Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Textbook 2020Latest edition Springer Nature Switzerland AG 202

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书目名称Clinical Cardiogenetics影响因子(影响力)




书目名称Clinical Cardiogenetics影响因子(影响力)学科排名




书目名称Clinical Cardiogenetics网络公开度




书目名称Clinical Cardiogenetics网络公开度学科排名




书目名称Clinical Cardiogenetics被引频次




书目名称Clinical Cardiogenetics被引频次学科排名




书目名称Clinical Cardiogenetics年度引用




书目名称Clinical Cardiogenetics年度引用学科排名




书目名称Clinical Cardiogenetics读者反馈




书目名称Clinical Cardiogenetics读者反馈学科排名

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Clinical Geneticsc aspects of disease. Genetic counselors are Masters-level university-trained health professionals who deal in the psychosocial and genetic aspects of familial diseases. Both are specifically trained in communicating the implications of genetic information and genetic disease to patients and their f

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Introduction to Hereditary Cardiomyopathiese, hypertension, valvular heart disease, and congenital heart disease sufficient to explain the observed myocardial abnormality. We describe five main cardiomyopathy subtypes as outlined by the European Society of Cardiology: hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic cardio

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Hypertrophic Cardiomyopathy is left ventricular hypertrophy in the absence of cardiac or systemic disease that may cause hypertrophy. The disease can present at any age and is highly variable. Patients can remain asymptomatic throughout their life, but HCM is also associated with adverse clinical events, like heart failure, s

febrile

Dilated Cardiomyopathyades, remarkable progress has been made in understanding the genetic basis of idiopathic dilated cardiomyopathy (iDCM). Rare variants in >50 genes, some also involved in other cardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produc

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Abjure

Left Ventricular Noncompactionwith no or slow progression, to severe disabling, rapidly progressive heart failure. Initial presentation includes the triad of heart failure, (potentially lethal) arrhythmias and/or thrombo-embolism. LVNC may occur at all ages, even prenatally. In childhood, clinical features are often more severe

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Restrictive Cardiomyopathyincreased stiffness of the myocardium, causing a rapid increase in ventricular pressure upon only small increases in volume. Biventricular chamber size, wall thickness and systolic function are usually normal or near-normal until later stages of the disease. Differentiation from constrictive pericar

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