Impact of Updated Diagnostic Criteria for Long QT Syndrome on Clinical Detection of Diseased Patients: Results From a Study of Patients Carrying Gene Mutations.

[1]  Qing Huang,et al.  Diagnostic accuracy of high resolution melting analysis for detection of KRAS mutations: a systematic review and meta-analysis , 2014, Scientific Reports.

[2]  K. Hayashi,et al.  Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects , 2014, Heart and Vessels.

[3]  C. Tracy,et al.  HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. , 2013, Heart rhythm.

[4]  Michael J Ackerman,et al.  Impact of genetics on the clinical management of channelopathies. , 2013, Journal of the American College of Cardiology.

[5]  P. Schwartz,et al.  QTc behavior during exercise and genetic testing for the long-QT syndrome. , 2011, Circulation.

[6]  M. Ackerman,et al.  The diagnostic utility of recovery phase QTc during treadmill exercise stress testing in the evaluation of long QT syndrome. , 2011, Heart rhythm.

[7]  K. Hayashi,et al.  Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations. , 2009, Clinical science.

[8]  D. Tester,et al.  Congenital Long QT Syndrome , 2008 .

[9]  P. Schwartz.  The congenital long QT syndromes from genotype to phenotype: clinical implications , 2006, Journal of internal medicine.

[10]  D. Tester,et al.  Effect of clinical phenotype on yield of long QT syndrome genetic testing. , 2005, Journal of the American College of Cardiology.

[11]  D. Roden.  Drug-induced prolongation of the QT interval. , 2004, The New England journal of medicine.

[12]  Carlo Napolitano,et al.  Risk stratification in the long-QT syndrome. , 2003, The New England journal of medicine.

[13]  S. Priori,et al.  Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome. , 2003, Journal of the American College of Cardiology.

[14]  W. Shimizu,et al.  Exercise Stress Test Amplifies Genotype-Phenotype Correlation in the LQT1 and LQT2 Forms of the Long-QT Syndrome , 2003, Circulation.

[15]  W. Shen,et al.  Epinephrine-induced QT interval prolongation: a gene-specific paradoxical response in congenital long QT syndrome. , 2002, Mayo Clinic proceedings.

[16]  K. Hayashi,et al.  Characterization of a novel missense mutation E637K in the pore-S6 loop of HERG in a patient with long QT syndrome. , 2002, Cardiovascular research.

[17]  S. Priori,et al.  Low penetrance in the long-QT syndrome: clinical impact. , 1999, Circulation.

[18]  Peter J. Schwartz,et al.  Diagnostic Criteria for the Long QT Syndrome An Update , 1993, Circulation.

[19]  A. Moss,et al.  The Long QT Syndrome: Prospective Longitudinal Study of 328 Families , 1991, Circulation.

[20]  G. Vincent,et al.  Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome. , 1991, The American journal of cardiology.

[21]  P. Schwartz,et al.  Idiopathic long QT syndrome: progress and questions. , 1985, American heart journal.