| scholarly article | Q13442814 |
| P356 | DOI | 10.2217/14796678.5.2.191 |
| P698 | PubMed publication ID | 19371192 |
| P50 | author | Simone N Santos | Q57400783 |
| P2093 | author name string | Guilherme Fenelon | |
| Paula G Macedo | |||
| Benhur D Henz | |||
| Luiz R Leite | |||
| André Zanatta | |||
| Fernando E S Cruz Filho | |||
| José R Barreto | |||
| P2860 | cites work | Molecular basis of catecholaminergic polymorphic ventricular tachycardia | Q37361927 |
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| Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations | Q45273441 | ||
| Association of bidirectional ventricular tachycardia with familial sudden death syndrome | Q46558516 | ||
| Adenosine triphosphate terminates bidirectional ventricular tachycardia in a patient with catecholaminergic polymorphic ventricular tachycardia | Q46723257 | ||
| Effects of unilateral cardiac sympathetic denervation on the ventricular fibrillation threshold | Q58011821 | ||
| Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death | Q24674590 | ||
| Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia | Q28142708 | ||
| Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia | Q28201561 | ||
| A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel | Q28204838 | ||
| Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia | Q28279395 | ||
| Catecholaminergic polymorphic ventricular tachycardia | Q28287523 | ||
| Successful treatment of catecholaminergic polymorphic ventricular tachycardia with bilateral thoracoscopic sympathectomy | Q28292607 | ||
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| Catecholaminergic polymorphic ventricular tachycardia. An important diagnosis in children with syncope and normal heart | Q31929262 | ||
| Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts | Q33145152 | ||
| Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. | Q33146000 | ||
| Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21. | Q33146452 | ||
| Catecholaminergic polymorphic ventricular tachyarrhythmias in children | Q33147649 | ||
| Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. | Q33147854 | ||
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| Catecholaminergic polymorphic ventricular tachycardia detected by an insertable loop recorder in a pediatric patient with exercise syncopal episodes | Q33151469 | ||
| Catecholaminergic polymorphic ventricular tachycardia. | Q33152560 | ||
| The molecular basis of catecholaminergic polymorphic ventricular tachycardia: what are the different hypotheses regarding mechanisms? | Q33155204 | ||
| Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia | Q33155477 | ||
| ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the ACC/AHA/NASPE 2002 Gui | Q33156283 | ||
| Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients | Q33173888 | ||
| Short-coupled variant of torsade de pointes. A new electrocardiographic entity in the spectrum of idiopathic ventricular tachyarrhythmias | Q33174331 | ||
| Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome | Q34232976 | ||
| Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes | Q35909999 | ||
| The role of molecular autopsy in unexplained sudden cardiac death | Q36443125 | ||
| Bidirectional tachycardia in a child. A study using His bundle electrography | Q36822217 | ||
| P433 | issue | 2 | |
| P921 | main subject | catecholaminergic polymorphic ventricular tachycardia | Q1649897 |
| ventricular tachycardia | Q56002 | ||
| tachycardia | Q209583 | ||
| P304 | page(s) | 191-199 | |
| P577 | publication date | 2009-03-01 | |
| P1433 | published in | Future Cardiology | Q15765184 |
| P1476 | title | Catecholaminergic polymorphic ventricular tachycardia: a current overview | |
| P478 | volume | 5 |
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