189 results on '"Beckmann, Britt-Maria"'
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2. Postmortale Genetik nach einem plötzlichen Herztod: Hintergründe, Vorgehen und Zukunft
3. Telemedical monitoring in patients with inborn cardiac disease – experience of a tertiary care centre
4. Correction: Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion
5. Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion
6. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
7. Sudden unexpected death in the young — Value of massive parallel sequencing in postmortem genetic analyses
8. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
9. Characterization of an N-terminal Nav1.5 channel variant – a potential risk factor for arrhythmias and sudden death?
10. Manual versus Automatic Assessment of the QT-Interval and QTc
11. Relevance of molecular testing in patients with a family history of sudden death
12. Manual vs. automatic assessment of the QT-interval and corrected QT.
13. Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome KCNQ1 Variants
14. Telemedical monitoring in patients with inborn cardiac disease – experience of a tertiary care centre
15. Fetal Bradycardia Caused by Monogenic Disorders—A Review of the Literature
16. Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations
17. Variant interpretation in molecular autopsy: a useful dilemma
18. Early repolarization pattern is the strongest predictor of arrhythmia recurrence in patients with idiopathic ventricular fibrillation: results from a single centre long-term follow-up over 20 years†
19. Usefulness of Short-Term Variability of QT Intervals as a Predictor for Electrical Remodeling and Proarrhythmia in Patients With Nonischemic Heart Failure
20. Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by involving an Integrin-αVβ6/TGF-β Signaling Cascade
21. Relation of Increased Short-Term Variability of QT Interval to Congenital Long-QT Syndrome
22. Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness
23. Clinical utility gene card for: Long-QT syndrome
24. Molekulargenetische Diagnostik bei hereditären Arrhythmiesyndromen heute und in Zukunft
25. Left-ventricular innervation assessed by ¹²³I-SPECT/CT is associated with cardiac events in inherited arrhythmia syndromes
26. Recurrent torsades de pointes after catheter ablation of incessant ventricular bigeminy in combination with QT prolongation
27. Left-ventricular innervation assessed by 123I-SPECT/CT is associated with cardiac events in inherited arrhythmia syndromes
28. Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study
29. Atrial Arrhythmias in Long-QT Syndrome under Daily Life Conditions: A Nested Case Control Study
30. The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)
31. Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: a case control pilot study
32. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?
33. Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry
34. Bedeutung und Probleme bei der Anwendung des Gendiagnostikgesetzes im klinischen Alltag
35. Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients
36. Association of Early Repolarization Pattern on ECG with Risk of Cardiac and All-Cause Mortality: A Population-Based Prospective Cohort Study (MONICA/KORA)
37. Seizures on hearing the alarm clock
38. Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients
39. Genetische Arrhythmiesyndrome – Teil 2
40. Genetische Arrhythmiesyndrome ohne strukturelle Herzerkrankung
41. Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia
42. Correspondence (reply): In Reply
43. Inherited Cardiac Arrhythmias: Diagnosis, Treatment, and Prevention
44. Purkinje-related ventricular fibrillation associated with a homozygous H558R polymorphism in the sodium channel SCN5A gene
45. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
46. Laminopathy presenting as familial atrial fibrillation
47. Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility
48. Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome:a case control pilot study
49. Clinical utility gene card for: Long-QT Syndrome (types 1–13)
50. Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants
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