Add to ORKGAims Clinical observations in patients with long QT syndrome carrying sodium channel mutations (LQT3) suggest that bra-dycardia caused by parasympathetic stimulation may provoke torsades de pointes (TdP). b-Adrenoceptor blockers appear less effective in LQT3 than in other forms of the disease. Methods and result
Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval prolongation...
The congenital familial long QT syndrome (LQTS) is characterized by QT interval prolongation on ECG ...
Long QT syndrome (LQTS) is an arrhythmogenic cardio-vascular disorder resulting from mutations in ca...
Aims Clinical observations in patients with long QT syndrome carrying sodium channel mutations (LQT3...
he idiopathic long QT syndrome (LQTS) is an unusual clinical disorder characterized by a prolongatio...
Congenital long QT syndrome (LQTS) is one of the most common cardiac channelopathies and is characte...
The long QT syndrome (LQTS) is a familial disease characterized by abnormally prolonged ventricular ...
The long QT syndrome (LQTS) is a familial disease characterized by prolonged ventricular repolarizat...
The idiopathic long QT syndrome is a congenital disease characterized by prolongation of the QT inte...
The hereditary long QT syndrome (LQTS) is a genetic channelopathy with variable penetrance that is a...
Congenital long-QT syndrome (LQTS) is a group ofinherited disorders that is associated with a prolon...
BACKGROUND: The genes for the long QT syndrome (LQTS) linked to chromosomes 3 (LQT3) and 7 (LQT2) w...
Abstract — The long QT syndrome type-3 (LQT3) is an inherited cardiac disorder caused by mutations i...
Long QT syndrome (LQTS) is a cardiovascular disorder characterized by an abnormality in cardiac repo...
RATIONALE: Sodium channel blockers are used as gene-specific treatments in long-QT syndrome type 3, ...
Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval prolongation...
The congenital familial long QT syndrome (LQTS) is characterized by QT interval prolongation on ECG ...
Long QT syndrome (LQTS) is an arrhythmogenic cardio-vascular disorder resulting from mutations in ca...
Aims Clinical observations in patients with long QT syndrome carrying sodium channel mutations (LQT3...
he idiopathic long QT syndrome (LQTS) is an unusual clinical disorder characterized by a prolongatio...
Congenital long QT syndrome (LQTS) is one of the most common cardiac channelopathies and is characte...
The long QT syndrome (LQTS) is a familial disease characterized by abnormally prolonged ventricular ...
The long QT syndrome (LQTS) is a familial disease characterized by prolonged ventricular repolarizat...
The idiopathic long QT syndrome is a congenital disease characterized by prolongation of the QT inte...
The hereditary long QT syndrome (LQTS) is a genetic channelopathy with variable penetrance that is a...
Congenital long-QT syndrome (LQTS) is a group ofinherited disorders that is associated with a prolon...
BACKGROUND: The genes for the long QT syndrome (LQTS) linked to chromosomes 3 (LQT3) and 7 (LQT2) w...
Abstract — The long QT syndrome type-3 (LQT3) is an inherited cardiac disorder caused by mutations i...
Long QT syndrome (LQTS) is a cardiovascular disorder characterized by an abnormality in cardiac repo...
RATIONALE: Sodium channel blockers are used as gene-specific treatments in long-QT syndrome type 3, ...
Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval prolongation...
The congenital familial long QT syndrome (LQTS) is characterized by QT interval prolongation on ECG ...
Long QT syndrome (LQTS) is an arrhythmogenic cardio-vascular disorder resulting from mutations in ca...