標題: Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Textbook 2020Latest edition Springer Nature Switzerland AG 202 [打印本頁] 作者: 自治 時間: 2025-3-21 18:34
書目名稱Clinical Cardiogenetics影響因子(影響力)
作者: 使人煩燥 時間: 2025-3-21 20:13
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作者: Antagonist 時間: 2025-3-22 00:44
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作者: 場所 時間: 2025-3-22 06:56
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作者: febrile 時間: 2025-3-22 10:32
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作者: Abjure 時間: 2025-3-22 14:50 作者: Abjure 時間: 2025-3-22 19:49
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 作者: 治愈 時間: 2025-3-22 22:16
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作者: 強壯 時間: 2025-3-23 03:50 作者: 脆弱帶來 時間: 2025-3-23 06:08 作者: SUE 時間: 2025-3-23 12:26
Mitochondrial Cardiomyopathiespresent in the majority of patients with cardiomyopathy, arrhythmias, and conduction defects being the most prevalent. Hypertrophic cardiomyopathy is the most frequently encountered cardiomyopathy in PMD but also dilated cardiomyopathy and left ventricular non-compaction can occur. Cardiac symptoms 作者: ANN 時間: 2025-3-23 14:05 作者: 非實體 時間: 2025-3-23 20:17 作者: Conspiracy 時間: 2025-3-24 00:26 作者: 果仁 時間: 2025-3-24 02:54
Catecholaminergic Polymorphic Ventricularclude polymorphic VT reproducibly induced during exercise test, isoproterenol infusion or emotion and exercise. CPVT occurs in children and adolescents and causes syncope and sudden cardiac death at a young age, in absence of structural heart disease. The resting electrocardiogram (ECG), including t作者: CRAB 時間: 2025-3-24 07:55 作者: Intervention 時間: 2025-3-24 11:27 作者: 黑豹 時間: 2025-3-24 15:21 作者: set598 時間: 2025-3-24 20:45 作者: slow-wave-sleep 時間: 2025-3-25 02:50
https://doi.org/10.1007/978-3-642-20144-8me also involved in other cardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produce a final DCM phenotype. Recommendations on genetic screening and cardiac screening are provided in this chapter.作者: 捐助 時間: 2025-3-25 06:52
https://doi.org/10.1007/978-3-319-54413-7d QT interval (QTc) on the surface electrocardiogram (ECG). This chapter reviews the clinical presentation of LQTS, its diagnosis, and principles of management in the context of recent clinical advances and molecular genetics, with a focus on the most common forms of LQTS—LQT1, LQT2, and LQT3.作者: Canary 時間: 2025-3-25 10:03 作者: 極小量 時間: 2025-3-25 14:08
Dilated Cardiomyopathyme also involved in other cardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produce a final DCM phenotype. Recommendations on genetic screening and cardiac screening are provided in this chapter.作者: 無可爭辯 時間: 2025-3-25 17:31 作者: irreducible 時間: 2025-3-25 23:40 作者: 彎曲道理 時間: 2025-3-26 01:46 作者: 引水渠 時間: 2025-3-26 05:50 作者: 改革運動 時間: 2025-3-26 12:29 作者: 愛管閑事 時間: 2025-3-26 14:00 作者: bizarre 時間: 2025-3-26 16:58 作者: cinder 時間: 2025-3-27 00:24
Representing Position and Orientationditis is important, but can be challenging. RCM can result from an inherited or acquired disease. Besides general supportive measures, treatment of RCM depends on the underlying cause of RCM. In this chapter, several disorders that can manifest as RCM will be addressed in more detail.作者: 出沒 時間: 2025-3-27 03:00
Textbook 2020Latest edition these conditions. It continues to provide the expertise that all cardiologists, clinical and molecular geneticists, and related medical professionals require to provide optimal care for patients with cardiac disease of genetic origin and for their relatives. Topics covered include the different car作者: 來這真柔軟 時間: 2025-3-27 09:10
Restrictive Cardiomyopathyditis is important, but can be challenging. RCM can result from an inherited or acquired disease. Besides general supportive measures, treatment of RCM depends on the underlying cause of RCM. In this chapter, several disorders that can manifest as RCM will be addressed in more detail.作者: thrombosis 時間: 2025-3-27 12:20 作者: 符合你規(guī)定 時間: 2025-3-27 14:09 作者: happiness 時間: 2025-3-27 21:09 作者: elastic 時間: 2025-3-27 22:53 作者: landmark 時間: 2025-3-28 03:29 作者: 閃光東本 時間: 2025-3-28 09:28 作者: 受傷 時間: 2025-3-28 11:49
https://doi.org/10.1007/978-3-642-20144-8with 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 作者: 教義 時間: 2025-3-28 15:18
Representing Position and Orientationincreased 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作者: 流利圓滑 時間: 2025-3-28 20:56 作者: BULLY 時間: 2025-3-29 01:22 作者: cochlea 時間: 2025-3-29 04:11
https://doi.org/10.1007/978-3-319-54413-7present in the majority of patients with cardiomyopathy, arrhythmias, and conduction defects being the most prevalent. Hypertrophic cardiomyopathy is the most frequently encountered cardiomyopathy in PMD but also dilated cardiomyopathy and left ventricular non-compaction can occur. Cardiac symptoms 作者: frenzy 時間: 2025-3-29 10:06 作者: 通知 時間: 2025-3-29 13:43 作者: Anthrp 時間: 2025-3-29 19:11 作者: Rheumatologist 時間: 2025-3-29 21:36 作者: 返老還童 時間: 2025-3-30 01:56
Vladimir Serebrenny,Madin Shereuzhev from sudden cardiac death (SCD). IVF may contain multiple forms by clinical manifestations and possible pathogenetic backgrounds. In this Chapter, IVF is described as two groups: early repolarization syndrome (ERS), and IVF in a narrow sense excluding ERS. Although the early repolarization pattern 作者: 場所 時間: 2025-3-30 05:24
Hubert F. Baars,Pieter A. F. M. Doevendans,J. PeteRepresents a practical cardiac genetics textbook for the clinician and trainee in cardiology.Contains detailed information on disease-causing genes.Features a bench-to-bedside approach to enable reade作者: FRAUD 時間: 2025-3-30 08:43 作者: BROTH 時間: 2025-3-30 16:02
https://doi.org/10.1007/978-3-030-45457-9Hypertrophic cardiomyopathy; Short QT-syndrome; Brugada syndrome; Sudden cardiac death; Congenital heart作者: Spinal-Tap 時間: 2025-3-30 17:31 作者: 膽小鬼 時間: 2025-3-30 23:13
Introduction to Molecular Geneticsenes in Families and Populations” section. Although NGS is becoming the most widely used technique to identify mutations, still several other techniques are being applied, and in the “Molecular Genetic Techniques” section, an overview of all currently used methods is provided. With the use of the af作者: 遺棄 時間: 2025-3-31 01:15 作者: Climate 時間: 2025-3-31 05:57 作者: 冥界三河 時間: 2025-3-31 10:02
Left Ventricular Noncompactione most prevalent disease gene. The nonisolated forms of LVNC are caused by a range of rare genetic defects. Until now, in half of familial isolated LVNC, the genetic defect remains unknown. Genetic defects in a large number of sarcomere and other cardiomyopathy genes and in genes primarily associate作者: 擴張 時間: 2025-3-31 14:59
Metabolic Cardiomyopathyseases..Most IEM are inherited as autosomal recessive traits, however, some highly prevalent diseases with cardiac involvement are X-linked (Anderson Fabry disease, Hunter syndrome—type II mucopolysaccharidosis, Danon disease)..Cardiomyopathies caused by IEM are phenotypically heterogeneous, most of作者: 他很靈活 時間: 2025-3-31 18:03
Cardiac Amyloidosisfailure (often with preserved ejection fraction in its earliest stage), and electrical conduction delay. Recent development of novel therapies to stabilize the protein complexes or diminish the production of pathological proteins has enormous potential to improve outcomes for people with cardiac amy
