메뉴 건너뛰기




Volumn 105, Issue 8, 2009, Pages 721-723

Editorial: Cardiac metabolic state and brugada syndrome: A link revealed

Author keywords

Brugada syndrome; Cardiac arrhythmias; NADH; Nav1.5; SCN5A

Indexed keywords

BRUGADA SYNDROME; EDITORIAL; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; ST SEGMENT ELEVATION; SUDDEN DEATH; ANIMAL; CELL LINE; DOWN REGULATION; DRUG ANTAGONISM; DRUG EFFECT; GENETICS; HEART MUSCLE; HEART VENTRICLE TACHYCARDIA; HUMAN; METABOLISM; MOUSE; MUTATION; NOTE; OXIDATION REDUCTION REACTION; RAT;

EID: 70350133633     PISSN: 00097330     EISSN: 15244571     Source Type: Journal    
DOI: 10.1161/CIRCRESAHA.109.208405     Document Type: Editorial
Times cited : (2)

References (17)
  • 1
    • 0026466921 scopus 로고
    • Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome
    • Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. J Am Coll Cardiol. 1992;20:1391-1396.
    • (1992) J Am Coll Cardiol , vol.20 , pp. 1391-1396
    • Brugada, P.1    Brugada, J.2
  • 3
    • 0030889337 scopus 로고    scopus 로고
    • Sudden unexplained death syndrome in Southeast Asia
    • Nademanee K. Sudden unexplained death syndrome in Southeast Asia. Am J Cardiol. 1997;79:10-11.
    • (1997) Am J Cardiol , vol.79 , pp. 10-11
    • Nademanee, K.1
  • 7
    • 63349104489 scopus 로고    scopus 로고
    • Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome
    • Cordeiro JM, Marieb M, Pfeiffer R, Calloe K, Burashnikov E, Antzelevitch C. Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome. J Mol Cell Cardiol. 2009;46:695-703.
    • (2009) J Mol Cell Cardiol , vol.46 , pp. 695-703
    • Cordeiro, J.M.1    Marieb, M.2    Pfeiffer, R.3    Calloe, K.4    Burashnikov, E.5    Antzelevitch, C.6
  • 10
    • 52749086867 scopus 로고    scopus 로고
    • Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome
    • Makiyama T, Akao M, Haruna Y, Tsuji K, Doi T, Ohno S, Nishio Y, Kita T, Horie M. Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome. Circ J. 2008;72:1705-1706.
    • (2008) Circ J , vol.72 , pp. 1705-1706
    • Makiyama, T.1    Akao, M.2    Haruna, Y.3    Tsuji, K.4    Doi, T.5    Ohno, S.6    Nishio, Y.7    Kita, T.8    Horie, M.9
  • 12
    • 2442698830 scopus 로고    scopus 로고
    • Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis
    • Antzelevitch C. Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis. Ann Med. 2004;36 Suppl 1:5-14.
    • (2004) Ann Med , vol.36 , Issue.SUPPL 1 , pp. 5-14
    • Antzelevitch, C.1
  • 13
    • 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 DW, Valdivia CR, Tester DJ, Ueda K, London B, Mak-ielski JC, Ackerman MJ. Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome. Circulation. 2007;116: 2253-2259.
    • (2007) Circulation , vol.116 , pp. 2253-2259
    • Van Norstrand, D.W.1    Valdivia, C.R.2    Tester, D.J.3    Ueda, K.4    London, B.5    Mak-Ielski, J.C.6    Ackerman, M.J.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.