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Volumn 61, Issue 1, 2014, Pages 127-148

Conduction Defects/Cardiomyopathies

Author keywords

Cardiac arrhythmias; Cardiomyopathies; Conduction disorders; Inherited diseases; Sudden death

Indexed keywords

ARRHYTHMIAS, CARDIAC; CARDIOMYOPATHIES; CHILD; CONGENITAL MALFORMATION; DIAGNOSTIC IMAGING; HEART MUSCLE CONDUCTION SYSTEM; HEART RATE; HUMAN; PATHOPHYSIOLOGY; PROCEDURES;

EID: 84904278950     PISSN: 00653101     EISSN: None     Source Type: Book Series    
DOI: 10.1016/j.yapd.2014.03.001     Document Type: Review
Times cited : (2)

References (99)
  • 1
    • 0015468602 scopus 로고
    • Congenital complete heart block: an international study of the natural history
    • Michaelsson M., Engle M. Congenital complete heart block: an international study of the natural history. Cardiovasc Clin 1972, 4:85-101.
    • (1972) Cardiovasc Clin , vol.4 , pp. 85-101
    • Michaelsson, M.1    Engle, M.2
  • 2
    • 0008752270 scopus 로고
    • Inherited disorders of cardiac rhythm and conduction
    • Gruntheroth W.G., Motolsky A.G. Inherited disorders of cardiac rhythm and conduction. Prog Med Genet 1983, 5:581.
    • (1983) Prog Med Genet , vol.5 , pp. 581
    • Gruntheroth, W.G.1    Motolsky, A.G.2
  • 3
    • 0017645262 scopus 로고
    • Congenital heart block in newborns of mothers with connective tissue disease
    • McCue C.M., Mantakas M.E., Tingelstad J.B., et al. Congenital heart block in newborns of mothers with connective tissue disease. Circulation 1977, 56(1):82-90.
    • (1977) Circulation , vol.56 , Issue.1 , pp. 82-90
    • McCue, C.M.1    Mantakas, M.E.2    Tingelstad, J.B.3
  • 4
    • 0015398581 scopus 로고
    • Pathogenesis of congenital atrioventricular block
    • Lev M. Pathogenesis of congenital atrioventricular block. Prog Cardiovasc Dis 1972, 15(2):145-157.
    • (1972) Prog Cardiovasc Dis , vol.15 , Issue.2 , pp. 145-157
    • Lev, M.1
  • 5
    • 0018744859 scopus 로고
    • Fetal cardiac arrhythmias
    • Shenker L. Fetal cardiac arrhythmias. Obstet Gynecol Surv 1979, 34(8):561-572.
    • (1979) Obstet Gynecol Surv , vol.34 , Issue.8 , pp. 561-572
    • Shenker, L.1
  • 6
    • 0016428340 scopus 로고
    • The heart in systemic lupus erythematosus and the changes induced in it by corticosteroid therapy. A study of 36 necropsy patients
    • Bulkley B.H., Roberts W.C. The heart in systemic lupus erythematosus and the changes induced in it by corticosteroid therapy. A study of 36 necropsy patients. Am J Med 1975, 58(2):243-264.
    • (1975) Am J Med , vol.58 , Issue.2 , pp. 243-264
    • Bulkley, B.H.1    Roberts, W.C.2
  • 7
    • 0020621909 scopus 로고
    • Connective-tissue disease, antibodies to ribonucleoprotein, and congenital heart block
    • Scott J.S., Maddison P.J., Taylor P.V., et al. Connective-tissue disease, antibodies to ribonucleoprotein, and congenital heart block. NEngl J Med 1983, 309(4):209-212.
    • (1983) NEngl J Med , vol.309 , Issue.4 , pp. 209-212
    • Scott, J.S.1    Maddison, P.J.2    Taylor, P.V.3
  • 8
    • 0021940551 scopus 로고
    • Maternal connective tissue disease and congenital heart block. Demonstration of immunoglobulin in cardiac tissue
    • Litsey S.E., Noonan J.A., O'Connor W.N., et al. Maternal connective tissue disease and congenital heart block. Demonstration of immunoglobulin in cardiac tissue. NEngl J Med 1985, 312(2):98-100.
    • (1985) NEngl J Med , vol.312 , Issue.2 , pp. 98-100
    • Litsey, S.E.1    Noonan, J.A.2    O'Connor, W.N.3
  • 10
    • 0031054075 scopus 로고    scopus 로고
    • Anovel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
    • Neyroud N., Tesson F., Denjoy I., et al. Anovel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nat Genet 1997, 15(2):186-189.
    • (1997) Nat Genet , vol.15 , Issue.2 , pp. 186-189
    • Neyroud, N.1    Tesson, F.2    Denjoy, I.3
  • 11
    • 0029831629 scopus 로고    scopus 로고
    • Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium
    • Compton S.J., Lux R.L., Ramsey M.R., et al. Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium. Circulation 1996, 94(5):1018-1022.
    • (1996) Circulation , vol.94 , Issue.5 , pp. 1018-1022
    • Compton, S.J.1    Lux, R.L.2    Ramsey, M.R.3
  • 12
    • 0028784917 scopus 로고
    • Prevention of class III-induced proarrhythmias by flecainide in an animal model of the acquired long QT syndrome
    • Hallman K., Carlsson L. Prevention of class III-induced proarrhythmias by flecainide in an animal model of the acquired long QT syndrome. Pharmacol Toxicol 1995, 77(4):250-254.
    • (1995) Pharmacol Toxicol , vol.77 , Issue.4 , pp. 250-254
    • Hallman, K.1    Carlsson, L.2
  • 13
    • 0029028063 scopus 로고
    • Nicorandil suppresses a hump on the monophasic action potential and torsade de pointes in a patient with idiopathic long QT syndrome
    • Chinushi M., Aizawa Y., Furushima H., et al. Nicorandil suppresses a hump on the monophasic action potential and torsade de pointes in a patient with idiopathic long QT syndrome. Jpn Heart J 1995, 36(4):477-481.
    • (1995) Jpn Heart J , vol.36 , Issue.4 , pp. 477-481
    • Chinushi, M.1    Aizawa, Y.2    Furushima, H.3
  • 14
    • 25044450042 scopus 로고    scopus 로고
    • Effects of potassium channel opener in KVLQT1 long QT gene carriers
    • Vincent G., Fox J., Zhang L. Effects of potassium channel opener in KVLQT1 long QT gene carriers. JAm Coll Cardiol 1997, 29:183A.
    • (1997) JAm Coll Cardiol , vol.29
    • Vincent, G.1    Fox, J.2    Zhang, L.3
  • 15
    • 0029021031 scopus 로고
    • Early afterdepolarization abolished by potassium channel opener in a patient with idiopathic long QT syndrome
    • Sato T., Hata Y., Yamamoto M., et al. Early afterdepolarization abolished by potassium channel opener in a patient with idiopathic long QT syndrome. JCardiovasc Electrophysiol 1995, 6(4):279-282.
    • (1995) JCardiovasc Electrophysiol , vol.6 , Issue.4 , pp. 279-282
    • Sato, T.1    Hata, Y.2    Yamamoto, M.3
  • 16
    • 0028839535 scopus 로고
    • Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndrome
    • Shimizu W., Ohe T., Kurita T., et al. Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndrome. JAm Coll Cardiol 1995, 26(5):1299-1309.
    • (1995) JAm Coll Cardiol , vol.26 , Issue.5 , pp. 1299-1309
    • Shimizu, W.1    Ohe, T.2    Kurita, T.3
  • 17
    • 0029887380 scopus 로고    scopus 로고
    • Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome
    • Priori S.G., Napolitano C., Cantu F., et al. Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome. Circ Res 1996, 78(6):1009-1015.
    • (1996) Circ Res , vol.78 , Issue.6 , pp. 1009-1015
    • Priori, S.G.1    Napolitano, C.2    Cantu, F.3
  • 18
    • 0028874658 scopus 로고
    • Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy
    • Schwartz P.J., Priori S.G., Locati E.H., et al. Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy. Circulation 1995, 92(12):3381-3386.
    • (1995) Circulation , vol.92 , Issue.12 , pp. 3381-3386
    • Schwartz, P.J.1    Priori, S.G.2    Locati, E.H.3
  • 20
    • 0020974404 scopus 로고
    • An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leukocytes
    • Barth P.G., Scholte J.A., Berden J.A., et al. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leukocytes. J Neurol Sci 1983, 62:327-355.
    • (1983) J Neurol Sci , vol.62 , pp. 327-355
    • Barth, P.G.1    Scholte, J.A.2    Berden, J.A.3
  • 21
    • 0023201949 scopus 로고
    • Endocardial fibroelastosis: possible X linked inheritance
    • Hodgson S., Child A., Dyson M. Endocardial fibroelastosis: possible X linked inheritance. JMed Genet 1987, 24(4):210-214.
    • (1987) JMed Genet , vol.24 , Issue.4 , pp. 210-214
    • Hodgson, S.1    Child, A.2    Dyson, M.3
  • 22
    • 0018393867 scopus 로고
    • An X-linked recessive cardiomyopathy with abnormal mitochondria
    • Neustein H.B., Lurie P.R., Dahms B., et al. An X-linked recessive cardiomyopathy with abnormal mitochondria. Pediatrics 1979, 64(1):24-29.
    • (1979) Pediatrics , vol.64 , Issue.1 , pp. 24-29
    • Neustein, H.B.1    Lurie, P.R.2    Dahms, B.3
  • 23
    • 4243935828 scopus 로고
    • X-linked cardiomyopathy, neutropenia and increased urinary levels of 3-methylglutaconic and 2-ethylhydracrylic acids
    • Kelly R., Clark B., Morton D., et al. X-linked cardiomyopathy, neutropenia and increased urinary levels of 3-methylglutaconic and 2-ethylhydracrylic acids. Am J Hum Genet 1989, 45(Suppl).
    • (1989) Am J Hum Genet , vol.45 , Issue.SUPPL
    • Kelly, R.1    Clark, B.2    Morton, D.3
  • 24
    • 0025951140 scopus 로고
    • X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria
    • Kelley R.I., Cheatham J.P., Clark B.J., et al. X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria. JPediatr 1991, 119(5):738-747.
    • (1991) JPediatr , vol.119 , Issue.5 , pp. 738-747
    • Kelley, R.I.1    Cheatham, J.P.2    Clark, B.J.3
  • 25
    • 0027414356 scopus 로고
    • Possible X linked congenital mitochondrial cardiomyopathy in three families
    • Orstavik K.H., Skjorten F., Hellebostad M., et al. Possible X linked congenital mitochondrial cardiomyopathy in three families. JMed Genet 1993, 30(4):269-272.
    • (1993) JMed Genet , vol.30 , Issue.4 , pp. 269-272
    • Orstavik, K.H.1    Skjorten, F.2    Hellebostad, M.3
  • 26
    • 0020974404 scopus 로고
    • An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes
    • Barth P.G., Scholte H.R., Berden J.A., et al. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes. JNeurol Sci 1983, 62(1-3):327-355.
    • (1983) JNeurol Sci , vol.62 , Issue.1-3 , pp. 327-355
    • Barth, P.G.1    Scholte, H.R.2    Berden, J.A.3
  • 27
    • 0026019727 scopus 로고
    • Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28
    • Bolhuis P.A., Hensels G.W., Hulsebos T.J., et al. Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28. Am J Hum Genet 1991, 48(3):481-485.
    • (1991) Am J Hum Genet , vol.48 , Issue.3 , pp. 481-485
    • Bolhuis, P.A.1    Hensels, G.W.2    Hulsebos, T.J.3
  • 28
    • 0029963145 scopus 로고    scopus 로고
    • Anovel X-linked gene, G4.5. is responsible for Barth syndrome
    • Bione S., D'Adamo P., Maestrini E., et al. Anovel X-linked gene, G4.5. is responsible for Barth syndrome. Nat Genet 1996, 12(4):385-389.
    • (1996) Nat Genet , vol.12 , Issue.4 , pp. 385-389
    • Bione, S.1    D'Adamo, P.2    Maestrini, E.3
  • 29
    • 2142765298 scopus 로고    scopus 로고
    • X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update
    • Barth P.G., Valianpour F., Bowen V.M., et al. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update. Am J Med Genet A 2004, 126A(4):349-354.
    • (2004) Am J Med Genet A , vol.126 A , Issue.4 , pp. 349-354
    • Barth, P.G.1    Valianpour, F.2    Bowen, V.M.3
  • 30
    • 0031204998 scopus 로고    scopus 로고
    • Barth syndrome may be due to an acyltransferase deficiency
    • Neuwald A.F. Barth syndrome may be due to an acyltransferase deficiency. Curr Biol 1997, 7(8):R465-R466.
    • (1997) Curr Biol , vol.7 , Issue.8
    • Neuwald, A.F.1
  • 31
    • 0034694802 scopus 로고    scopus 로고
    • Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome
    • Vreken P., Valianpour F., Nijtmans L.G., et al. Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome. Biochem Biophys Res Commun 2000, 279(2):378-382.
    • (2000) Biochem Biophys Res Commun , vol.279 , Issue.2 , pp. 378-382
    • Vreken, P.1    Valianpour, F.2    Nijtmans, L.G.3
  • 32
    • 0036228186 scopus 로고    scopus 로고
    • Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome
    • Schhlame M., Towbin J., Jehle R., et al. Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome. Ann Neurol 2002, 51:634-637.
    • (2002) Ann Neurol , vol.51 , pp. 634-637
    • Schhlame, M.1    Towbin, J.2    Jehle, R.3
  • 33
    • 0025106446 scopus 로고
    • Isolated noncompaction of left ventricular myocardium. A study of eight cases
    • Chin T.K., Perloff J.K., Williams R.G., et al. Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation 1990, 82(2):507-513.
    • (1990) Circulation , vol.82 , Issue.2 , pp. 507-513
    • Chin, T.K.1    Perloff, J.K.2    Williams, R.G.3
  • 34
    • 0031428848 scopus 로고    scopus 로고
    • Isolated noncompaction of the myocardium in adults
    • Ritter M., Oechslin E., Sutsch G., et al. Isolated noncompaction of the myocardium in adults. Mayo Clin Proc 1997, 72(1):26-31.
    • (1997) Mayo Clin Proc , vol.72 , Issue.1 , pp. 26-31
    • Ritter, M.1    Oechslin, E.2    Sutsch, G.3
  • 35
    • 0035185141 scopus 로고    scopus 로고
    • Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy
    • Jenni R., Oechslin E., Schneider J., et al. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy. Heart 2001, 86(6):666-671.
    • (2001) Heart , vol.86 , Issue.6 , pp. 666-671
    • Jenni, R.1    Oechslin, E.2    Schneider, J.3
  • 36
    • 0344844423 scopus 로고    scopus 로고
    • Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy
    • Pignatelli R.H., McMahon C.J., Dreyer W.J., et al. Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy. Circulation 2003, 108(21):2672-2678.
    • (2003) Circulation , vol.108 , Issue.21 , pp. 2672-2678
    • Pignatelli, R.H.1    McMahon, C.J.2    Dreyer, W.J.3
  • 37
    • 0031746624 scopus 로고    scopus 로고
    • Pathological case of the month. Noncompaction of the left ventricular myocardium
    • Michel R.S., Carpenter M.A., Lovell M.A. Pathological case of the month. Noncompaction of the left ventricular myocardium. Arch Pediatr Adolesc Med 1998, 152(7):709-710.
    • (1998) Arch Pediatr Adolesc Med , vol.152 , Issue.7 , pp. 709-710
    • Michel, R.S.1    Carpenter, M.A.2    Lovell, M.A.3
  • 38
    • 1442324783 scopus 로고    scopus 로고
    • Review: metabolic cardiomyopathy and conduction system defects in children
    • Gilbert-Barness E. Review: metabolic cardiomyopathy and conduction system defects in children. Ann Clin Lab Sci 2004, 34(1):15-34.
    • (2004) Ann Clin Lab Sci , vol.34 , Issue.1 , pp. 15-34
    • Gilbert-Barness, E.1
  • 39
    • 0020611002 scopus 로고
    • Arrhythmogenic right ventricular dysplasia: a generalized cardiomyopathy?
    • Manyari D.E., Klein G.J., Gulamhusein S., et al. Arrhythmogenic right ventricular dysplasia: a generalized cardiomyopathy?. Circulation 1983, 68(2):251-257.
    • (1983) Circulation , vol.68 , Issue.2 , pp. 251-257
    • Manyari, D.E.1    Klein, G.J.2    Gulamhusein, S.3
  • 40
    • 0030976714 scopus 로고    scopus 로고
    • Familial incidence of late ventricular potentials and electrocardiographic abnormalities in arrhythmogenic right ventricular dysplasia
    • Hermida J.S., Minassian A., Jarry G., et al. Familial incidence of late ventricular potentials and electrocardiographic abnormalities in arrhythmogenic right ventricular dysplasia. Am J Cardiol 1997, 79(10):1375-1380.
    • (1997) Am J Cardiol , vol.79 , Issue.10 , pp. 1375-1380
    • Hermida, J.S.1    Minassian, A.2    Jarry, G.3
  • 41
    • 18644363134 scopus 로고    scopus 로고
    • Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy
    • Rampazzo A., Nava A., Malacrida S., et al. Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet 2002, 71(5):1200-1206.
    • (2002) Am J Hum Genet , vol.71 , Issue.5 , pp. 1200-1206
    • Rampazzo, A.1    Nava, A.2    Malacrida, S.3
  • 42
    • 0022483542 scopus 로고
    • Cardiac abnormalities in familial palmoplantar keratosis
    • Protonotarios N., Tsatsopoulou A., Patsourakos P., et al. Cardiac abnormalities in familial palmoplantar keratosis. Br Heart J 1986, 56(4):321-326.
    • (1986) Br Heart J , vol.56 , Issue.4 , pp. 321-326
    • Protonotarios, N.1    Tsatsopoulou, A.2    Patsourakos, P.3
  • 43
    • 0028243281 scopus 로고
    • The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24
    • Rampazzo A., Nava A., Danieli P., et al. The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24. Hum Molec Genet 1994, 3:959-962.
    • (1994) Hum Molec Genet , vol.3 , pp. 959-962
    • Rampazzo, A.1    Nava, A.2    Danieli, P.3
  • 44
    • 0028807911 scopus 로고
    • Anew locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43
    • Rampazzo A., Nava A., Erne P., et al. Anew locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43. Hum Mol Genet 1995, 4(11):2151-2154.
    • (1995) Hum Mol Genet , vol.4 , Issue.11 , pp. 2151-2154
    • Rampazzo, A.1    Nava, A.2    Erne, P.3
  • 45
    • 0030050430 scopus 로고    scopus 로고
    • Anew locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14
    • Severini G.M., Krajinovic M., Pinamonti B., et al. Anew locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14. Genomics 1996, 31(2):193-200.
    • (1996) Genomics , vol.31 , Issue.2 , pp. 193-200
    • Severini, G.M.1    Krajinovic, M.2    Pinamonti, B.3
  • 46
    • 0030724006 scopus 로고    scopus 로고
    • ARVD4, a new focus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm
    • Rampazzo A., Nava A., Miorin M., et al. ARVD4, a new focus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. Genomics 1997, 45(2):259-263.
    • (1997) Genomics , vol.45 , Issue.2 , pp. 259-263
    • Rampazzo, A.1    Nava, A.2    Miorin, M.3
  • 47
    • 0032578962 scopus 로고    scopus 로고
    • Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23
    • Ahmad F., Li D., Karibe A., et al. Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23. Circulation 1998, 98(25):2791-2795.
    • (1998) Circulation , vol.98 , Issue.25 , pp. 2791-2795
    • Ahmad, F.1    Li, D.2    Karibe, A.3
  • 48
    • 19944433030 scopus 로고    scopus 로고
    • The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)
    • Hodgkinson K.A., Parfrey P.S., Bassett A.S., et al. The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5). JAm Coll Cardiol 2005, 45(3):400-408.
    • (2005) JAm Coll Cardiol , vol.45 , Issue.3 , pp. 400-408
    • Hodgkinson, K.A.1    Parfrey, P.S.2    Bassett, A.S.3
  • 49
    • 0033910196 scopus 로고    scopus 로고
    • The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14
    • Li D., Ahmad F., Gardner M.J., et al. The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14. Am J Hum Genet 2000, 66(1):148-156.
    • (2000) Am J Hum Genet , vol.66 , Issue.1 , pp. 148-156
    • Li, D.1    Ahmad, F.2    Gardner, M.J.3
  • 50
    • 0032701867 scopus 로고    scopus 로고
    • Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q
    • Melberg A., Oldfors A., Blomstrom-Lundqvist C., et al. Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q. Ann Neurol 1999, 46(5):684-692.
    • (1999) Ann Neurol , vol.46 , Issue.5 , pp. 684-692
    • Melberg, A.1    Oldfors, A.2    Blomstrom-Lundqvist, C.3
  • 51
    • 11444264507 scopus 로고    scopus 로고
    • Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
    • Gerull B., Heuser A., Wichter T., et al. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nat Genet 2004, 36(11):1162-1164.
    • (2004) Nat Genet , vol.36 , Issue.11 , pp. 1162-1164
    • Gerull, B.1    Heuser, A.2    Wichter, T.3
  • 53
    • 0029020780 scopus 로고
    • Right ventricular dysplasia: the Mayo Clinic experience
    • Kullo L., Edwards W., Seward J. Right ventricular dysplasia: the Mayo Clinic experience. Mayo Clin Proc 1995, 70:541-548.
    • (1995) Mayo Clin Proc , vol.70 , pp. 541-548
    • Kullo, L.1    Edwards, W.2    Seward, J.3
  • 54
    • 13244292435 scopus 로고    scopus 로고
    • Implantable cardioverter-defibrillator therapy in arrhythmogenic right ventricular cardiomyopathy. A role for genotyping in decision-making?
    • Wichter T., Breithardt G. Implantable cardioverter-defibrillator therapy in arrhythmogenic right ventricular cardiomyopathy. A role for genotyping in decision-making?. JAm Coll Cardiol 2005, 45:409.
    • (2005) JAm Coll Cardiol , vol.45 , pp. 409
    • Wichter, T.1    Breithardt, G.2
  • 55
    • 0027485942 scopus 로고
    • Histiocytoid cardiomyopathy: case report and literature review
    • Prahlow J.A., Teot L.A. Histiocytoid cardiomyopathy: case report and literature review. JForensic Sci 1993, 38(6):1427-1435.
    • (1993) JForensic Sci , vol.38 , Issue.6 , pp. 1427-1435
    • Prahlow, J.A.1    Teot, L.A.2
  • 56
    • 0018103562 scopus 로고
    • Foamy myocardial transformation of infancy: 'lipid' or 'histiocytoid' myocardiopathy
    • Witzleben C.L., Pinto M. Foamy myocardial transformation of infancy: 'lipid' or 'histiocytoid' myocardiopathy. Arch Pathol Lab Med 1978, 102(6):306-311.
    • (1978) Arch Pathol Lab Med , vol.102 , Issue.6 , pp. 306-311
    • Witzleben, C.L.1    Pinto, M.2
  • 57
    • 0023099292 scopus 로고
    • Foamy myocardial transformation of infancy: an inherited disease
    • Suarez V., Fuggle W.J., Cameron A.H., et al. Foamy myocardial transformation of infancy: an inherited disease. JClin Pathol 1987, 40(3):329-334.
    • (1987) JClin Pathol , vol.40 , Issue.3 , pp. 329-334
    • Suarez, V.1    Fuggle, W.J.2    Cameron, A.H.3
  • 58
    • 0024203274 scopus 로고
    • Oncocytic cardiomyopathy syndrome
    • Franciosi R.A., Singh A. Oncocytic cardiomyopathy syndrome. Hum Pathol 1988, 19(11):1361-1362.
    • (1988) Hum Pathol , vol.19 , Issue.11 , pp. 1361-1362
    • Franciosi, R.A.1    Singh, A.2
  • 59
    • 0028062710 scopus 로고
    • Infantile histiocytoid cardiomyopathy: three cases and literature review
    • Malhotra V., Ferrans V.J., Virmani R. Infantile histiocytoid cardiomyopathy: three cases and literature review. Am Heart J 1994, 128(5):1009-1021.
    • (1994) Am Heart J , vol.128 , Issue.5 , pp. 1009-1021
    • Malhotra, V.1    Ferrans, V.J.2    Virmani, R.3
  • 60
    • 3242730113 scopus 로고    scopus 로고
    • Orthotopic heart transplantation in a child with histiocytoid cardiomyopathy
    • Zangwill S.D., Trost B.A., Zlotocha J., et al. Orthotopic heart transplantation in a child with histiocytoid cardiomyopathy. JHeart Lung Transplant 2004, 23(7):902-904.
    • (2004) JHeart Lung Transplant , vol.23 , Issue.7 , pp. 902-904
    • Zangwill, S.D.1    Trost, B.A.2    Zlotocha, J.3
  • 61
    • 0031598518 scopus 로고    scopus 로고
    • Histiocytoid cardiomyopathy: three new cases and a review of the literature
    • Shehata B.M., Patterson K., Thomas J.E., et al. Histiocytoid cardiomyopathy: three new cases and a review of the literature. Pediatr Dev Pathol 1998, 1(1):56-69.
    • (1998) Pediatr Dev Pathol , vol.1 , Issue.1 , pp. 56-69
    • Shehata, B.M.1    Patterson, K.2    Thomas, J.E.3
  • 62
    • 0027944925 scopus 로고
    • Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy?
    • Bird L.M., Krous H.F., Eichenfield L.F., et al. Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy?. Am J Med Genet 1994, 53(2):141-148.
    • (1994) Am J Med Genet , vol.53 , Issue.2 , pp. 141-148
    • Bird, L.M.1    Krous, H.F.2    Eichenfield, L.F.3
  • 63
    • 0035344419 scopus 로고    scopus 로고
    • Test and teach. Ill-defined subendocardial nodules in an infant. Histiocytoid cardiomyopathy
    • Baillie T., Chan Y.F., Koelmeyer T.D., et al. Test and teach. Ill-defined subendocardial nodules in an infant. Histiocytoid cardiomyopathy. Pathology 2001, 33(2):230-234.
    • (2001) Pathology , vol.33 , Issue.2 , pp. 230-234
    • Baillie, T.1    Chan, Y.F.2    Koelmeyer, T.D.3
  • 64
    • 6044248965 scopus 로고    scopus 로고
    • Acase of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation
    • Vallance H.D., Jeven G., Wallace D.C., et al. Acase of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation. Pediatr Cardiol 2004, 25(5):538-540.
    • (2004) Pediatr Cardiol , vol.25 , Issue.5 , pp. 538-540
    • Vallance, H.D.1    Jeven, G.2    Wallace, D.C.3
  • 65
    • 0028940244 scopus 로고
    • Pathological case of the month. Histiocytoid (oncocytic) cardiomyopathy
    • Heifetz S.A., Faught P.R., Bauman M. Pathological case of the month. Histiocytoid (oncocytic) cardiomyopathy. Arch Pediatr Adolesc Med 1995, 149(4):464-465.
    • (1995) Arch Pediatr Adolesc Med , vol.149 , Issue.4 , pp. 464-465
    • Heifetz, S.A.1    Faught, P.R.2    Bauman, M.3
  • 66
    • 0017226321 scopus 로고
    • Infantile cardiomyopathy with histiocytoid change in cardiac muscle cells. Report of six patients
    • Ferrans V.J., McAllister H.A., Haese W.H. Infantile cardiomyopathy with histiocytoid change in cardiac muscle cells. Report of six patients. Circulation 1976, 53(4):708-719.
    • (1976) Circulation , vol.53 , Issue.4 , pp. 708-719
    • Ferrans, V.J.1    McAllister, H.A.2    Haese, W.H.3
  • 67
    • 0020527386 scopus 로고
    • Histiocytoid cardiomyopathy: a cause of sudden death in apparently healthy infants
    • Saffitz J.E., Ferrans V.J., Rodriguez E.R., et al. Histiocytoid cardiomyopathy: a cause of sudden death in apparently healthy infants. Am J Cardiol 1983, 52(1):215-217.
    • (1983) Am J Cardiol , vol.52 , Issue.1 , pp. 215-217
    • Saffitz, J.E.1    Ferrans, V.J.2    Rodriguez, E.R.3
  • 68
    • 0019964047 scopus 로고
    • Congenital "histiocytoid" cardiomyopathy: evidence suggesting a developmental disorder of the Purkinje cell system of the heart
    • Zimmerman A., Diem P., Cottier H. Congenital "histiocytoid" cardiomyopathy: evidence suggesting a developmental disorder of the Purkinje cell system of the heart. Virchows Arch A Pathol Anat Histol 1982, 396:187-195.
    • (1982) Virchows Arch A Pathol Anat Histol , vol.396 , pp. 187-195
    • Zimmerman, A.1    Diem, P.2    Cottier, H.3
  • 69
    • 0024403675 scopus 로고
    • Pathologic anatomy of the dilated cardiomyopathies
    • Ferrans V.J. Pathologic anatomy of the dilated cardiomyopathies. Am J Cardiol 1989, 64(6):9C-11C.
    • (1989) Am J Cardiol , vol.64 , Issue.6
    • Ferrans, V.J.1
  • 70
    • 0015498573 scopus 로고
    • Idiopathic infantile cardiomyopathy with involvement of the conduction system
    • Kauffman S.L., Chandra N., Peress N.S., et al. Idiopathic infantile cardiomyopathy with involvement of the conduction system. Am J Cardiol 1972, 30(6):648-652.
    • (1972) Am J Cardiol , vol.30 , Issue.6 , pp. 648-652
    • Kauffman, S.L.1    Chandra, N.2    Peress, N.S.3
  • 71
    • 0028726746 scopus 로고
    • Radiofrequency catheter ablation of cardiac arrhythmias in pediatric patients
    • Van Hare G.F. Radiofrequency catheter ablation of cardiac arrhythmias in pediatric patients. Adv Pediatr 1994, 41:83-109.
    • (1994) Adv Pediatr , vol.41 , pp. 83-109
    • Van Hare, G.F.1
  • 72
    • 0034487308 scopus 로고    scopus 로고
    • Idiopathic short QT interval: a new clinical syndrome?
    • Gussak I., Brugada P., Brugada J., et al. Idiopathic short QT interval: a new clinical syndrome?. Cardiology 2000, 94(2):99-102.
    • (2000) Cardiology , vol.94 , Issue.2 , pp. 99-102
    • Gussak, I.1    Brugada, P.2    Brugada, J.3
  • 73
    • 33749454557 scopus 로고    scopus 로고
    • Short QT syndrome: clinical findings and diagnostic-therapeutic implications
    • Giustetto C., Di Monte F., Wolpert C., et al. Short QT syndrome: clinical findings and diagnostic-therapeutic implications. Eur Heart J 2006, 27(20):2440-2447.
    • (2006) Eur Heart J , vol.27 , Issue.20 , pp. 2440-2447
    • Giustetto, C.1    Di Monte, F.2    Wolpert, C.3
  • 74
    • 20344369318 scopus 로고    scopus 로고
    • Short QT syndrome: mechanisms, diagnosis and treatment
    • Bjerregaard P., Gussak I. Short QT syndrome: mechanisms, diagnosis and treatment. Nat Clin Pract Cardiovasc Med 2005, 2(2):84-87.
    • (2005) Nat Clin Pract Cardiovasc Med , vol.2 , Issue.2 , pp. 84-87
    • Bjerregaard, P.1    Gussak, I.2
  • 75
    • 0346727397 scopus 로고    scopus 로고
    • Sudden death associated with short-QT syndrome linked to mutations in HERG
    • Brugada R., Hong K., Dumaine R., et al. Sudden death associated with short-QT syndrome linked to mutations in HERG. Circulation 2004, 109(1):30-35.
    • (2004) Circulation , vol.109 , Issue.1 , pp. 30-35
    • Brugada, R.1    Hong, K.2    Dumaine, R.3
  • 76
    • 2542491002 scopus 로고    scopus 로고
    • Mutation in the KCNQ1 gene leading to the short QT-interval syndrome
    • Bellocq C., van Ginneken A.C., Bezzina C.R., et al. Mutation in the KCNQ1 gene leading to the short QT-interval syndrome. Circulation 2004, 109(20):2394-2397.
    • (2004) Circulation , vol.109 , Issue.20 , pp. 2394-2397
    • Bellocq, C.1    van Ginneken, A.C.2    Bezzina, C.R.3
  • 77
    • 17044424224 scopus 로고    scopus 로고
    • Short QT syndrome and atrial fibrillation caused by mutation in KCNH2
    • Hong K., Bjerregaard P., Gussak I., et al. Short QT syndrome and atrial fibrillation caused by mutation in KCNH2. JCardiovasc Electrophysiol 2005, 16(4):394-396.
    • (2005) JCardiovasc Electrophysiol , vol.16 , Issue.4 , pp. 394-396
    • Hong, K.1    Bjerregaard, P.2    Gussak, I.3
  • 78
    • 0034975654 scopus 로고    scopus 로고
    • I(Kr): the hERG channel
    • Tseng G.N. I(Kr): the hERG channel. JMol Cell Cardiol 2001, 33(5):835-849.
    • (2001) JMol Cell Cardiol , vol.33 , Issue.5 , pp. 835-849
    • Tseng, G.N.1
  • 79
    • 0042859880 scopus 로고    scopus 로고
    • Short QT syndrome: a familial cause of sudden death
    • Gaita F., Giustetto C., Bianchi F., et al. Short QT syndrome: a familial cause of sudden death. Circulation 2003, 108(8):965-970.
    • (2003) Circulation , vol.108 , Issue.8 , pp. 965-970
    • Gaita, F.1    Giustetto, C.2    Bianchi, F.3
  • 80
    • 0025355667 scopus 로고
    • Familial ventricular tachycardia: a report of four families
    • Wren C., Rowland E., Burn J., et al. Familial ventricular tachycardia: a report of four families. Br Heart J 1990, 63(3):169-174.
    • (1990) Br Heart J , vol.63 , Issue.3 , pp. 169-174
    • Wren, C.1    Rowland, E.2    Burn, J.3
  • 81
    • 0028957403 scopus 로고
    • Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients
    • Leenhardt A., Lucet V., Denjoy I., et al. Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients. Circulation 1995, 91(5):1512-1519.
    • (1995) Circulation , vol.91 , Issue.5 , pp. 1512-1519
    • Leenhardt, A.1    Lucet, V.2    Denjoy, I.3
  • 82
    • 0033452339 scopus 로고
    • Familial polymorphic ventricular arrhythmias: a quarter century of successful medical treatment based on serial exercise-pharmacologic testing
    • Fisher J.D., Krikler D., Hallidie-Smith K.A. Familial polymorphic ventricular arrhythmias: a quarter century of successful medical treatment based on serial exercise-pharmacologic testing. JAm Coll Cardiol 1993, 94:2015-2022.
    • (1993) JAm Coll Cardiol , vol.94 , pp. 2015-2022
    • Fisher, J.D.1    Krikler, D.2    Hallidie-Smith, K.A.3
  • 83
    • 0036645605 scopus 로고    scopus 로고
    • Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia
    • Priori S.G., Napolitano C., Memmi M., et al. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. Circulation 2002, 106(1):69-74.
    • (2002) Circulation , vol.106 , Issue.1 , pp. 69-74
    • Priori, S.G.1    Napolitano, C.2    Memmi, M.3
  • 84
    • 0033405388 scopus 로고    scopus 로고
    • Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
    • Swan H., Piippo K., Viitasalo M., et al. Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts. JAm Coll Cardiol 1999, 34(7):2035-2042.
    • (1999) JAm Coll Cardiol , vol.34 , Issue.7 , pp. 2035-2042
    • Swan, H.1    Piippo, K.2    Viitasalo, M.3
  • 85
    • 0035895322 scopus 로고    scopus 로고
    • Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
    • Priori S.G., Napolitano C., Tiso N., et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 2001, 103(2):196-200.
    • (2001) Circulation , vol.103 , Issue.2 , pp. 196-200
    • Priori, S.G.1    Napolitano, C.2    Tiso, N.3
  • 86
    • 0035969990 scopus 로고    scopus 로고
    • Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
    • Laitinen P.J., Brown K.M., Piippo K., et al. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 2001, 103(4):485-490.
    • (2001) Circulation , vol.103 , Issue.4 , pp. 485-490
    • Laitinen, P.J.1    Brown, K.M.2    Piippo, K.3
  • 87
    • 0035205336 scopus 로고    scopus 로고
    • Amissense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
    • Lahat H., Pras E., Olender T., et al. Amissense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Am J Hum Genet 2001, 69(6):1378-1384.
    • (2001) Am J Hum Genet , vol.69 , Issue.6 , pp. 1378-1384
    • Lahat, H.1    Pras, E.2    Olender, T.3
  • 88
    • 0348223717 scopus 로고    scopus 로고
    • Anovel form of familial bidirectional ventricular tachycardia
    • Nof E., Lahat H., Constantini N., et al. Anovel form of familial bidirectional ventricular tachycardia. Am J Cardiol 2004, 93(2):231-234.
    • (2004) Am J Cardiol , vol.93 , Issue.2 , pp. 231-234
    • Nof, E.1    Lahat, H.2    Constantini, N.3
  • 89
    • 0037708928 scopus 로고    scopus 로고
    • FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death
    • Wehrens X.H., Lehnart S.E., Huang F., et al. FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death. Cell 2003, 113(7):829-840.
    • (2003) Cell , vol.113 , Issue.7 , pp. 829-840
    • Wehrens, X.H.1    Lehnart, S.E.2    Huang, F.3
  • 90
    • 0035849570 scopus 로고    scopus 로고
    • Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21
    • Lahat H., Eldar M., Levy-Nissenbaum E., et al. Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21. Circulation 2001, 103(23):2822-2827.
    • (2001) Circulation , vol.103 , Issue.23 , pp. 2822-2827
    • Lahat, H.1    Eldar, M.2    Levy-Nissenbaum, E.3
  • 91
    • 33748512585 scopus 로고    scopus 로고
    • Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia
    • di Barletta M.R., Viatchenko-Karpinski S., Nori A., et al. Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia. Circulation 2006, 114(10):1012-1019.
    • (2006) Circulation , vol.114 , Issue.10 , pp. 1012-1019
    • di Barletta, M.R.1    Viatchenko-Karpinski, S.2    Nori, A.3
  • 92
    • 0028927058 scopus 로고
    • Sudden cardiac death and polymorphous ventricular tachycardia in patients with normal QT intervals and normal systolic cardiac function
    • Eisenberg S.J., Scheinman M.M., Dullet N.K., et al. Sudden cardiac death and polymorphous ventricular tachycardia in patients with normal QT intervals and normal systolic cardiac function. Am J Cardiol 1995, 75(10):687-692.
    • (1995) Am J Cardiol , vol.75 , Issue.10 , pp. 687-692
    • Eisenberg, S.J.1    Scheinman, M.M.2    Dullet, N.K.3
  • 93
    • 43249085697 scopus 로고    scopus 로고
    • Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia
    • Wilde A.A., Bhuiyan Z.A., Crotti L., et al. Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia. NEngl J Med 2008, 358(19):2024-2029.
    • (2008) NEngl J Med , vol.358 , Issue.19 , pp. 2024-2029
    • Wilde, A.A.1    Bhuiyan, Z.A.2    Crotti, L.3
  • 94
    • 41349112275 scopus 로고    scopus 로고
    • Exercise-induced polymorphic ventricular tachycardia in adults without structural heart disease
    • Tan J.H., Scheinman M.M. Exercise-induced polymorphic ventricular tachycardia in adults without structural heart disease. Am J Cardiol 2008, 101(8):1142-1146.
    • (2008) Am J Cardiol , vol.101 , Issue.8 , pp. 1142-1146
    • Tan, J.H.1    Scheinman, M.M.2
  • 95
    • 0019830914 scopus 로고
    • Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy
    • Tripp M.E., Katcher M.L., Peters H.A., et al. Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy. NEngl J Med 1981, 305(7):385-390.
    • (1981) NEngl J Med , vol.305 , Issue.7 , pp. 385-390
    • Tripp, M.E.1    Katcher, M.L.2    Peters, H.A.3
  • 96
    • 0019949555 scopus 로고
    • Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transport
    • Waber L.J., Valle D., Neill C., et al. Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transport. JPediatr 1982, 101(5):700-705.
    • (1982) JPediatr , vol.101 , Issue.5 , pp. 700-705
    • Waber, L.J.1    Valle, D.2    Neill, C.3
  • 97
    • 0021024932 scopus 로고
    • Carnitine-metabolism and functions
    • Bremer J. Carnitine-metabolism and functions. Physiol Rev 1983, 63(4):1420-1480.
    • (1983) Physiol Rev , vol.63 , Issue.4 , pp. 1420-1480
    • Bremer, J.1
  • 98
    • 0016441684 scopus 로고
    • The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiologic features
    • Karpati G., Carpenter S., Engel A.G., et al. The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiologic features. Neurology 1975, 25(1):16-24.
    • (1975) Neurology , vol.25 , Issue.1 , pp. 16-24
    • Karpati, G.1    Carpenter, S.2    Engel, A.G.3


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