P. Laitinen

发表

Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.

M. Viitasalo, L. Toivonen, K. Kontula, 1999, Journal of the American College of Cardiology.

Epidemiology of Pacemaker Procedures Among Medicare Enrollees in 1990, 1995, and 2000

L. Toivonen, K. Kontula, L. Oikarinen, 2005 .

Familial polymorphic ventricular tachycardia--intracellular calcium channel disorder.

H. Swan, P. Laitinen, 2002, Cardiac electrophysiology review.

Temporal repolarization lability differences among genotyped patients with the long QT syndrome.

B. Fetics, R. Berger, M. Viitasalo, 2004, The American journal of cardiology.

Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in water

A. Sajantila, K. Kontula, P. Laitinen, 2003, International Journal of Legal Medicine.

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns.

A. Sajantila, M. Viitasalo, L. Toivonen, 2000, Journal of the American College of Cardiology.

unctional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH 2 ( HERG )

M. Viitasalo, L. Toivonen, K. Kontula, 2003 .

Beta1-adrenergic receptor polymorphisms, QTc interval and occurrence of symptoms in type 1 of long QT syndrome.

M. Viitasalo, L. Toivonen, S. Sarna, 2007, International Journal of Cardiology.

Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects

J. Kaprio, M. Viitasalo, L. Toivonen, 2000, Human mutation.

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia

S. Priori, M. Memmi, A. Marks, 2002, Journal of cellular physiology.

Ambulatory Electrocardiographic Evidence of Transmural Dispersion of Repolarization in Patients With Long-QT Syndrome Type 1 and 2

Lauri Toivonen, Lasse Oikarinen, Matti Viitasalo, 2002, Circulation.

Response of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndrome

M. Viitasalo, L. Toivonen, L. Hokkanen, 2001, Heart.

Four potassium channel mutations account for 73% of the genetic spectrum underlying long‐QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

M. Viitasalo, L. Toivonen, K. Kontula, 2004, Annals of medicine.

Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG).

M. Viitasalo, L. Toivonen, K. Kontula, 2003, Cardiovascular research.

β1-Adrenergic receptor polymorphisms, QTc interval and occurrence of symptoms in type 1 of long QT syndrome

M. Viitasalo, L. Toivonen, S. Sarna, 2007 .

Calcium Channel Antagonism Reduces Exercise‐Induced Ventricular Arrhythmias in Catecholaminergic Polymorphic Ventricular Tachycardia Patients with RyR2 Mutations

L. Toivonen, K. Kontula, H. Swan, 2005, Journal of cardiovascular electrophysiology.

Volatile Anesthetics and Succinylcholine in Cardiac Ryanodine Receptor Defects

L. Toivonen, H. Swan, P. Laitinen, 2004, Anesthesia and analgesia.

Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia

K. Brown, D. Stephan, E. A. Donarum, 2001, Circulation.

Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia

M. Viitasalo, L. Toivonen, K. Kontula, 2004, Annals of medicine.

Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms

K. Kontula, H. Swan, P. Laitinen, 2003, European Journal of Human Genetics.

Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia

K. Brown, D. Stephan, E. A. Donarum, 2001, Circulation.

Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insights.

M. Viitasalo, L. Toivonen, K. Kontula, 2005, Cardiovascular research.

Sudden Death in Familial Polymorphic Ventricular Tachycardia Associated With Calcium Release Channel (Ryanodine Receptor) Leak

S. Reiken, A. Marks, S. Lehnart, 2004, Circulation.

Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women.

H. Huikuri, M. Savolainen, Y. Kesäniemi, 2002, Journal of the American College of Cardiology.