265 results on '"Gray, Belinda"'
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2. Vigorous exercise and sports participation in individuals with hypertrophic cardiomyopathy
3. The role of genetic testing in management and prognosis of individuals with inherited cardiomyopathies
4. A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship
5. The New South Wales Sudden Cardiac Arrest Registry: A Data Linkage Cohort Study
6. The assessment of undergraduate bachelor of nursing students in the collaborative clusters education model: A qualitative descriptive design
7. Feasibility of supporting newly qualified nurses: Nominal group technique of the perspectives of nursing stakeholders
8. Athletic Activity for Patients With Hypertrophic Cardiomyopathy and Other Inherited Cardiovascular Diseases: JACC Focus Seminar 3/4
9. The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic
10. Longitudinal Assessment of Structural Phenotype in Brugada Syndrome Using Cardiac Magnetic Resonance Imaging
11. International Criteria for Reporting Study Quality for Sudden Cardiac Arrest/Death Tool
12. Recurrent immunosuppressive-responsive myocarditis in a patient with desmoplakin cardiomyopathy: a case report
13. Medical Evaluation of Athletes: Genetic Testing
14. Biventricular Myocardial Fibrosis and Sudden Death in Patients With Brugada Syndrome
15. Comparison of conventional autopsy with post-mortem magnetic resonance, computed tomography in determining the cause of unexplained death
16. Patients With Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement
17. A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia
18. A balanced translocation disrupting SCN5A in a family with Brugada syndrome and sudden cardiac death
19. Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome
20. A case series of patients with filamin-C truncating variants attending a specialized cardiac genetic clinic
21. Development of a website support intervention for families after sudden cardiac death
22. The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy
23. Noncardiac genetic predisposition in sudden infant death syndrome
24. Abstract 14500: Physical Activity in Individuals With the Long Qt Syndrome: Baseline Data From the Lifestyle and Exercise in Long Qt Study (live Lqts)
25. Variant Location Is a Novel Risk Factor for Individuals with Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant
26. Variant Location Is a Novel Risk Factor for Individuals with Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant
27. Type 1 Brugada Pattern May Be Provoked by Ajmaline in Some Healthy Subjects: Results From a Clinical Trial.
28. Evaluation After Sudden Death in the Young: A Global Approach
29. Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
30. Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant
31. Longitudinal assessment of structural phenotype in Brugada syndrome using cardiac magnetic resonance imaging
32. Social determinants of health in the setting of hypertrophic cardiomyopathy
33. Radiation Exposure During Cardiac Catheterisation is Similar for Both Femoral and Radial Approaches
34. Additional file 1 of The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic
35. Liver function parameters, cholesterol, and phospholipid α-linoleic acid are associated with adipokine levels in overweight and obese adults
36. Feasibility of supporting newly qualified nurses: Nominal group technique of the perspectives of nursing stakeholders
37. Liver enzymes but not free fatty acid levels predict markers of insulin sensitivity in overweight and obese, nondiabetic adults
38. LB-469807-01 IMPACT OF VIGOROUS EXERCISE IN THE LONG QT SYNDROME BY GENOTYPE, AGE, AND SEX: DATA FROM THE LIFESTYLE AND EXERCISE IN LONG QT SYNDROME REGISTRY (LIVE-LQTS)
39. Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT Syndrome
40. Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT Syndrome
41. Treatment of Chronic Stuttering: Outcomes from a Student Training Clinic
42. ECG changes in athletes What is normal and when should I worry?
43. Vigorous Exercise in Patients With Hypertrophic Cardiomyopathy
44. The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic
45. Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT Syndrome
46. Andersen–Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity
47. NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy
48. Abstract 9544: Physical Activity in Individuals With Hypertrophic Cardiomyopathy: Baseline Data From the Prospective "Lifestyle and Exercise in Hcm" (live-hcm) Study
49. Variant location is a novel risk factor for individuals with arrhythmogenic cardiomyopathy due to a desmoplakin (DSP) truncating variant
50. Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands
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