Suhr, O.B.1
Larsson, M.2
Ericzon, B.G.3
Wilczek, H.E.4
-
36
-
-
84888071980
-
Genotype, echocardiography, and survival in familial transthyretin amyloidosis
-
COI: 1:CAS:528:DC%2BC3sXhsl2htb7K
-
Arruda-Olson AM, Zeldenrust SR, Dispenzieri A et al (2013) Genotype, echocardiography, and survival in familial transthyretin amyloidosis. Amyloid: the international journal of experimental and clinical investigation: the official journal of the International Society of Amyloidosis 20:263–268
-
(2013)
Amyloid: the international journal of experimental and clinical investigation: the official journal of the International Society of Amyloidosis
, vol.20
, pp. 263-268
-
-
Arruda-Olson, A.M.1
Zeldenrust, S.R.2
Dispenzieri, A.3
-
37
-
-
84994501751
-
Natural history of wild-type transthyretin cardiac amyloidosis and risk stratification using a novel staging system
-
PID: 27585505
-
Grogan M, Scott CG, Kyle RA et al (2016) Natural history of wild-type transthyretin cardiac amyloidosis and risk stratification using a novel staging system. J Am Coll Cardiol 68:1014–1020
-
(2016)
J Am Coll Cardiol
, vol.68
, pp. 1014-1020
-
-
Grogan, M.1
Scott, C.G.2
Kyle, R.A.3
-
38
-
-
84928418312
-
Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs
-
COI: 1:CAS:528:DC%2BC2cXitVWksLbE, PID: 25408161
-
Castano A, Drachman BM, Judge D, Maurer MS (2015) Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs. Heart Fail Rev 20:163–178
-
(2015)
Heart Fail Rev
, vol.20
, pp. 163-178
-
-
Castano, A.1
Drachman, B.M.2
Judge, D.3
Maurer, M.S.4
-
39
-
-
80053283839
-
Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I
-
COI: 1:CAS:528:DC%2BC3MXhsVSqtbjL, PID: 21820994
-
Rowczenio D, Dogan A, Theis JD et al (2011) Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I. Am J Pathol 179:1978–1987
-
(2011)
Am J Pathol
, vol.179
, pp. 1978-1987
-
-
Rowczenio, D.1
Dogan, A.2
Theis, J.D.3
-
40
-
-
36148995393
-
Evaluation and management of the cardiac amyloidosis
-
COI: 1:CAS:528:DC%2BD2sXhtlGiu7rK, PID: 18036445
-
Selvanayagam JB, Hawkins PN, Paul B, Myerson SG, Neubauer S (2007) Evaluation and management of the cardiac amyloidosis. J Am Coll Cardiol 50:2101–2110
-
(2007)
J Am Coll Cardiol
, vol.50
, pp. 2101-2110
-
-
Selvanayagam, J.B.1
Hawkins, P.N.2
Paul, B.3
Myerson, S.G.4
Neubauer, S.5
-
44
-
-
84970857837
-
Cardiac transplantation for AL amyloidosis
-
COI: 1:STN:280:DyaK2M%2FnvVKitw%3D%3D
-
Hall R, Hawkins PN (1994) Cardiac transplantation for AL amyloidosis. BMJ (Clinical research ed) 309:1135–1137
-
(1994)
BMJ (Clinical research ed)
, vol.309
, pp. 1135-1137
-
-
Hall, R.1
Hawkins, P.N.2
-
45
-
-
0023877241
-
Heart transplantation for cardiac amyloidosis: successful one-year outcome despite recurrence of the disease
-
COI: 1:STN:280:DyaL1c3hsVGruw%3D%3D, PID: 3284989
-
Conner R, Hosenpud JD, Norman DJ, Pantely GA, Cobanoglu A, Starr A (1988) Heart transplantation for cardiac amyloidosis: successful one-year outcome despite recurrence of the disease. The Journal of heart transplantation 7:165–167
-
(1988)
The Journal of heart transplantation
, vol.7
, pp. 165-167
-
-
Conner, R.1
Hosenpud, J.D.2
Norman, D.J.3
Pantely, G.A.4
Cobanoglu, A.5
Starr, A.6
-
47
-
-
84976354847
-
Cardiac amyloid load: a prognostic and predictive biomarker in patients with light-chain amyloidosis
-
COI: 1:CAS:528:DC%2BC28XhtVyht7%2FO, PID: 27364045
-
Kristen AV, Brokbals E, Aus dem Siepen F et al (2016) Cardiac amyloid load: a prognostic and predictive biomarker in patients with light-chain amyloidosis. J Am Coll Cardiol 68:13–24
-
(2016)
J Am Coll Cardiol
, vol.68
, pp. 13-24
-
-
Kristen, A.V.1
Brokbals, E.2
Aus dem Siepen, F.3
-
48
-
-
78249290790
-
Cardiac transplantation followed by dose-intensive melphalan and autologous stem-cell transplantation for light chain amyloidosis and heart failure
-
COI: 1:CAS:528:DC%2BC3cXhtlSqu73P, PID: 20733534
-
Dey BR, Chung SS, Spitzer TR et al (2010) Cardiac transplantation followed by dose-intensive melphalan and autologous stem-cell transplantation for light chain amyloidosis and heart failure. Transplantation 90:905–911
-
(2010)
Transplantation
, vol.90
, pp. 905-911
-
-
Dey, B.R.1
Chung, S.S.2
Spitzer, T.R.3
-
50
-
-
84966495692
-
Does survival on the heart transplant waiting list depend on the underlying heart disease?
-
Hsich EM, Rogers JG, McNamara DM et al. (2016) Does survival on the heart transplant waiting list depend on the underlying heart disease? JACC Heart failure
-
(2016)
JACC Heart failure
-
-
Hsich, E.M.1
Rogers, J.G.2
McNamara, D.M.3
-
51
-
-
2042480728
-
Heart transplantation in patients with amyloidosis: single-center experience
-
COI: 1:STN:280:DC%2BD2c3hsVajtw%3D%3D, PID: 15110619
-
Alloni A, Pellegrini C, Ragni T et al (2004) Heart transplantation in patients with amyloidosis: single-center experience. Transplant Proc 36:643–644
-
(2004)
Transplant Proc
, vol.36
, pp. 643-644
-
-
Alloni, A.1
Pellegrini, C.2
Ragni, T.3
-
52
-
-
0026261681
-
Progression of systemic disease and reduced long-term survival in patients with cardiac amyloidosis undergoing heart transplantation. Follow-up results of a multicenter survey
-
COI: 1:STN:280:DyaK38%2FjsFGitw%3D%3D, PID: 1934428
-
Hosenpud JD, DeMarco T, Frazier OH et al (1991) Progression of systemic disease and reduced long-term survival in patients with cardiac amyloidosis undergoing heart transplantation. Follow-up results of a multicenter survey. Circulation 84:III338–III343
-
(1991)
Circulation
, vol.84
, pp. III338-III343
-
-
Hosenpud, J.D.1
DeMarco, T.2
Frazier, O.H.3
-
53
-
-
31544436321
-
Sequential heart and autologous stem cell transplantation for systemic AL amyloidosis
-
COI: 1:CAS:528:DC%2BD28Xht1Ontbg%3D, PID: 16210334
-
Gillmore JD, Goodman HJ, Lachmann HJ et al (2006) Sequential heart and autologous stem cell transplantation for systemic AL amyloidosis. Blood 107:1227–1229
-
(2006)
Blood
, vol.107
, pp. 1227-1229
-
-
Gillmore, J.D.1
Goodman, H.J.2
Lachmann, H.J.3
-
54
-
-
84957415044
-
Current indications, strategies, and outcomes with cardiac transplantation for cardiac amyloidosis and sarcoidosis
-
COI: 1:CAS:528:DC%2BC2MXhsFWns7vK, PID: 26262459
-
Rosenbaum AN, Edwards BS (2015) Current indications, strategies, and outcomes with cardiac transplantation for cardiac amyloidosis and sarcoidosis. Curr Opin Organ Transplant 20:584–592
-
(2015)
Curr Opin Organ Transplant
, vol.20
, pp. 584-592
-
-
Rosenbaum, A.N.1
Edwards, B.S.2
-
57
-
-
70349675875
-
Staged heart transplantation and chemotherapy as a treatment option in patients with severe cardiac light-chain amyloidosis
-
COI: 1:CAS:528:DC%2BD1MXht1Wru7jO, PID: 19789405
-
Kristen AV, Sack FU, Schonland SO et al (2009) Staged heart transplantation and chemotherapy as a treatment option in patients with severe cardiac light-chain amyloidosis. Eur J Heart Fail 11:1014–1020
-
(2009)
Eur J Heart Fail
, vol.11
, pp. 1014-1020
-
-
Kristen, A.V.1
Sack, F.U.2
Schonland, S.O.3
-
58
-
-
85011650987
-
Long term outcomes of cardiac transplant for immunoglobulin light chain amyloidosis: the Mayo Clinic experience
-
PID: 27358783
-
Grogan M, Gertz M, McCurdy A et al (2016) Long term outcomes of cardiac transplant for immunoglobulin light chain amyloidosis: the Mayo Clinic experience. World J Transplant 6:380–388
-
(2016)
World J Transplant
, vol.6
, pp. 380-388
-
-
Grogan, M.1
Gertz, M.2
McCurdy, A.3
-
59
-
-
84857048094
-
Heart transplantation and cardiac amyloidosis: approach to screening and novel management strategies
-
Varr BC, Liedtke M, Arai S, Lafayette RA, Schrier SL, Witteles RM (2012) Heart transplantation and cardiac amyloidosis: approach to screening and novel management strategies. The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation 31:325–331
-
(2012)
The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation
, vol.31
, pp. 325-331
-
-
Varr, B.C.1
Liedtke, M.2
Arai, S.3
Lafayette, R.A.4
Schrier, S.L.5
Witteles, R.M.6
-
62
-
-
33845350244
-
Long-term survival in a patient with AL amyloidosis after cardiac transplantation followed by autologous stem cell transplantation
-
COI: 1:STN:280:DC%2BD28npslWlsQ%3D%3D
-
Perz JB, Kristen AV, Rahemtulla A et al (2006) Long-term survival in a patient with AL amyloidosis after cardiac transplantation followed by autologous stem cell transplantation. Clinical research in cardiology: official journal of the German Cardiac Society 95:671–674
-
(2006)
Clinical research in cardiology: official journal of the German Cardiac Society
, vol.95
, pp. 671-674
-
-
Perz, J.B.1
Kristen, A.V.2
Rahemtulla, A.3
-
63
-
-
33947331862
-
Cardiac transplantation using extended-donor criteria organs for systemic amyloidosis complicated by heart failure
-
PID: 17353770
-
Maurer MS, Raina A, Hesdorffer C et al (2007) Cardiac transplantation using extended-donor criteria organs for systemic amyloidosis complicated by heart failure. Transplantation 83:539–545
-
(2007)
Transplantation
, vol.83
, pp. 539-545
-
-
Maurer, M.S.1
Raina, A.2
Hesdorffer, C.3
-
64
-
-
38349057368
-
Treatment options for severe cardiac amyloidosis: heart transplantation combined with chemotherapy and stem cell transplantation for patients with AL-amyloidosis and heart and liver transplantation for patients with ATTR-amyloidosis
-
Sack FU, Kristen A, Goldschmidt H et al (2008) Treatment options for severe cardiac amyloidosis: heart transplantation combined with chemotherapy and stem cell transplantation for patients with AL-amyloidosis and heart and liver transplantation for patients with ATTR-amyloidosis. European journal of cardio-thoracic surgery: official journal of the European Association for Cardio-thoracic Surgery 33:257–262
-
(2008)
European journal of cardio-thoracic surgery: official journal of the European Association for Cardio-thoracic Surgery
, vol.33
, pp. 257-262
-
-
Sack, F.U.1
Kristen, A.2
Goldschmidt, H.3
-
65
-
-
71049187207
-
Cardiac transplantation should be considered in selected patients with either AL or hereditary forms of amyloidosis: the UK National Amyloidosis Centre experience
-
COI: 1:STN:280:DC%2BD1MjmtVCqtw%3D%3D, PID: 19912412, author reply 787-8
-
Gibbs SD, Sattianayagam PT, Hawkins PN, Gillmore JD (2009) 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 39:786–787 author reply 787-8
-
(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
-
66
-
-
77955486307
-
Heart transplantation in patients with amyloidosis
-
PID: 20430206
-
Luo JM, Chou NK, Chi NH et al (2010) Heart transplantation in patients with amyloidosis. Transplant Proc 42:927–929
-
(2010)
Transplant Proc
, vol.42
, pp. 927-929
-
-
Luo, J.M.1
Chou, N.K.2
Chi, N.H.3
-
67
-
-
57849120727
-
Heart transplantation in systemic (AL) amyloidosis: a retrospective study of eight French patients
-
PID: 19041836
-
Mignot A, Varnous S, Redonnet M et al (2008) Heart transplantation in systemic (AL) amyloidosis: a retrospective study of eight French patients. Archives of cardiovascular diseases 101:523–532
-
(2008)
Archives of cardiovascular diseases
, vol.101
, pp. 523-532
-
-
Mignot, A.1
Varnous, S.2
Redonnet, M.3
-
68
-
-
66249101178
-
Outcomes of heart transplantation for cardiac amyloidosis: subanalysis of the Spanish registry for heart transplantation
-
COI: 1:STN:280:DC%2BD1Mrjs1SitQ%3D%3D
-
Roig E, Almenar L, Gonzalez-Vilchez F et al (2009) Outcomes of heart transplantation for cardiac amyloidosis: subanalysis of the Spanish registry for heart transplantation. Am J Transplant Off J Am Soc Transplant Am Soc Transplant Surg 9:1414–1419
-
(2009)
Am J Transplant Off J Am Soc Transplant Am Soc Transplant Surg
, vol.9
, pp. 1414-1419
-
-
Roig, E.1
Almenar, L.2
Gonzalez-Vilchez, F.3
-
70
-
-
45449090807
-
Current state of combined heart-liver transplantation in the United States
-
Te HS, Anderson AS, Millis JM, Jeevanandam V, Jensen DM (2008) Current state of combined heart-liver transplantation in the United States. The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation 27:753–759
-
(2008)
The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation
, vol.27
, pp. 753-759
-
-
Te, H.S.1
Anderson, A.S.2
Millis, J.M.3
Jeevanandam, V.4
Jensen, D.M.5
-
71
-
-
0025990675
-
Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30)
-
COI: 1:STN:280:DyaK387islyktw%3D%3D, PID: 1685359
-
Holmgren G, Steen L, Ekstedt J et al (1991) Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30). Clin Genet 40:242–246
-
(1991)
Clin Genet
, vol.40
, pp. 242-246
-
-
Holmgren, G.1
Steen, L.2
Ekstedt, J.3
-
74
-
-
84940745072
-
Liver transplantation for hereditary transthyretin amyloidosis: after 20 years still the best therapeutic alternative?
-
COI: 1:CAS:528:DC%2BC2MXhs1Ogu7%2FE, PID: 26308415
-
Ericzon BG, Wilczek HE, Larsson M et al (2015) Liver transplantation for hereditary transthyretin amyloidosis: after 20 years still the best therapeutic alternative? Transplantation 99:1847–1854
-
(2015)
Transplantation
, vol.99
, pp. 1847-1854
-
-
Ericzon, B.G.1
Wilczek, H.E.2
Larsson, M.3
-
75
-
-
84869088603
-
A review of the United States experience with combined heart-liver transplantation
-
Cannon RM, Hughes MG, Jones CM, Eng M, Marvin MR (2012) A review of the United States experience with combined heart-liver transplantation. Transplant international: official journal of the European Society for Organ Transplantation 25:1223–1228
-
(2012)
Transplant international: official journal of the European Society for Organ Transplantation
, vol.25
, pp. 1223-1228
-
-
Cannon, R.M.1
Hughes, M.G.2
Jones, C.M.3
Eng, M.4
Marvin, M.R.5
-
77
-
-
84889238225
-
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy
-
COI: 1:CAS:528:DC%2BC3sXhtl2jurfI, PID: 23974642
-
Coelho T, Maia LF, da Silva AM et al (2013) Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy. J Neurol 260:2802–2814
-
(2013)
J Neurol
, vol.260
, pp. 2802-2814
-
-
Coelho, T.1
Maia, L.F.2
da Silva, A.M.3
-
81
-
-
0038350962
-
Combined heart and liver transplantation for familial amyloidotic polyneuropathy
-
PID: 12771895
-
Arpesella G, Chiappini B, Marinelli G et al (2003) Combined heart and liver transplantation for familial amyloidotic polyneuropathy. J Thorac Cardiovasc Surg 125:1165–1166
-
(2003)
J Thorac Cardiovasc Surg
, vol.125
, pp. 1165-1166
-
-
Arpesella, G.1
Chiappini, B.2
Marinelli, G.3
-
83
-
-
11144355964
-
Combined heart and liver transplantation in four adults with familial amyloidosis: experience of a single center
-
COI: 1:STN:280:DC%2BD2c3hsVajtA%3D%3D, PID: 15110620
-
Nardo B, Beltempo P, Bertelli R et al (2004) Combined heart and liver transplantation in four adults with familial amyloidosis: experience of a single center. Transplant Proc 36:645–647
-
(2004)
Transplant Proc
, vol.36
, pp. 645-647
-
-
Nardo, B.1
Beltempo, P.2
Bertelli, R.3
-
84
-
-
68249116301
-
Combined heart and liver transplantation: a single-center experience
-
PID: 19623017
-
Raichlin E, Daly RC, Rosen CB et al (2009) Combined heart and liver transplantation: a single-center experience. Transplantation 88:219–225
-
(2009)
Transplantation
, vol.88
, pp. 219-225
-
-
Raichlin, E.1
Daly, R.C.2
Rosen, C.B.3
-
86
-
-
84876094177
-
Long-term outcome in patients treated with combined heart and liver transplantation for familial amyloidotic cardiomyopathy
-
Nelson LM, Penninga L, Sander K et al (2013) Long-term outcome in patients treated with combined heart and liver transplantation for familial amyloidotic cardiomyopathy. Clin Transpl 27:203–209
-
(2013)
Clin Transpl
, vol.27
, pp. 203-209
-
-
Nelson, L.M.1
Penninga, L.2
Sander, K.3
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