作者: hematuria 時(shí)間: 2025-3-21 21:24 作者: meretricious 時(shí)間: 2025-3-22 02:38
Idiopathic Right Ventricular Outflow Tract Tachycardia,normal heart (idiopathic VT). However, it is also a focus of arrhythmias due to arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D). These two conditions can be easily confused, especially if myocardial abnormalities are mild or minimal as in patients with ARVC/D in its early stage [.].作者: 豐富 時(shí)間: 2025-3-22 07:00 作者: 躲債 時(shí)間: 2025-3-22 09:09 作者: abject 時(shí)間: 2025-3-22 15:50
https://doi.org/10.1007/978-88-470-0490-0Ablation; angiography; biopsy; cell; echocardiography; genes; genetics; heart; human genetics; radiology作者: syring 時(shí)間: 2025-3-22 20:39 作者: expdient 時(shí)間: 2025-3-22 23:37 作者: 誤傳 時(shí)間: 2025-3-23 02:34 作者: Inflated 時(shí)間: 2025-3-23 06:55 作者: 魅力 時(shí)間: 2025-3-23 11:04
The Cathedral of French Sciencetricular arrhythmias, heart failure, and sudden death [., .]. The pathological process consists of progressive loss of ventricular myocardium with fibrofatty replacement [.]. The right ventricle is mostly involved [.] but presentation of disease with predominantly left ventricular involvement has been recently reported [.].作者: ostracize 時(shí)間: 2025-3-23 13:54 作者: Cloudburst 時(shí)間: 2025-3-23 18:50
The Cathedral of French Sciencemajor advancements in the basic knowledge of the disease as well as a better understanding of the diagnosis and treatment. A workshop was held in Venice, Italy on October 3, 2005, where research on various aspects of this disease, both biological and clinical was presented.作者: agonist 時(shí)間: 2025-3-24 00:16
Metro-Goldwyn-Mayer Meets the Atom Bomb“silent” cardiomyopathic abnormalities localized in the right ventricle in asymptomatic victims of sudden death; (b) “overt” disease characterized by segmental or global right ventricular structural changes, often associated with histological evidence of left ventricular involvement and underlying s作者: 直覺好 時(shí)間: 2025-3-24 05:49 作者: 吊胃口 時(shí)間: 2025-3-24 09:38
Metro-Goldwyn-Mayer Meets the Atom Bombasing number of subjects, providing better knowledge of the diagnostic criteria, natural history, and ethiopathogenesis of the disease. Three different groups of genes have been found to be linked to ARVC/D: the ryanodine receptor-2 gene (RyR2), the gene encoding for the growth factor TGFbeta 3 and 作者: 隱藏 時(shí)間: 2025-3-24 14:38
The Cathedral of French Scienceracterized by progressive fibrofatty replacement of right ventricular myocardium, initially with typical regional and later global right and some left ventricular involvement, with relative sparing of the septum [.]. The residual myocytes interspersed among adipocytes and fibrous tissue provides the作者: TOM 時(shí)間: 2025-3-24 15:01 作者: 招募 時(shí)間: 2025-3-24 20:26
Exposure Routes of Environmental Toxicants,early in the course of disease with later-onset left ventricular (LV) disease [.]. Clinically, the disease is classically characterized by ventricular arrhythmias of RV origin, as noted by ventricular tachycardia (VT) with a left bundle branch block (LBBB) morphology, commonly associated with syncop作者: 付出 時(shí)間: 2025-3-25 03:02 作者: 四牛在彎曲 時(shí)間: 2025-3-25 03:50 作者: 他一致 時(shí)間: 2025-3-25 09:51
Benedikt Cramer,Hans-Ulrich Humpfs arising from the right ventricle in the presence of subtle or diffuse morphological changes [.–.]. Histologically the condition is characterized by myocyte loss with fatty or fibrofatty replacement [.]. The reclassification of cardiomyopathies by the World Health Organization/International Society作者: 慌張 時(shí)間: 2025-3-25 12:40 作者: 館長 時(shí)間: 2025-3-25 17:00
https://doi.org/10.1007/978-3-319-61688-9normal heart (idiopathic VT). However, it is also a focus of arrhythmias due to arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D). These two conditions can be easily confused, especially if myocardial abnormalities are mild or minimal as in patients with ARVC/D in its early stage [.作者: 場所 時(shí)間: 2025-3-25 22:10 作者: 貪心 時(shí)間: 2025-3-26 01:50
Carla Viegas,Susana Viegas,Raquel Sabino. Global or regional abnormalities of right ventricular (RV) structure and function are an important component of the Task Force of the Working Group on Cardiomyopathies diagnostic criteria [.]. The criterion for RV structure and function currently lacks quantitative cut points for clinicians to use作者: 花費(fèi) 時(shí)間: 2025-3-26 04:52 作者: Ischemia 時(shí)間: 2025-3-26 09:53
Science Networks. Historical Studiescture and function and ventricular tachyarrhythmias including sudden death [., .]. It is an inheritable cardiomyopathy predominantly affecting the myocardium of the RV free wall. Progressive atrophy and loss of myocytes with subsequent fatty and/or fibrous tissue replacement and interspersed survivi作者: 誘導(dǎo) 時(shí)間: 2025-3-26 14:07
https://doi.org/10.1007/3-7643-7593-0V) involvement and risk of arrhythmic sudden death [.–.]. Distinctive pathologic feature is RV myocardial atrophy with replacement by fibrofatty tissue [.–.]. The condition was initially believed to be a developmental defect of the RV myocardium, leading to the original designation of “dysplasia” [.作者: 連鎖,連串 時(shí)間: 2025-3-26 19:44
https://doi.org/10.1007/3-7643-7593-0ients and athletes with apparently normal hearts. The disease is characterized by localized or diffuse atrophy of predominantly right ventricular myocardium with subsequent replacement by fatty and fibrous tissue. As a result of these pathomorphological alterations, global and regional right (and le作者: languid 時(shí)間: 2025-3-27 00:33 作者: Suggestions 時(shí)間: 2025-3-27 04:09 作者: aptitude 時(shí)間: 2025-3-27 07:30
Carla Viegas,Susana Viegas,Raquel Sabinoily members of affected individuals or those who may have a subclinical form of the disease, is limited by the lack of a gold standard for the diagnosis of ARVC/D. Additionally, the echocardiographic natural history of the disease has not yet been defined.作者: 出沒 時(shí)間: 2025-3-27 10:05
Advances in Genetics: Dominant Forms,ilure and eventually requiring heart transplantation [.]. A scoring system to establish the diagnosis of ARVC/D has been developed on the basis of the presence of major and minor criteria encompassing structural, histological, electrocardiographic, arrhythmic, and genetic features of the disease [.].作者: 流出 時(shí)間: 2025-3-27 16:29
Genotype-Phenotype Correlations,all these genes lead to the pathogenetic process that is the basis of the disease, consisting of myocyte death followed by myocardial atrophy and fibrofatty replacement [., .] (Fig. 3.1). These discoveries have confirmed the genetic heterogeneity of ARVC/D [.].作者: Wordlist 時(shí)間: 2025-3-27 18:55
Echocardiography,ily members of affected individuals or those who may have a subclinical form of the disease, is limited by the lack of a gold standard for the diagnosis of ARVC/D. Additionally, the echocardiographic natural history of the disease has not yet been defined.作者: 窩轉(zhuǎn)脊椎動物 時(shí)間: 2025-3-27 23:10
Possible Causative or Contributing Role of Viruses,d and shown to be a disease of the desmosome [.]. Mutations in desmoplakin, plakoglobin, plakophilin, desmoglein, and desmocollin have been identified, along with the desmosome modifying gene TGF-β3 [.–.].作者: 公社 時(shí)間: 2025-3-28 05:10 作者: 存在主義 時(shí)間: 2025-3-28 08:08 作者: INCH 時(shí)間: 2025-3-28 13:03
https://doi.org/10.1007/3-7643-7593-0ardium with subsequent replacement by fatty and fibrous tissue. As a result of these pathomorphological alterations, global and regional right (and left) ventricular dysfunction and ventricular tachyarrhythmias due to areas of slow conduction and dispersion of refractoriness are the major clinical findings and manifestations of ARVC/D [.–.].作者: MILK 時(shí)間: 2025-3-28 17:47 作者: modish 時(shí)間: 2025-3-28 21:43
Benedikt Cramer,Hans-Ulrich Humpfar involvement, with relative sparing of the septum. Familial disease is common, with autosomal dominant inheritance and incomplete penetrance; a recessive form is described. Presentation with arrhythmias and sudden death is common, particularly in the young” [.].作者: Flawless 時(shí)間: 2025-3-29 01:56 作者: 伸展 時(shí)間: 2025-3-29 04:03 作者: 盤旋 時(shí)間: 2025-3-29 09:17
Book 20071st edition muscle d- ease which is a major threat to the life of affected young people. It summarizes ne- ly 25 years of investigation on the etiology, genetics, pathology, clinical features, - agnosis, and treatment of ARVC/D. In particular, a 5-year research program supported by grants from both the Europea作者: 征服 時(shí)間: 2025-3-29 11:58 作者: 關(guān)節(jié)炎 時(shí)間: 2025-3-29 17:13
Science Networks. Historical Studiesng myocyte fibers provide the morphological substrate for re-entrant arrhythmias and regional (segmental) or global (diffuse) abnormalities of RV structure and function. In the advanced stages of ARVC/D, clinical signs of right or global heart failure and left ventricular (LV) involvement may develop [.].作者: Spongy-Bone 時(shí)間: 2025-3-29 21:12
Introduction: Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Clarified,major advancements in the basic knowledge of the disease as well as a better understanding of the diagnosis and treatment. A workshop was held in Venice, Italy on October 3, 2005, where research on various aspects of this disease, both biological and clinical was presented.作者: Pulmonary-Veins 時(shí)間: 2025-3-30 00:01 作者: TEM 時(shí)間: 2025-3-30 05:18 作者: 使迷惑 時(shí)間: 2025-3-30 09:43
Genotype-Phenotype Correlations,asing number of subjects, providing better knowledge of the diagnostic criteria, natural history, and ethiopathogenesis of the disease. Three different groups of genes have been found to be linked to ARVC/D: the ryanodine receptor-2 gene (RyR2), the gene encoding for the growth factor TGFbeta 3 and 作者: 修正案 時(shí)間: 2025-3-30 15:18
Autopsy and Endomyocardial Biopsy Findings,racterized by progressive fibrofatty replacement of right ventricular myocardium, initially with typical regional and later global right and some left ventricular involvement, with relative sparing of the septum [.]. The residual myocytes interspersed among adipocytes and fibrous tissue provides the作者: 壓迫 時(shí)間: 2025-3-30 18:07 作者: Coterminous 時(shí)間: 2025-3-30 22:37 作者: Dysplasia 時(shí)間: 2025-3-31 02:02 作者: 鄙視讀作 時(shí)間: 2025-3-31 07:14
Possible Causative or Contributing Role of Viruses, of the right ventricle and clinically by life-threatening ventricular arrhythmias in apparently healthy people [.]. The disease results in a high risk of sudden death, particularly in young people [.] and athletes [.]. Over the past several years, the genetic basis of this disease has been unravele作者: CERE 時(shí)間: 2025-3-31 12:15 作者: 保全 時(shí)間: 2025-3-31 16:29 作者: 多骨 時(shí)間: 2025-3-31 18:58 作者: 瑣碎 時(shí)間: 2025-4-1 00:22
Electrocardiographic Manifestations,cardiomyopathy/dysplasia (ARVC/D) [.–.]. Typically, ARVC/D is considered in a young or middle-aged individual with a history of ventricular arrhythmias who does not have evidence of ischemic heart disease. The suspicion of ARVC/D is increased if the standard 12-lead ECG shows features suggestive of 作者: 可耕種 時(shí)間: 2025-4-1 04:04
Echocardiography,. Global or regional abnormalities of right ventricular (RV) structure and function are an important component of the Task Force of the Working Group on Cardiomyopathies diagnostic criteria [.]. The criterion for RV structure and function currently lacks quantitative cut points for clinicians to use作者: 柔美流暢 時(shí)間: 2025-4-1 07:30
MR and CT Imaging,ricle (RV), which leads to progressive RV failure and ventricular arrhythmias [., .]. The disease presents between the second and fifth decades of life either with symptoms of palpitations and/or syncope associated with ventricular tachycardia or with SCD. The exact prevalence of this condition is n作者: right-atrium 時(shí)間: 2025-4-1 11:31
Diagnostic Role of Angiography,cture and function and ventricular tachyarrhythmias including sudden death [., .]. It is an inheritable cardiomyopathy predominantly affecting the myocardium of the RV free wall. Progressive atrophy and loss of myocytes with subsequent fatty and/or fibrous tissue replacement and interspersed survivi作者: 鉤針織物 時(shí)間: 2025-4-1 17:32
