A. Medina

发表

Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?

B. Kerem, R. Kass, J. Benhorin, 2000, Circulation.

Spectrum of ST-T–Wave Patterns and Repolarization Parameters in Congenital Long-QT Syndrome: ECG Findings Identify Genotypes

Wojciech Zareba, Li Zhang, Carlo Napolitano, 2000, Circulation.

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.

Li Zhang, Wojciech Zareba, Derick R. Peterson, 2003, Journal of the American College of Cardiology.

Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

S. Priori, A. Moss, P. Schwartz, 2000, Circulation.

Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits.

B. Kerem, R. Kass, J. Benhorin, 1998, Circulation research.

Clinical Implications for Affected Parents and Siblings of Probands With Long-QT Syndrome

S. Priori, A. Moss, P. Schwartz, 2001, Circulation.

Novel LQT-3 Mutation Affects Na (cid:49) Channel Activity Through Interactions Between (cid:97) - and (cid:98) 1 -Subunits

B. Kerem, R. Kass, J. Benhorin, 1998 .

Brain natriuretic peptide and the risk of ventricular tachyarrhythmias in mildly symptomatic heart failure patients enrolled in MADIT-CRT.

Paul J. Wang, A. Moss, W. Zareba, 2016, Heart rhythm.

Images in clinical medicine. Congenital long-QT syndrome.

J. Benhorin, A. Medina, 1997, The New England journal of medicine.

Increased Risk of Arrhythmic Events in Long-QT Syndrome With Mutations in the Pore Region of the Human Ether-a-go-go–Related Gene Potassium Channel

Derick R. Peterson, E. Kaufman, S. Priori, 2002, Circulation.

Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome.

S. Priori, A. Moss, P. Schwartz, 2000, The American journal of cardiology.

Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.

S. Priori, A. Moss, P. Schwartz, 1999, The American journal of cardiology.

Evidence of genetic heterogeneity in the long QT syndrome.

B. Kerem, J. Blangero, J. Towbin, 1993, Science.

Novel LQT-3 Mutation Affects Na+ Channel Activity Through Interactions Between α- and β1-Subunits

B. Kerem, R. Kass, J. Benhorin, 1998 .

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

S. Priori, A. Moss, P. Schwartz, 1998, The New England journal of medicine.