短QT间期综合征的诊治进展(2)
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[7]Mazzanti A, Kanthan A, Monteforte N, et al. Novel Insight Into the Natural History of Short QT Syndrome[J]. J Am Coll Cardiol,2014,63(13):1300-1308.
[8]Priori SG, Pandit SV, Rivolta I, et al. A novel form of short QT syndmme (SQT3)is caused by amutafion in the KCNJ2 gene[J]. Circ Res,2005,96(7):800-807.
[9]Antzelevitch C, Pollevick GD, Cordeiro JM, 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[J]. Circutation,2007,115(4):442-449.
[10]Brugada R, Hong K, Dumaine R, et al. Sudden death associated with short QT syndmme linked to mutations in HERG[J].Circulation,2004,109(1):30-35.
[11]Tülümen E, Giustetto C, Wolpert C, et al. PQ segment depression in patients with short QT syndrome: A novel marker for diagnosing short QT syndrome[J]? Heart Rhythm,2014,11(6):1024-1030.
[12]Gollob MH, Redpath CJ, Roberts JD. The short QT syndrome: proposed diagnostic criteria[J]. J Am Coll Cardiol,2011,57(7):802-812.
[13]Villafane J, Atallah J, Gollob MH, et al. Long_term follow_up of a pediatric cohort with short QT syndrome[J]. J Am Coll Cardiol,2013,61(11):1183-1191.
[14]Giustetto C, Schimpf R, Mazzanti A, et al. Long_Term Follow_Up of Patients With Short QT Syndrome[J]. J Am Coll Cardiol,2011,58(6):587-595.
[15]郭成军,张英川,方东平,等.短QT综合征多频率室性心动过速和心室颤动的机制与消融治疗[J].中国心脏起博与心电生理杂志,2005,19(1):23-28.
(收稿日期:2014_8_18)
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