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42 results found

no	title	author	magazine	year	volume	issue	page(s)	type
1	A Model for Collaboration: Sudden Death Pathway	Thompson, T.			31	S1	p. S19-S20	article
2	Analysis of Athlete QT Intervals by Age: Fridericia and Hodges Heart Rate Correction Methods Outperform the Bazett's Method for Athlete ECG Screening	Orchard, J.			31	S1	p. S15	article
3	A Young Patient With a Cardiomyopathy Caused by Mutations in the TAF1A Gene?	Helderman-van den Enden, A.			31	S1	p. S8	article
4	Bioinformatic Re-analysis of Data From the Australian Genomics Cardiovascular Genetic Disorders Flagship	Chang, Y.			31	S1	p. S6	article
5	Brugada Syndrome in New Zealand: The Experience of the National Cardiac Inherited Disease Group	Gelbart, D.			31	S1	p. S7	article
6	Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) – The paediatric experience in New South Wales (NSW)	Fitzgerald, N.			31	S1	p. S7	article
7	Comparison of Methods for Correcting QT Interval in Athletes and Young People: A Systematic Literature Review	Mahendran, S.			31	S1	p. S13	article
8	Contribution and Functional Characterisation of Splice-Disrupting Variants in Inherited Heart Disease and Sudden Cardiac Death	Singer, E.			31	S1	p. S2	article
9	COPESCD — An Online Community Supporting Families After Sudden Cardiac Death in the Young: A Protocol for a Pilot Study	Yeates, L.			31	S1	p. S20	article
10	Diagnostic Yield of Panel Genetic Testing in a Cohort of >200 Patients With Congenital Heart Disease	Zilliacus, E.			31	S1	p. S21	article
11	Disproportionate Elevations of Cardiac Troponin in Fabry Disease: A Case Series of False Positives due to Macrotroponin	Moussa, Y.			31	S1	p. S15	article
12	Efficient CRISPR-editing of Pluripotent Stem Cells for Modelling CPVT in Human Cardiac Organoids	Pocock, M.			31	S1	p. S16	article
13	Embedding Genetic Counselling Into Cardiology Clinics: Case Studies From a Queensland Cardiology Genomics Service	Rutstein, A.			31	S1	p. S18	article
14	End Unexplained Cardiac Death (EndUCD) NSW Registry: A Data Linkage Cohort Study Protocol	Leslie, F.			31	S1	p. S11	article
15	Evaluating the Clinical Utility of Polygenic Risk Score for Heart Failure	Mo, X.			31	S1	p. S1-S2	article
16	Further Characterisation of the Cardiac Desminopathy Phenotype	Mahmoodi, E.			31	S1	p. S13	article
17	Genetic Basis of Childhood Cardiomyopathy	Bagnall, R.			31	S1	p. S2-S3	article
18	Genetic Testing for Pulmonary Arterial Hypertension: Diagnostic Yield and Findings From a Cohort of Patients Referred for Targeted Panel Testing	Hathaway, J.			31	S1	p. S8	article
19	Genetic Testing Outcomes in a Cohort of 21,159 Children With Heart Disease	Schonrock, N.			31	S1	p. S18-S19	article
20	Getting to the Heart of Genomics: Mainstreaming Cardiology Genomics in Queensland	Baldini, M.			31	S1	p. S3	article
21	Longitudinal CMR Assessment of Structural Phenotype in Brugada Syndrome	Isbister, J.			31	S1	p. S9-S10	article
22	miR-151-3p and miR-214 Expression Associate With Clinical Phenotypes in BAV Aortopathy	Portelli, S.			31	S1	p. S16	article
23	NSW HEARTS: The NSW Inherited Cardiomyopathy Cohort Study protocol	Butters, A.			31	S1	p. S4	article
24	Outcomes of Clinical Genetic Testing in Congenital Heart Disease – A Single-Site Audit Study	Morrish, A.			31	S1	p. S14	article
25	Patching the Gap Between Variant Identification and Risk Stratification for SCN5A-Associated Cardiac Diseases	Ma, J.			31	S1	p. S12-S13	article
26	Population Genomic Screening of Young Adults for Familial Hypercholesterolaemia: A Cost-Effectiveness Analysis	Lacaze, P.			31	S1	p. S1	article
27	Practise Changing Research – Adding DNAH11 to a Congenital Heart Disease Panel	Thompson, T.			31	S1	p. S19	article
28	Precision Medicine Opportunities for Familial Arrhythmias and Cardiomyopathies Identified When Cost of Genetic Testing is Removed as a Barrier	Schonrock, N.			31	S1	p. S19	article
29	Prevalence of Mitochondrial Genome Variants in an Inherited Heart Disease Cohort	Crowe, J.			31	S1	p. S6-S7	article
30	Reclassifying a LAMP2 Splicing Variant of Uncertain Significance to Pathogenic Following Familial Segregation and Functional RNA Diagnostics	Horton, A.			31	S1	p. S9	article
31	Recurrent GJA1 Mutation Causing Infantile Arrhythmic Cardiomyopathy Fills Gap in Knowledge of the Junction	Ronan, A.			31	S1	p. S17	article
32	Sex Disaggregated Analysis of Risk Factors for Adverse Outcomes in Hypertrophic Cardiomyopathy	Butters, A.			31	S1	p. S5	article
33	Slow Conduction Velocity Revealed in Hypertrophic Cardiomyopathy Modelled With Patient-Derived Induced Pluripotent Stem Cell Cardiomyocytes	Lim, S.			31	S1	p. S11-S12	article
34	Tango 2 Case Series: Cardiac Manifestations	Jardine, K.			31	S1	p. S10	article
35	The Congenital Heart Disease Genetics Clinic: Evolving the Model of Care	Morrish, A.			31	S1	p. S14	article
36	The Elusive Hearts Study: Seeking Genetic Diagnoses in Gene-elusive Cases of Rare Monogenic Cardiovascular Diseases	Richardson, E.			31	S1	p. S17	article
37	The Introduction and Development of a Genetic Counsellor-led Cardiac Genetics Service in a Metropolitan Hospital	Chalinor, H.			31	S1	p. S5-S6	article
38	The Role of Genetic Testing in Diagnosis and Care of Inherited Cardiac Conditions in a Specialised Multidisciplinary Clinic	Krishnan, N.			31	S1	p. S10-S11	article
39	This abstract has been withdrawn				31	S1	p. S15	article
40	Troponin I Autoantibodies in a Patient with Desmoplakin Cardiomyopathy/Myocarditis Overlap Syndrome	Rowe, S.			31	S1	p. S17-S18	article
41	Use of Advanced Echocardiographic Modalities to Discriminate Preclinical Hypertrophic Cardiomyopathy Mutation Carriers From Non-Carriers	Lo, A.			31	S1	p. S12	article
42	Victorian Inherited Cardiac Disorders Family Initiative (VicDFI)—Creating a Shared Cardiac Clinical Database Across the Life Spectrum	Zentner, D.			31	S1	p. S20-S21	article

42 results found

Koninklijke Bibliotheek - National Library of the Netherlands