G. M. Vincent

发表

Diagnostic Criteria for the Long QT Syndrome An Update

Peter J. Schwartz, Arthur J. Moss, A. Moss, 1993, Circulation.

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

A. Moss, P. Schwartz, J. Towbin, 1994, Nature Genetics.

Impact of Laboratory Molecular Diagnosis on Contemporary Diagnostic Criteria for Genetically Transmitted Cardiovascular Diseases : Hypertrophic Cardiomyopathy , Long-QT Syndrome , and Marfan Syndrome

J. Towbin, Maron, Moller, 1998 .

Clinical implications for patients with long QT syndrome who experience a cardiac event during infancy.

E. Kaufman, S. Priori, A. Moss, 2009, Journal of the American College of Cardiology.

Mutations in Cytoplasmic Loops of the Kcnq1 Channel and the Risk of Life-threatening Events Implications for Mutation-specific Response to ␤-blocker Therapy in Type 1 Long-qt Syndrome Methods Study Sample Phenotype Characterization Genotype Characterization Barsheshet Et Al Mutations in Cytoplasmic

E. Kaufman, J. Towbin, W. Zareba, 2022 .

Risk of Syncope in Family Members Who Are Genotype-Negative for a Family-Associated Long-QT Syndrome Mutation

E. Kaufman, A. Moss, J. Towbin, 2011, Circulation. Cardiovascular genetics.

Congenital Long QT syndrome.

K. Timothy, Li Zhang, G. M. Vincent, 2002, Cardiac electrophysiology review.

Electrocardiographic Features in Andersen-Tawil Syndrome Patients With KCNJ2 Mutations: Characteristic T-U–Wave Patterns Predict the KCNJ2 Genotype

P. Schwartz, M. Ackerman, G. Vincent, 2005, Circulation.

Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome.

Michael J Ackerman, Wojciech Zareba, Wataru Shimizu, 2011, Heart rhythm.