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http://scihub22266oqcxt.onion/ 1348867!ä!1348867 Warning: Undefined variable $yww in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 538 Warning: Undefined variable $yww in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 538       Kokyu+To+Junkan 1992 ; 40 (2): 195-8 Nephropedia Template TP {{tp|p=1348867|t=1992. A case of congenital long QT syndrome associated with T wave alternans |pdf=|usr=}}{{1348867}} gab.com Text A case of congenital long QT syndrome associated with T wave alternans JO: Kokyu To Junkan http://www.kidney.de/pget.php?&tw=1&pmid=1348867 #FOAvip A case was presented in which a rare T wave alternans occurred in association with congenital long QT syndrome. A 71-year-old woman, who had experienced several syncopal attacks per year for the previous forty years, was admitted for further evaluation of the syncope. She had a family history of sudden death (sister) and QT prolongation (son). Electrocardiogram showed a corrected QT interval of 0.68 seconds. Treadmill exercise-tolerance test revealed both T wave alternans immediately after exercise and torsades de pointes 150 seconds after exercise. The syncope was induced by the mental excitation. A prolonged corrected QT interval reduced from 0.70 seconds to 0.58 seconds by the correction of her serum potassium and magnesium. The effect of propranolol, verapamil, phenytoin or mexiletine on T wave alternans and ventricular arrhythmia was evaluated by the treadmill exercise-tolerance test. The treatment with propranolol was most effective. Twit Text FOAVip A case of congenital long QT syndrome associated with T wave alternans ????Kokyu To Junkan http://www.kidney.de/pget.php?&tw=1&pmid=1348867 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=1348867 #FOAvip English Wikipedia <ref>{{Cite pmid|1348867}}</ref> A case of congenital long QT syndrome associated with T wave alternans #MMPMID1348867 Motoyasu M; Nishikawa H; Shimizu Y; Aoki T; Ono N; Unno M; Kakuta Y; Yazu T; Kasai A; Yamakado T; et al. Kokyu To Junkan 1992[Feb]; 40 (2): 195-8 PMID1348867show ga A case was presented in which a rare T wave alternans occurred in association with congenital long QT syndrome. A 71-year-old woman, who had experienced several syncopal attacks per year for the previous forty years, was admitted for further evaluation of the syncope. She had a family history of sudden death (sister) and QT prolongation (son). Electrocardiogram showed a corrected QT interval of 0.68 seconds. Treadmill exercise-tolerance test revealed both T wave alternans immediately after exercise and torsades de pointes 150 seconds after exercise. The syncope was induced by the mental excitation. A prolonged corrected QT interval reduced from 0.70 seconds to 0.58 seconds by the correction of her serum potassium and magnesium. The effect of propranolol, verapamil, phenytoin or mexiletine on T wave alternans and ventricular arrhythmia was evaluated by the treadmill exercise-tolerance test. The treatment with propranolol was most effective. |*Electrocardiography[MESH] |Adrenergic beta-Antagonists/therapeutic use[MESH] |Aged[MESH] |Exercise Test[MESH] |Female[MESH] |Humans[MESH] |Long QT Syndrome/*congenital/drug therapy/physiopathology[MESH] |Propranolol/therapeutic use[MESH] |Syncope/drug therapy/etiology[MESH] A case of congenital long QT syndrome associated with T wave alternan(epmc).pdf DeepDyve Pubget Overpricing