Clinical cardiogenetics /
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Imprint: | London : Springer, ©2011. |
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Description: | 1 online resource (xv, 455 pages) : illustrations (some color) |
Language: | English |
Subject: | |
Format: | E-Resource Book |
URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/11269907 |
Table of Contents:
- Introduction to molecular genetics
- Clinical genetics
- Hypertrophic cardiomyopathy
- Familial dilated cardiomyopathy
- Arrhythmogenic right ventricular dysplasia/cardiomyopathy from desmosome to disease
- Noncompaction cardiomyopathy
- Mitochondrial cardiomyopathy
- Restrictive cardiomyopathy
- Congenital long QT-syndrome
- The Brugada syndrome
- Short QT syndrome
- Catecholaminergic polymorphic ventricular tachycardia
- A molecular genetic perspective on atrial fibrillation
- Idiopathic ventricular fibrillation
- The genetics of mitral valve prolapse
- Atrioventricular (AV) reentry tachycardia
- Hereditary cardiac conduction diseases
- Connective tissue disorders and smooth muscle disorders in cardiology
- Genetics of congenital heart defects
- Genetic disorders of the lipoprotein metabolism: diagnosis and management
- Novel insights into genetics of arterial thrombosis
- The pharmacogenetics of atherosclerosis
- Genetics of (premature) coronary artery disease
- Heredity neuromuscular diseases and cardiac involvement
- Sudden cardiac death in the young: epidemiology and cardiogenetic evaluation of victims and their relatives
- The outpatient clinics for cardiogenetics
- Abdominal aortic aneurysm
- Future of cardiogenetics.