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Volumn 11, Issue 3, 2014, Pages 168-179

Treatment of dystrophin cardiomyopathies

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOTENSIN RECEPTOR ANTAGONIST; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CALCIUM; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; DYSTROPHIN; MINERALOCORTICOID ANTAGONIST; NITRIC OXIDE; STEROID; UTROPHIN;

EID: 84896701493     PISSN: 17595002     EISSN: 17595010     Source Type: Journal    
DOI: 10.1038/nrcardio.2013.213     Document Type: Review
Times cited : (54)

References (147)
  • 1
    • 84881218944 scopus 로고    scopus 로고
    • Cardiac and respiratory dysfunction in Duchenne muscular dystrophy and the role of second messengers
    • Mosqueira, M., Zeiger, U., Frderer, M., Brinkmeier, H. & Fink, R. H. Cardiac and respiratory dysfunction in Duchenne muscular dystrophy and the role of second messengers. Med. Res. Rev. 33, 1174-1213 (2013).
    • (2013) Med. Res. Rev , vol.33 , pp. 1174-1213
    • Mosqueira, M.1    Zeiger, U.2    Frderer, M.3    Brinkmeier, H.4    Fink, R.H.5
  • 2
    • 77950362202 scopus 로고    scopus 로고
    • Cardiomyopathy in Duchenne muscular dystrophy: Pathogenesis and therapeutics
    • Fayssoil, A., Nardi, O., Orlikowski, D. & Annane, D. Cardiomyopathy in Duchenne muscular dystrophy: pathogenesis and therapeutics. Heart Fail. Rev. 15, 103-107 (2010).
    • (2010) Heart Fail. Rev , vol.15 , pp. 103-107
    • Fayssoil, A.1    Nardi, O.2    Orlikowski, D.3    Annane, D.4
  • 3
    • 84891829592 scopus 로고    scopus 로고
    • Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapy
    • van den Bergen, J. C. et al. Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapy. J. Neurol. Neurosurg. Psychiatry 85, 92-98 (2014).
    • (2014) J. Neurol. Neurosurg. Psychiatry , vol.85 , pp. 92-98
    • Van Den Bergen, J.C.1
  • 4
    • 84858975848 scopus 로고    scopus 로고
    • The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy
    • Neri, M. et al. The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy. BMC Med. Genet. 13, 20 (2012).
    • (2012) BMC Med. Genet , vol.13 , Issue.20
    • Neri, M.1
  • 5
    • 77449155277 scopus 로고    scopus 로고
    • Familial dilated cardiomyopathy secondary to dystrophin splice site mutation
    • Obler, D. et al. Familial dilated cardiomyopathy secondary to dystrophin splice site mutation. J. Card. Fail. 16, 194-199 (2010).
    • (2010) J. Card. Fail , vol.16 , pp. 194-199
    • Obler, D.1
  • 6
    • 84869160655 scopus 로고    scopus 로고
    • Improvement of survival in Duchenne muscular dystrophy: Retrospective analysis of 835 patients
    • Passamano, L. et al. Improvement of survival in Duchenne muscular dystrophy: retrospective analysis of 835 patients. Acta Myol. 31, 121-125 (2012).
    • (2012) Acta Myol , vol.31 , pp. 121-125
    • Passamano, L.1
  • 7
    • 54449083388 scopus 로고    scopus 로고
    • Cardiac involvement in Becker muscular dystrophy
    • Finsterer, J. & Stllberger, C. Cardiac involvement in Becker muscular dystrophy. Can. J. Cardiol. 24, 786-792 (2008).
    • (2008) Can. J. Cardiol , vol.24 , pp. 786-792
    • Finsterer, J.1    Stllberger, C.2
  • 8
    • 84881611731 scopus 로고    scopus 로고
    • Comparison of X-chromosome inactivation in Duchenne muscle/myocardium- manifesting carriers, non-manifesting carriers and related daughters
    • Viggiano, E., Picillo, E., Cirillo, A. & Politano, L. Comparison of X-chromosome inactivation in Duchenne muscle/myocardium-manifesting carriers, non-manifesting carriers and related daughters. Clin. Genet. 84, 265-270 (2012).
    • (2012) Clin. Genet , vol.84 , pp. 265-270
    • Viggiano, E.1    Picillo, E.2    Cirillo, A.3    Politano, L.4
  • 9
    • 61949145164 scopus 로고    scopus 로고
    • NO may prompt calcium leakage in dystrophic muscle
    • Tidball, J. G. & Villalta, S. A. NO may prompt calcium leakage in dystrophic muscle. Nat. Med. 15, 243-244 (2009).
    • (2009) Nat. Med , vol.15 , pp. 243-244
    • Tidball, J.G.1    Villalta, S.A.2
  • 10
    • 84864516708 scopus 로고    scopus 로고
    • Variable phenotype of del45-55 Becker patients correlated with nNOS? Mislocalization and RYR1 hypernitrosylation
    • Gentil, C. et al. Variable phenotype of del45-55 Becker patients correlated with nNOS? mislocalization and RYR1 hypernitrosylation. Hum. Mol. Genet. 21, 3449-3460 (2012).
    • (2012) Hum. Mol. Genet , vol.21 , pp. 3449-3460
    • Gentil, C.1
  • 11
    • 84885133772 scopus 로고    scopus 로고
    • Exon skipping and gene transfer restore dystrophin expression in human induced pluripotent stem cells-cardiomyocytes harboring DMD mutations
    • Dick, E. et al. Exon skipping and gene transfer restore dystrophin expression in human induced pluripotent stem cells-cardiomyocytes harboring DMD mutations. Stem Cells Dev. 15, 2714-2724 (2013).
    • (2013) Stem Cells Dev , vol.15 , pp. 2714-2724
    • Dick, E.1
  • 12
    • 84861660093 scopus 로고    scopus 로고
    • Treatment of dystrophinopathic cardiomyopathy: Review of the literature and personal results
    • Politano, L. & Nigro, G. Treatment of dystrophinopathic cardiomyopathy: review of the literature and personal results. Acta Myol. 31, 24-30 (2012).
    • (2012) Acta Myol , vol.31 , pp. 24-30
    • Politano, L.1    Nigro, G.2
  • 13
    • 0034219353 scopus 로고    scopus 로고
    • Muscular dystrophy
    • Roland, E. H. Muscular dystrophy. Pediatr. Rev. 21, 233-237 (2000).
    • (2000) Pediatr. Rev , vol.21 , pp. 233-237
    • Roland, E.H.1
  • 14
    • 0037304994 scopus 로고    scopus 로고
    • 107th ENMC international workshop: The management of cardiac involvement in muscular dystrophy and myotonic dystrophy
    • Bushby, K., Mutoni, F. & Bourke, J. P. 107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. Neuromuscul. Disord. 13, 166-172 (2003).
    • (2003) Neuromuscul. Disord , vol.13 , pp. 166-172
    • Bushby, K.1    Mutoni, F.2    Bourke, J.P.3
  • 15
    • 0029971310 scopus 로고    scopus 로고
    • Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies
    • Politano, L. et al. Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies. JAMA 275, 1335-1338 (1996).
    • (1996) JAMA , vol.275 , pp. 1335-1338
    • Politano, L.1
  • 16
    • 78649668751 scopus 로고    scopus 로고
    • Cardiac assessment in Duchenne and Becker muscular dystrophies
    • Romfh, A. & McNally, E. M. Cardiac assessment in Duchenne and Becker muscular dystrophies. Curr. Heart Fail. Rep. 7, 212-218 (2010).
    • (2010) Curr. Heart Fail. Rep , vol.7 , pp. 212-218
    • Romfh, A.1    McNally, E.M.2
  • 17
    • 77957830378 scopus 로고    scopus 로고
    • Cardiac resynchronization therapy in Becker muscular dystrophy: For which patients?
    • Fayssoil, A. & Abasse, S. Cardiac resynchronization therapy in Becker muscular dystrophy: for which patients? Hellenic J. Cardiol. 51, 377-378 (2010).
    • (2010) Hellenic J. Cardiol , vol.51 , pp. 377-378
    • Fayssoil, A.1    Abasse, S.2
  • 18
    • 67649871434 scopus 로고    scopus 로고
    • Somatic mosaicism for Duchenne dystrophy: Evidence for genetic normalization mitigating muscle symptoms
    • Kesari, A. et al. Somatic mosaicism for Duchenne dystrophy: evidence for genetic normalization mitigating muscle symptoms. Am. J. Med. Genet. A 149A, 1499-1503 (2009).
    • (2009) Am. J. Med. Genet. A , vol.149 , pp. 1499-1503
    • Kesari, A.1
  • 19
    • 8044224015 scopus 로고    scopus 로고
    • Myocardial involvement is very frequent among patients affected with subclinical Beckers muscular dystrophy
    • Melacini, P. et al. Myocardial involvement is very frequent among patients affected with subclinical Beckers muscular dystrophy. Circulation 94, 3168-3175 (1996).
    • (1996) Circulation , vol.94 , pp. 3168-3175
    • Melacini, P.1
  • 20
    • 80051486151 scopus 로고    scopus 로고
    • Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
    • Schade van Westrum, S. M. et al. Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy. Neurology 77, 62-66 (2011).
    • (2011) Neurology , vol.77 , pp. 62-66
    • Schade Van Westrum, S.M.1
  • 21
    • 0028819577 scopus 로고
    • Evaluation of the cardiomyopathy in Becker muscular dystrophy
    • Nigro, G. et al. Evaluation of the cardiomyopathy in Becker muscular dystrophy. Muscle Nerve 18, 283-291 (1995).
    • (1995) Muscle Nerve , vol.18 , pp. 283-291
    • Nigro, G.1
  • 22
    • 0035178452 scopus 로고    scopus 로고
    • Spontaneous left ventricular hypertrabeculation in dystrophin duplication based Beckers muscular dystrophy
    • Finsterer, J. & Stllberger, C. Spontaneous left ventricular hypertrabeculation in dystrophin duplication based Beckers muscular dystrophy. Herz 26, 477-481 (2001).
    • (2001) Herz , vol.26 , pp. 477-481
    • Finsterer, J.1    Stllberger, C.2
  • 23
    • 35948966373 scopus 로고    scopus 로고
    • Characteristics of cardiomyopathy in recessive X-linked myodystrophy with a rapid and slow course [Russian]
    • Vikentev, V. V. & Grinio, L. P. Characteristics of cardiomyopathy in recessive X-linked myodystrophy with a rapid and slow course [Russian]. Ter. Arkh. 79, 49-53 (2007).
    • (2007) Ter. Arkh , vol.79 , pp. 49-53
    • Vikentev, V.V.1    Grinio, L.P.2
  • 24
    • 36549078038 scopus 로고    scopus 로고
    • Revising the cardiac phenotype of Duchenne muscular dystrophy
    • Markham, L. W. et al. Revising the cardiac phenotype of Duchenne muscular dystrophy. Neuromuscul. Disord. 16, 699 (2006).
    • (2006) Neuromuscul. Disord , vol.16 , pp. 699
    • Markham, L.W.1
  • 25
    • 84867841437 scopus 로고    scopus 로고
    • Correlation of heart rate and cardiac dysfunction in Duchenne muscular dystrophy
    • Thomas, T. O., Morgan, T. M., Burnette, W. B. & Markham, L. W. Correlation of heart rate and cardiac dysfunction in Duchenne muscular dystrophy. Pediatr. Cardiol. 33, 1175-1179 (2012).
    • (2012) Pediatr. Cardiol , vol.33 , pp. 1175-1179
    • Thomas, T.O.1    Morgan, T.M.2    Burnette, W.B.3    Markham, L.W.4
  • 26
    • 69749085715 scopus 로고    scopus 로고
    • Pericardial effusion with cardiac tamponade as a cardiac manifestation of Duchenne muscular dystrophy
    • Lin, J. J. et al. Pericardial effusion with cardiac tamponade as a cardiac manifestation of Duchenne muscular dystrophy. Muscle Nerve 40, 476-480 (2009).
    • (2009) Muscle Nerve , vol.40 , pp. 476-480
    • Lin, J.J.1
  • 27
    • 84896738731 scopus 로고    scopus 로고
    • Electrocardiographic abnormalities in Duchenne muscular dystrophy prior to the onset of cardiac dysfunction
    • James, J., Kinnett, K., Wang, Y., Ittenbach, R. & Cripe, L. Electrocardiographic abnormalities in Duchenne muscular dystrophy prior to the onset of cardiac dysfunction. Neuromuscul. Disord. 20, 661 (2010).
    • (2010) Neuromuscul. Disord , vol.20 , Issue.661
    • James, J.1    Kinnett, K.2    Wang, Y.3    Ittenbach, R.4    Cripe, L.5
  • 28
    • 0016719224 scopus 로고
    • Echocardiographic evaluation of posterior left ventricular wall motion in muscular dystrophy
    • Kovick, R. B., Fogelman, A. M., Abbasi, A. D., Peter, J. B. & Pearce, M. L. Echocardiographic evaluation of posterior left ventricular wall motion in muscular dystrophy. Circulation 52, 447-454 (1975).
    • (1975) Circulation , vol.52 , pp. 447-454
    • Kovick, R.B.1    Fogelman, A.M.2    Abbasi, A.D.3    Peter, J.B.4    Pearce, M.L.5
  • 29
    • 81155122953 scopus 로고    scopus 로고
    • Myocardial performance index and atrial ejection force in patients with Duchennes muscular dystrophy
    • Shabanian, R. et al. Myocardial performance index and atrial ejection force in patients with Duchennes muscular dystrophy. Echocardiography 28, 1088-1094 (2011).
    • (2011) Echocardiography , vol.28 , pp. 1088-1094
    • Shabanian, R.1
  • 30
    • 80052766582 scopus 로고    scopus 로고
    • Pathophysiology and therapy of cardiac dysfunction in Duchenne muscular dystrophy
    • Judge, D. P., Kass, D. A., Thompson, W. R. & Wagner, K. R. Pathophysiology and therapy of cardiac dysfunction in Duchenne muscular dystrophy. Am. J. Cardiovasc. Drugs 11, 287-294 (2011).
    • (2011) Am. J. Cardiovasc. Drugs , vol.11 , pp. 287-294
    • Judge, D.P.1    Kass, D.A.2    Thompson, W.R.3    Wagner, K.R.4
  • 31
    • 33750336564 scopus 로고    scopus 로고
    • Is heart rate variability a valid parameter to predict sudden death in patients with Beckers muscular dystrophy?
    • Ammendola, E., Russo, V., Politano, L., Santangelo, L. & Calabr, R. Is heart rate variability a valid parameter to predict sudden death in patients with Beckers muscular dystrophy? Heart 92, 1686-1687 (2006).
    • (2006) Heart , vol.92 , pp. 1686-1687
    • Ammendola, E.1    Russo, V.2    Politano, L.3    Santangelo, L.4    Calabr, R.5
  • 32
    • 84860390502 scopus 로고    scopus 로고
    • Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects
    • Diegoli, M. et al. Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects. J. Am. Coll. Cardiol. 58, 925-934 (2011).
    • (2011) J. Am. Coll. Cardiol , vol.58 , pp. 925-934
    • Diegoli, M.1
  • 33
    • 76549098001 scopus 로고    scopus 로고
    • Leaky RyR2 trigger ventricular arrhythmias in Duchenne muscular dystrophy
    • Fauconnier, J. et al. Leaky RyR2 trigger ventricular arrhythmias in Duchenne muscular dystrophy. Proc. Natl Acad. Sci. USA 107, 1559-1564 (2010).
    • (2010) Proc. Natl Acad. Sci. USA , vol.107 , pp. 1559-1564
    • Fauconnier, J.1
  • 34
    • 84881475183 scopus 로고    scopus 로고
    • Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy
    • Mourkioti, F. et al. Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy. Nat. Cell Biol. 15, 895-904 (2013).
    • (2013) Nat. Cell Biol , vol.15 , pp. 895-904
    • Mourkioti, F.1
  • 35
    • 0142042349 scopus 로고    scopus 로고
    • Cardiomyopathy in muscular dystrophies
    • Muntoni, F. Cardiomyopathy in muscular dystrophies. Curr. Opin. Neurol. 16, 577-583 (2003).
    • (2003) Curr. Opin. Neurol , vol.16 , pp. 577-583
    • Muntoni, F.1
  • 36
    • 0027305755 scopus 로고
    • Ventricular arrhythmia in Duchenne muscular dystrophy: Prevalence, significance and prognosis
    • Chenard, A. A., Becane, H. M., Tertrain, F., de Kermadec, J. M. & Weiss, Y. A. Ventricular arrhythmia in Duchenne muscular dystrophy: prevalence, significance and prognosis. Neuromuscul. Disord. 3, 201-206 (1993).
    • (1993) Neuromuscul. Disord , vol.3 , pp. 201-206
    • Chenard, A.A.1    Becane, H.M.2    Tertrain, F.3    De Kermadec, J.M.4    Weiss, Y.A.5
  • 37
    • 84876130733 scopus 로고    scopus 로고
    • CMR detects subclinical cardiomyopathy in mother-carriers of Duchenne and Becker muscular dystrophy
    • Mavrogeni, S. et al. CMR detects subclinical cardiomyopathy in mother-carriers of Duchenne and Becker muscular dystrophy. JACC Cardiovasc. Imaging 6, 526-528 (2013).
    • (2013) JACC Cardiovasc. Imaging , vol.6 , pp. 526-528
    • Mavrogeni, S.1
  • 38
    • 65449122304 scopus 로고    scopus 로고
    • Current understanding and management of dilated cardiomyopathy in Duchenne and Becker muscular dystrophy
    • Kaspar, R. W., Allen, H. D. & Montanaro, F. Current understanding and management of dilated cardiomyopathy in Duchenne and Becker muscular dystrophy. J. Am. Acad. Nurse Pract. 21, 241-249 (2009).
    • (2009) J. Am. Acad. Nurse Pract , vol.21 , pp. 241-249
    • Kaspar, R.W.1    Allen, H.D.2    Montanaro, F.3
  • 39
    • 58749093466 scopus 로고    scopus 로고
    • Cardiac involvement in patients with Becker muscular dystrophy: New diagnostic and pathophysiological insights by a CMR approach
    • Yilmaz, A. et al. Cardiac involvement in patients with Becker muscular dystrophy: new diagnostic and pathophysiological insights by a CMR approach. J. Cardiovasc. Magn. Reson. 10, 50 (2008).
    • (2008) J. Cardiovasc. Magn. Reson , vol.10 , pp. 50
    • Yilmaz, A.1
  • 40
    • 84885614369 scopus 로고    scopus 로고
    • Prognosis of Duchenne/Becker muscular dystrophy with noncompaction is worse than without noncompaction
    • Stllberger, C. & Finsterer, J. Prognosis of Duchenne/Becker muscular dystrophy with noncompaction is worse than without noncompaction. Int. J. Cardiol. 168, 2915-2916 (2013).
    • (2013) Int. J. Cardiol , vol.168 , pp. 2915-2916
    • Stllberger, C.1    Finsterer, J.2
  • 41
    • 78650186613 scopus 로고    scopus 로고
    • Use of corticosteroids in a population-based cohort of boys with Duchenne and Becker muscular dystrophy
    • Matthews, D. J. et al. Use of corticosteroids in a population-based cohort of boys with Duchenne and Becker muscular dystrophy. J. Child Neurol. 25, 1319-1324 (2010).
    • (2010) J. Child Neurol , vol.25 , pp. 1319-1324
    • Matthews, D.J.1
  • 42
    • 84879399461 scopus 로고    scopus 로고
    • Long-term ventilation of patients with Duchenne muscular dystrophy: Experiences at the Neuromuscular Centre Ulm
    • Wollinsky, K. H., Kutter, B. & Geiger, P. M. Long-term ventilation of patients with Duchenne muscular dystrophy: experiences at the Neuromuscular Centre Ulm. Acta Myol. 31, 170-178 (2012).
    • (2012) Acta Myol , vol.31 , pp. 170-178
    • Wollinsky, K.H.1    Kutter, B.2    Geiger, P.M.3
  • 43
    • 27844561168 scopus 로고    scopus 로고
    • Evolving therapeutic strategies for dystrophinopathies: Potential for conflict between cardiac and skeletal needs
    • Colan, S. D. Evolving therapeutic strategies for dystrophinopathies: potential for conflict between cardiac and skeletal needs. Circulation 112, 2756-2758 (2005).
    • (2005) Circulation , vol.112 , pp. 2756-2758
    • Colan, S.D.1
  • 44
    • 42549128181 scopus 로고    scopus 로고
    • Emergent dilated cardiomyopathy caused by targeted repair of dystrophic skeletal muscle
    • Townsend, D., Yasuda, S., Li, S., Chamberlain, J. S. & Metzger, J. M. Emergent dilated cardiomyopathy caused by targeted repair of dystrophic skeletal muscle. Mol. Ther. 16, 832-835 (2008).
    • (2008) Mol. Ther , vol.16 , pp. 832-835
    • Townsend, D.1    Yasuda, S.2    Li, S.3    Chamberlain, J.S.4    Metzger, J.M.5
  • 45
    • 84868377982 scopus 로고    scopus 로고
    • Novel approaches to corticosteroid treatment in Duchenne muscular dystrophy
    • Hoffman, E. P. et al. Novel approaches to corticosteroid treatment in Duchenne muscular dystrophy. Phys. Med. Rehabil. Clin. N. Am. 23, 821-828 (2012).
    • (2012) Phys. Med. Rehabil. Clin. N. Am , vol.23 , pp. 821-828
    • Hoffman, E.P.1
  • 46
    • 43449112637 scopus 로고    scopus 로고
    • Corticosteroid treatment retards development of ventricular dysfunction in Duchenne muscular dystrophy
    • Markham, L. W., Kinnett, K., Wong, B. L., Woodrow Benson, D. & Cripe, L. H. Corticosteroid treatment retards development of ventricular dysfunction in Duchenne muscular dystrophy. Neuromuscul. Disord. 18, 365-370 (2008).
    • (2008) Neuromuscul. Disord , vol.18 , pp. 365-370
    • Markham, L.W.1    Kinnett, K.2    Wong, B.L.3    Woodrow Benson, D.4    Cripe, L.H.5
  • 47
    • 84877594408 scopus 로고    scopus 로고
    • Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy
    • Ricotti, V. et al. Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy. J. Neurol. Neurosurg. Psychiatry 84, 698-705 (2013).
    • (2013) J. Neurol. Neurosurg. Psychiatry , vol.84 , pp. 698-705
    • Ricotti, V.1
  • 48
    • 84884509873 scopus 로고    scopus 로고
    • The impact of deflazacort on puberty in Duchenne muscular dystrophy
    • Dooley, J. M., Bobbitt, S. A. & Cummings, E. A. The impact of deflazacort on puberty in Duchenne muscular dystrophy. Pediatr. Neurol. 49, 292-293 (2013).
    • (2013) Pediatr. Neurol , vol.49 , pp. 292-293
    • Dooley, J.M.1    Bobbitt, S.A.2    Cummings, E.A.3
  • 49
    • 84870393032 scopus 로고    scopus 로고
    • Bone health in boys with Duchenne muscular dystrophy on long-term daily deflazacort therapy
    • Mayo, A. L., Craven, B. C., McAdam, L. C. & Biggar, W. D. Bone health in boys with Duchenne muscular dystrophy on long-term daily deflazacort therapy. Neuromuscul. Disord. 22, 1040-1045 (2012).
    • (2012) Neuromuscul. Disord , vol.22 , pp. 1040-1045
    • Mayo, A.L.1    Craven, B.C.2    McAdam, L.C.3    Biggar, W.D.4
  • 50
    • 84861702194 scopus 로고    scopus 로고
    • The Canadian experience with long-term deflazacort treatment in Duchenne muscular dystrophy
    • McAdam, L. C., Mayo, A. L., Alman, B. A. & Biggar, W. D. The Canadian experience with long-term deflazacort treatment in Duchenne muscular dystrophy. Acta Myol. 31, 16-20 (2012).
    • (2012) Acta Myol , vol.31 , pp. 16-20
    • McAdam, L.C.1    Mayo, A.L.2    Alman, B.A.3    Biggar, W.D.4
  • 51
    • 84870393322 scopus 로고    scopus 로고
    • Growth hormone treatment in boys with Duchenne muscular dystrophy and glucocorticoid-induced growth failure
    • Rutter, M. M. et al. Growth hormone treatment in boys with Duchenne muscular dystrophy and glucocorticoid-induced growth failure. Neuromuscul. Disord. 22, 1046-1056 (2012).
    • (2012) Neuromuscul. Disord , vol.22 , pp. 1046-1056
    • Rutter, M.M.1
  • 53
    • 84879551364 scopus 로고    scopus 로고
    • Corticosteroids in Duchenne muscular dystrophy: Major variations in practice
    • Griggs, R. C. et al. Corticosteroids in Duchenne muscular dystrophy: major variations in practice. Muscle Nerve 48, 27-31 (2013).
    • (2013) Muscle Nerve , vol.48 , pp. 27-31
    • Griggs, R.C.1
  • 54
    • 84875416473 scopus 로고    scopus 로고
    • Steroid therapy effectively delays Duchennes cardiomyopathy
    • Dec, G. W. Steroid therapy effectively delays Duchennes cardiomyopathy. J. Am. Coll. Cardiol. 61, 955-956 (2013).
    • (2013) J. Am. Coll. Cardiol , vol.61 , pp. 955-956
    • Dec, G.W.1
  • 55
    • 57449111767 scopus 로고    scopus 로고
    • Effect of deflazacort on cardiac and sternocleidomastoid muscles in Duchenne muscular dystrophy: A magnetic resonance imaging study
    • Mavrogeni, S. et al. Effect of deflazacort on cardiac and sternocleidomastoid muscles in Duchenne muscular dystrophy: a magnetic resonance imaging study. Eur. J. Paediatr. Neurol. 13, 34-40 (2009).
    • (2009) Eur. J. Paediatr. Neurol , vol.13 , pp. 34-40
    • Mavrogeni, S.1
  • 56
    • 0037443583 scopus 로고    scopus 로고
    • Effects of deflazacort on left ventricular function in patients with Duchenne muscular dystrophy
    • Silverside, C. K., Webb, G. D., Harris, V. A. & Biggar, D. W. Effects of deflazacort on left ventricular function in patients with Duchenne muscular dystrophy. Am. J. Cardiol. 91, 769-772 (2003).
    • (2003) Am. J. Cardiol , vol.91 , pp. 769-772
    • Silverside, C.K.1    Webb, G.D.2    Harris, V.A.3    Biggar, D.W.4
  • 57
    • 31144470666 scopus 로고    scopus 로고
    • Steroid therapy and cardiac function in Duchenne muscular dystrophy
    • Markham, L. W. et al. Steroid therapy and cardiac function in Duchenne muscular dystrophy. Pediatr. Cardiol. 26, 768-771 (2005).
    • (2005) Pediatr. Cardiol , vol.26 , pp. 768-771
    • Markham, L.W.1
  • 58
    • 38949092529 scopus 로고    scopus 로고
    • Deflazacort use in Duchenne muscular dystrophy: An 8-year follow-up
    • Houde, S. et al. Deflazacort use in Duchenne muscular dystrophy: an 8-year follow-up. Pediatr. Neurol. 38, 200-206 (2008).
    • (2008) Pediatr. Neurol , vol.38 , pp. 200-206
    • Houde, S.1
  • 59
    • 84884673254 scopus 로고    scopus 로고
    • Oral corticosteroids and onset of cardiomyopathy in Duchenne muscular dystrophy
    • Barber, B. J. et al. Oral corticosteroids and onset of cardiomyopathy in Duchenne muscular dystrophy. J. Pediatr. 163, 1080-1084 (2013).
    • (2013) J. Pediatr , vol.163 , pp. 1080-1084
    • Barber, B.J.1
  • 60
    • 84875444308 scopus 로고    scopus 로고
    • All-cause mortality and cardiovascular outcomes with prophylactic steroid therapy in Duchenne muscular dystrophy
    • Schram, G. et al. All-cause mortality and cardiovascular outcomes with prophylactic steroid therapy in Duchenne muscular dystrophy. J. Am. Coll. Cardiol. 61, 948-954 (2013).
    • (2013) J. Am. Coll. Cardiol , vol.61 , pp. 948-954
    • Schram, G.1
  • 61
    • 66249136309 scopus 로고    scopus 로고
    • Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy
    • Bauer, R., Straub, V., Blain, A., Bushby, K. & MacGowan, G. A. Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy. Eur. J. Heart Fail. 11, 463-471 (2009).
    • (2009) Eur. J. Heart Fail , vol.11 , pp. 463-471
    • Bauer, R.1    Straub, V.2    Blain, A.3    Bushby, K.4    Macgowan, G.A.5
  • 62
    • 52449087790 scopus 로고    scopus 로고
    • Steroid treatment causes deterioration of myocardial function in the ?-sarcoglycan-deficient mouse model for dilated cardiomyopathy
    • Bauer, R., Macgowan, G. A., Blain, A., Bushby, K. & Straub, V. Steroid treatment causes deterioration of myocardial function in the ?-sarcoglycan-deficient mouse model for dilated cardiomyopathy. Cardiovasc. Res. 79, 652-661 (2008).
    • (2008) Cardiovasc. Res , vol.79 , pp. 652-661
    • Bauer, R.1    Macgowan, G.A.2    Blain, A.3    Bushby, K.4    Straub, V.5
  • 63
    • 80052635987 scopus 로고    scopus 로고
    • Worsening of cardiomyopathy using deflazacort in an animal model rescued by gene therapy
    • Rotundo, I. L. et al. Worsening of cardiomyopathy using deflazacort in an animal model rescued by gene therapy. PLoS ONE 6, e24729 (2011).
    • (2011) PLoS ONE , vol.6
    • Rotundo, I.L.1
  • 64
    • 84882416839 scopus 로고    scopus 로고
    • Effects of glucocorticoids and idebenone on respiratory function in patients with duchenne muscular dystrophy
    • Buyse, G. M., Goemans, N., van den Hauwe, M. & Meier, T. Effects of glucocorticoids and idebenone on respiratory function in patients with duchenne muscular dystrophy. Pediatr. Pulmonol. 48, 912-920 (2013).
    • (2013) Pediatr. Pulmonol , vol.48 , pp. 912-920
    • Buyse, G.M.1    Goemans, N.2    Van Den Hauwe, M.3    Meier, T.4
  • 65
    • 14844318046 scopus 로고    scopus 로고
    • Effect of perindopril on the onset and progression of left ventricular dysfunction in Duchenne muscular dystrophy
    • Duboc, D. et al. Effect of perindopril on the onset and progression of left ventricular dysfunction in Duchenne muscular dystrophy. J. Am. Coll. Cardiol. 45, 855-857 (2005).
    • (2005) J. Am. Coll. Cardiol , vol.45 , pp. 855-857
    • Duboc, D.1
  • 66
    • 80051552743 scopus 로고    scopus 로고
    • Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice
    • Rafael-Fortney, J. A. et al. Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice. Circulation 124, 582-588 (2011).
    • (2011) Circulation , vol.124 , pp. 582-588
    • Rafael-Fortney, J.A.1
  • 67
    • 80054989179 scopus 로고    scopus 로고
    • Enalapril treatment discloses an early role of angiotensin II in inflammation- and oxidative stress-related muscle damage in dystrophic mdx mice
    • Cozzoli, A. et al. Enalapril treatment discloses an early role of angiotensin II in inflammation- and oxidative stress-related muscle damage in dystrophic mdx mice. Pharmacol. Res. 64, 482-492 (2011).
    • (2011) Pharmacol. Res , vol.64 , pp. 482-492
    • Cozzoli, A.1
  • 68
    • 33748062315 scopus 로고    scopus 로고
    • Left ventricular function and response to enalapril in patients with Duchenne muscular dystrophy during the second decade of life
    • Ramaciotti, C. et al. Left ventricular function and response to enalapril in patients with Duchenne muscular dystrophy during the second decade of life. Am. J. Cardiol. 98, 825-827 (2006).
    • (2006) Am. J. Cardiol , vol.98 , pp. 825-827
    • Ramaciotti, C.1
  • 69
    • 34547934811 scopus 로고    scopus 로고
    • Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years follow-up
    • Duboc, D. et al. Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years follow-up. Am. Heart J. 154, 596-602 (2007).
    • (2007) Am. Heart J , vol.154 , pp. 596-602
    • Duboc, D.1
  • 70
    • 84859921451 scopus 로고    scopus 로고
    • The effect of enalapril and carvedilol on left ventricular dysfunction in middle childhood and adolescent patients with muscular dystrophy
    • Kwon, H. W. et al. The effect of enalapril and carvedilol on left ventricular dysfunction in middle childhood and adolescent patients with muscular dystrophy. Korean Circ. J. 42, 184-191 (2012).
    • (2012) Korean Circ. J , vol.42 , pp. 184-191
    • Kwon, H.W.1
  • 71
    • 79951479823 scopus 로고    scopus 로고
    • Losartan decreases cardiac muscle fibrosis and improves cardiac function in dystrophin-deficient mdx mice
    • Spurney, C. F. et al. Losartan decreases cardiac muscle fibrosis and improves cardiac function in dystrophin-deficient mdx mice. J. Cardiovasc. Pharmacol. Ther. 16, 87-95 (2011).
    • (2011) J. Cardiovasc. Pharmacol. Ther , vol.16 , pp. 87-95
    • Spurney, C.F.1
  • 72
    • 79959442500 scopus 로고    scopus 로고
    • Chronic losartan administration reduces mortality and preserves cardiac but not skeletal muscle function in dystrophic mice
    • Bish, L. T. et al. Chronic losartan administration reduces mortality and preserves cardiac but not skeletal muscle function in dystrophic mice. PLoS ONE 6, e20856 (2011).
    • (2011) Plos One , vol.6
    • Bish, L.T.1
  • 73
    • 84874260796 scopus 로고    scopus 로고
    • Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy
    • Blain, A. et al. Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy. PLoS ONE 8, e57260 (2013).
    • (2013) Plos One , vol.8
    • Blain, A.1
  • 74
    • 33746709342 scopus 로고    scopus 로고
    • Beta-blocker therapy for cardiac dysfunction in patients with muscular dystrophy
    • Kajimoto, H. et al. Beta-blocker therapy for cardiac dysfunction in patients with muscular dystrophy. Circ. J. 70, 991-994 (2006).
    • (2006) Circ. J , vol.70 , pp. 991-994
    • Kajimoto, H.1
  • 75
    • 58249134742 scopus 로고    scopus 로고
    • Beneficial effects of beta-blockers and angiotensin-converting enzyme inhibitors in Duchenne muscular dystrophy
    • Ogata, H., Ishikawa, Y., Ishikawa, Y. & Minami, R. Beneficial effects of beta-blockers and angiotensin-converting enzyme inhibitors in Duchenne muscular dystrophy. J. Cardiol. 53, 72-78 (2009).
    • (2009) J. Cardiol , vol.53 , pp. 72-78
    • Ogata, H.1    Ishikawa, Y.2    Ishikawa, Y.3    Minami, R.4
  • 76
    • 79151475205 scopus 로고    scopus 로고
    • Recovery of systolic dysfunction in Duchenne muscular dystrophy due to the point mutation c.4213C >t
    • Finsterer, J., Stllberger, C. & Holinski-Feder, E. Recovery of systolic dysfunction in Duchenne muscular dystrophy due to the point mutation c.4213C >T. Cardiology 117, 265-267 (2010).
    • (2010) Cardiology , vol.117 , pp. 265-267
    • Finsterer, J.1    Stllberger, C.2    Holinski-Feder, E.3
  • 77
    • 79958821082 scopus 로고    scopus 로고
    • Presence of mechanical dyssynchrony in Duchenne muscular dystrophy
    • Hor, K. N. et al. Presence of mechanical dyssynchrony in Duchenne muscular dystrophy. J. Cardiovasc. Magn. Reson. 13, 12 (2011).
    • (2011) J. Cardiovasc. Magn. Reson , vol.13 , Issue.12
    • Hor, K.N.1
  • 78
    • 84878592126 scopus 로고    scopus 로고
    • Duchenne muscular dystrophy fibroblast nodules: A cell-based assay for screening anti-fibrotic agents
    • Zanotti, S., Gibertini, S., Savadori, P., Mantegazza, R. & Mora, M. Duchenne muscular dystrophy fibroblast nodules: a cell-based assay for screening anti-fibrotic agents. Cell Tissue Res. 352, 659-670 (2013).
    • (2013) Cell Tissue Res , vol.352 , pp. 659-670
    • Zanotti, S.1    Gibertini, S.2    Savadori, P.3    Mantegazza, R.4    Mora, M.5
  • 79
    • 80051552743 scopus 로고    scopus 로고
    • Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice
    • Rafael-Fortney, J. A. et al. Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice. Circulation 124, 582-588 (2011).
    • (2011) Circulation , vol.124 , pp. 582-588
    • Rafael-Fortney, J.A.1
  • 80
    • 62549124069 scopus 로고    scopus 로고
    • Cardiac magnetic resonance imaging and management of dilated cardiomyopathy in a Duchenne muscular dystrophy manifesting carrier
    • Barison, A. et al. Cardiac magnetic resonance imaging and management of dilated cardiomyopathy in a Duchenne muscular dystrophy manifesting carrier. J. Neurol. 256, 283-284 (2009).
    • (2009) J. Neurol , vol.256 , pp. 283-284
    • Barison, A.1
  • 81
    • 84868210193 scopus 로고    scopus 로고
    • Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: A possible contributor of progressive muscledegeneration
    • Weber, M. A. et al. Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscledegeneration. J. Neurol. 259, 2385-2392 (2012).
    • (2012) J. Neurol , vol.259 , pp. 2385-2392
    • Weber, M.A.1
  • 82
    • 84861659184 scopus 로고    scopus 로고
    • Rationale for treating oedema in Duchenne muscular dystrophy with eplerenone
    • Lehmann-Horn, F. et al. Rationale for treating oedema in Duchenne muscular dystrophy with eplerenone. Acta Myol. 31, 31-39 (2012).
    • (2012) Acta Myol , vol.31 , pp. 31-39
    • Lehmann-Horn, F.1
  • 83
    • 84864477617 scopus 로고    scopus 로고
    • ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC
    • McMurray, J. J. et al. ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. Eur. J. Heart Fail. 14, 803-869 (2012).
    • (2012) Eur. J. Heart Fail , vol.14 , pp. 803-869
    • McMurray, J.J.1
  • 84
    • 0032908603 scopus 로고    scopus 로고
    • Cardioprotection for Duchennes muscular dystrophy
    • Ishikawa, Y., Bach, J. R. & Minami, R. Cardioprotection for Duchennes muscular dystrophy. Am. Heart J. 137, 895-902 (1999).
    • (1999) Am. Heart J , vol.137 , pp. 895-902
    • Ishikawa, Y.1    Bach, J.R.2    Minami, R.3
  • 85
    • 40949086482 scopus 로고    scopus 로고
    • Safety and efficacy of carvedilol therapy for patients with dilated cardiomyopathy secondary to muscular dystrophy
    • Rhodes, J. et al. Safety and efficacy of carvedilol therapy for patients with dilated cardiomyopathy secondary to muscular dystrophy. Pediatr. Cardiol. 29, 343-351 (2008).
    • (2008) Pediatr. Cardiol , vol.29 , pp. 343-351
    • Rhodes, J.1
  • 86
    • 77954996985 scopus 로고    scopus 로고
    • Carvedilol can prevent cardiac events in Duchenne muscular dystrophy
    • Matsumura, T., Tamura, T., Kuru, S., Kikuchi, Y. & Kawai, M. Carvedilol can prevent cardiac events in Duchenne muscular dystrophy. Intern. Med. 49, 1357-1363 (2010).
    • (2010) Intern. Med , vol.49 , pp. 1357-1363
    • Matsumura, T.1    Tamura, T.2    Kuru, S.3    Kikuchi, Y.4    Kawai, M.5
  • 87
    • 0035740111 scopus 로고    scopus 로고
    • Carvedilol effectiveness for left ventricular-insufficient patients with Duchenne muscular dystrophy [Japanese]
    • Saito, T., Matsumura, T., Miyai, I., Nozaki, S. & Shinno, S. Carvedilol effectiveness for left ventricular-insufficient patients with Duchenne muscular dystrophy [Japanese]. Rinsho Shinkeigaku 41, 691-694 (2001).
    • (2001) Rinsho Shinkeigaku , vol.41 , pp. 691-694
    • Saito, T.1    Matsumura, T.2    Miyai, I.3    Nozaki, S.4    Shinno, S.5
  • 88
    • 84867850252 scopus 로고    scopus 로고
    • Beneficial effect of ivabradine in dilated cardiomyopathy from Becker muscular dystrophy
    • Finsterer, J., Stllberger, C. & Berger, E. Beneficial effect of ivabradine in dilated cardiomyopathy from Becker muscular dystrophy. Herz 37, 702-705 (2012).
    • (2012) Herz , vol.37 , pp. 702-705
    • Finsterer, J.1    Stllberger, C.2    Berger, E.3
  • 89
    • 85026832570 scopus 로고    scopus 로고
    • Cardiac transplantation in Duchenne muscular dystrophy: A case report
    • Cripe, L. et al. Cardiac transplantation in Duchenne muscular dystrophy: a case report. Neuromuscul. Disord. 21, 645 (2011).
    • (2011) Neuromuscul. Disord , vol.21 , Issue.645
    • Cripe, L.1
  • 90
    • 0032887613 scopus 로고    scopus 로고
    • Effective milrinone therapy to a Duchenne muscular dystrophy patient with advanced congestive heart failure [Japanese]
    • Matsumura, T., Saito, T., Miyai, I., Nozaki, S. & Kang, J. Effective milrinone therapy to a Duchenne muscular dystrophy patient with advanced congestive heart failure [Japanese]. Rinsho Shinkeigaku 39, 643-648 (1999).
    • (1999) Rinsho Shinkeigaku , vol.39 , pp. 643-648
    • Matsumura, T.1    Saito, T.2    Miyai, I.3    Nozaki, S.4    Kang, J.5
  • 91
    • 77953983399 scopus 로고    scopus 로고
    • Pacemaker implantation for sinus node dysfunction in a young patient with Duchenne muscular dystrophy
    • Fayssoil, A., Orlikowski, D., Nardi, O. & Annane, D. Pacemaker implantation for sinus node dysfunction in a young patient with Duchenne muscular dystrophy. Congest. Heart Fail. 16, 127-128 (2010).
    • (2010) Congest. Heart Fail , vol.16 , pp. 127-128
    • Fayssoil, A.1    Orlikowski, D.2    Nardi, O.3    Annane, D.4
  • 92
  • 93
    • 55249090419 scopus 로고    scopus 로고
    • Complete atrioventricular block in Duchenne muscular dystrophy
    • Fayssoil, A., Orlikowski, D., Nardi, O. & Annane, D. Complete atrioventricular block in Duchenne muscular dystrophy. Europace 10, 1351-1352 (2008).
    • (2008) Europace , vol.10 , pp. 1351-1352
    • Fayssoil, A.1    Orlikowski, D.2    Nardi, O.3    Annane, D.4
  • 94
    • 0030782124 scopus 로고    scopus 로고
    • A case of pacemaker implantation for complete atrioventricular block associated with Duchenne muscular dystrophy [Japanese]
    • Takano, N., Honke, K., Hasui, M., Ohno, I. & Takemura, H. A case of pacemaker implantation for complete atrioventricular block associated with Duchenne muscular dystrophy [Japanese]. No To Hattatsu 29, 476-480 (1997).
    • (1997) No to Hattatsu , vol.29 , pp. 476-480
    • Takano, N.1    Honke, K.2    Hasui, M.3    Ohno, I.4    Takemura, H.5
  • 95
    • 74449091265 scopus 로고    scopus 로고
    • Cardiac involvement in a female carrier of Duchenne muscular dystrophy
    • Walcher, T. et al. Cardiac involvement in a female carrier of Duchenne muscular dystrophy. Int. J. Cardiol. 138, 302-305 (2010).
    • (2010) Int. J. Cardiol , vol.138 , pp. 302-305
    • Walcher, T.1
  • 96
    • 84872287018 scopus 로고    scopus 로고
    • 2012 ACCF/AHA/HRS focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities: A report of the American College of cardiology foundation/american heart association task force on practice guidelines and the heart rhythm society
    • Epstein, A. E. et al. 2012 ACCF/AHA/HRS focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society. J. Am. Coll. Cardiol. 61, e6-e75 (2013).
    • (2013) J. Am. Coll. Cardiol , vol.61
    • Epstein, A.E.1
  • 97
    • 84878166794 scopus 로고    scopus 로고
    • Cardiac resynchronization therapy in Becker muscular dystrophy
    • Andrikopoulos, G. et al. Cardiac resynchronization therapy in Becker muscular dystrophy. Hellenic J. Cardiol. 54, 227-229 (2013).
    • (2013) Hellenic J. Cardiol , vol.54 , pp. 227-229
    • Andrikopoulos, G.1
  • 98
    • 24644476131 scopus 로고    scopus 로고
    • Left ventricular synchronization by biventricular pacing in Becker muscular dystrophy as assessed by tissue Doppler imaging
    • Stllberger, C. & Finsterer, J. Left ventricular synchronization by biventricular pacing in Becker muscular dystrophy as assessed by tissue Doppler imaging. Heart Lung 34, 317-320 (2005).
    • (2005) Heart Lung , vol.34 , pp. 317-320
    • Stllberger, C.1    Finsterer, J.2
  • 99
    • 0034935340 scopus 로고    scopus 로고
    • Cardiomyopathy in a carrier of Duchennes muscular dystrophy
    • Davies, J. E. et al. Cardiomyopathy in a carrier of Duchennes muscular dystrophy. J. Heart Lung Transplant. 20, 781-784 (2001).
    • (2001) J. Heart Lung Transplant , vol.20 , pp. 781-784
    • Davies, J.E.1
  • 100
    • 25144517141 scopus 로고    scopus 로고
    • CardioWest total artificial heart in a moribund adolescent with left ventricular thrombi
    • Smith, M. C. et al. CardioWest total artificial heart in a moribund adolescent with left ventricular thrombi. Ann. Thorac. Surg. 80, 1490-1492 (2005).
    • (2005) Ann. Thorac. Surg , vol.80 , pp. 1490-1492
    • Smith, M.C.1
  • 101
    • 85047695763 scopus 로고    scopus 로고
    • Anaesthesia for non-cardiac surgery in patient with Beckers muscular dystrophy supported with a left ventricular assist device
    • Webb, S. T., Patil, V. & Vuylsteke, A. Anaesthesia for non-cardiac surgery in patient with Beckers muscular dystrophy supported with a left ventricular assist device. Eur. J. Anaesthesiol. 24, 640-642 (2007).
    • (2007) Eur. J. Anaesthesiol , vol.24 , pp. 640-642
    • Webb, S.T.1    Patil, V.2    Vuylsteke, A.3
  • 102
    • 0036298651 scopus 로고    scopus 로고
    • Successful bridge to transplantation in a patient with Becker muscular dystrophy-associated cardiomyopathy
    • Leprince, P. et al. Successful bridge to transplantation in a patient with Becker muscular dystrophy-associated cardiomyopathy. J. Heart Lung Transplant. 21, 822-824 (2002).
    • (2002) J. Heart Lung Transplant , vol.21 , pp. 822-824
    • Leprince, P.1
  • 103
    • 84869509282 scopus 로고    scopus 로고
    • Left ventricular assist device in Duchenne cardiomyopathy: Can we change the natural history of cardiac disease?
    • Amodeo, A. & Adorisio, R. Left ventricular assist device in Duchenne cardiomyopathy: can we change the natural history of cardiac disease? Int. J. Cardiol. 161, e43 (2012).
    • (2012) Int. J. Cardiol , vol.161
    • Amodeo, A.1    Adorisio, R.2
  • 104
    • 84867150155 scopus 로고    scopus 로고
    • Inappropriate use of neurally adjusted ventilator assist
    • bcr1020115029
    • Iodice, F., Testa, G., Amodeo, A. & Cogo, P. Inappropriate use of neurally adjusted ventilator assist. BMJ Case Rep. 2012, bcr1020115029 (2012).
    • (2012) BMJ Case Rep , vol.2012
    • Iodice, F.1    Testa, G.2    Amodeo, A.3    Cogo, P.4
  • 105
    • 0032718905 scopus 로고    scopus 로고
    • Cardiac involvement in Beckers muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvement
    • Finsterer, J., Bittner, R. E. & Grimm, M. Cardiac involvement in Beckers muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvement. Neuromuscul. Disord. 9, 598-600 (1999).
    • (1999) Neuromuscul. Disord , vol.9 , pp. 598-600
    • Finsterer, J.1    Bittner, R.E.2    Grimm, M.3
  • 106
    • 0035078071 scopus 로고    scopus 로고
    • Heart transplantation in patients with inherited myopathies associated with end-stage cardiomyopathy: Molecular and biochemical defects on cardiac and skeletal muscle
    • Melacini, P. et al. Heart transplantation in patients with inherited myopathies associated with end-stage cardiomyopathy: molecular and biochemical defects on cardiac and skeletal muscle. Transplant. Proc. 33, 1596-1599 (2001).
    • (2001) Transplant. Proc , vol.33 , pp. 1596-1599
    • Melacini, P.1
  • 108
    • 4544272373 scopus 로고    scopus 로고
    • Respiratory care of the patient with Duchenne muscular dystrophy: ATS consensus statement
    • Finder, J. D. et al. Respiratory care of the patient with Duchenne muscular dystrophy: ATS consensus statement. Am. J. Respir. Crit. Care Med. 170, 456-465 (2004).
    • (2004) Am. J. Respir. Crit. Care Med , vol.170 , pp. 456-465
    • Finder, J.D.1
  • 109
    • 84884209816 scopus 로고    scopus 로고
    • Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011
    • Kieny, P. et al. Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011. Ann. Phys. Rehabil. Med. 56, 443-454 (2013).
    • (2013) Ann. Phys. Rehabil. Med , vol.56 , pp. 443-454
    • Kieny, P.1
  • 110
    • 55349084415 scopus 로고    scopus 로고
    • Update on the management of Duchenne muscular dystrophy
    • Manzur, A. Y., Kinali, M. & Muntoni, F. Update on the management of Duchenne muscular dystrophy. Arch. Dis. Child. 93, 986-990 (2008).
    • (2008) Arch. Dis. Child , vol.93 , pp. 986-990
    • Manzur, A.Y.1    Kinali, M.2    Muntoni, F.3
  • 111
    • 79960665553 scopus 로고    scopus 로고
    • Duchenne muscular dystrophy: Continuous noninvasive ventilatory support prolongs survival
    • Bach, J. R. & Martinez, D. Duchenne muscular dystrophy: continuous noninvasive ventilatory support prolongs survival. Respir. Care 56, 744-750 (2011).
    • (2011) Respir. Care , vol.56 , pp. 744-750
    • Bach, J.R.1    Martinez, D.2
  • 112
    • 76549130473 scopus 로고    scopus 로고
    • Diagnosis and management of Duchenne muscular dystrophy, part 2: Implementation of multidisciplinary care
    • Bushby, K. et al. Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol. 9, 177-189 (2010).
    • (2010) Lancet Neurol , vol.9 , pp. 177-189
    • Bushby, K.1
  • 113
    • 33644986339 scopus 로고    scopus 로고
    • Muscular Dystrophy Campaign funded workshop on management of scoliosis in Duchenne muscular dystrophy 24 January 2005 London, UK
    • Muntoni, F., Bushby, K. & Manzur, A. Y. Muscular Dystrophy Campaign funded workshop on management of scoliosis in Duchenne muscular dystrophy 24 January 2005 London, UK. Neuromuscul. Disord. 16, 210-219 (2006).
    • (2006) Neuromuscul. Disord , vol.16 , pp. 210-219
    • Muntoni, F.1    Bushby, K.2    Manzur, A.Y.3
  • 114
    • 84881559374 scopus 로고    scopus 로고
    • Cardiac considerations in the operative management of the patient with Duchenne or Becker muscular dystrophy
    • Cripe, L. H. & Tobias, J. D. Cardiac considerations in the operative management of the patient with Duchenne or Becker muscular dystrophy. Paediatr. Anaesth. 23, 777-784 (2013).
    • (2013) Paediatr. Anaesth , vol.23 , pp. 777-784
    • Cripe, L.H.1    Tobias, J.D.2
  • 116
    • 84866342088 scopus 로고    scopus 로고
    • Gene therapy for Duchenne muscular dystrophy
    • Verhaart, I. E. & Aartsma-Rus, A. Gene therapy for Duchenne muscular dystrophy. Curr. Opin. Neurol. 25, 588-596 (2012).
    • (2012) Curr. Opin. Neurol , vol.25 , pp. 588-596
    • Verhaart, I.E.1    Aartsma-Rus, A.2
  • 117
    • 84874301993 scopus 로고    scopus 로고
    • Exon skipping quantification by quantitative reverse-transcription polymerase chain reaction in Duchenne muscular dystrophy patients treated with the antisense oligomer eteplirsen
    • Anthony, K. et al. Exon skipping quantification by quantitative reverse-transcription polymerase chain reaction in Duchenne muscular dystrophy patients treated with the antisense oligomer eteplirsen. Hum. Gene Ther. Methods 23, 336-345 (2012).
    • (2012) Hum. Gene Ther. Methods , vol.23 , pp. 336-345
    • Anthony, K.1
  • 118
    • 84877872340 scopus 로고    scopus 로고
    • Clinical trials using antisense oligonucleotides in Duchenne muscular dystrophy
    • Koo, T. & Wood, M. J. Clinical trials using antisense oligonucleotides in Duchenne muscular dystrophy. Hum. Gene Ther. 24, 479-488 (2013).
    • (2013) Hum. Gene Ther , vol.24 , pp. 479-488
    • Koo, T.1    Wood, M.J.2
  • 119
    • 37549034298 scopus 로고    scopus 로고
    • Local dystrophin restoration with antisense oligonucleotide PRO051
    • van Deutekom, J. C. et al. Local dystrophin restoration with antisense oligonucleotide PRO051. N. Engl. J. Med. 357, 2677-2686 (2007).
    • (2007) N. Engl. J. Med , vol.357 , pp. 2677-2686
    • Van Deutekom, J.C.1
  • 120
    • 69949107887 scopus 로고    scopus 로고
    • Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: A single-blind, placebo-controlled, dose-escalation, proof-of-concept study
    • Kinali, M. et al. Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study. Lancet Neurol. 8, 918-928 (2009).
    • (2009) Lancet Neurol , vol.8 , pp. 918-928
    • Kinali, M.1
  • 121
    • 84868371403 scopus 로고    scopus 로고
    • Pip6-PMO, a new generation of peptide-oligonucleotide conjugates with improved cardiac exon skipping activity for DMD treatment
    • Betts, C. et al. Pip6-PMO, a new generation of peptide-oligonucleotide conjugates with improved cardiac exon skipping activity for DMD treatment. Mol. Ther. Nucleic Acids 1, e38 (2012).
    • (2012) Mol. Ther. Nucleic Acids , vol.1
    • Betts, C.1
  • 122
    • 84857793829 scopus 로고    scopus 로고
    • Long-term restoration of cardiac dystrophin expression in golden retriever muscular dystrophy following rAAV6-mediated exon skipping
    • Bish, L. T. et al. Long-term restoration of cardiac dystrophin expression in golden retriever muscular dystrophy following rAAV6-mediated exon skipping. Mol. Ther. 20, 580-589 (2012).
    • (2012) Mol. Ther , vol.20 , pp. 580-589
    • Bish, L.T.1
  • 123
    • 74349109205 scopus 로고    scopus 로고
    • Dose-dependent restoration of dystrophin expression in cardiac muscle of dystrophic mice by systemically delivered morpholino
    • Wu, B. et al. Dose-dependent restoration of dystrophin expression in cardiac muscle of dystrophic mice by systemically delivered morpholino. Gene Ther. 17, 132-140 (2010).
    • (2010) Gene Ther , vol.17 , pp. 132-140
    • Wu, B.1
  • 124
    • 79959995255 scopus 로고    scopus 로고
    • Pip5 transduction peptides direct high efficiency oligonucleotide- mediated dystrophin exon skipping in heart and phenotypic correction in mdx mice
    • Yin, H. et al. Pip5 transduction peptides direct high efficiency oligonucleotide-mediated dystrophin exon skipping in heart and phenotypic correction in mdx mice. Mol. Ther. 19, 1295-1303 (2011).
    • (2011) Mol. Ther , vol.19 , pp. 1295-1303
    • Yin, H.1
  • 125
    • 80052213474 scopus 로고    scopus 로고
    • Long-term systemic administration of unconjugated morpholino oligomers for therapeutic expression of dystrophin by exon skipping in skeletal muscle: Implications for cardiac muscle integrity
    • Malerba, A., Boldrin, L. & Dickson, G. Long-term systemic administration of unconjugated morpholino oligomers for therapeutic expression of dystrophin by exon skipping in skeletal muscle: implications for cardiac muscle integrity. Nucleic Acid Ther. 21, 293-298 (2011).
    • (2011) . Nucleic Acid Ther , vol.21 , pp. 293-298
    • Malerba, A.1    Boldrin, L.2    Dickson, G.3
  • 126
    • 84883713705 scopus 로고    scopus 로고
    • Anti-dystrophin T-cell responses in Duchenne muscular dystrophy: Prevalence and a glucocorticoid treatment effect
    • Flanigan, K. M. et al. Anti-dystrophin T-cell responses in Duchenne muscular dystrophy: prevalence and a glucocorticoid treatment effect. Hum. Gene Ther. 24, 797-806 (2013).
    • (2013) Hum. Gene Ther , vol.24 , pp. 797-806
    • Flanigan, K.M.1
  • 127
    • 84864370685 scopus 로고    scopus 로고
    • Long-term preservation of cardiac structure and function after adeno-associated virus serotype 9-mediated microdystrophin gene transfer in mdx mice
    • Schinkel, S. et al. Long-term preservation of cardiac structure and function after adeno-associated virus serotype 9-mediated microdystrophin gene transfer in mdx mice. Hum. Gene Ther. 23, 566-575 (2012).
    • (2012) Hum. Gene Ther , vol.23 , pp. 566-575
    • Schinkel, S.1
  • 128
    • 84865794295 scopus 로고    scopus 로고
    • Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy
    • Kayali, R. et al. Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy. Hum. Mol. Genet. 21, 4007-4020 (2012).
    • (2012) Hum. Mol. Genet , vol.21 , pp. 4007-4020
    • Kayali, R.1
  • 129
    • 0034982292 scopus 로고    scopus 로고
    • Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations
    • Wagner, K. R. et al. Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations. Ann. Neurol. 49, 706-711 (2001).
    • (2001) Ann. Neurol , vol.49 , pp. 706-711
    • Wagner, K.R.1
  • 130
    • 84878756939 scopus 로고    scopus 로고
    • Arginine butyrate: A therapeutic candidate for Duchenne muscular dystrophy
    • Vianello, S. et al. Arginine butyrate: a therapeutic candidate for Duchenne muscular dystrophy. FASEB J. 27, 2256-2269 (2013).
    • (2013) FASEB J , vol.27 , pp. 2256-2269
    • Vianello, S.1
  • 131
    • 0033179005 scopus 로고    scopus 로고
    • Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
    • Fanin, M., Melacini, P., Angelini, C. & Danieli, G. A. Could utrophin rescue the myocardium of patients with dystrophin gene mutations? J. Mol. Cell. Cardiol. 31, 1501-1508 (1999).
    • (1999) J. Mol. Cell. Cardiol , vol.31 , pp. 1501-1508
    • Fanin, M.1    Melacini, P.2    Angelini, C.3    Danieli, G.A.4
  • 132
    • 84873472020 scopus 로고    scopus 로고
    • Injection of vessel-derived stem cells prevents dilated cardiomyopathy and promotes angiogenesis and endogenous cardiac stem cell proliferation in mdx/utrn-/- but not aged mdx mouse models for duchenne muscular dystrophy
    • Chun, J. L., OBrien, R., Song, M. H., Wondrasch, B. F. & Berry, S. E. Injection of vessel-derived stem cells prevents dilated cardiomyopathy and promotes angiogenesis and endogenous cardiac stem cell proliferation in mdx/utrn-/- but not aged mdx mouse models for duchenne muscular dystrophy. Stem Cells Transl. Med. 2, 68-80 (2013).
    • (2013) Stem Cells Transl. Med , vol.2 , pp. 68-80
    • Chun, J.L.1    Obrien, R.2    Song, M.H.3    Wondrasch, B.F.4    Berry, S.E.5
  • 133
    • 84862836692 scopus 로고    scopus 로고
    • Bradykinin restores left ventricular function, sarcomeric protein phosphorylation, and e/nNOS levels in dogs with Duchenne muscular dystrophy cardiomyopathy
    • Su, J. B. et al. Bradykinin restores left ventricular function, sarcomeric protein phosphorylation, and e/nNOS levels in dogs with Duchenne muscular dystrophy cardiomyopathy. Cardiovasc. Res. 95, 86-96 (2012).
    • (2012) Cardiovasc. Res , vol.95 , pp. 86-96
    • Su, J.B.1
  • 134
    • 33846989762 scopus 로고    scopus 로고
    • ACE inhibitor bulks up muscle
    • Chamberlain, J. S. ACE inhibitor bulks up muscle. Nat. Med. 13, 125-126 (2007).
    • (2007) Nat. Med , vol.13 , pp. 125-126
    • Chamberlain, J.S.1
  • 135
    • 80052668815 scopus 로고    scopus 로고
    • Osteopontin-stimulated expression of matrix metalloproteinase-9 causes cardiomyopathy in the mdx model of Duchenne muscular dystrophy
    • Dahiya, S. et al. Osteopontin-stimulated expression of matrix metalloproteinase-9 causes cardiomyopathy in the mdx model of Duchenne muscular dystrophy. J. Immunol. 187, 2723-2731 (2011).
    • (2011) J Immunol , vol.187 , pp. 2723-2731
    • Dahiya, S.1
  • 136
    • 77951187476 scopus 로고    scopus 로고
    • Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs
    • Townsend, D. et al. Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs. J. Clin. Invest. 120, 1140-1150 (2010).
    • (2010) J Clin. Invest , vol.120 , pp. 1140-1150
    • Townsend, D.1
  • 137
    • 84874287712 scopus 로고    scopus 로고
    • Resveratrol improves cardiomyopathy in dystrophin-deficient mice through SIRT1 protein-mediated modulation of p300 protein
    • Kuno, A. et al. Resveratrol improves cardiomyopathy in dystrophin-deficient mice through SIRT1 protein-mediated modulation of p300 protein. J. Biol. Chem. 288, 5963-5972 (2013).
    • (2013) J. Biol. Chem , vol.288 , pp. 5963-5972
    • Kuno, A.1
  • 138
    • 80052144579 scopus 로고    scopus 로고
    • Resveratrol ameliorates muscular pathology in the dystrophic mdx mouse, a model for Duchenne muscular dystrophy
    • Hori, Y. S. et al. Resveratrol ameliorates muscular pathology in the dystrophic mdx mouse, a model for Duchenne muscular dystrophy. J. Pharmacol. Exp. Ther. 338, 784-794 (2011).
    • (2011) J Pharmacol. Exp. Ther , vol.338 , pp. 784-794
    • Hori, Y.S.1
  • 139
    • 78650474571 scopus 로고    scopus 로고
    • Sildenafil reverses cardiac dysfunction in the mdx mouse model of Duchenne muscular dystrophy
    • Adamo, C. M. et al. Sildenafil reverses cardiac dysfunction in the mdx mouse model of Duchenne muscular dystrophy. Proc. Natl Acad. Sci. USA 107, 19079-19083 (2010).
    • (2010) Proc. Natl Acad. Sci. USA , vol.107 , pp. 19079-19083
    • Adamo, C.M.1
  • 140
    • 58149173164 scopus 로고    scopus 로고
    • Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: Cardiac protection and improved exercise performance
    • Buyse, G. M. et al. Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: cardiac protection and improved exercise performance. Eur. Heart J. 30, 116-124 (2009).
    • (2009) Eur. Heart J , vol.30 , pp. 116-124
    • Buyse, G.M.1
  • 141
    • 84891924161 scopus 로고    scopus 로고
    • Suramin attenuates dystrophin-deficient cardiomyopathy in the mdx mouse model of Duchenne muscular dystrophy
    • de Oliveira Moreira, D. et al. Suramin attenuates dystrophin-deficient cardiomyopathy in the mdx mouse model of Duchenne muscular dystrophy. Muscle Nerve 48, 911-919 (2013).
    • (2013) Muscle Nerve , vol.48 , pp. 911-919
    • De Oliveira Moreira, D.1
  • 142
    • 84862906115 scopus 로고    scopus 로고
    • AAV micro-dystrophin gene therapy alleviates stress-induced cardiac death but not myocardial fibrosis in >21-m-old mdx mice, an end-stage model of Duchenne muscular dystrophy cardiomyopathy
    • Bostick, B. et al. AAV micro-dystrophin gene therapy alleviates stress-induced cardiac death but not myocardial fibrosis in >21-m-old mdx mice, an end-stage model of Duchenne muscular dystrophy cardiomyopathy. J. Mol. Cell. Cardiol. 53, 217-222 (2012).
    • (2012) J. Mol. Cell. Cardiol , vol.53 , pp. 217-222
    • Bostick, B.1
  • 143
    • 84864370685 scopus 로고    scopus 로고
    • Long-term preservation of cardiac structure and function after adeno-associated virus serotype 9-mediated microdystrophin gene transfer in mdx mice
    • Kleinschmidt, J. A., Katus, H. A. & Mller, O. J. Long-term preservation of cardiac structure and function after adeno-associated virus serotype 9-mediated microdystrophin gene transfer in mdx mice. Hum. Gene Ther. 23, 566-575 (2012).
    • (2012) Hum. Gene Ther , vol.23 , pp. 566-575
    • Kleinschmidt, J.A.1    Katus, H.A.2    Mller, O.J.3
  • 144
    • 63749122186 scopus 로고    scopus 로고
    • Disease rescue and increased lifespan in a model of cardiomyopathy and muscular dystrophy by combined AAV treatments
    • Vitiello, C. et al. Disease rescue and increased lifespan in a model of cardiomyopathy and muscular dystrophy by combined AAV treatments. PLoS ONE 4, e5051 (2009).
    • (2009) Plos One , vol.4
    • Vitiello, C.1
  • 145
    • 23944526782 scopus 로고    scopus 로고
    • A novel approach to identify Duchenne muscular dystrophy patients for aminoglycoside antibiotics therapy
    • Kimura, S. et al. A novel approach to identify Duchenne muscular dystrophy patients for aminoglycoside antibiotics therapy. Brain Dev. 27, 400-405 (2005).
    • (2005) Brain Dev , vol.27 , pp. 400-405
    • Kimura, S.1
  • 146
    • 84861716968 scopus 로고    scopus 로고
    • Drug treatment of Duchenne muscular dystrophy: Available evidence and perspectives
    • Beyta Mde, L., Vry, J. & Kirschner, J. Drug treatment of Duchenne muscular dystrophy: available evidence and perspectives. Acta Myol. 31, 4-8 (2012).
    • (2012) Acta Myol , vol.31 , pp. 4-8
    • Beyta Mde, L.1    Vry, J.2    Kirschner, J.3
  • 147
    • 84863442061 scopus 로고    scopus 로고
    • Sustaining cardiac claudin-5 levels prevents functional hallmarks of cardiomyopathy in a muscular dystrophy mouse model
    • Delfn, D. A. et al. Sustaining cardiac claudin-5 levels prevents functional hallmarks of cardiomyopathy in a muscular dystrophy mouse model. Mol. Ther. 20, 1378-1383 (2012).
    • (2012) Mol. Ther , vol.20 , pp. 1378-1383
    • Delfn, D.A.1


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