作者: 傲慢人 時(shí)間: 2025-3-21 21:18
https://doi.org/10.1007/978-3-031-06469-2y prolongation of the heart rate . (QTc) on the 12-lead electrocardiogram (ECG). In affected family members, it is associated with recurrent syncope, seizures, and . due to . (. and .), which typically follow a precipitating event such as exertion, extreme emotion, swimming and diving, or auditory stimulation.作者: instill 時(shí)間: 2025-3-22 04:16 作者: Infusion 時(shí)間: 2025-3-22 05:05
H.F. Baars,P.A.F.M. Doevendans,J.J. van der SmagtPractical cardiac genetics textbook for the clinician.Contains detailed information on disease-causing genes.Bench-to-bedside approach.Includes supplementary material: 作者: 頑固 時(shí)間: 2025-3-22 12:48
http://image.papertrans.cn/c/image/227836.jpg作者: 開始從未 時(shí)間: 2025-3-22 15:35 作者: 開始從未 時(shí)間: 2025-3-22 17:56 作者: expdient 時(shí)間: 2025-3-23 00:29 作者: Epidural-Space 時(shí)間: 2025-3-23 02:21 作者: 步履蹣跚 時(shí)間: 2025-3-23 05:45
Benedikt Kolbeinsson,Krystian Mikolajczyk. is a disease characterized by progressive fibrofatty replacement of primarily the . (RV). .作者: Bridle 時(shí)間: 2025-3-23 11:28
Weapon Detection Using PTZ Cameras,Noncompaction of the left ventricle or . (.) is a relatively new clinicopathologic entity, first described by Feldt et al.作者: 夜晚 時(shí)間: 2025-3-23 17:08
Representing Position and OrientationIn 2000, Gussak et al. described an idiopathic short QT interval associated with atrial fibrillation in a family and sudden death in an unrelated individual. Three years later, in 2003, Gaita et al. reported the association of a short QT interval and sudden cardiac death in two unrelated European families.作者: FIN 時(shí)間: 2025-3-23 20:57 作者: 營養(yǎng) 時(shí)間: 2025-3-23 23:07
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. is a disease characterized by progressive fibrofatty replacement of primarily the . (RV). .作者: 檢查 時(shí)間: 2025-3-24 05:57
Noncompaction CardiomyopathyNoncompaction of the left ventricle or . (.) is a relatively new clinicopathologic entity, first described by Feldt et al.作者: NUL 時(shí)間: 2025-3-24 10:29
Short QT SyndromeIn 2000, Gussak et al. described an idiopathic short QT interval associated with atrial fibrillation in a family and sudden death in an unrelated individual. Three years later, in 2003, Gaita et al. reported the association of a short QT interval and sudden cardiac death in two unrelated European families.作者: 盡管 時(shí)間: 2025-3-24 14:25 作者: 蘆筍 時(shí)間: 2025-3-24 18:26
Joachim von Braun,Heike Baumüllern gathered as a result of the human genome project and large-scale resequencing projects at a rapid pace.. The genetic cause of the vast majority of important monogenic disorders is nowadays known, and more rare disorders are being unraveled quickly. Developments in genomics and sequencing technolog作者: angina-pectoris 時(shí)間: 2025-3-24 19:18
https://doi.org/10.1007/978-3-030-54173-6c aspects of disease. They are specifically trained in communicating the implications of genetic information and genetic disease to patients and their families. In addition, they are trained in syndrome diagnosis and clinical dysmorphology.作者: Calculus 時(shí)間: 2025-3-25 02:57
Ján Chudy,Nestor Popov,Pavel Surynek further study of the disease, and dissections of victims of sudden death revealed bulky hearts. 1 Nowadays, HCM is still a major cause of sudden cardiac death (SCD) in the young, and the most common monogenetic heart disease. . This chapter discusses not only the epidemiology, diagnosis, pathophysi作者: 固執(zhí)點(diǎn)好 時(shí)間: 2025-3-25 03:47 作者: agitate 時(shí)間: 2025-3-25 10:54 作者: padding 時(shí)間: 2025-3-25 13:48
Lecture Notes in Electrical Engineeringof impaired diastolic filling. In the early stages, systolic function may be normal, but when the disease progresses, systolic function usually declines as well. There is an overlap with other types of cardiomyopathy, such as hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), and left 作者: Interstellar 時(shí)間: 2025-3-25 17:47
https://doi.org/10.1007/978-3-031-06469-2y prolongation of the heart rate . (QTc) on the 12-lead electrocardiogram (ECG). In affected family members, it is associated with recurrent syncope, seizures, and . due to . (. and .), which typically follow a precipitating event such as exertion, extreme emotion, swimming and diving, or auditory s作者: admission 時(shí)間: 2025-3-25 20:16 作者: 確定 時(shí)間: 2025-3-26 02:34
Springer Tracts in Advanced Roboticsorphic ventricular tachycardia (VT) and ventricular fibrillation (VF) during physical or emotional stress in structurally normal hearts. This disease is illustrative of the progress that has been made in the field of cardiogenetics in the last decennia.作者: faculty 時(shí)間: 2025-3-26 04:38
Representing Position and Orientationincidental finding within asymptomatic patients to dramatic cases with severe mitral regurgitation, heart failure, bacterial endocarditis, or even sudden cardiac death. Mitral valve prolapse appears to be one of the most common Mendelian cardiovascular abnormalities in humans. This chapter briefly d作者: 爭(zhēng)論 時(shí)間: 2025-3-26 12:17 作者: NATAL 時(shí)間: 2025-3-26 14:47
Representing Position and Orientationden cardiac death. Mitral valve prolapse appears to be one of the most common Mendelian cardiovascular abnormalities in humans. This chapter briefly discusses the epidemiologic aspects of mitral valve prolapse, its pathophysiology, and the current status of genetic knowledge of this intriguing valvular disorder.作者: 加入 時(shí)間: 2025-3-26 20:47
The Genetics of Mitral Valve Prolapseden cardiac death. Mitral valve prolapse appears to be one of the most common Mendelian cardiovascular abnormalities in humans. This chapter briefly discusses the epidemiologic aspects of mitral valve prolapse, its pathophysiology, and the current status of genetic knowledge of this intriguing valvular disorder.作者: PANIC 時(shí)間: 2025-3-26 22:13
Book 20111st editionh a genetic disease. With detailed discussion of the basic science of cardiogenetics in order to assist in the clinical understanding of the topic....The genetic causes of various cardiovascular diseases are explained in a concise clinical way that reinforces the current management doctrine in a pra作者: 機(jī)密 時(shí)間: 2025-3-27 04:31 作者: 大雨 時(shí)間: 2025-3-27 07:32
Hypertrophic Cardiomyopathyology, and therapy of HCM but also deals with topics specific for cardiogenetic diseases like the genetic background, risk stratification for SCD, and the screening strategies in HCM families. It is intended to be of help for all involved in the care for HCM patients and their families.作者: 肥料 時(shí)間: 2025-3-27 12:49
Restrictive Cardiomyopathyventricular noncompaction. Indeed, an autosomal dominantly segregating cardiomyopathy has been described where a single sarcomere gene mutation caused idiopathic RCM in some and HCM in other family members. 1作者: Ingratiate 時(shí)間: 2025-3-27 13:40 作者: 豐滿有漂亮 時(shí)間: 2025-3-27 20:34
Ján Chudy,Nestor Popov,Pavel Surynekology, and therapy of HCM but also deals with topics specific for cardiogenetic diseases like the genetic background, risk stratification for SCD, and the screening strategies in HCM families. It is intended to be of help for all involved in the care for HCM patients and their families.作者: ectropion 時(shí)間: 2025-3-27 22:00 作者: corpuscle 時(shí)間: 2025-3-28 05:32 作者: paltry 時(shí)間: 2025-3-28 09:42 作者: vitreous-humor 時(shí)間: 2025-3-28 12:59 作者: Exposition 時(shí)間: 2025-3-28 16:46
The Brugada Syndromesease, but remaining questions still propel today a large research activity on the subject. This chapter reviews the current knowledge on clinical, genetic, and molecular features of the Brugada syndrome, and provides updated information supplied by recent clinical and basic studies.作者: catagen 時(shí)間: 2025-3-28 20:23
a table describing the genes involved in each. Each chapter will also contain specific illustrations, cumulatively giving a complete, practical review of each cardiogenetic disea978-1-4471-5703-8978-1-84996-471-5作者: Carcinogenesis 時(shí)間: 2025-3-28 23:40
A Molecular Genetic Perspective on Atrial Fibrillation作者: Parley 時(shí)間: 2025-3-29 07:05 作者: 背帶 時(shí)間: 2025-3-29 09:55
https://doi.org/10.1007/978-3-031-19650-8 the function of a number of proteins encoded by candidate genes is still unknown. To date, over 20 genes have been shown to play a pivotal role in the origin of DCM. This diversity of genetic etiologies in DCM explains why patients sometimes exhibit additional clinical manifestations, including def作者: 繁忙 時(shí)間: 2025-3-29 11:36 作者: 大約冬季 時(shí)間: 2025-3-29 18:25 作者: 開始沒有 時(shí)間: 2025-3-29 20:00 作者: 迷住 時(shí)間: 2025-3-30 00:16
