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Publications by Päivi J. Laitinen-Forsblom
Clinical and Molecular Genetic Risk Determinants in Adult Long QT Syndrome Type 1 and 2 Patients
BMC Medical Genetics
Genetics
Gain-Of-Function Mutation of the SCN5A Gene Causes Exercise-Induced Polymorphic Ventricular Arrhythmias
Circulation: Cardiovascular Genetics
Related publications
Non Genetic Risk Factors of Long-Qt Syndrome
Open Journal of Genetics
Long Qt Syndrome. Part 1
Journal of the Grodno State Medical University
R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Statin Therapy in Long QT Syndrome Type II
Biophysical Journal
Biophysics
Oral Contraceptive Use and the Risk of Cardiac Events in Patients With Long QT Syndrome
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Association of a Congenital Long QT Syndrome Type 1 With Takotsubo Cardiomyopathy
Clinical Case Reports
Medicine
Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-Qt Syndrome
Circulation: Cardiovascular Genetics
Clinical, Genetic, and Biophysical Characterization of a Homozygous HERG Mutation Causing Severe Neonatal Long QT Syndrome
Pediatric Research
Child Health
Pediatrics
Perinatology
Variability of Action Potential Duration in Pharmacologically Induced Long QT Syndrome Type 1
