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(VP094) ROLE OF MEDICAL THERAPY TO REDUCE THE RATE OF AORTIC DILATATION IN CHILDREN WITH BICUSPID AORTIC VALVE

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(CCSP019) 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

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(CCSP020) ACUTE KIDNEY INJURY AND RENAL RECOVERY FOLLOWING FONTAN SURGERY

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(CCSP021) ARCH MORPHOLOGY IS ASSOCIATED WITH LEFT VENTRICULAR OUTFLOW TRACT DIAMETER AND OBSTRUCTION RISK IN INTERRUPTED AORTIC ARCH

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(CCSP022) HIGH INTENSITY INTERVAL TRAINING IN YOUTH WITH CONGENITAL HEART DISEASE: A CLINICAL TRIAL OF A NOVEL TELEMEDICINE VIDEO GAME-LINKED EXERCISE PLATFORM

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(CCSP023) INFLUENCE OF AORTIC VALVE PHENOTYPE, MORPHOLOGY AND SEX ON ASCENDING AORTA DILATION

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(CCSP024) ISOLATING THE EFFECT OF A SYSTEMIC RIGHT VENTRICLE WITH BI-VENTRICULAR CIRCULATION ON CARDIORESPIRATORY FITNESS

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(CCSP025) LESS LONG-TERM MIGRAINE IN CHILDREN FOLLOWING OCCLUTECH PERCUTANEOUS ATRIAL SEPTAL DEFECT CLOSURE VS THE AMPLATZ

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(CCSP026) MACHINE LEARNING ALGORITHMS TO PREDICT OUTCOME OF FETAL CARDIAC DISEASE

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(CCSP028) QTC PROLONGATION AND ITS ASSOCIATION WITH ELECTROLYTE ABNORMALITIES AND PSYCHOTROPIC DRUG USE AMONG PATIENTS WITH EATING DISORDERS

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(CCSP029) RISK FACTORS AND LONG-TERM OUTCOMES OF TETRALOGY OF FALLOT PATIENTS LOST TO CARDIOLOGY

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(CCSP030) THE QUEBEC CONGENITAL HEART DISEASE REGISTRY: DEVELOPMENT OF A PROSPECTIVE DATABANK TO FACILITATE RESEARCH IN CONGENITAL HEART DISEASE

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(CCSP031) TWO-YEAR OUTCOMES IN AN EXPANDED COHORT OF HARMONY TRANSCATHETER PULMONARY VALVE RECIPIENTS

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