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  2. Sodium channel dysfunction in inherited and acquired cardiac diseases

Sodium channel dysfunction in inherited and acquired cardiac diseases

Open Access
Authors
  • S. Casini
Supervisors
  • J.M.T. de Bakker
Cosupervisors
  • H.L. Tan
  • M.W. Veldkamp
Award date 12-06-2008
ISBN
  • 9788860391001
Number of pages 198
Publisher Masso delle Fate Edizioni
Organisations
  • Faculty of Medicine (AMC-UvA)
Document type PhD thesis
Note Research conducted at: Universiteit van Amsterdam
Language English
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Thesis
Cover
Titlepage
Contents
Chapter 1 General Introduction / Aim of the thesis
Chapter 2 Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S5 linker in slow inactivation
Chapter 3 Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome : a combined electrophysiological, genetic, histopathologic, and computational study
Chapter 4 Tubulin polymerization modifies cardiac sodium channel expression and gating
Chapter 5 Intracellular calcium modulation of voltage-gated sodium channels ventricular myocytes
Chapter 6 Summary/Samenvatting
Dankwoord
List of publications
Curriculum Vitae
Editorial data
Cover
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