Arrhythmogenic RV Cardiomyopathy/Dysplasia: Recent Advances
Editat de Frank I. Marcus, Andrea Nava, Gaetano Thieneen Limba Engleză Paperback – 13 dec 2014
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Specificații
ISBN-13: 9788847056213
ISBN-10: 8847056217
Pagini: 232
Ilustrații: XIII, 217 p.
Dimensiuni: 193 x 260 x 12 mm
Ediția:2007
Editura: Springer
Colecția Springer
Locul publicării:Milano, Italy
ISBN-10: 8847056217
Pagini: 232
Ilustrații: XIII, 217 p.
Dimensiuni: 193 x 260 x 12 mm
Ediția:2007
Editura: Springer
Colecția Springer
Locul publicării:Milano, Italy
Public țintă
Professional/practitionerCuprins
Introduction: Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Clarified.- Advances in Genetics: Dominant Forms.- Advances in Genetics: Recessive Forms.- Genotype-Phenotype Correlations.- Autopsy and Endomyocardial Biopsy Findings.- Cell Adhesion Pathology.- Ultrastructural Substrates.- Transgenic Animal Models.- Spontaneous Animal Models.- Possible Causative or Contributing Role of Viruses.- Diagnosis: Task Force Criteria including Modifications for Family Members.- Strengths and Weaknesses of the Task Force Criteria — Proposed Modifications.- Idiopathic Right Ventricular Outflow Tract Tachycardia.- Electrocardiographic Manifestations.- Echocardiography.- MR and CT Imaging.- Diagnostic Role of Angiography.- Electrophysiologic Study including Electroanatomic Mapping.- Risk Stratification and Antiarrhythmic Drug Therapy.- Catheter Ablation of Ventricular Tachycardia.- The Role of the Implantable Cardiac Defibrillator in the Management.- Management of Heart Failure.- Sudden Death in Young Athletes.
Textul de pe ultima copertă
This book covers all aspects (biological, pathological, genetic, clinical and therapeutical) of arrhythmogenic right ventricular cardiomyopathy/dysplasia, a recent cardiomyopathy which represents a very high risk of sudden death in the young and in athletes. The monograph presents the results of 5-year research program on ARVC/D supported by grants of both the European Commission and the NIH, which enabled the discovery of seven disease-causing genes, thus opening new avenues for the early identification of affected patients and for sudden death prevention.
A panel of top scientists, both European and Americans, contributed to this volume, which will be an essential reference for professionals and residents in cardiology, radiology, human genetics, and sport medicine.
A panel of top scientists, both European and Americans, contributed to this volume, which will be an essential reference for professionals and residents in cardiology, radiology, human genetics, and sport medicine.
Caracteristici
Covers all aspects of arrhythmogenic right ventricular cardiomyopathy/dysplasia Gathers the results of a research program promoted by European Commission and NIH, focused on early identification of affected patients and for sudden death prevention in the young and the athletes Essential reference for professionals and residents in cardiology, radiology, human genetics, and sport medicine