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

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書(shū)目名稱Noncompaction Cardiomyopathy影響因子(影響力)




書(shū)目名稱Noncompaction Cardiomyopathy影響因子(影響力)學(xué)科排名




書(shū)目名稱Noncompaction Cardiomyopathy網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱Noncompaction Cardiomyopathy網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱Noncompaction Cardiomyopathy被引頻次




書(shū)目名稱Noncompaction Cardiomyopathy被引頻次學(xué)科排名




書(shū)目名稱Noncompaction Cardiomyopathy年度引用




書(shū)目名稱Noncompaction Cardiomyopathy年度引用學(xué)科排名




書(shū)目名稱Noncompaction Cardiomyopathy讀者反饋




書(shū)目名稱Noncompaction Cardiomyopathy讀者反饋學(xué)科排名

性行為放縱者

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.

廣口瓶

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

詞根詞綴法

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.

鴿子

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.

分開(kāi)如此和諧

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.

冷淡周邊

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