메뉴 건너뛰기




Volumn 32, Issue SUPPL. 2, 2009, Pages

Hypertrophic cardiomyopathy

Author keywords

Echocardiography; Electrophysiology clinical; Hemodynamics; Pathology; Pediatrics

Indexed keywords

ADENYLATE KINASE; ATENOLOL; CANDESARTAN; CAPTOPRIL; CARVEDILOL; ENALAPRIL; LOSARTAN; PROPRANOLOL; VERAPAMIL;

EID: 68249149715     PISSN: 01478389     EISSN: 15408159     Source Type: Journal    
DOI: 10.1111/j.1540-8159.2009.02381.x     Document Type: Review
Times cited : (30)

References (110)
  • 1
    • 0037070514 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy: A systemic review
    • Maron BJ. Hypertrophic cardiomyopathy: A systemic review. JAMA 2002 287 : 1308 1320.
    • (2002) JAMA , vol.287 , pp. 1308-1320
    • Maron, B.J.1
  • 2
    • 2942530660 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy
    • Elliott P, McKenna WJ. Hypertrophic cardiomyopathy. Lancet 2004 363 : 188 189.
    • (2004) Lancet , vol.363 , pp. 188-189
    • Elliott, P.1    McKenna, W.J.2
  • 4
    • 0036153781 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy: Management, risk stratification, and prevention of sudden death
    • McKenna WJ, Behr ER. Hypertrophic cardiomyopathy: Management, risk stratification, and prevention of sudden death. Heart 2002 87 : 169 176.
    • (2002) Heart , vol.87 , pp. 169-176
    • McKenna, W.J.1    Behr, E.R.2
  • 5
    • 1942436225 scopus 로고    scopus 로고
    • Assessing the risk of sudden cardiac death in a patient with hypertrophic cardiomyopathy
    • Frenneaux MP. Assessing the risk of sudden cardiac death in a patient with hypertrophic cardiomyopathy. Heart 2004 90 : 570 575.
    • (2004) Heart , vol.90 , pp. 570-575
    • Frenneaux, M.P.1
  • 7
    • 0034538027 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy and sudden death: New perspective on risk stratification and prevention with the implantable cardioverter-defibrillator
    • Maron BJ. Hypertrophic cardiomyopathy and sudden death: New perspective on risk stratification and prevention with the implantable cardioverter- defibrillator. Eur Heart J 2000 21 : 1979 1983.
    • (2000) Eur Heart J , vol.21 , pp. 1979-1983
    • Maron, B.J.1
  • 8
    • 0023269245 scopus 로고
    • Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilation in hypertrophic cardiomyopathy
    • Spirito P, Maron BJ, Bonow RO, Epstein SE. Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilation in hypertrophic cardiomyopathy. Am J Cardiol 1987 60 : 123 139.
    • (1987) Am J Cardiol , vol.60 , pp. 123-139
    • Spirito, P.1    Maron, B.J.2    Bonow, R.O.3    Epstein, S.E.4
  • 10
    • 1542358948 scopus 로고    scopus 로고
    • Left ventricular diastolic dysfunction and diastolic heart failure
    • Gaasch WH, Zile MR. Left ventricular diastolic dysfunction and diastolic heart failure. Annu Rev Med 2004 55 : 373 394.
    • (2004) Annu Rev Med , vol.55 , pp. 373-394
    • Gaasch, W.H.1    Zile, M.R.2
  • 11
  • 12
    • 0029083650 scopus 로고
    • Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 411 subjects in the CARDIA study
    • Maron BJ, Gardin JM, Flack JM, Gidding SS, Kurosaki TT, Bild DE. 1995. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 411 subjects in the CARDIA study. Circulation 92 : 785 789.
    • (1995) Circulation , vol.92 , pp. 785-789
    • Maron, B.J.1    Gardin, J.M.2    Flack, J.M.3    Gidding, S.S.4    Kurosaki, T.T.5    Bild, D.E.6
  • 13
    • 0037133660 scopus 로고    scopus 로고
    • New concepts in diastolic dysfunction and diastolic heart failure. Part I. Diagnosis, prognosis, and measurements of diastolic function
    • Zile MR, Brutsaert DL. New concepts in diastolic dysfunction and diastolic heart failure. Part I. Diagnosis, prognosis, and measurements of diastolic function. Circulation 2002 105 : 1387 1393.
    • (2002) Circulation , vol.105 , pp. 1387-1393
    • Zile, M.R.1    Brutsaert, D.L.2
  • 14
    • 0037425535 scopus 로고    scopus 로고
    • Burden of systolic and diastolic ventricular dysfunction in the community: Appreciating the scope of the heart failure epidemic
    • Redfield MM, Jacobsen SJ, Burnett JC Jr., Mahoney DW, Barley KR, Rodeheffer RJ. Burden of systolic and diastolic ventricular dysfunction in the community: Appreciating the scope of the heart failure epidemic. JAMA 2003 289 : 194 202.
    • (2003) JAMA , vol.289 , pp. 194-202
    • Redfield, M.M.1    Jacobsen, S.J.2    Burnett Jr., J.C.3    Mahoney, D.W.4    Barley, K.R.5    Rodeheffer, R.J.6
  • 15
    • 0000024141 scopus 로고
    • Contribution à l'étude des rétrécissements de l'orifice ventriculo-aortique
    • Vulpian A. Contribution à l'étude des rétré cissements de l'orifice ventriculo-aortique. Arch Physiol 1868 3 : 220 222.
    • (1868) Arch Physiol , vol.3 , pp. 220-222
    • Vulpian, A.1
  • 16
    • 0037453073 scopus 로고    scopus 로고
    • Genetic clues to disease pathways in hypertrophic and dilated cardiomyopathies
    • Watkins H. Genetic clues to disease pathways in hypertrophic and dilated cardiomyopathies. Circulation 2003 107 : 1344 1346.
    • (2003) Circulation , vol.107 , pp. 1344-1346
    • Watkins, H.1
  • 19
    • 0030765610 scopus 로고    scopus 로고
    • Mutations in the cardiac troponin i gene associated with hypertrophic cardiomyopathy
    • Kimura A, Harada H, Park JE, Nishi H, Satoh M, Takahashi M, Hiroi S, et al. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nat Genet 1997 16 : 379 382.
    • (1997) Nat Genet , vol.16 , pp. 379-382
    • Kimura, A.1    Harada, H.2    Park, J.E.3    Nishi, H.4    Satoh, M.5    Takahashi, M.6    Hiroi, S.7
  • 21
    • 15844400653 scopus 로고    scopus 로고
    • Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
    • Poetter K, Jiang H, Hassanzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, et al. Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nat Genet 1996 13 : 63 69.
    • (1996) Nat Genet , vol.13 , pp. 63-69
    • Poetter, K.1    Jiang, H.2    Hassanzadeh, S.3    Master, S.R.4    Chang, A.5    Dalakas, M.C.6    Rayment, I.7
  • 22
    • 0035838393 scopus 로고    scopus 로고
    • Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy
    • Nagueh SF, Bachinski LL, Meyer D, Hill R, Zoghbi WA, Tam JW, Quinones MA, et al. Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy. Circulation 2001 104 : 128 130.
    • (2001) Circulation , vol.104 , pp. 128-130
    • Nagueh, S.F.1    Bachinski, L.L.2    Meyer, D.3    Hill, R.4    Zoghbi, W.A.5    Tam, J.W.6    Quinones, M.A.7
  • 23
    • 0034687163 scopus 로고    scopus 로고
    • Tissue Doppler imaging consistently detects myocardial contraction and relaxation abnormalities, irrespective of cardiac hypertrophy, in a transgenic rabbit model of human hypertrophic cardiomyopathy
    • Nagueh SF, Kopelen HA, Lim DS, Zoghbi WA, Quinones MA, Roberts R, Marian AJ. Tissue Doppler imaging consistently detects myocardial contraction and relaxation abnormalities, irrespective of cardiac hypertrophy, in a transgenic rabbit model of human hypertrophic cardiomyopathy. Circulation 2000 102 : 1346 1350.
    • (2000) Circulation , vol.102 , pp. 1346-1350
    • Nagueh, S.F.1    Kopelen, H.A.2    Lim, D.S.3    Zoghbi, W.A.4    Quinones, M.A.5    Roberts, R.6    Marian, A.J.7
  • 24
    • 11144355765 scopus 로고    scopus 로고
    • Characterization of left ventricular diastolic function by tissue Doppler imaging and clinical status in children with hypertrophic cardiomyopathy
    • McMahon CJ, Nagueh SF, Pignatelli RH, Denfield SW, Dreyer WJ, Price JF, Clunie S, et al. Characterization of left ventricular diastolic function by tissue Doppler imaging and clinical status in children with hypertrophic cardiomyopathy. Circulation 109 : 1756 1762.
    • Circulation , vol.109 , pp. 1756-1762
    • McMahon, C.J.1    Nagueh, S.F.2    Pignatelli, R.H.3    Denfield, S.W.4    Dreyer, W.J.5    Price, J.F.6    Clunie, S.7
  • 25
    • 0344844423 scopus 로고    scopus 로고
    • Clinical characterization of left ventricular noncompaction in children. A relatively common form of cardiomyopathy
    • Pignatelli RH, McMahon CJ, Dreyer WJ, Denfield SW, Price J, Belmont JW, Craigen WJ, et al. Clinical characterization of left ventricular noncompaction in children. A relatively common form of cardiomyopathy. Circulation 2003 108 : 2672 2678.
    • (2003) Circulation , vol.108 , pp. 2672-2678
    • Pignatelli, R.H.1    McMahon, C.J.2    Dreyer, W.J.3    Denfield, S.W.4    Price, J.5    Belmont, J.W.6    Craigen, W.J.7
  • 27
    • 0035872209 scopus 로고    scopus 로고
    • Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: Evidence for a central role of energy compromise in disease pathogenesis
    • Blair E, Redwood C, Ashrafian H, Oliveira M, Broxholme J, Kerr B, Salmon A, et al. Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: Evidence for a central role of energy compromise in disease pathogenesis. Hum Mol Genet 2001 10 : 1215 1220.
    • (2001) Hum Mol Genet , vol.10 , pp. 1215-1220
    • Blair, E.1    Redwood, C.2    Ashrafian, H.3    Oliveira, M.4    Broxholme, J.5    Kerr, B.6    Salmon, A.7
  • 28
    • 0034702928 scopus 로고    scopus 로고
    • Sudden death and cardiovascular collapse in children with restrictive cardiomyopathies
    • Rivenes SM, Towbin JA, Gajarski RJ, Price JK, Denfield SW. Sudden death and cardiovascular collapse in children with restrictive cardiomyopathies. Circulation 2000 102 : 876 882.
    • (2000) Circulation , vol.102 , pp. 876-882
    • Rivenes, S.M.1    Towbin, J.A.2    Gajarski, R.J.3    Price, J.K.4    Denfield, S.W.5
  • 29
    • 0036194934 scopus 로고    scopus 로고
    • Sudden death in children with restrictive cardiomyopathy
    • Denfield SW. Sudden death in children with restrictive cardiomyopathy. Card Electrophysiol Rev 2002 6 : 163 167.
    • (2002) Card Electrophysiol Rev , vol.6 , pp. 163-167
    • Denfield, S.W.1
  • 30
    • 0029038349 scopus 로고
    • Idiopathic restrictive cardiomyopathy in childhood: Diagnostic features and clinical course
    • Cetta F, O'Leary PW, Seward JB, Driscoll DJ. Idiopathic restrictive cardiomyopathy in childhood: Diagnostic features and clinical course. Mayo Clin Proc 1995 70 : 634 640.
    • (1995) Mayo Clin Proc , vol.70 , pp. 634-640
    • Cetta, F.1    O'Leary, P.W.2    Seward, J.B.3    Driscoll, D.J.4
  • 31
    • 0026642655 scopus 로고
    • Clinical profile and outcome of restrictive cardiomyopathy in children
    • Lewis AB. Clinical profile and outcome of restrictive cardiomyopathy in children. Am Heart J 1992 123 : 1589 1593.
    • (1992) Am Heart J , vol.123 , pp. 1589-1593
    • Lewis, A.B.1
  • 32
    • 0036167225 scopus 로고    scopus 로고
    • Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy
    • Arad M, Benson DW, Perez-Atayde AR, McKenna WJ, Sparks EA, Kanter RJ, McGarry K, et al. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy. J Clin Invest 2002 107 : 357 362.
    • (2002) J Clin Invest , vol.107 , pp. 357-362
    • Arad, M.1    Benson, D.W.2    Perez-Atayde, A.R.3    McKenna, W.J.4    Sparks, E.A.5    Kanter, R.J.6    McGarry, K.7
  • 33
    • 0036951869 scopus 로고    scopus 로고
    • Desmin filaments and cardiac disease: Establishing causality
    • Wang X, Osinska H, Gerdes AM, Robbins J. Desmin filaments and cardiac disease: Establishing causality. J Card Fail 2002 8 : S287 S292.
    • (2002) J Card Fail , vol.8
    • Wang, X.1    Osinska, H.2    Gerdes, A.M.3    Robbins, J.4
  • 35
    • 0030046902 scopus 로고    scopus 로고
    • Contractile protein mutations and heart disease
    • Vikstrom KL, Leinwand LA. Contractile protein mutations and heart disease. Curr Opin Cell Biol 1996 8 : 97 105.
    • (1996) Curr Opin Cell Biol , vol.8 , pp. 97-105
    • Vikstrom, K.L.1    Leinwand, L.A.2
  • 36
    • 0026573969 scopus 로고
    • Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
    • Watkins H, Rosenweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Engl J Med 1992 326 : 1108 1114.
    • (1992) N Engl J Med , vol.326 , pp. 1108-1114
    • Watkins, H.1    Rosenweig, A.2    Hwang, D.S.3    Levi, T.4    McKenna, W.5    Seidman, C.E.6    Seidman, J.G.7
  • 37
    • 0037058868 scopus 로고    scopus 로고
    • Prevalence and severity of "benign" mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy
    • Van Driest SL, Ackerman MJ, Ommen SR, Shakur R, Will ML, Nishimura RA, Tajik AJ, et al. Prevalence and severity of "benign" mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy. Circulation 2002 106 : 3085 3090.
    • (2002) Circulation , vol.106 , pp. 3085-3090
    • Van Driest, S.L.1    Ackerman, M.J.2    Ommen, S.R.3    Shakur, R.4    Will, M.L.5    Nishimura, R.A.6    Tajik, A.J.7
  • 38
    • 3843094224 scopus 로고    scopus 로고
    • Diastolic heart failure abnormalities in active relaxation and passive stiffness of the left ventricle
    • Zile MR, Baicu CF, Gaasch WH. Diastolic heart failure abnormalities in active relaxation and passive stiffness of the left ventricle. N Engl J Med 2004 350 : 1953 1959.
    • (2004) N Engl J Med , vol.350 , pp. 1953-1959
    • Zile, M.R.1    Baicu, C.F.2    Gaasch, W.H.3
  • 44
    • 0029143611 scopus 로고
    • Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White Syndrome maps to a locus on chromosome 7q3
    • MacRae CA, Ghaisas N, Kass S, Donnelly S, Basson CT, Watkins HC, Anan R, et al. Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White Syndrome maps to a locus on chromosome 7q3. J Clin Invest 1995 96 : 1216 1220.
    • (1995) J Clin Invest , vol.96 , pp. 1216-1220
    • MacRae, C.A.1    Ghaisas, N.2    Kass, S.3    Donnelly, S.4    Basson, C.T.5    Watkins, H.C.6    Anan, R.7
  • 45
    • 15844400653 scopus 로고    scopus 로고
    • Mutation in either the essential regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
    • Poetter K, Jiang H, Hassanzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, et al. Mutation in either the essential regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nat Genet 1996 13 : 63 69.
    • (1996) Nat Genet , vol.13 , pp. 63-69
    • Poetter, K.1    Jiang, H.2    Hassanzadeh, S.3    Master, S.R.4    Chang, A.5    Dalakas, M.C.6    Rayment, I.7
  • 46
    • 0030765610 scopus 로고    scopus 로고
    • Mutations in the cardiac troponin i gene associated with hypertrophic cardiomyopathy
    • Kimura A, Harada H, Park JE, Nishi H, Satoh M, Takahashi M, Hiroi S, et al. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nat Genet 1997 16 : 379 382.
    • (1997) Nat Genet , vol.16 , pp. 379-382
    • Kimura, A.1    Harada, H.2    Park, J.E.3    Nishi, H.4    Satoh, M.5    Takahashi, M.6    Hiroi, S.7
  • 48
    • 0033610050 scopus 로고    scopus 로고
    • Structural analysis of the titin gene in hypertrophic cardiomyopathy: Identification of a novel disease gene
    • Satoh M, Takahashi M, Sakamoto T, Hiroe M, Marumo F, Kimura A. Structural analysis of the titin gene in hypertrophic cardiomyopathy: Identification of a novel disease gene. Biochem Biophys Res Commun 1999 2625 : 411 417.
    • (1999) Biochem Biophys Res Commun , vol.2625 , pp. 411-417
    • Satoh, M.1    Takahashi, M.2    Sakamoto, T.3    Hiroe, M.4    Marumo, F.5    Kimura, A.6
  • 49
    • 0037453074 scopus 로고    scopus 로고
    • Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy
    • Geier C, Perrot A, Ozcelik C, Binner P, Counsell D, Hoffmann K, Pilz B, et al. Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy. Circulation 2003 107 : 1390 1395.
    • (2003) Circulation , vol.107 , pp. 1390-1395
    • Geier, C.1    Perrot, A.2    Ozcelik, C.3    Binner, P.4    Counsell, D.5    Hoffmann, K.6    Pilz, B.7
  • 50
    • 1942437588 scopus 로고    scopus 로고
    • Novel association of hypertrophic cardiomyopathy, sensorineural deafness and a mutation in unconventional myosin VI (MYO6)
    • Mohiddin SA, Ahmed ZM, Griffith AJ, Tripodi D, Friedman TB, Fananapazir L, Morrell RJ. Novel association of hypertrophic cardiomyopathy, sensorineural deafness and a mutation in unconventional myosin VI (MYO6). J Med Genet 2004 41 : 309 314.
    • (2004) J Med Genet , vol.41 , pp. 309-314
    • Mohiddin, S.A.1    Ahmed, Z.M.2    Griffith, A.J.3    Tripodi, D.4    Friedman, T.B.5    Fananapazir, L.6    Morrell, R.J.7
  • 51
    • 10744220034 scopus 로고    scopus 로고
    • Identification and functional and of caveolin-3 mutation associated with familial hypertrophic cardiomyopathy
    • Hayashi T, Armimura T, Ueda K, Shibata H, Hohda S, Takahashi M, Hori H, et al. Identification and functional and of caveolin-3 mutation associated with familial hypertrophic cardiomyopathy. Biochem Biophys Res Commun 2004 313 : 178 184.
    • (2004) Biochem Biophys Res Commun , vol.313 , pp. 178-184
    • Hayashi, T.1    Armimura, T.2    Ueda, K.3    Shibata, H.4    Hohda, S.5    Takahashi, M.6    Hori, H.7
  • 52
    • 0035936792 scopus 로고    scopus 로고
    • The genetic basis for cardiomyopathy from mutation identification to mechanistic paradigms
    • Seidman JG, Seidman C. The genetic basis for cardiomyopathy from mutation identification to mechanistic paradigms. Cell 2001 108 : 557 567.
    • (2001) Cell , vol.108 , pp. 557-567
    • Seidman, J.G.1    Seidman, C.2
  • 53
    • 0037050022 scopus 로고    scopus 로고
    • The failing heart
    • Towbin JA, Bowles NE. The failing heart. Nature 2002 415 : 227 233.
    • (2002) Nature , vol.415 , pp. 227-233
    • Towbin, J.A.1    Bowles, N.E.2
  • 54
    • 0029896830 scopus 로고    scopus 로고
    • Molecular diversity of myofibrillar proteins: Gene regulation and functional significant
    • Schiaffiino S, Reggiani C. Molecular diversity of myofibrillar proteins: Gene regulation and functional significant. Physiol Rev 1996 76 : 371 423.
    • (1996) Physiol Rev , vol.76 , pp. 371-423
    • Schiaffiino, S.1    Reggiani, C.2
  • 55
    • 0026573969 scopus 로고
    • Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
    • Watkins H, Rosenzweig T, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Engl J Med 1992 326 : 1108 1114.
    • (1992) N Engl J Med , vol.326 , pp. 1108-1114
    • Watkins, H.1    Rosenzweig, T.2    Hwang, D.S.3    Levi, T.4    McKenna, W.5    Seidman, C.E.6    Seidman, J.G.7
  • 58
    • 0028886136 scopus 로고
    • Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
    • Bonne G, Carrier L, Bercovici J, Cruaud C, Richard P, Hainque B, Gautel M, et al. Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nat Genet 1995 11 : 438 440.
    • (1995) Nat Genet , vol.11 , pp. 438-440
    • Bonne, G.1    Carrier, L.2    Bercovici, J.3    Cruaud, C.4    Richard, P.5    Hainque, B.6    Gautel, M.7
  • 59
    • 0028844204 scopus 로고
    • Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
    • Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, et al. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat Genet 1995 11 : 434 437.
    • (1995) Nat Genet , vol.11 , pp. 434-437
    • Watkins, H.1    Conner, D.2    Thierfelder, L.3    Jarcho, J.A.4    MacRae, C.5    McKenna, W.J.6    Maron, B.J.7
  • 61
    • 0032499634 scopus 로고    scopus 로고
    • Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to cardiac myosin-binding protein C gene
    • Charron P, Dubourg O, Desnos M, Bennaceur M, Carrier L, Camproux AC, Isnard R, et al. Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to cardiac myosin-binding protein C gene. Circulation 1998 97 : 2230 2236.
    • (1998) Circulation , vol.97 , pp. 2230-2236
    • Charron, P.1    Dubourg, O.2    Desnos, M.3    Bennaceur, M.4    Carrier, L.5    Camproux, A.C.6    Isnard, R.7
  • 62
    • 0028784754 scopus 로고
    • Angiotensin-converting enzyme gene polymorphism in Japanese patients with hypertrophic cardiomyopathy
    • Yoneya K, Okamoto H, Machida M, Onozuka H, Noguchi M, Mikami T, Kawaguchi H, et al. Angiotensin-converting enzyme gene polymorphism in Japanese patients with hypertrophic cardiomyopathy. Am Heart J 1995 130 : 1089 1093.
    • (1995) Am Heart J , vol.130 , pp. 1089-1093
    • Yoneya, K.1    Okamoto, H.2    MacHida, M.3    Onozuka, H.4    Noguchi, M.5    Mikami, T.6    Kawaguchi, H.7
  • 63
    • 0031080069 scopus 로고    scopus 로고
    • The influence of the angiotensin i converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation
    • Tesson F, Dufour C, Moolman JC, Carrier L, al-Mahdawi S, Chojnowska L, Dubourg O, et al. The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation. J Mol Cell Cardiol 1997 29 : 831 838.
    • (1997) J Mol Cell Cardiol , vol.29 , pp. 831-838
    • Tesson, F.1    Dufour, C.2    Moolman, J.C.3    Carrier, L.4    Al-Mahdawi, S.5    Chojnowska, L.6    Dubourg, O.7
  • 64
    • 0036178004 scopus 로고    scopus 로고
    • Genetic polymorphisms in the rennin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: A study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene
    • Ortlepp JR, Vosberg HP, Reith S, Ohme F, Mahon NG, Schroder D, Klues HG, et al. Genetic polymorphisms in the rennin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: A study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene. Heart 2002 87 : 270 275.
    • (2002) Heart , vol.87 , pp. 270-275
    • Ortlepp, J.R.1    Vosberg, H.P.2    Reith, S.3    Ohme, F.4    Mahon, N.G.5    Schroder, D.6    Klues, H.G.7
  • 65
    • 0023144759 scopus 로고
    • Comparative effects of calcium-channel blockers and beta-adrenergic blocker on early diastolic time intervals and A-wave ratio in patients with hypertrophic cardiomyopathy
    • Doiuchi J, Hamada M, Ito T, Kokubu T. Comparative effects of calcium-channel blockers and beta-adrenergic blocker on early diastolic time intervals and A-wave ratio in patients with hypertrophic cardiomyopathy. Clin Cardiol 1987 10 : 26 30.
    • (1987) Clin Cardiol , vol.10 , pp. 26-30
    • Doiuchi, J.1    Hamada, M.2    Ito, T.3    Kokubu, T.4
  • 66
    • 0021922353 scopus 로고
    • Use of calcium channel blockers in hypertrophic cardiomyopathy
    • Lorell BH. Use of calcium channel blockers in hypertrophic cardiomyopathy. Am J Med 1985 78 : 43 54.
    • (1985) Am J Med , vol.78 , pp. 43-54
    • Lorell, B.H.1
  • 67
    • 0032113264 scopus 로고    scopus 로고
    • Verapamil therapy in infants with hypertrophic cardiomyopathy
    • Moran AM, Colan SD. Verapamil therapy in infants with hypertrophic cardiomyopathy. Cardiol Young 1998 8 : 310 319.
    • (1998) Cardiol Young , vol.8 , pp. 310-319
    • Moran, A.M.1    Colan, S.D.2
  • 70
    • 0033600550 scopus 로고    scopus 로고
    • Cardiac pacing. An alternative treatment for selected patients with hypertrophic cardiomyopathy and adjunctive therapy for certain patients with dilated cardiomyopathy
    • O'Rourke RA. Cardiac pacing. An alternative treatment for selected patients with hypertrophic cardiomyopathy and adjunctive therapy for certain patients with dilated cardiomyopathy. Circulation 1999 100 : 786 788.
    • (1999) Circulation , vol.100 , pp. 786-788
    • O'Rourke, R.A.1
  • 71
    • 0030027221 scopus 로고    scopus 로고
    • Appraisal of dual-chamber pacing therapy in hypertrophic cardiomyopathy: Too soon for a rush to judgment?
    • Maron BJ. Appraisal of dual-chamber pacing therapy in hypertrophic cardiomyopathy: Too soon for a rush to judgment? J Am Coll Cardiol 1996 27 : 431 432.
    • (1996) J Am Coll Cardiol , vol.27 , pp. 431-432
    • Maron, B.J.1
  • 72
    • 0035165517 scopus 로고    scopus 로고
    • Dual chamber pacemaker therapy for mid-cavity obstructive hypertrophic cardiomyopathy
    • Begley D, Mohiddin S, Fananapazir L. Dual chamber pacemaker therapy for mid-cavity obstructive hypertrophic cardiomyopathy. Pacing Clin Electrophysiol 2001 24 : 1639 1644.
    • (2001) Pacing Clin Electrophysiol , vol.24 , pp. 1639-1644
    • Begley, D.1    Mohiddin, S.2    Fananapazir, L.3
  • 73
    • 1342288505 scopus 로고    scopus 로고
    • Predictors of outcome after alcohol septal ablation therapy in patients with hypertrophic obstructive cardiomyopathy
    • Chang SM, Lakkis NM, Franklin J, Spencer WH III., Nagueh SF. Predictors of outcome after alcohol septal ablation therapy in patients with hypertrophic obstructive cardiomyopathy. Circulation 2004 109 : 824 827.
    • (2004) Circulation , vol.109 , pp. 824-827
    • Chang, S.M.1    Lakkis, N.M.2    Franklin, J.3    Spencer, III.W.H.4    Nagueh, S.F.5
  • 74
    • 0038546823 scopus 로고    scopus 로고
    • Nonsurgical septal reduction therapy for hypertrophic obstructive cardiomyopathy: Short-term results in 50 consecutive procedures
    • Nielsen CD, Killip D, Spencer WH III. Nonsurgical septal reduction therapy for hypertrophic obstructive cardiomyopathy: Short-term results in 50 consecutive procedures. Clin Cardiol 2003 26 : 275 279.
    • (2003) Clin Cardiol , vol.26 , pp. 275-279
    • Nielsen, C.D.1    Killip, D.2    Spencer, III.W.H.3
  • 75
    • 0037162385 scopus 로고    scopus 로고
    • Acute effect of nonsurgical septal reduction therapy on regional left ventricular asynchrony in patients with hypertrophic obstructive cardiomyopathy
    • Park TH, Lakkis NM, Middleton KJ, Franklin J, Zoghbi WA, Quinones MA, Spencer WH III., et al. Acute effect of nonsurgical septal reduction therapy on regional left ventricular asynchrony in patients with hypertrophic obstructive cardiomyopathy. Circulation 2002 106 : 412 415.
    • (2002) Circulation , vol.106 , pp. 412-415
    • Park, T.H.1    Lakkis, N.M.2    Middleton, K.J.3    Franklin, J.4    Zoghbi, W.A.5    Quinones, M.A.6    Spencer, III.W.H.7
  • 76
    • 8144226241 scopus 로고    scopus 로고
    • New treatment strategies for hypertrophic obstructive cardiomyopathy
    • Hess OM, Sigwart U. New treatment strategies for hypertrophic obstructive cardiomyopathy. J Am Coll Cardiol 2004 44 : 2054 2055.
    • (2004) J Am Coll Cardiol , vol.44 , pp. 2054-2055
    • Hess, O.M.1    Sigwart, U.2
  • 77
    • 0020052713 scopus 로고
    • Fabry disease: Impaired autonomic function
    • Cable WJ, Kolodny EH, Adams RD. Fabry disease: Impaired autonomic function. Neurology 1982 32 : 498 502.
    • (1982) Neurology , vol.32 , pp. 498-502
    • Cable, W.J.1    Kolodny, E.H.2    Adams, R.D.3
  • 79
    • 0000243356 scopus 로고
    • Glycogen storage diseases
    • Scriver, C.R. Beaudet, A.L. Sly, W.S. Valle, D. eds. New York. McGraw-Hill. pp.
    • Hers HG, van Hoof F, de Barsy T. Glycogen storage diseases. In : Scriver CR, Beaudet AL, Sly WS, Valle D (eds. The Metabolic Basis of Inherited Disease. 6th Ed. New York, McGraw-Hill, 1989, pp. 425 452.
    • (1989) The Metabolic Basis of Inherited Disease. 6th Ed. , pp. 425-452
    • Hers, H.G.1    Van Hoof, F.2    De Barsy, T.3
  • 80
    • 0027215234 scopus 로고
    • Molecular genetic aspects of cardiomyopathy
    • Towbin JA. Molecular genetic aspects of cardiomyopathy. Biochem Med Metab Biol 1993 49 : 283 320.
    • (1993) Biochem Med Metab Biol , vol.49 , pp. 283-320
    • Towbin, J.A.1
  • 81
    • 0018646407 scopus 로고
    • Genetics of type II glycogenosis: Assignment of the human gene for acid α-glucosidase to chromosome 17
    • D'Ancona GG, Wurm J, Croce CM. Genetics of type II glycogenosis: Assignment of the human gene for acid α-glucosidase to chromosome 17. Proc Natl Acad Sci USA 1979 76 : 4526 4529.
    • (1979) Proc Natl Acad Sci USA , vol.76 , pp. 4526-4529
    • D'Ancona, G.G.1    Wurm, J.2    Croce, C.M.3
  • 82
    • 0020655515 scopus 로고
    • Genetic heterogeneity in acid α-glucosidase deficiency
    • Beratis NG, LaBadie GU, Hirschhorn K. Genetic heterogeneity in acid α-glucosidase deficiency. Am J Hum Genet 1983 35 : 21 33.
    • (1983) Am J Hum Genet , vol.35 , pp. 21-33
    • Beratis, N.G.1    Labadie, G.U.2    Hirschhorn, K.3
  • 83
    • 0026006438 scopus 로고
    • Identification of a missense mutation in one allele of a patient with Pompe disease and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele
    • Zhong N, Martiniuk F, Tzall S, Hirschhorn R. Identification of a missense mutation in one allele of a patient with Pompe disease and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele. Am J Hum Genet 1991 49 : 635 645.
    • (1991) Am J Hum Genet , vol.49 , pp. 635-645
    • Zhong, N.1    Martiniuk, F.2    Tzall, S.3    Hirschhorn, R.4
  • 85
    • 5044228518 scopus 로고    scopus 로고
    • Fabry disease: A review
    • DOI 10.1016/j.jbspin.2003.10.015, PII S1297319X03002355
    • Masson C, Cisse I, Simon V, Insalaco P, Audran M. Fabry disease: A review. Joint Bone Spine 2004 71 : 381 383. (Pubitemid 39335671)
    • (2004) Joint Bone Spine , vol.71 , Issue.5 , pp. 381-383
    • Masson, C.1    Cisse, I.2    Simon, V.3    Insalaco, P.4    Audran, M.5
  • 87
    • 0016716506 scopus 로고
    • Cardiac manifestations of Fabry's disease: Report of a case with mitral insufficiency and electrocardiographic evidence of myocardial infarction
    • Becker AE, Schoorl R, Balk AG, van der Heide RM. Cardiac manifestations of Fabry's disease: Report of a case with mitral insufficiency and electrocardiographic evidence of myocardial infarction. Am J Cardiol 1975 36 : 829 835.
    • (1975) Am J Cardiol , vol.36 , pp. 829-835
    • Becker, A.E.1    Schoorl, R.2    Balk, A.G.3    Van Der Heide, R.M.4
  • 91
    • 17044440789 scopus 로고    scopus 로고
    • Primary LAMP-2 deficiency causes X-linked vascular cardiomyopathy and myopathy (Danon Disease)
    • Nishino I, Fu J, Tanji K, Yamada T, Shimojo S, Koori T, Mora M, et al. Primary LAMP-2 deficiency causes X-linked vascular cardiomyopathy and myopathy (Danon Disease). Nature 2000 406 : 906 909.
    • (2000) Nature , vol.406 , pp. 906-909
    • Nishino, I.1    Fu, J.2    Tanji, K.3    Yamada, T.4    Shimojo, S.5    Koori, T.6    Mora, M.7
  • 93
    • 0034654362 scopus 로고    scopus 로고
    • Characterization of AMP-activated protein kinase gamma-subunit isoforms and their role in AMP binding
    • Cheung PC, Salt IP, Davies SP, Hardie DG, Carling D. Characterization of AMP-activated protein kinase gamma-subunit isoforms and their role in AMP binding. Biochem J 2000 346 : 659 669.
    • (2000) Biochem J , vol.346 , pp. 659-669
    • Cheung, P.C.1    Salt, I.P.2    Davies, S.P.3    Hardie, D.G.4    Carling, D.5
  • 95
    • 0037782349 scopus 로고    scopus 로고
    • Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy
    • Arad M, Moskowitz IP, Patel VV, Ahmad F, Perez-Atayde AR, Sawyer DB, Walter M, et al. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy. Circulation 2003 107 : 2850 2856.
    • (2003) Circulation , vol.107 , pp. 2850-2856
    • Arad, M.1    Moskowitz, I.P.2    Patel, V.V.3    Ahmad, F.4    Perez-Atayde, A.R.5    Sawyer, D.B.6    Walter, M.7
  • 96
    • 0022751029 scopus 로고    scopus 로고
    • The elucidation of the human mitochondrial genome: A historical perspective
    • Attardi G. The elucidation of the human mitochondrial genome: A historical perspective. Bioessays 1996 5 : 34 39.
    • (1996) Bioessays , vol.5 , pp. 34-39
    • Attardi, G.1
  • 97
    • 0024163051 scopus 로고
    • Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease
    • Wallace DC, Zheng X, Lott MT, Shoffner JM, Hodge JA, Kelley RI, Epstein CM, et al. Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease. Cell 1988 55 : 601 610.
    • (1988) Cell , vol.55 , pp. 601-610
    • Wallace, D.C.1    Zheng, X.2    Lott, M.T.3    Shoffner, J.M.4    Hodge, J.A.5    Kelley, R.I.6    Epstein, C.M.7
  • 98
    • 0023003310 scopus 로고
    • The clinical features of mitochondrial myopathy
    • Petty RKH, Harding AE, Morgan-Hughes JA. The clinical features of mitochondrial myopathy. Brain 1986 109 : 915 938.
    • (1986) Brain , vol.109 , pp. 915-938
    • Petty, R.K.H.1    Harding, A.E.2    Morgan-Hughes, J.A.3
  • 99
    • 0028258728 scopus 로고
    • Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNALeu(UUR) mutation associated with maternally inherited myopathy and cardiomyopathy
    • Mariotti C, Tiranti V, Carrara F, Dallapiccola B, DiDonato S, Zeviani M. Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNALeu(UUR) mutation associated with maternally inherited myopathy and cardiomyopathy. J Clin Invest 1994 93 : 1102 1107.
    • (1994) J Clin Invest , vol.93 , pp. 1102-1107
    • Mariotti, C.1    Tiranti, V.2    Carrara, F.3    Dallapiccola, B.4    Didonato, S.5    Zeviani, M.6
  • 100
    • 0035096954 scopus 로고    scopus 로고
    • Mitochondrial myopathies and the role of the pathologist in the molecular era
    • Vogel H. Mitochondrial myopathies and the role of the pathologist in the molecular era. J Neuropathol Exp Neurol 2001 60 : 217 227.
    • (2001) J Neuropathol Exp Neurol , vol.60 , pp. 217-227
    • Vogel, H.1
  • 101
    • 0023915528 scopus 로고
    • Complexity and tissue specificity of the mitochondrial respiratory chain
    • Capaldi RA, Halphen DG, Zhang YZ, Yanamura W. Complexity and tissue specificity of the mitochondrial respiratory chain. J Bioenerg Biomembr 1988 20 : 291 311.
    • (1988) J Bioenerg Biomembr , vol.20 , pp. 291-311
    • Capaldi, R.A.1    Halphen, D.G.2    Zhang, Y.Z.3    Yanamura, W.4
  • 102
    • 0025004427 scopus 로고
    • Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy
    • Ozawa T, Tanaka M, Sugiyama S, Hattori K, Ito T, Oho K, Takahashi A, et al. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy. Biochem Biophys Res Commun 1990 170 : 830 836.
    • (1990) Biochem Biophys Res Commun , vol.170 , pp. 830-836
    • Ozawa, T.1    Tanaka, M.2    Sugiyama, S.3    Hattori, K.4    Ito, T.5    Oho, K.6    Takahashi, A.7
  • 104
    • 0025106446 scopus 로고
    • Isolated noncompaction of left ventricular myocardium. A study of eight cases
    • Chin TK, Perloff JK, Williams RG, Jue K, Mohrmann R. Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation 1990 82 : 507 513.
    • (1990) Circulation , vol.82 , pp. 507-513
    • Chin, T.K.1    Perloff, J.K.2    Williams, R.G.3    Jue, K.4    Mohrmann, R.5
  • 105
    • 0037108211 scopus 로고    scopus 로고
    • Left ventricular hypertrabeculation/ noncompaction and association with additional cardiac abnormalities and neuromuscular disorders
    • Stollberger C, Finsterer J, Blazek G. Left ventricular hypertrabeculation/ noncompaction and association with additional cardiac abnormalities and neuromuscular disorders. Am J Cardiol 2002 90 : 899 902.
    • (2002) Am J Cardiol , vol.90 , pp. 899-902
    • Stollberger, C.1    Finsterer, J.2    Blazek, G.3
  • 106
    • 17044449684 scopus 로고    scopus 로고
    • Left ventricular hypertrabeculation/ noncompaction
    • Stollberger C, Finsterer J. Left ventricular hypertrabeculation/ noncompaction. J Am Soc Echocardiogr 2004 17 : 91 100.
    • (2004) J Am Soc Echocardiogr , vol.17 , pp. 91-100
    • Stollberger, C.1    Finsterer, J.2
  • 107
    • 0033165683 scopus 로고    scopus 로고
    • Clinical features of isolated noncompaction of the ventricular myocardium: Long-term clinical course, hemodynamic properties and genetic background
    • Ichida F, Hamamichi Y, Miyawaki T, Ono Y, Kamiya T, Akagi T, Hamada H, et al. Clinical features of isolated noncompaction of the ventricular myocardium: Long-term clinical course, hemodynamic properties and genetic background. J Am Coll Cardiol 1999 34 : 233 240.
    • (1999) J Am Coll Cardiol , vol.34 , pp. 233-240
    • Ichida, F.1    Hamamichi, Y.2    Miyawaki, T.3    Ono, Y.4    Kamiya, T.5    Akagi, T.6    Hamada, H.7
  • 108
  • 110
    • 0344873698 scopus 로고    scopus 로고
    • Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction
    • Vatta M, Mohapatra B, Jimenez S, Sanchez X, Faulkner G, Perles Z, Sinagra G, et al. Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J Am Coll Cardiol 2003 42 : 2014 2027.
    • (2003) J Am Coll Cardiol , vol.42 , pp. 2014-2027
    • Vatta, M.1    Mohapatra, B.2    Jimenez, S.3    Sanchez, X.4    Faulkner, G.5    Perles, Z.6    Sinagra, G.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.