45 results on '"Wilde, Arthur A M"'
Search Results
2. Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic review
3. The Dutch Idiopathic Ventricular Fibrillation Registry: progress report on the quest to identify the unidentifiable
4. Multimodal explainable artificial intelligence identifies patients with non-ischaemic cardiomyopathy at risk of lethal ventricular arrhythmias
5. Assessment of ICD eligibility in non-ischaemic cardiomyopathy patients: a position statement by the Task Force of the Dutch Society of Cardiology
6. A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients
7. Importance of exercise stress testing in evaluation of unexplained cardiac arrest survivor
8. Timing and mid-term outcomes of using leadless pacemakers as replacement for infected cardiac implantable electronic devices
9. Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
10. The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant
11. MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset
12. SCN5A-1795insD founder variant: a unique Dutch experience spanning 7 decades
13. Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathy
14. Real-world long-term battery longevity of Micra leadless pacemakers
15. Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity?
16. A deep learning approach identifies new ECG features in congenital long QT syndrome
17. Clinical utility gene card for: Long-QT syndrome
18. How to study the role of volunteer responders in the chain of survival
19. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
20. Epidemiology of inherited arrhythmias
21. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy
22. Inherited cardiac arrhythmias
23. A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in Children
24. Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
25. Relationship Between Cardiac Dysfunction and Cerebral Perfusion in Patients with Aneurysmal Subarachnoid Hemorrhage
26. Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel
27. Scar tissue and microvolt T-wave alternans
28. hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities
29. Genetic testing for inherited cardiac disease
30. Electrocardiographic P wave changes after thoracoscopic pulmonary vein isolation for atrial fibrillation
31. Late Sodium Current Inhibition in Acquired and Inherited Ventricular (dys)function and Arrhythmias
32. The Chemical Compound PTC124 Does Not Affect Cellular Electrophysiology of Cardiac Ventricular Myocytes
33. Genetic Basis of Ventricular Arrhythmias
34. The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome
35. Prevalence and Characterization of ECG Abnormalities After Intracerebral Hemorrhage
36. Implantable cardioverter defibrillator as a bridge to recovery in an infant with cardiac rhabdomyoma
37. Clinical and Genetic Analysis of Long QT Syndrome in Children from Six Families in Saudi Arabia: Are They Different?
38. Syncope during exercise, documented with continuous blood pressure monitoring during ergometer testing
39. Exercise related syncope, when it’s not the heart
40. Brugada syndrome: in search of a genotype-phenotype relationship
41. Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3
42. Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period
43. The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene
44. Role of ATP-sensitive K+ channel current in ischemic arrhythmias
45. Exercise related syncope: when it’s not the heart
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