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Volumn 6, Issue 2, 2009, Pages 272-278

Sudden infant death syndrome: Do ion channels play a role?

Author keywords

Electrocardiogram; Genetics; Ion channels; Long QT syndrome; QT interval; Sudden infant death syndrome

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; ION CHANNEL; MEXILETINE; PROPRANOLOL;

EID: 58849160795     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2008.07.028     Document Type: Article
Times cited : (40)

References (59)
  • 1
    • 0017264676 scopus 로고
    • Cardiac sympathetic innervation and the sudden infant death syndrome: a possible pathogenic link
    • 167172
    • Schwartz P.J. Cardiac sympathetic innervation and the sudden infant death syndrome: a possible pathogenic link. Am J Med 60 (1976) 167172
    • (1976) Am J Med , vol.60
    • Schwartz, P.J.1
  • 2
    • 0017145176 scopus 로고
    • Potential role of QT interval prolongation in sudden infant death syndrome
    • 423430
    • Maron B.J., Clark C.E., Goldstein R.E., et al. Potential role of QT interval prolongation in sudden infant death syndrome. Circulation 54 (1976) 423430
    • (1976) Circulation , vol.54
    • Maron, B.J.1    Clark, C.E.2    Goldstein, R.E.3
  • 3
    • 3042798289 scopus 로고    scopus 로고
    • Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach
    • Krous H.F., Beckwith J.B., Byard R.W., et al. Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach. Pediatrics 114 (2004) 234-238
    • (2004) Pediatrics , vol.114 , pp. 234-238
    • Krous, H.F.1    Beckwith, J.B.2    Byard, R.W.3
  • 4
    • 0037127415 scopus 로고    scopus 로고
    • Evaluation of diagnostic tools applied in the examination of sudden unexpected deaths in infancy and early childhood
    • Arnestad M., Vege A., and Rognum T.O. Evaluation of diagnostic tools applied in the examination of sudden unexpected deaths in infancy and early childhood. Forensic Sci Int 125 (2002) 262-268
    • (2002) Forensic Sci Int , vol.125 , pp. 262-268
    • Arnestad, M.1    Vege, A.2    Rognum, T.O.3
  • 5
    • 0033497543 scopus 로고    scopus 로고
    • Sudden unexpected deaths in infancy: what are the causes?
    • Cote A., Russo P., and Michaud J. Sudden unexpected deaths in infancy: what are the causes?. J Pediatr 135 (1999) 437-443
    • (1999) J Pediatr , vol.135 , pp. 437-443
    • Cote, A.1    Russo, P.2    Michaud, J.3
  • 6
    • 0037347308 scopus 로고    scopus 로고
    • Defining the sudden infant death syndrome
    • Beckwith J.B. Defining the sudden infant death syndrome. Arch Pediatr Adolesc Med 157 (2003) 286-290
    • (2003) Arch Pediatr Adolesc Med , vol.157 , pp. 286-290
    • Beckwith, J.B.1
  • 7
    • 33745655821 scopus 로고    scopus 로고
    • Sudden infant death syndrome
    • Hunt C.E., and Hauck F.R. Sudden infant death syndrome. CMAJ 174 (2006) 1861-1869
    • (2006) CMAJ , vol.174 , pp. 1861-1869
    • Hunt, C.E.1    Hauck, F.R.2
  • 8
    • 34347386731 scopus 로고    scopus 로고
    • Infant mortality statistics from the 2004 period linked birth/infant death data set
    • Mathews T.J., and MacDorman M.F. Infant mortality statistics from the 2004 period linked birth/infant death data set. Natl Vital Stat Rep 55 (2007) 1-32
    • (2007) Natl Vital Stat Rep , vol.55 , pp. 1-32
    • Mathews, T.J.1    MacDorman, M.F.2
  • 9
    • 34147129252 scopus 로고    scopus 로고
    • Sudden infant death syndrome: review of implicated genetic factors
    • Weese-Mayer D.E., Ackerman M.J., Marazita M.L., et al. Sudden infant death syndrome: review of implicated genetic factors. Am J Med Genet A 143 (2007) 771-788
    • (2007) Am J Med Genet A , vol.143 , pp. 771-788
    • Weese-Mayer, D.E.1    Ackerman, M.J.2    Marazita, M.L.3
  • 10
    • 33750518186 scopus 로고    scopus 로고
    • Multiple serotonergic brainstem abnormalities in sudden infant death syndrome
    • Paterson D.S., Trachtenberg F.L., Thompson E.G., et al. Multiple serotonergic brainstem abnormalities in sudden infant death syndrome. JAMA 296 (2006) 2124-2132
    • (2006) JAMA , vol.296 , pp. 2124-2132
    • Paterson, D.S.1    Trachtenberg, F.L.2    Thompson, E.G.3
  • 11
    • 0037522034 scopus 로고    scopus 로고
    • Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene
    • Weese-Mayer D.E., Berry-Kravis E.M., Maher B.S., et al. Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene. Am J Med Genet A 117A (2003) 268-274
    • (2003) Am J Med Genet A , vol.117 A , pp. 268-274
    • Weese-Mayer, D.E.1    Berry-Kravis, E.M.2    Maher, B.S.3
  • 12
    • 17644435180 scopus 로고    scopus 로고
    • Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life
    • Boles R.G., Buck E.A., Blitzer M.G., et al. Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life. J Pediatr 132 (1998) 924-933
    • (1998) J Pediatr , vol.132 , pp. 924-933
    • Boles, R.G.1    Buck, E.A.2    Blitzer, M.G.3
  • 13
    • 41749086869 scopus 로고    scopus 로고
    • Ion channel diseases in children: manifestations and management
    • Schwartz P.J., and Crotti L. Ion channel diseases in children: manifestations and management. Curr Opin Cardiol 23 (2008) 184-191
    • (2008) Curr Opin Cardiol , vol.23 , pp. 184-191
    • Schwartz, P.J.1    Crotti, L.2
  • 14
    • 0031916794 scopus 로고    scopus 로고
    • The long QT syndrome: ion channel diseases of the heart
    • Ackerman M.J. The long QT syndrome: ion channel diseases of the heart. Mayo Clin Proc 73 (1998) 250-269
    • (1998) Mayo Clin Proc , vol.73 , pp. 250-269
    • Ackerman, M.J.1
  • 15
    • 0034609531 scopus 로고    scopus 로고
    • Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
    • Splawski I., Shen J., Timothy K.W., et al. Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 102 (2000) 1178-1185
    • (2000) Circulation , vol.102 , pp. 1178-1185
    • Splawski, I.1    Shen, J.2    Timothy, K.W.3
  • 16
    • 17144415220 scopus 로고    scopus 로고
    • Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing
    • Tester D.J., Will M.L., Haglund C.M., et al. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing. Heart Rhythm 2 (2005) 507-517
    • (2005) Heart Rhythm , vol.2 , pp. 507-517
    • Tester, D.J.1    Will, M.L.2    Haglund, C.M.3
  • 17
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
    • Wang Q., Curran M.E., Splawski I., et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 12 (1996) 17-23
    • (1996) Nat Genet , vol.12 , pp. 17-23
    • Wang, Q.1    Curran, M.E.2    Splawski, I.3
  • 18
    • 0028914969 scopus 로고
    • A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
    • Curran M.E., Splawski I., Timothy K.W., et al. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 80 (1995) 795-803
    • (1995) Cell , vol.80 , pp. 795-803
    • Curran, M.E.1    Splawski, I.2    Timothy, K.W.3
  • 19
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • Wang Q., Shen J., Splawski I., et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 80 (1995) 805-811
    • (1995) Cell , vol.80 , pp. 805-811
    • Wang, Q.1    Shen, J.2    Splawski, I.3
  • 20
    • 0242464931 scopus 로고    scopus 로고
    • Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death
    • Mohler P.J., Schott J.-J., Gramolini A.O., et al. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Nature 421 (2003) 634-639
    • (2003) Nature , vol.421 , pp. 634-639
    • Mohler, P.J.1    Schott, J.-J.2    Gramolini, A.O.3
  • 22
    • 0033574273 scopus 로고    scopus 로고
    • MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia
    • Abbott G.W., Sesti F., Splawski I., et al. MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia. Cell 97 (1999) 175-187
    • (1999) Cell , vol.97 , pp. 175-187
    • Abbott, G.W.1    Sesti, F.2    Splawski, I.3
  • 23
    • 0035907032 scopus 로고    scopus 로고
    • Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
    • Plaster N.M., Tawil R., Tristani-Firouzi M., et al. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. Cell 105 (2001) 511-519
    • (2001) Cell , vol.105 , pp. 511-519
    • Plaster, N.M.1    Tawil, R.2    Tristani-Firouzi, M.3
  • 24
    • 5344223383 scopus 로고    scopus 로고
    • Cav1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
    • Splawski I., Timothy K.W., Sharpe L.M., et al. Cav1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. Cell 119 (2004) 19-31
    • (2004) Cell , vol.119 , pp. 19-31
    • Splawski, I.1    Timothy, K.W.2    Sharpe, L.M.3
  • 25
    • 33751016041 scopus 로고    scopus 로고
    • Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome
    • Vatta M., Ackerman M.J., Ye B., et al. Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome. Circulation 114 (2006) 2104-2112
    • (2006) Circulation , vol.114 , pp. 2104-2112
    • Vatta, M.1    Ackerman, M.J.2    Ye, B.3
  • 26
    • 34447307435 scopus 로고    scopus 로고
    • SCN4B-encoded sodium channel beta 4 subunit in congenital long-QT syndrome
    • Medeiros-Domingo A., Kaku T., Tester D.J., et al. SCN4B-encoded sodium channel beta 4 subunit in congenital long-QT syndrome. Circulation 116 (2007) 134-142
    • (2007) Circulation , vol.116 , pp. 134-142
    • Medeiros-Domingo, A.1    Kaku, T.2    Tester, D.J.3
  • 27
    • 38049169040 scopus 로고    scopus 로고
    • Mutation of an A-kinase-anchoring protein causes long-QT syndrome
    • Chen L., Marquardt M.L., Tester D.J., et al. Mutation of an A-kinase-anchoring protein causes long-QT syndrome. Proc Natl Acad Sci U S A 104 (2007) 20990-20995
    • (2007) Proc Natl Acad Sci U S A , vol.104 , pp. 20990-20995
    • Chen, L.1    Marquardt, M.L.2    Tester, D.J.3
  • 28
    • 48249148221 scopus 로고    scopus 로고
    • Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex
    • Ueda K., Valdivia C.R., Medeiros-Domingo A., et al. Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex. Proc Natl Acad Sci U S A 105 (2008) 9355-9360
    • (2008) Proc Natl Acad Sci U S A , vol.105 , pp. 9355-9360
    • Ueda, K.1    Valdivia, C.R.2    Medeiros-Domingo, A.3
  • 29
    • 0026466921 scopus 로고
    • Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report
    • Brugada P., and Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol 20 (1992) 1391-1396
    • (1992) J Am Coll Cardiol , vol.20 , pp. 1391-1396
    • Brugada, P.1    Brugada, J.2
  • 30
    • 0036471801 scopus 로고    scopus 로고
    • Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome
    • Vatta M., Dumaine R., Varghese G., et al. Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome. Hum Mol Genet 11 (2002) 337-345
    • (2002) Hum Mol Genet , vol.11 , pp. 337-345
    • Vatta, M.1    Dumaine, R.2    Varghese, G.3
  • 31
    • 20144388932 scopus 로고    scopus 로고
    • Brugada syndrome: report of the Second Consensus Conference
    • Antzelevitch C., Brugada P., Borggrefe M., et al. Brugada syndrome: report of the Second Consensus Conference. Heart Rhythm 2 (2005) 429-440
    • (2005) Heart Rhythm , vol.2 , pp. 429-440
    • Antzelevitch, C.1    Brugada, P.2    Borggrefe, M.3
  • 33
    • 33846627787 scopus 로고    scopus 로고
    • Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death
    • Antzelevitch C., Pollevick G.D., Cordeiro J.M., et al. Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death. Circulation 115 (2007) 442-449
    • (2007) Circulation , vol.115 , pp. 442-449
    • Antzelevitch, C.1    Pollevick, G.D.2    Cordeiro, J.M.3
  • 34
    • 34147146134 scopus 로고    scopus 로고
    • A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors
    • Tester D.J., Dura M., Carturan E., et al. A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors. Heart Rhythm 4 (2007) 733-739
    • (2007) Heart Rhythm , vol.4 , pp. 733-739
    • Tester, D.J.1    Dura, M.2    Carturan, E.3
  • 35
    • 25144503454 scopus 로고    scopus 로고
    • Genetics of cardiac arrhythmias
    • Wilde A.A., and Bezzina C.R. Genetics of cardiac arrhythmias. Heart 91 (2005) 1352-1358
    • (2005) Heart , vol.91 , pp. 1352-1358
    • Wilde, A.A.1    Bezzina, C.R.2
  • 36
    • 26944485507 scopus 로고    scopus 로고
    • Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing
    • Tester D.J., Kopplin L.J., Will M.L., et al. Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing. Heart Rhythm 2 (2005) 1099-1105
    • (2005) Heart Rhythm , vol.2 , pp. 1099-1105
    • Tester, D.J.1    Kopplin, L.J.2    Will, M.L.3
  • 37
    • 13844297632 scopus 로고    scopus 로고
    • Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation
    • Allouis M., Probst V., Jaafar P., et al. Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation. Am J Cardiol 95 (2005) 700-702
    • (2005) Am J Cardiol , vol.95 , pp. 700-702
    • Allouis, M.1    Probst, V.2    Jaafar, P.3
  • 38
    • 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 103 (2001) 196-200
    • (2001) Circulation , vol.103 , pp. 196-200
    • Priori, S.G.1    Napolitano, C.2    Tiso, N.3
  • 39
    • 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 106 (2002) 69-74
    • (2002) Circulation , vol.106 , pp. 69-74
    • Priori, S.G.1    Napolitano, C.2    Memmi, M.3
  • 40
    • 17144450747 scopus 로고    scopus 로고
    • Prolongation of the QT interval and the sudden infant death syndrome
    • Schwartz P.J., Stramba-Badiale M., Segantini A., et al. Prolongation of the QT interval and the sudden infant death syndrome. N Engl J Med 338 (1998) 1709-1714
    • (1998) N Engl J Med , vol.338 , pp. 1709-1714
    • Schwartz, P.J.1    Stramba-Badiale, M.2    Segantini, A.3
  • 41
    • 0032988240 scopus 로고    scopus 로고
    • Comments on a sudden infant death article in another journal
    • Lucey J.F. Comments on a sudden infant death article in another journal. Pediatrics 103 (1999) 812
    • (1999) Pediatrics , vol.103 , pp. 812
    • Lucey, J.F.1
  • 42
    • 0034721235 scopus 로고    scopus 로고
    • A molecular link between the sudden infant death syndrome and the long-QT syndrome
    • Schwartz P.J., Priori S.G., Dumaine R., et al. A molecular link between the sudden infant death syndrome and the long-QT syndrome. N Engl J Med 343 (2000) 262-267
    • (2000) N Engl J Med , vol.343 , pp. 262-267
    • Schwartz, P.J.1    Priori, S.G.2    Dumaine, R.3
  • 43
    • 0035806944 scopus 로고    scopus 로고
    • De novo mutation in the SCN5A gene associated with early onset of sudden infant death
    • Wedekind H., Smits J.P., Schulze-Bahr E., et al. De novo mutation in the SCN5A gene associated with early onset of sudden infant death. Circulation 104 (2001) 1158-1164
    • (2001) Circulation , vol.104 , pp. 1158-1164
    • Wedekind, H.1    Smits, J.P.2    Schulze-Bahr, E.3
  • 44
    • 0035922697 scopus 로고    scopus 로고
    • Molecular diagnosis in a child with sudden infant death syndrome
    • Schwartz P.J., Priori S.G., Bloise R., et al. Molecular diagnosis in a child with sudden infant death syndrome. Lancet 358 (2001) 1342-1343
    • (2001) Lancet , vol.358 , pp. 1342-1343
    • Schwartz, P.J.1    Priori, S.G.2    Bloise, R.3
  • 45
    • 0035860984 scopus 로고    scopus 로고
    • Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome
    • Ackerman M.J., Siu B.L., Sturner W.Q., et al. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome. JAMA 286 (2001) 2264-2269
    • (2001) JAMA , vol.286 , pp. 2264-2269
    • Ackerman, M.J.1    Siu, B.L.2    Sturner, W.Q.3
  • 46
    • 22544474319 scopus 로고    scopus 로고
    • Sudden infant death syndrome: how significant are the cardiac channelopathies?
    • Tester D.J., and Ackerman M.J. Sudden infant death syndrome: how significant are the cardiac channelopathies?. Cardiovasc Res 67 (2005) 388-396
    • (2005) Cardiovasc Res , vol.67 , pp. 388-396
    • Tester, D.J.1    Ackerman, M.J.2
  • 47
    • 33846046495 scopus 로고    scopus 로고
    • Prevalence of long-QT syndrome gene variants in sudden infant death syndrome
    • Arnestad M., Crotti L., Rognum T.O., et al. Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation 115 (2007) 361-367
    • (2007) Circulation , vol.115 , pp. 361-367
    • Arnestad, M.1    Crotti, L.2    Rognum, T.O.3
  • 48
    • 33846425740 scopus 로고    scopus 로고
    • Cardiac sodium channel dysfunction in sudden infant death syndrome
    • Wang D.W., Desai R.R., Crotti L., et al. Cardiac sodium channel dysfunction in sudden infant death syndrome. Circulation 115 (2007) 368-376
    • (2007) Circulation , vol.115 , pp. 368-376
    • Wang, D.W.1    Desai, R.R.2    Crotti, L.3
  • 49
    • 40649125752 scopus 로고    scopus 로고
    • Cardiac potassium channel dysfunction in sudden infant death syndrome
    • Rhodes T.E., Abraham R.L., Welch R.C., et al. Cardiac potassium channel dysfunction in sudden infant death syndrome. J Mol Cell Cardiol 44 (2008) 571-581
    • (2008) J Mol Cell Cardiol , vol.44 , pp. 571-581
    • Rhodes, T.E.1    Abraham, R.L.2    Welch, R.C.3
  • 50
    • 33846510967 scopus 로고    scopus 로고
    • Novel mechanism for sudden infant death syndrome: Persistent late sodium current secondary to mutations in caveolin-3
    • Cronk L.B., Ye B., Kaku T., et al. Novel mechanism for sudden infant death syndrome: Persistent late sodium current secondary to mutations in caveolin-3. Heart Rhythm 4 (2007) 161-166
    • (2007) Heart Rhythm , vol.4 , pp. 161-166
    • Cronk, L.B.1    Ye, B.2    Kaku, T.3
  • 51
    • 36048965546 scopus 로고    scopus 로고
    • Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome
    • Van Norstrand D.W., Valdivia C.R., Tester D.J., et al. Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome. Circulation 116 (2007) 2253-2259
    • (2007) Circulation , vol.116 , pp. 2253-2259
    • Van Norstrand, D.W.1    Valdivia, C.R.2    Tester, D.J.3
  • 52
    • 7744243863 scopus 로고    scopus 로고
    • Spectrum and prevalence of cardiac sodium channel variants among Black, White, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/Long QT Syndrome genetic testing
    • Ackerman M.J., Splawski I., Makielski J.C., et al. Spectrum and prevalence of cardiac sodium channel variants among Black, White, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/Long QT Syndrome genetic testing. Heart Rhythm 1 (2004) 600-607
    • (2004) Heart Rhythm , vol.1 , pp. 600-607
    • Ackerman, M.J.1    Splawski, I.2    Makielski, J.C.3
  • 53
    • 33645809963 scopus 로고    scopus 로고
    • Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study
    • Wedekind H., Bajanowski T., Friederich P., et al. Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study. Int J Legal Med 120 (2006) 129-137
    • (2006) Int J Legal Med , vol.120 , pp. 129-137
    • Wedekind, H.1    Bajanowski, T.2    Friederich, P.3
  • 54
    • 18544383162 scopus 로고    scopus 로고
    • Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia
    • Splawski I., Timothy K.W., Tateyama M., et al. Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia. Science 297 (2002) 1333-1336
    • (2002) Science , vol.297 , pp. 1333-1336
    • Splawski, I.1    Timothy, K.W.2    Tateyama, M.3
  • 55
    • 23844527207 scopus 로고    scopus 로고
    • Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks
    • Burke A., Creighton W., Mont E., et al. Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks. Circulation 112 (2005) 798-802
    • (2005) Circulation , vol.112 , pp. 798-802
    • Burke, A.1    Creighton, W.2    Mont, E.3
  • 56
    • 32444436881 scopus 로고    scopus 로고
    • A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y
    • Plant L.D., Bowers P.N., Liu Q.Y., et al. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. J Clin Invest 116 (2006) 430-435
    • (2006) J Clin Invest , vol.116 , pp. 430-435
    • Plant, L.D.1    Bowers, P.N.2    Liu, Q.Y.3
  • 57
    • 42649091103 scopus 로고    scopus 로고
    • Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome
    • Van Norstrand D.W., Tester D.J., and Ackerman M.J. Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome. Heart Rhythm 5 (2008) 712-715
    • (2008) Heart Rhythm , vol.5 , pp. 712-715
    • Van Norstrand, D.W.1    Tester, D.J.2    Ackerman, M.J.3
  • 58
    • 0037133593 scopus 로고    scopus 로고
    • Natural history of Brugada syndrome: insights for risk stratification and management
    • Priori S.G., Napolitano C., Gasparini M., et al. Natural history of Brugada syndrome: insights for risk stratification and management. Circulation 105 (2002) 1342-1347
    • (2002) Circulation , vol.105 , pp. 1342-1347
    • Priori, S.G.1    Napolitano, C.2    Gasparini, M.3
  • 59
    • 47649133621 scopus 로고    scopus 로고
    • Highly malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional SCN5A mutation successfully treated with mexiletine and propranolol
    • Abstr
    • Wang D.W., Crotti L., Ferrandi C., et al. Highly malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional SCN5A mutation successfully treated with mexiletine and propranolol. Circulation 116 Suppl (2007) II_54-II_55 Abstr
    • (2007) Circulation , vol.116 , Issue.SUPPL
    • Wang, D.W.1    Crotti, L.2    Ferrandi, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.