Titlebook: Noncompaction Cardiomyopathy; Kadir Caliskan,Osama I. Soliman,Folkert J. ten Cat Book 2019 Springer Nature Switzerland AG 2019 Noncompacti

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书目名称Noncompaction Cardiomyopathy影响因子(影响力)




书目名称Noncompaction Cardiomyopathy影响因子(影响力)学科排名




书目名称Noncompaction Cardiomyopathy网络公开度




书目名称Noncompaction Cardiomyopathy网络公开度学科排名




书目名称Noncompaction Cardiomyopathy被引频次




书目名称Noncompaction Cardiomyopathy被引频次学科排名




书目名称Noncompaction Cardiomyopathy年度引用




书目名称Noncompaction Cardiomyopathy年度引用学科排名




书目名称Noncompaction Cardiomyopathy读者反馈




书目名称Noncompaction Cardiomyopathy读者反馈学科排名

性行为放纵者

Book 2019l resource for all medical professionals managing these patients, including clinicians in cardiology, electrophysiology, clinical and molecular genetics, pediatrics, pathology, neurology and general practitioners.  . .

埋葬

Congenital Heart Disease and Noncompaction Cardiomyopathy,uspide aortic valve (1%). Medical and surgical teams caring for patients with CHD should be aware that NCCM can be associated with all forms of CHD and may be associated with poor outcomes and increased adverse events.

广口瓶

meshwork and deep intertrabecular recesses.Collates answers .This book provides a comprehensive but concise overview of noncompaction cardiomyopathy. Information on congestive heart failure, thromboembolic events, (potentially lethal) arrhythmias, and sudden cardiac death is presented. Topics covere

Prosaic

infringe

词根词缀法

Neuromuscular Disorders and Noncompaction Cardiomyopathy,ssociated with complications and the outcome of LVHT patients depends on the presence/absence of an NMD, it is essential that all patients with a NMD are prospectively investigated for LVHT and that all patients with LVHT are prospectively investigated for a NMD. Management of LVHT depends on the presence/absence of a NMD.

鸽子

Genetics and Family Screening for Noncompaction Cardiomyopathy,erited cardiomyopathies, timely identification and treatment of relatives at risk is important. This chapter focusses on the process of identifying a genetic cause, predicting risk for relatives, informing index cases and relatives on subsequent recommendations for family screening.

分开如此和谐

Future Perspectives,tomatic disease to severe, disabling, progressive heart failure. However, the prevalence, histo-pathological and molecular base of this yet rare, orphan disease is largely unknown. Strategies to improve the accurate diagnosis and outcome should come from large prospective international registries and randomized-controlled trials.

冷淡周边

978-3-030-17722-5Springer Nature Switzerland AG 2019