571 results on '"Sanatani, S."'
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2. PHENOTYPIC DIFFERENCES BETWEEN "COMMON” LONG QT TYPE 1 VARIANT CARRIERS IN THE NATIONAL HIRO REGISTRY
3. HIGH RISK NON-CLASSICAL LQTS GENOTYPES: SPECTRUM OF GENETIC AND PHENOTYPIC FEATURES OF LONG QT SYNDROME
4. A MILD PHENOTYPE ASSOCIATED WITH KCNQ1 P.V205M MEDIATED LONG QT SYNDROME IN FIRST NATIONS CHILDREN OF NORTHERN BRITISH COLUMBIA: EFFECT OF ADDITIONAL VARIANTS AND CONSIDERATIONS FOR MANAGEMENT
5. Phospholamban cardiomyopathy: a Canadian perspective on a unique population
6. Flecainide is associated with a reduction in arrhythmic events in a large cohort of patients with catecholaminergic polymorphic ventricular tachycardia
7. DIAGNOSTIC UTILITY OF HOLTER MONITORING IN CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA
8. Response Letter to ‘Optimising physiology for adolescents with dysautonomia’
9. SUPRAVENTRICULAR TACHYCARDIA IN INFANTS: DOES MEDICATION CHOICE MATTER?
10. LONG-TERM ARRHYTHMIC OUTCOMES AMONG CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)
11. NEW VIEW OF THE CARDIAC RYANODINE RECEPTOR ARRANGEMENTS AND THEIR FUNCTIONAL CORRELATION: 368
12. Cardiac risk assessment before the use of stimulant medications in children and youth: A joint position statement by the Canadian Paediatric Society, the Canadian Cardiovascular Society, and the Canadian Academy of Child and Adolescent Psychiatry
13. At-home determination of 24-h urine sodium excretion: Validation of chloride test strips and multiple spot samples
14. Recurrent Congestive Heart Failure in a Child Due to Probable Myocarditis
15. A MILD PHENOTYPE ASSOCIATED WITH KCNQ1 P.V205M MEDIATED LONG QT SYNDROME IN FIRST NATIONS CHILDREN OF NORTHERN BRITISH COLUMBIA: EFFECT OF ADDITIONAL VARIANTS AND CONSIDERATIONS FOR MANAGEMENT
16. PHENOTYPIC DIFFERENCES BETWEEN "COMMON” LONG QT TYPE 1 VARIANT CARRIERS IN THE NATIONAL HIRO REGISTRY
17. HIGH RISK NON-CLASSICAL LQTS GENOTYPES: SPECTRUM OF GENETIC AND PHENOTYPIC FEATURES OF LONG QT SYNDROME
18. Medications Used to Manage Supraventricular Tachycardia in the Infant A North American Survey
19. Dilated Cardiomyopathy Masquerading as Long QT Syndrome
20. Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
21. Post-hoc Diagnosis of Congenital Long QT Syndrome in Patients with Tetralogy of Fallot
22. Evolution of Heart Rate Control After Transplantation: Conduction Versus Autonomic Innervation
23. Predictors of Refractory Tachycardia in Infants with Supraventricular Tachycardia
24. Balloon Angioplasty of Right Ventricular Outflow Tract Conduits
25. Atenolol is not effective in reducing ventricular arrhythmia severity on exercise stress test in patients with catecholaminergic polymorphic ventricular tachycardia
26. THE EFFECT OF ISOPROTERENOL USE ON ACCESSORY PATHWAY CONDUCTION CHARACTERISTICS IN WOLFF-PARKINSON-WHITE SYNDROME IN CHILDREN
27. VARIANT RE-INTERPRETATION IN SURVIVORS OF CARDIAC ARREST WITH PRESERVED EJECTION FRACTION (CASPER REGISTRY) BY CLINICIANS AND CLINICAL COMMERCIAL LABORATORIES
28. Coronary vessel involvement by chronic graft-versus-host disease presenting as sudden cardiac death
29. OUTCOME OF PEDIATRIC UNEXPLAINED CARDIAC ARREST SURVIVORS: A REPORT FROM THE CANADIAN PEDIATRIC HEART RHYTHM NETWORK
30. The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry
31. SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
32. DOES THE EXERCISE STRESS TEST OVER DIAGNOSE LONG QT IN PEDIATRIC PATIENTS?
33. ARRHYTHMIC OUTCOMES IN CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)
34. MULTIPLE GENETIC VARIANTS IN CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: A CLINICAL AND MOLECULAR REPORT FROM THE PACES CPVT REGISTRY
35. Ischemia-reperfusion destabilizes rhythmicity in immature atrioventricular pacemakers: A predisposing factor for postoperative arrhythmias in neonate rabbits
36. IMPLANTABLE CARDIOVERTER DEFIBRILLATOR USE IN CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: A SYSTEMATIC REVIEW
37. CARDIAC OUTCOMES DURING PREGNANT AND NON-PREGNANT PERIODS IN CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA
38. Exercise and the multidisciplinary holistic approach to adolescent dysautonomia
39. ACCESS AND BARRIERS TO GENETIC TESTING FOR SUDDEN UNEXPECTED DEATH CONDITIONS: EXAMINING THE INTERDISCIPLINARY CLINIC MODEL FOR INHERITED ARRHYTHMIA AND CARDIOMYOPATHY IN CANADA
40. PREVALENCE AND OUTCOMES OF SYNCOPE IN CHILDREN AND ADOLESCENTS EVALUATED IN CANADIAN EMERGENCY DEPARTMENTS: A POPULATION-BASED STUDY OF 9,830 PATIENTS
41. PHOSPHOLAMBAN CARDIOMYOPATHY: A CANADIAN PERSPECTIVE ON A UNIQUE DUTCH FOUNDER POPULATION
42. YOUNG INVESTIGATORS COMPETITION1GENETIC ANALYSIS IN THE EVALUATION OF UNEXPLAINED CARDIAC ARREST: FROM THE CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)2IN-VIVO WHOLE HEART CONTACT MAPPING DATA AND A SIMPLE MATHEMATICAL FRAMEWORK TO UNDERSTAND THE INTERACTIONS BETWEEN ACTIVATION AND REPOLARIZATION RESITUTION DYNAMICS IN THE INTACT HUMAN HEART3THE K(ATP) CHANNEL OPENER DIAZOXIDE REDUCES AUTOMATICITY IN AN IN VITRO ATRIAL CELL MODEL - POTENTIAL FOR K(ATP) CHANNELS AS A DRUG TARGET FOR ATRIAL ARRHYTHMIAS4LONG-TERM OUTCOMES AFTER CATHETER ABLATION OF VENTRICULAR TACHYCARDIA IN PATIENTS WITH STRUCTURAL HEART DISEASE: A MULTICENTRE UK STUDY5THE BURDEN OF ARRHYTHMIAS IN LIFE-LONG ENDURANCE ATHLETES6CARDIAC MAGNETIC RESONANCE IMAGING RISK STRATIFICATION USING MARKERS OF REGIONAL AND DIFFUSE FIBROSIS FOR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR THERAPY: THE VALUE OF T1 MAPPING IN NON-ISCHEMIC PATIENTS
43. The effect of phenomenological three-body forces on the saturation of binding energies of light nuclei
44. On planar group diagrams
45. EARLY REPOLARIZATION INHERITANCE PATTERN IN CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)
46. NOVEL ARRHYTHMIC TRIGGERS AND CALSEQUESTRIN-2 VARIANTS IN CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: SHIFTING PARADIGMS IN PREVENTING SUDDEN CARDIAC DEATH
47. DOES AN 8-WEEK LOWER BODY EXERCISE PROGRAM IMPROVE QUALITY OF LIFE IN TEENAGERS WITH DYSAUTONOMIA?
48. FLECAINIDE AS MONOTHERAPY FOR CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: A NOVEL STRATEGY FOR AN OFTEN DEADLY ARRHYTHMIA?
49. CARDIAC ABNORMALITIES IN RELATIVES OF SUDDEN CARDIAC ARREST VICTIMS: A REPORT FROM THE CASPER REGISTRY
50. THE UTILITY AND INCREMENTAL VALUE OF THE SIGNAL AVERAGED ECG: A NOVEL MODEL FOR STRATIFYING PATIENTS WITH SUSPECTED BRUGADA SYNDROME
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