Description

Book Synopsis

Section I: BASIC CONCEPTS - Introduction, Introduction to molecular genetics, Molecular genetics in cardiology, Clinical Genetics of cardiac diseases.- Section II: CARDIOMYOPATHY - Hypertrophic cardiomyopathy.- Dilated cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, Other cardiomyopathies.- Section III: PRIMARY ELECTRICAL HEART DISEASES - Congenital long QT-syndrome, Brugada syndrome, Short QT-syndrome, Catecholamine induced polymorphic ventricular tachycardia, Familial atrial fibrillation, Hereditary conduction diseases, Connective tissue disorders and smooth muscle disorders, Genetics of congenital heart diseases, Genetics of hypertension and clinical aspects, Genetics of the lipoprotein metabolism and clinical aspects, Genetics of homocysteine metabolism and clinical aspects, Genetic markers of hemostatic factors, The pharmacogenetics of atherosclerosis, Genetics of (premature) coronary artery disease, Cardiac involvement in hereditary neuromuscular diseases,

Table of Contents

Section I: BASIC CONCEPTS - Introduction, Introduction to molecular genetics, Molecular genetics in cardiology, Clinical Genetics of cardiac diseases

Section II: CARDIOMYOPATHY - Hypertrophic cardiomyopathy. Dilated cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, Other cardiomyopathies

Section III: PRIMARY ELECTRICAL HEART DISEASES - Congenital long QT-syndrome, Brugada syndrome, Short QT-syndrome, Catecholamine induced polymorphic ventricular tachycardia, Familial atrial fibrillation, Hereditary conduction diseases, Connective tissue disorders and smooth muscle disorders, Genetics of congenital heart diseases, Genetics of hypertension and clinical aspects, Genetics of the lipoprotein metabolism and clinical aspects, Genetics of homocysteine metabolism and clinical aspects, Genetic markers of hemostatic factors, The pharmacogenetics of atherosclerosis, Genetics of (premature) coronary artery disease, Cardiac involvement in hereditary neuromuscular diseases, Sudden cardiac death < 40 years, The outpatient clinic for cardiogenetics, The future of cardiogenetics

Clinical Cardiogenetics

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A Paperback by H.F. Baars, P.A.F.M. Doevendans, J.J. van der Smagt

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    View other formats and editions of Clinical Cardiogenetics by H.F. Baars

    Publisher: Springer
    Publication Date: 12/13/2014 12:00:00 AM
    ISBN13: 9781447157038, 978-1447157038
    ISBN10: 1447157036

    Description

    Book Synopsis

    Section I: BASIC CONCEPTS - Introduction, Introduction to molecular genetics, Molecular genetics in cardiology, Clinical Genetics of cardiac diseases.- Section II: CARDIOMYOPATHY - Hypertrophic cardiomyopathy.- Dilated cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, Other cardiomyopathies.- Section III: PRIMARY ELECTRICAL HEART DISEASES - Congenital long QT-syndrome, Brugada syndrome, Short QT-syndrome, Catecholamine induced polymorphic ventricular tachycardia, Familial atrial fibrillation, Hereditary conduction diseases, Connective tissue disorders and smooth muscle disorders, Genetics of congenital heart diseases, Genetics of hypertension and clinical aspects, Genetics of the lipoprotein metabolism and clinical aspects, Genetics of homocysteine metabolism and clinical aspects, Genetic markers of hemostatic factors, The pharmacogenetics of atherosclerosis, Genetics of (premature) coronary artery disease, Cardiac involvement in hereditary neuromuscular diseases,

    Table of Contents

    Section I: BASIC CONCEPTS - Introduction, Introduction to molecular genetics, Molecular genetics in cardiology, Clinical Genetics of cardiac diseases

    Section II: CARDIOMYOPATHY - Hypertrophic cardiomyopathy. Dilated cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, Other cardiomyopathies

    Section III: PRIMARY ELECTRICAL HEART DISEASES - Congenital long QT-syndrome, Brugada syndrome, Short QT-syndrome, Catecholamine induced polymorphic ventricular tachycardia, Familial atrial fibrillation, Hereditary conduction diseases, Connective tissue disorders and smooth muscle disorders, Genetics of congenital heart diseases, Genetics of hypertension and clinical aspects, Genetics of the lipoprotein metabolism and clinical aspects, Genetics of homocysteine metabolism and clinical aspects, Genetic markers of hemostatic factors, The pharmacogenetics of atherosclerosis, Genetics of (premature) coronary artery disease, Cardiac involvement in hereditary neuromuscular diseases, Sudden cardiac death < 40 years, The outpatient clinic for cardiogenetics, The future of cardiogenetics

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