758 results on '"Schulze-Bahr, Eric"'
Search Results
2. Case report: cosegregation of a TPM1 in-frame deletion (p.Lys7del) with familial non-compaction cardiomyopathy (NCCM)
3. Human Genetics of Cardiac Arrhythmias
4. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation: A THESIS Substudy
5. Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome
6. An International Multicenter Evaluation of Type 5 Long QT Syndrome
7. KCNQ1 is an essential mediator of the sex-dependent perception of moderate cold temperatures
8. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation
9. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
10. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
11. Clinical utility gene card for: Long-QT syndrome
12. Comments on the 2023 guidelines of the ESC on management of cardiomyopathies
13. Short QT Syndrome
14. SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes
15. POPDC2 a novel susceptibility gene for conduction disorders
16. A MATLAB algorithm to automatically estimate the QT interval and other ECG parameters and validation using a machine learning approach in congenital long-QT syndrome
17. Case Report: Hypertrophic cardiomyopathy with recurrent episodes of ventricular fibrillation and concurrent sinus arrest
18. Acral keratoderma and sudden death
19. A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations
20. Arrhythmogenic right ventricular cardiomyopathy: Evolving from unique clinical features to a complex pathophysiological concept
21. Körperliche Aktivität, Sport, Genetik und kardiovaskuläre Erkrankungen
22. Einführung in das Herz-Kreislauf-System
23. Interdisciplinary safety precautions protocol for electroconvulsive therapy (ECT) in a patient with treatment-resistant major depression and Brugada ECG
24. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
25. The W101C KCNJ5 Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived Cardiomyocytes
26. Patient-derived stem cell line UKMi005-A (hiPSC) harboring a non-synonymous heterozygous KCNJ5 gene variant
27. Possible Causes and Clinical Relevance of a “Ring-Like” Late Gadolinium Enhancement Pattern
28. Management of Congenital Long-QT Syndrome: Commentary From the Experts
29. Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing
30. Acral keratoderma and sudden death.
31. Possible Causes and Clinical Relevance of a “Ring-Like” Late Gadolinium Enhancement Pattern
32. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
33. Case report: cosegregation of a TPM1 in-frame deletion (p.Lys7del) with familial non-compaction cardiomyopathy (NCCM)
34. Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing
35. Principles of molecular genetic testing
36. Basic principles of genetic disease
37. TASK-1 and TASK-3 may form heterodimers in human atrial cardiomyocytes
38. Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome
39. Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy
40. Single Nucleotide Polymorphisms in Health and Cardiac Disease
41. Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: Disease mechanisms and pharmacological rescue
42. Generation of a patient-specific hiPS cell line with heterozygous GNB2 mutation (UKMi003-A) causative for human sinus node dysfunction and a corresponding CRISPR/Cas9-corrected isogenic control (UKMi004-A)
43. Single Nucleotide Polymorphisms in Health and Cardiac Disease
44. Einführung in das Herz-Kreislauf-System
45. Körperliche Aktivität, Sport, Genetik und kardiovaskuläre Erkrankungen
46. Abstract 19832: De Novo Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Are Rare and Associated With Large Deletions
47. Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning Models
48. Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning Models
49. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
50. Connexin Expression Patterns in Arrhythmogenic Right Ventricular Cardiomyopathy
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.