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64 results on '"Schott, Jean-Jacques"'

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1. Functional Epicardial Conduction Disturbances Due to a SCN5A Variant Associated With Brugada Syndrome

2. Left Ventricular Abnormal Substrate in Brugada Syndrome

3. EN-452414-5 VENTRICULAR CONDUCTION IS A MARKER FOR ARRHYTHMIC RISK IN OVERLAP SODIUM CHANNEL DISEASE

4. Machine Learning–Based Phenogrouping in Mitral Valve Prolapse Identifies Profiles Associated With Myocardial Fibrosis and Cardiovascular Events

5. Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a new syndromic cardiac disorder

6. Mitral Valve Dystrophy: What role do leukocytes play?

7. BS-515-01 NON-CODING DELETION INDUCES 3D CHROMATIN REMODELLING AND PITX2 EXPRESSION DYSREGULATION ASSOCIATED WITH A SYNDROMIC CARDIAC DISORDER

8. BS-513-02 GENOME-WIDE ASSOCIATION ANALYSES IDENTIFY NOVEL BRUGADA SYNDROME RISK LOCI AND HIGHLIGHT A NEW MECHANISM OF SODIUM CHANNEL REGULATION IN DISEASE SUSCEPTIBILITY

9. Heritability of aortic valve stenosis and bicuspid enrichment in families with aortic valve stenosis

10. Familial recurrence patterns in congenitally corrected transposition of the great arteries: An international study

11. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

12. Genetic and In Vitro Inhibition of PCSK9 and Calcific Aortic Valve Stenosis

14. SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups

15. Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm

16. Value of the sodium-channel blocker challenge in Brugada syndrome

17. Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity

18. The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway

19. Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation

21. Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia

23. Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I

24. 0131: A phenotypic study of ARHGAP24 mitral valve prolapse suggests a genetic origin for fibro elastic deficiency

27. 0186 : Genotype/phenotype relationship in a large cohort of long QT syndrome patients

28. 0207 : Functional explorations of genes near genetic risk loci for mitral valve prolapse involve TNS1 and LMCD1 in valve development and integrity

30. 0185 : Genetic screening identifies a high proportion of mutations in patients with idiopathic ventricular fibrillation and sudden cardiac death

31. 0077 : DOCK1 a new candidate gene in inherited form of mitral valve prolapse

32. 0210 : Effect of SCN5A mutations and SCN10A, SCN5A and HEY2 frequent variants on ECG of Brugada patients during ajmaline test

34. OP-071 Mutations in ARHGAP24 Encoding Filgap as a Cause of Mitral Valve Prolapse

36. Brugada Syndrome and Nav1.5

41. Identification of Large Families in Early Repolarization Syndrome

42. Multifocal Ectopic Purkinje-Related Premature Contractions

43. 325 Clinical presentation and long-term clinical outcomes of non immune, isolated atrioventricular block diagnosed in utero or early childhood

46. 341 Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood non-immune isolated atrioventricular block

47. 294 Clinical presentation and long-term outcome of non immune and isolated atrioventricular block when congenital or diagnosed during childhood: a French multicentric study on 141 patients

48. 242 Clinical presentation and long-term outcome of non immune and isolated atrioventricular block when congenital or diagnosed during childhood: a French multicentric study on 141 patients

49. Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome

50. Early Repolarization Disease

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