Rare cardiac arrhythmias of the pediatric age. Repetitive paroxysmal tachycardia.. Minerva Pediatr, 15 , pp.
Cell, 80 , pp. Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.. Hum Mol Genet, 4 , pp. The long QT syndrome: ion channel diseases of the heart.. Mayo Clin Proc, 73 , pp.
Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders.. Circ Res, 94 , pp.
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Compendium of cardiac channel mutations in consecutive unrelated patients referred for long QT syndrome genetic testing.. Heart Rhythm, 2 , pp. Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.. JAMA, , pp. Low penetrance in the long-QT syndrome: clinical impact.. Circulation, 99 , pp.
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Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.. Circulation, , pp. Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome.. Mayo Clin Proc, 74 , pp.
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J Electrocardiol, 39 , pp. Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.. Heart Rhythm, 1 , pp. J Am Coll Cardiol, 46 , pp.
QT Prolongation and Malignant Arrhythmia: How Serious a Problem?
Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death.. Nature, , pp. Ankyrin-based cardiac arrhythmias: a new class of channelopathies due to loss of cellular targeting.. Curr Opin Cardiol, 20 , pp. A cardiac arrhythmia syndrome caused by loss of ankyrin-B function.. Nat Genet, 17 , pp. Cell, 97 , pp. Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies..
A new syndrome? Acta Paediatr Scand, 60 , pp. Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features.. Ann Neurol, 35 , pp. Mutations in Kir21 cause the developmental and episodic electrical phenotypes of Andersen's syndrome..
Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes
Cell, , pp. Andersen-Tawil syndrome: Prospective cohort analysis and expansion of the phenotype.. Am J Med Genet A, , pp. Ca V 12 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.. Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.. Heart Rhyth, 3 , pp. Nat Genet, 15 , pp. Diagnostic criteria for the long QT syndrome. An update..
Circulation, 88 , pp.
Prenatal diagnosis and treatment of fetal long QT syndrome: a case report.. Prenat Diagn, 22 , pp. Fetal cardiac repolarization abnormalities.. Am J Cardiol, 98 , pp. Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome.. Prenatal molecular genetic diagnosis of congenital long QT syndrome by strategic genotyping.. Am J Cardiol, 93 , pp. Importance of lead selection in QT interval measurement..
Am J Cardiol, 61 , pp. Eur Heart J. An analysis of the time-relations of electrocardiograms.. Heart, 7 , pp. Inaccurate electrocardiographic interpretation of long QT: the majority of physicians cannot recognize a long QT when they see one.. The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.. N Engl J Med, , pp. Repolarization dynamics in patients with long QT syndrome.. J Cardiovasc Electrophysiol, 13 , pp. T wave alternans in idiopathic long QT syndrome.. J Am Coll Cardiol, 23 , pp. T-wave alternans and the susceptibility to ventricular arrhythmias..
J Am Coll Cardiol, 47 , pp. Fetal sinus bradycardia and the long QT syndrome.. Am J Obstet Gynecol, , pp.
The Impact of LQTS
J Am Coll Cardiol, 43 , pp. Two:one atrioventricular block in infants with congenital long QT syndrome.. Am J Cardiol, 60 , pp. The long QT syndrome in children. An international study of patients..
Circulation, 87 , pp. Infants with long-QT syndrome and atrioventricular block.. Am Heart J, , pp.
Long QT Syndrome
The long QT syndrome with impaired atrioventricular conduction: a malignant variant in infants.. J Cardiovasc Electrophysiol, 9 , pp. Persistent functional atrioventricular block in two patients with prolonged QT intervals: elucidation of the mechanism of block.. Pacing Clin Electrophysiol, 13 , pp. Circ Res, 89 , pp. E Medline. Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns..
J Am Coll Cardiol, 35 , pp. Sodium channel Subunit mutation causes congenital long QT syndrome. Classification and mechanism of Torsade de Pointes initiation in patients with congenital long QT syndrome.. Eur Heart J, 25 , pp. The mechanism of pause-induced torsade de pointes in long QT syndrome.. J Cardiovasc Electrophysiol, 16 , pp. Arrhythmias in the congenital long QT syndrome:how often is torsade de pointes pause dependent? Heart, 83 , pp. Burst bicycle exercise facilitates diagnosis of latent long QT syndrome..
Am J Cardiol, 68 , pp. J Am Coll Cardiol, 34 , pp. Implications for gene-specific therapy.. Circulation, 92 , pp.
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