15 results on '"Schott, Jean-Jacques"'
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2. Abstract 4139829: New Insights in Non-syndromic Mitral Valve Dystrophy: Role of Inflammation and Macrophages
3. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
4. Abstract 12406: Mitral Valve Prolapse: Immune Response as a New Player
5. Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse
6. Abstract 17361: Phenotype of the Aortic Valve in Patients With Filamin-A Mutations: Echocardiographic Features and Clinical Outcomes
7. Abstract 18977: Non-Syndromic Mitral Valve Prolapse From Gene Mutations to Modifiable Mechanisms
8. Parental Electrocardiographic Screening Identifies a High Degree of Inheritance for Congenital and Childhood Nonimmune Isolated Atrioventricular Block
9. Abstract 8808: Early Repolarization Syndrome: Valsalva Maneuver in Familial Screening
10. Defects in Ankyrin-Based Membrane Protein Targeting Pathways Underlie Atrial Fibrillation
11. Clinical Aspects and Prognosis of Brugada Syndrome in Children
12. Defining the Cellular Phenotype of “Ankyrin-B Syndrome” Variants
13. Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy
14. Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France
15. Novel SCN5A Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family
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