메뉴 건너뛰기




Volumn 36, Issue 2, 2013, Pages 263-270

Management of mucopolysaccharidosis type IH (Hurler's syndrome) presenting in infancy with severe dilated cardiomyopathy: A single institution's experience

Author keywords

[No Author keywords available]

Indexed keywords

ALEMTUZUMAB; BUSULFAN; CYCLOPHOSPHAMIDE; CYCLOSPORIN A; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; DIURETIC AGENT; LARONIDASE; METHOTREXATE; PREDNISONE; THYMOCYTE ANTIBODY;

EID: 84879688298     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-012-9500-3     Document Type: Article
Times cited : (31)

References (39)
  • 1
    • 41849119871 scopus 로고    scopus 로고
    • The clinical outcome of Hurler syndrome after stem cell transplantation
    • 18410891 10.1016/j.bbmt.2008.01.009 1:CAS:528:DC%2BD1cXmtFSnsrc%3D
    • Aldenhoven M, Boelens JJ, de Koning TJ (2008) The clinical outcome of Hurler syndrome after stem cell transplantation. Biol Blood Marrow Transplant 14(5):485-498
    • (2008) Biol Blood Marrow Transplant , vol.14 , Issue.5 , pp. 485-498
    • Aldenhoven, M.1    Boelens, J.J.2    De Koning, T.J.3
  • 2
    • 0016892443 scopus 로고
    • Acute lethal carditis caused by high-dose combination chemotherapy. A unique clinical and pathological entity
    • 54581 10.1016/S0140-6736(76)90151-3 1:STN:280:DyaE28%2FpvFamtA%3D%3D
    • Appelbaum F, Strauchen JA, Graw RG et al (1976) Acute lethal carditis caused by high-dose combination chemotherapy. A unique clinical and pathological entity. Lancet 1(7950):58-62
    • (1976) Lancet , vol.1 , Issue.7950 , pp. 58-62
    • Appelbaum, F.1    Strauchen, J.A.2    Graw, R.G.3
  • 3
    • 34547147899 scopus 로고    scopus 로고
    • Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: A risk factor analysis for graft failure
    • 17529997 10.1038/sj.bmt.1705718 1:STN:280:DC%2BD2svhs1Ggtg%3D%3D
    • Boelens JJ, Wynn RF, O'meara A et al (2007) Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: a risk factor analysis for graft failure. Bone Marrow Transplant 40(3):225-233
    • (2007) Bone Marrow Transplant , vol.40 , Issue.3 , pp. 225-233
    • Boelens, J.J.1    Wynn, R.F.2    O'Meara, A.3
  • 4
    • 63749102158 scopus 로고    scopus 로고
    • Risk factor analysis of outcomes after unrelated cord blood transplantation in patients with hurler syndrome
    • 19361754 10.1016/j.bbmt.2009.01.020
    • Boelens JJ, Rocha V, Aldenhoven M et al (2009) Risk factor analysis of outcomes after unrelated cord blood transplantation in patients with hurler syndrome. Biol Blood Marrow Transplant 15(5):618-625
    • (2009) Biol Blood Marrow Transplant , vol.15 , Issue.5 , pp. 618-625
    • Boelens, J.J.1    Rocha, V.2    Aldenhoven, M.3
  • 5
    • 0141459294 scopus 로고    scopus 로고
    • Usefulness of bone marrow transplantation in the Hurler syndrome
    • 14516901 10.1016/S0002-9149(03)00909-3
    • Braunlin EA, Stauffer NR, Peters CH et al (2003) Usefulness of bone marrow transplantation in the Hurler syndrome. Am J Cardiol 92(7):882-886
    • (2003) Am J Cardiol , vol.92 , Issue.7 , pp. 882-886
    • Braunlin, E.A.1    Stauffer, N.R.2    Peters, C.H.3
  • 6
    • 33745943855 scopus 로고    scopus 로고
    • Cardiac findings after enzyme replacement therapy for mucopolysaccharidosis type i
    • 16860035 10.1016/j.amjcard.2006.02.047 1:CAS:528:DC%2BD28XntVWjtrw%3D
    • Braunlin EA, Berry JM, Whitley CB (2006) Cardiac findings after enzyme replacement therapy for mucopolysaccharidosis type I. Am J Cardiol 98(3):416-418
    • (2006) Am J Cardiol , vol.98 , Issue.3 , pp. 416-418
    • Braunlin, E.A.1    Berry, J.M.2    Whitley, C.B.3
  • 7
    • 82955163032 scopus 로고    scopus 로고
    • Cardiac disease in patients with mucopolysaccharidosis: Presentation, diagnosis and management
    • 21744090 10.1007/s10545-011-9359-8 1:CAS:528:DC%2BC3MXhsFyjt7%2FI
    • Braunlin EA, Harmatz PR, Scarpa M et al (2011) Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management. J Inherit Metab Dis 34(6):1183-1197
    • (2011) J Inherit Metab Dis , vol.34 , Issue.6 , pp. 1183-1197
    • Braunlin, E.A.1    Harmatz, P.R.2    Scarpa, M.3
  • 8
    • 0031834476 scopus 로고    scopus 로고
    • Cardiovascular changes in children with mucopolysaccharide storage diseases and related disorders-clinical and echocardiographic findings in 64 patients
    • 9686810 10.1007/s004310050872 1:STN:280:DyaK1czkvFGquw%3D%3D
    • Dangel JH (1998) Cardiovascular changes in children with mucopolysaccharide storage diseases and related disorders-clinical and echocardiographic findings in 64 patients. Eur J Pediatr 157(7):534-538
    • (1998) Eur J Pediatr , vol.157 , Issue.7 , pp. 534-538
    • Dangel, J.H.1
  • 10
    • 0027319246 scopus 로고
    • Cyclophosphamide cardiac injury mimicking acute myocardial infarction
    • 8401367 1:STN:280:DyaK2c%2FgsVOjsw%3D%3D
    • Dow E, Schulman H, Agura E (1993) Cyclophosphamide cardiac injury mimicking acute myocardial infarction. Bone Marrow Transplant 12(2):169-172
    • (1993) Bone Marrow Transplant , vol.12 , Issue.2 , pp. 169-172
    • Dow, E.1    Schulman, H.2    Agura, E.3
  • 11
    • 0029117050 scopus 로고
    • Cardiac involvement in mucopolysaccharidoses: Effects of allogeneic bone marrow transplantation
    • 7492172 10.1136/adc.73.3.259 1:STN:280:DyaK28%2FpsF2msQ%3D%3D
    • Gatzoulis MA, Vellodi A, Redington AN (1995) Cardiac involvement in mucopolysaccharidoses: effects of allogeneic bone marrow transplantation. Arch Dis Child 73(3):259-260
    • (1995) Arch Dis Child , vol.73 , Issue.3 , pp. 259-260
    • Gatzoulis, M.A.1    Vellodi, A.2    Redington, A.N.3
  • 12
    • 0036623690 scopus 로고    scopus 로고
    • Chemotherapy-induced cardiotoxicity: Current practice and prospects of prophylaxis
    • 12034146 10.1016/S1388-9842(01)00201-X 1:CAS:528:DC%2BD38XktVGju7k%3D
    • Gharib MI, Burnett AK (2002) Chemotherapy-induced cardiotoxicity: current practice and prospects of prophylaxis. Eur J Heart Fail 4(3):235-242
    • (2002) Eur J Heart Fail , vol.4 , Issue.3 , pp. 235-242
    • Gharib, M.I.1    Burnett, A.K.2
  • 13
    • 0022806838 scopus 로고
    • Cyclophosphamide cardiotoxicity: An analysis of dosing as a risk factor
    • 3533179 1:STN:280:DyaL2s%2Fis12ksQ%3D%3D
    • Goldberg MA, Antin JH, Guinan EC, Rappeport JM (1986) Cyclophosphamide cardiotoxicity: an analysis of dosing as a risk factor. Blood 68(5):1114-1118
    • (1986) Blood , vol.68 , Issue.5 , pp. 1114-1118
    • Goldberg, M.A.1    Antin, J.H.2    Guinan, E.C.3    Rappeport, J.M.4
  • 14
    • 84948007710 scopus 로고
    • Cardiotoxicity associated with high-dose cyclophosphamide therapy
    • 7235784 10.1001/archinte.1981.00340060066015 1:STN:280: DyaL3M3gs1ejtQ%3D%3D
    • Gottdiener JS, Appelbaum FR, Ferrans VJ, Deisseroth A, Ziegler J (1981) Cardiotoxicity associated with high-dose cyclophosphamide therapy. Arch Intern Med 141(6):758-763
    • (1981) Arch Intern Med , vol.141 , Issue.6 , pp. 758-763
    • Gottdiener, J.S.1    Appelbaum, F.R.2    Ferrans, V.J.3    Deisseroth, A.4    Ziegler, J.5
  • 15
    • 0023760034 scopus 로고
    • Echocardiographic abnormalities in the mucopolysaccharide storage diseases
    • 3122547 10.1016/0002-9149(88)91325-2 1:STN:280:DyaL1c7gtlehsQ%3D%3D
    • Gross DM, Williams JC, Caprioli C, Dominguez B, Howell RR (1988) Echocardiographic abnormalities in the mucopolysaccharide storage diseases. Am J Cardiol 61(1):170-176
    • (1988) Am J Cardiol , vol.61 , Issue.1 , pp. 170-176
    • Gross, D.M.1    Williams, J.C.2    Caprioli, C.3    Dominguez, B.4    Howell, R.R.5
  • 16
    • 0033888320 scopus 로고    scopus 로고
    • Impaired elastogenesis in Hurler disease: Dermatan sulfate accumulation linked to deficiency in elastin-binding protein and elastic fiber assembly
    • 10702409 10.1016/S0002-9440(10)64961-9 1:CAS:528:DC%2BD3cXitVeru7Y%3D
    • Hinek A, Wilson SE (2000) Impaired elastogenesis in Hurler disease: dermatan sulfate accumulation linked to deficiency in elastin-binding protein and elastic fiber assembly. Am J Pathol 156(3):925-938
    • (2000) Am J Pathol , vol.156 , Issue.3 , pp. 925-938
    • Hinek, A.1    Wilson, S.E.2
  • 17
    • 35448943425 scopus 로고    scopus 로고
    • Successful treatment of severe heart failure in an infant with Hurler syndrome
    • 17768668 10.1007/s10545-007-0613-z 1:STN:280:DC%2BD2sngtFyntw%3D%3D
    • Hirth A, Berg A, Greve G (2007) Successful treatment of severe heart failure in an infant with Hurler syndrome. J Inherit Metab Dis 30(5):820
    • (2007) J Inherit Metab Dis , vol.30 , Issue.5 , pp. 820
    • Hirth, A.1    Berg, A.2    Greve, G.3
  • 18
    • 0019466750 scopus 로고
    • Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation
    • 6116856 10.1016/S0140-6736(81)91046-1 1:STN:280:DyaL38%2FjsVOmtw%3D%3D
    • Hobbs JR, Hugh-Jones K, Barrett AJ et al (1981) Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation. Lancet 2(8249):709-712
    • (1981) Lancet , vol.2 , Issue.8249 , pp. 709-712
    • Hobbs, J.R.1    Hugh-Jones, K.2    Barrett, A.J.3
  • 19
    • 0029143678 scopus 로고
    • Microglia: The effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage diseases
    • 7582569 10.1016/0963-6897(95)00021-O 1:STN:280:DyaK28%2FptVehsw%3D%3D
    • Krivit W, Sung JH, Shapiro EG, Lockman LA (1995) Microglia: the effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage diseases. Cell Transplant 4(4):385-392
    • (1995) Cell Transplant , vol.4 , Issue.4 , pp. 385-392
    • Krivit, W.1    Sung, J.H.2    Shapiro, E.G.3    Lockman, L.A.4
  • 20
    • 77953550230 scopus 로고    scopus 로고
    • Echocardiographic study of paediatric patients with mucopolysaccharidosis
    • 20416133 10.1017/S104795110999062X
    • Leal GN, de Paula AC, Leone C, Kim CA (2010) Echocardiographic study of paediatric patients with mucopolysaccharidosis. Cardiol Young 20(3):254-261
    • (2010) Cardiol Young , vol.20 , Issue.3 , pp. 254-261
    • Leal, G.N.1    De Paula, A.C.2    Leone, C.3    Kim, C.A.4
  • 21
    • 52949116848 scopus 로고    scopus 로고
    • The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK
    • 18796143 10.1186/1750-1172-3-24
    • Moore D, Connock MJ, Wraith E, Lavery C (2008) The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK. Orphanet J Rare Dis 3:24
    • (2008) Orphanet J Rare Dis , vol.3 , pp. 24
    • Moore, D.1    Connock, M.J.2    Wraith, E.3    Lavery, C.4
  • 22
    • 0000869162 scopus 로고    scopus 로고
    • The mucopolysaccharidoses
    • Scriver CS, WS ed. New York: McGraw Hill
    • Neufield EM, J (2000) The mucopolysaccharidoses. In Scriver CS, WS ed. The metabolic and molecular bases of inherited disease: New York: McGraw Hill, 3421-3452
    • (2000) The Metabolic and Molecular Bases of Inherited Disease , pp. 3421-3452
    • Emj, N.1
  • 23
    • 78651341103 scopus 로고    scopus 로고
    • Cardiac disease in mucopolysaccharidosis type i attributed to catecholaminergic and hemodynamic deficiencies
    • 21076027 10.1152/ajpheart.00774.2010 1:CAS:528:DC%2BC3MXhslWnsrc%3D
    • Palpant NJ, Bedada FB, Peacock B, Blazar BR, Metzger JM, Tolar J (2011) Cardiac disease in mucopolysaccharidosis type I attributed to catecholaminergic and hemodynamic deficiencies. Am J Physiol Heart Circ Physiol 300(1):H356-365
    • (2011) Am J Physiol Heart Circ Physiol , vol.300 , Issue.1 , pp. 356-365
    • Palpant, N.J.1    Bedada, F.B.2    Peacock, B.3    Blazar, B.R.4    Metzger, J.M.5    Tolar, J.6
  • 24
    • 34047274124 scopus 로고    scopus 로고
    • The MPS i registry: Design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type i
    • 17336562 10.1016/j.ymgme.2007.01.011 1:CAS:528:DC%2BD2sXkt1ehuro%3D
    • Pastores GM, Arn P, Beck M et al (2007) The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I. Mol Genet Metab 91(1):37-47
    • (2007) Mol Genet Metab , vol.91 , Issue.1 , pp. 37-47
    • Pastores, G.M.1    Arn, P.2    Beck, M.3
  • 25
    • 0032055564 scopus 로고    scopus 로고
    • Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group
    • 9516162 1:CAS:528:DyaK1cXitF2hsbc%3D
    • Peters C, Shapiro EG, Anderson J et al (1998) Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group. Blood 91(7):2601-2608
    • (1998) Blood , vol.91 , Issue.7 , pp. 2601-2608
    • Peters, C.1    Shapiro, E.G.2    Anderson, J.3
  • 26
    • 84864532141 scopus 로고    scopus 로고
    • Hematopoietic stem cell transplantation ameliorates the high incidence of neutralizing allo-antibodies observed in MPSI-Hurler after pharmacological enzyme replacement therapy
    • doi: 10.3324/haematol.2011.058644
    • Saif MA, Bigger BW, Brookes KE, et al (2012) Hematopoietic stem cell transplantation ameliorates the high incidence of neutralizing allo-antibodies observed in MPSI-Hurler after pharmacological enzyme replacement therapy. Haematologica doi: 10.3324/haematol.2011.058644
    • (2012) Haematologica
    • Saif, M.A.1    Bigger, B.W.2    Brookes, K.E.3
  • 27
    • 0015458139 scopus 로고
    • The use of cyclophosphamide for clinical marrow transplantation
    • 4405147 1:STN:280:DyaE3s%2FntlKhsQ%3D%3D
    • Santos GW, Sensenbrenner LL, Burke PJ et al (1972) The use of cyclophosphamide for clinical marrow transplantation. Transplant Proc 4(4):559-564
    • (1972) Transplant Proc , vol.4 , Issue.4 , pp. 559-564
    • Santos, G.W.1    Sensenbrenner, L.L.2    Burke, P.J.3
  • 28
    • 0016828432 scopus 로고
    • Cardiac manifestations of the mucopolysaccharidoses
    • 10.1161/01.CIR.52.4.700 1:STN:280:DyaE28%2FgtFygsA%3D%3D
    • Schieken RM, Kerber RE, Ionasescu VV, Zellweger H (1975) Cardiac manifestations of the mucopolysaccharidoses. Circ 52(4):700-705
    • (1975) Circ , vol.52 , Issue.4 , pp. 700-705
    • Schieken, R.M.1    Kerber, R.E.2    Ionasescu, V.V.3    Zellweger, H.4
  • 29
    • 0029146242 scopus 로고
    • Neuropsychological outcomes of several storage diseases with and without bone marrow transplantation
    • 7494400 10.1007/BF00710053 1:STN:280:DyaK28%2Flt1yjsQ%3D%3D
    • Shapiro EG, Lockman LA, Balthazor M, Krivit W (1995) Neuropsychological outcomes of several storage diseases with and without bone marrow transplantation. J Inherit Metab Dis 18(4):413-429
    • (1995) J Inherit Metab Dis , vol.18 , Issue.4 , pp. 413-429
    • Shapiro, E.G.1    Lockman, L.A.2    Balthazor, M.3    Krivit, W.4
  • 30
    • 10744223978 scopus 로고    scopus 로고
    • Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources
    • 12796790 10.1038/sj.bmt.1704105 1:STN:280:DC%2BD3s3mvFKqtw%3D%3D
    • Souillet G, Guffon N, Maire I et al (2003) Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources. Bone Marrow Transplant 31(12):1105-1117
    • (2003) Bone Marrow Transplant , vol.31 , Issue.12 , pp. 1105-1117
    • Souillet, G.1    Guffon, N.2    Maire, I.3
  • 31
    • 0019823623 scopus 로고
    • Cardiac changes with cyclophosphamide
    • 7300803 10.1002/mpo.2950090502 1:STN:280:DyaL38%2FlslKrsQ%3D%3D
    • Steinherz LJ, Steinherz PG, Mangiacasale D et al (1981) Cardiac changes with cyclophosphamide. Med Pediatr Oncol 9(5):417-422
    • (1981) Med Pediatr Oncol , vol.9 , Issue.5 , pp. 417-422
    • Steinherz, L.J.1    Steinherz, P.G.2    Mangiacasale, D.3
  • 32
    • 0026511701 scopus 로고
    • Hypertrophic cardiomyopathy in mucopolysaccharidoses: Regression after bone marrow transplantation
    • 1614914 10.1007/BF00798216
    • Viñallonga X, Sanz N, Balaguer A, Miro L, Ortega JJ, Casaldaliga J (1992) Hypertrophic cardiomyopathy in mucopolysaccharidoses: regression after bone marrow transplantation. Pediatr Cardiol 13(2):107-109
    • (1992) Pediatr Cardiol , vol.13 , Issue.2 , pp. 107-109
    • Viñallonga, X.1    Sanz, N.2    Balaguer, A.3    Miro, L.4    Ortega, J.J.5    Casaldaliga, J.6
  • 33
    • 0027466761 scopus 로고
    • Long-term outcome of Hurler syndrome following bone marrow transplantation
    • 8484412 10.1002/ajmg.1320460222 1:STN:280:DyaK3s3kvV2nsw%3D%3D
    • Whitley CB, Belani KG, Chang PN et al (1993) Long-term outcome of Hurler syndrome following bone marrow transplantation. Am J Med Genet 46(2):209-218
    • (1993) Am J Med Genet , vol.46 , Issue.2 , pp. 209-218
    • Whitley, C.B.1    Belani, K.G.2    Chang, P.N.3
  • 34
    • 0035000479 scopus 로고    scopus 로고
    • Enzyme replacement therapy in mucopolysaccharidosis type I: Progress and emerging difficulties
    • 11405343 10.1023/A:1010379320378 1:CAS:528:DC%2BD3MXkslCrtrs%3D
    • Wraith JE (2001) Enzyme replacement therapy in mucopolysaccharidosis type I: progress and emerging difficulties. J Inherit Metab Dis 24(2):245-250
    • (2001) J Inherit Metab Dis , vol.24 , Issue.2 , pp. 245-250
    • Wraith, J.E.1
  • 35
    • 17144399564 scopus 로고    scopus 로고
    • The first 5 years of clinical experience with laronidase enzyme replacement therapy for mucopolysaccharidosis i
    • 15794739 10.1517/14656566.6.3.489 1:CAS:528:DC%2BD2MXjvVyrtrk%3D
    • Wraith JE (2005) The first 5 years of clinical experience with laronidase enzyme replacement therapy for mucopolysaccharidosis I. Expert Opin Pharmacother 6(3):489-506
    • (2005) Expert Opin Pharmacother , vol.6 , Issue.3 , pp. 489-506
    • Wraith, J.E.1
  • 36
    • 34447121276 scopus 로고    scopus 로고
    • Enzyme replacement therapy in patients who have mucopolysaccharidosis i and are younger than 5 years: Results of a multinational study of recombinant human alpha-L-iduronidase (laronidase)
    • 10.1542/peds.2006-2156
    • Wraith JE, Beck M, Lane R et al (2007) Enzyme replacement therapy in patients who have mucopolysaccharidosis I and are younger than 5 years: results of a multinational study of recombinant human alpha-L-iduronidase (laronidase). Pediatr 120(1):e37-46
    • (2007) Pediatr , vol.120 , Issue.1 , pp. 37-46
    • Wraith, J.E.1    Beck, M.2    Lane, R.3
  • 37
    • 62649094547 scopus 로고    scopus 로고
    • Improved metabolic correction in patients with lysosomal storage disease treated with hematopoietic stem cell transplant compared with enzyme replacement therapy
    • 19324223 10.1016/j.jpeds.2008.11.005 1:CAS:528:DC%2BD1MXjslOnt78%3D
    • Wynn RF, Wraith JE, Mercer J et al (2009) Improved metabolic correction in patients with lysosomal storage disease treated with hematopoietic stem cell transplant compared with enzyme replacement therapy. J Pediatr 154(4):609-611
    • (2009) J Pediatr , vol.154 , Issue.4 , pp. 609-611
    • Wynn, R.F.1    Wraith, J.E.2    Mercer, J.3
  • 38
    • 84881002836 scopus 로고    scopus 로고
    • Postmortem studies on a patient with mucopolysaccharidosis type I: Histopathological findings after one year of enzyme replacement therapy
    • Mar 27 (Epub ahead of print)
    • Yano S, Moseley K, Pavlova Z (2009) Postmortem studies on a patient with mucopolysaccharidosis type I: Histopathological findings after one year of enzyme replacement therapy. J Inherit Metab Dis Mar 27 (Epub ahead of print)
    • (2009) J Inherit Metab Dis
    • Yano, S.1    Moseley, K.2    Pavlova, Z.3
  • 39
    • 6044274062 scopus 로고    scopus 로고
    • Cardiovascular complications of cancer therapy: Diagnosis, pathogenesis, and management
    • 10.1161/01.CIR.0000133187.74800.B9
    • Yeh ETH, Tong AT, Lenihan DJ et al (2004) Cardiovascular complications of cancer therapy: diagnosis, pathogenesis, and management. Circ 109(25):3122-3131
    • (2004) Circ , vol.109 , Issue.25 , pp. 3122-3131
    • Yeh, E.T.H.1    Tong, A.T.2    Lenihan, D.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.