Current Concepts in Arrhythmogenic Right Ventricular by Corinna Brunckhorst, Firat Duru, Ardan M. Saguner

By Corinna Brunckhorst, Firat Duru, Ardan M. Saguner

Edited and written by way of across the world famous experts, present strategies in Arrhythmogenic correct Ventricular Cardiomyopathy/Dysplasia (ARVC/D) provides vital insights to all points of this certain disorder and may function a invaluable consultant to assist readers give you the absolute best deal with their sufferers. dialogue of ARVC/D through the specialists includes:

  • Basic and medical science.
  • Pathophysiology, molecular mechanisms, and genetic background.
  • The mechanisms of affliction development resulting in a range of affliction phenotypes.
  • Challenges within the scientific environment with admire to analysis, threat stratification, and therapy.

"The editors...have enlisted as authors those that first famous and named the sickness, and such a lot of these answerable for the new advances during this interesting quarter. the result's an outstanding, finished yet very readable textual content facing this more and more very important spectrum of illnesses. it's a designated publication that are meant to be came across at the cabinets of every body who seeks to control sufferers with cardiac arrhythmia simply because among those that consult there are guaranteed to be sufferers with this difficult disease."

- From the foreword by way of A. John Camm, MD

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Additional resources for Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy / Dysplasia

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10. Marcus FI, Fontaine G, Guiraudon G, et al. Right ventricular dysplasia: a report of 24 cases. Circulation. 1982;65:384-399. 16 Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia 11. Uhl HS. A previously undescribed congenital malformation of the heart: almost total absence of the myocardium of the right ventricle. Bull Johns Hopkins Hosp. 1952;91:197-205. 12. Thiene G, Nava A, Corrado D, Rossi L, Pennelli N. Right ventricular cardiomyopathy and sudden death in young people.

Rizzo S, Lodder EM, Verkerk AO, et al. Intercalated disc abnormalities, reduced Na+ current density and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes. Cardiovasc Res. 1093/cvr/cvs219. Noorman M, Hakim S, Kessler E, et al. Remodeling of the cardiac sodium channel, connexin43, and plakoglobin at the intercalated disk in patients with arrhythmogenic cardiomyopathy. Heart Rhythm. 2013;10: 412-419. Gomes J, Finlay M, Ahmed AK, et al. Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

26. 27. 28. 29. 30. From postnatal morphogenesis to paroxysmal arrhythmias. Circulation. 1994;90:556-573. Runge MS, Stouffer GA, Sheahan RG, Yamamoto S, Tsyplenkova VG, James TN. Morphological patterns of death by myocytes in arrhythmogenic right ventricular dysplasia. Am J Med Sci. 2000;320:310-319. Mallat Z, Tedgui A, Fontaliran F, Frank R, Durigon M, Fontaine G. Evidence of apoptosis in arrhythmogenic right ventricular dysplasia. N Engl J Med. 1996;335:1190-1196. Protonotarios N, Tsatsopoulou A, Patsourakos P, et al.

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