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(P065) ASSESSMENT OF RESOURCE AVAILABILITY AND USE FOR NEURODEVELOPMENTAL OUTCOMES IN CHILDREN WITH CONGENITAL HEART DISEASE IN NOVA SCOTIA
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(P081) TAILORING FETAL ECHOCARDIOGRAPHY INDICATIONS TO THE LIMITED RESOURCES IN SASKATCHEWAN
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(P066) CARDIAC MANIFESTATIONS IN CHILDREN AND ADULTS WITH LONG-CHAIN FATTY ACID OXIDATION DISORDERS (LC-FAOD): A UNITED STATES RETROSPECTIVE CLAIMS DATABASE ANALYSIS
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(P067) CHANGE IN PATIENT-REPORTED PHYSICAL AND MENTAL HEALTH AFTER ADULT CONGENITAL HEART DISEASE INTERVENTIONS
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(P068) CLINICAL FOLLOW-UP AND SURVEILLANCE IN FONTAN PATIENTS: REFLECTING ON THE ACC/AHA GUIDELINES
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(P069) DETERMINING ANTENATAL RISK FACTORS FOR PROGRESSION AND OUTCOME OF ATRIOVENTRICULAR VALVE REGURGITATION IN PATIENTS WITH ATRIOVENTRICULAR SEPTAL DEFECT
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(P070) FONTAN ASSOCIATED LIVER DISEASE: TRENDS OVER TIME
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(P071) HIGH HETEROGENEITY IN PRENATAL DETECTION RATES OF SEVERE CONGENTAL HEART DISEASE BETWEEN PHYSICIANS, HOSPITALS AND REGIONS
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(P072) INFECTIVE ENDOCARDITIS IN ADULTS WITH CONGENITAL HEART DISEASE (IE-ACHD): A REGISTRY
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(P073) KNOWLEDGE TO ACTION: IMPLEMENTATION OF A KNOWLEDGE TRANSLATION STRATEGY TO IDENTIFY AND TREAT FAMILIAL HYPERCHOLESTEROLEMIA
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(P074) META-ANALYSIS OF PRENATAL RISK FACTORS FOR CONGENITAL HEART DISEASE: PART 2 - MATERNAL ALCOHOL AND MEDICATION, ASSISTED REPRODUCTIVE TECHNOLOGIES, AND FAMILIAL AND FETAL FACTORS.
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(P075) OUTCOMES AFTER PEDIATRIC PULMONARY VALVE REPLACEMENT IN PATIENTS WITH TETRALOGY OF FALLOT
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(P076) PEDIATRIC CARDIOLOGY REFERRAL TRENDS IN THE MARITIMES: PRELIMINARY ANALYSIS
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(P077) PHARMACISTS CLINICAL ACTIVITIES AND PATIENT OUTCOMES IN ADULT CONGENTIAL HEART DISEASE PATIENTS
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(P078) PSYCHOLOGICAL IMPACTS OF FETAL ECHOCARDIOGRAPHY REFERRAL AND RESULTS ON THE EXPECTING PARENTS
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(P079) SANGUINEOUS CARDIOPULMONARY BYPASS PRIME ACCELERATES THE INFLAMMATORY RESPONSE DURING PEDIATRIC CARDIAC SURGERY
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(P080) SEX-BASED DIFFERENCES IN LONG-TERM OUTCOMES FOLLOWING TRANSCATHETER CLOSURE OF PATENT FORAMEN OVALE FOR CRYPTOGENIC STROKE
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(P082) THE IMPACT OF A FONTAN FAMILY CAMP ON CHILDREN AND THEIR FAMILIES
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(P083) THE QUALITY STUDY: LONGITUDINAL ASSESSMENT OF QUALITY OF LIFE IN CHILDREN AND YOUNG ADULTS WITH CONGENITAL HEART DEFECTS
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(P084) TIMELINE MAPPING CONGENITAL HEART DISEASE: A QUALITATIVE STUDY OF PARENTAL AND CLINICAL CARE PROVIDER EXPERIENCES
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(P085) UNDERSTANDING PATIENT/FAMILY PERSPECTIVES ON THE USE OF 3D PRINTED HEART MODELS OF CONGENITAL HEART DISEASE FOR FAMILY EDUCATION
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