大葉大學圖書館 |

Clinical cardiogenetics[electronic resource] /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
杜威分類號:	616.1042
書名/作者:	Clinical cardiogenetics/ edited by Hubert F. Baars ... [et al.].
其他作者:	Baars, Hubert F.
出版者:	Cham : : Springer International Publishing :, 2016.
面頁冊數:	viii, 405 p. : : ill., digital ;; 24 cm.
Contained By:	Springer eBooks
標題:	Cardiovascular system - Diseases
標題:	Medicine & Public Health.
標題:	Cardiology.
標題:	Human Genetics.
ISBN:	9783319442037
ISBN:	9783319442020
內容註:	Molecular Genetics -- Clinical genetics -- Differential diagnosis of cardiomyopathies -- Hypertrophic Cardiomyopathy -- Dilated Cardiomyopathy -- Arrhythmogenic Cardiomyopathy -- Non-Compaction Cardiomyopathy -- Hereditary neuromuscular diseases and cardiac involvement -- Fabry disease -- Long QT Syndrome -- Brugada Syndrome -- Short QT Syndrome -- Cathecholaminergic Polymorphic VT -- Sudden death and Idiopathic Ventricular Fibrillation -- Thoracic Aortic Aneurysm Dissection -- Bicuspid aortic valve -- Premature coronary artery disease.
摘要、提要註:	This extensively revised second edition provides a thorough basic knowledge on the genetic aspects of cardiovascular disorders. Many cardiologists have not been specifically trained in genetics, let alone in explaining genetics to their patients. While clinics for cardiogenetic disorders have been established in many academic teaching hospitals, it is neither desirable nor feasible that the care for this large group of patients and their relatives remains solely restricted to this small number of centers. This book reviews the expertise that all cardiologists, clinical and molecular geneticists, genetic nurses, and social workers need to provide optimal care for individuals with cardiac disease of probable genetic origin and their family members. Clinical Cardiogenetics, Second Edition, compiles the huge amount of information available in a single easy-to-read textbook. It does not require prior expert genetic knowledge and provides a practical clinical primer for cardiologists and other physicians involved in the management of these patients. With the continuing increase in genetic knowledge, and the expanding possibilities to prevent fatal arrhythmias in those individuals at high risk, a steady increase in questions regarding genetics from patients and their relatives in the years to come should be expected. This comprehensive textbook is a valuable tool in dealing with such questions.
電子資源:	http://dx.doi.org/10.1007/978-3-319-44203-7

Clinical cardiogenetics[electronic resource] /
Clinical cardiogenetics[electronic resource] /edited by Hubert F. Baars ... [et al.]. - 2nd ed. - Cham :Springer International Publishing :2016. - viii, 405 p. :ill., digital ;24 cm.

Molecular Genetics -- Clinical genetics -- Differential diagnosis of cardiomyopathies -- Hypertrophic Cardiomyopathy -- Dilated Cardiomyopathy -- Arrhythmogenic Cardiomyopathy -- Non-Compaction Cardiomyopathy -- Hereditary neuromuscular diseases and cardiac involvement -- Fabry disease -- Long QT Syndrome -- Brugada Syndrome -- Short QT Syndrome -- Cathecholaminergic Polymorphic VT -- Sudden death and Idiopathic Ventricular Fibrillation -- Thoracic Aortic Aneurysm Dissection -- Bicuspid aortic valve -- Premature coronary artery disease.

This extensively revised second edition provides a thorough basic knowledge on the genetic aspects of cardiovascular disorders. Many cardiologists have not been specifically trained in genetics, let alone in explaining genetics to their patients. While clinics for cardiogenetic disorders have been established in many academic teaching hospitals, it is neither desirable nor feasible that the care for this large group of patients and their relatives remains solely restricted to this small number of centers. This book reviews the expertise that all cardiologists, clinical and molecular geneticists, genetic nurses, and social workers need to provide optimal care for individuals with cardiac disease of probable genetic origin and their family members. Clinical Cardiogenetics, Second Edition, compiles the huge amount of information available in a single easy-to-read textbook. It does not require prior expert genetic knowledge and provides a practical clinical primer for cardiologists and other physicians involved in the management of these patients. With the continuing increase in genetic knowledge, and the expanding possibilities to prevent fatal arrhythmias in those individuals at high risk, a steady increase in questions regarding genetics from patients and their relatives in the years to come should be expected. This comprehensive textbook is a valuable tool in dealing with such questions.

ISBN: 9783319442037

Standard No.: 10.1007/978-3-319-44203-7doiSubjects--Topical Terms:

688427
Cardiovascular system
--Diseases

LC Class. No.: RC669

Dewey Class. No.: 616.1042

Clinical cardiogenetics[electronic resource] /
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520 $a This extensively revised second edition provides a thorough basic knowledge on the genetic aspects of cardiovascular disorders. Many cardiologists have not been specifically trained in genetics, let alone in explaining genetics to their patients. While clinics for cardiogenetic disorders have been established in many academic teaching hospitals, it is neither desirable nor feasible that the care for this large group of patients and their relatives remains solely restricted to this small number of centers. This book reviews the expertise that all cardiologists, clinical and molecular geneticists, genetic nurses, and social workers need to provide optimal care for individuals with cardiac disease of probable genetic origin and their family members. Clinical Cardiogenetics, Second Edition, compiles the huge amount of information available in a single easy-to-read textbook. It does not require prior expert genetic knowledge and provides a practical clinical primer for cardiologists and other physicians involved in the management of these patients. With the continuing increase in genetic knowledge, and the expanding possibilities to prevent fatal arrhythmias in those individuals at high risk, a steady increase in questions regarding genetics from patients and their relatives in the years to come should be expected. This comprehensive textbook is a valuable tool in dealing with such questions.
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