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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    £999.99

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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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