找回密碼
 To register

QQ登錄

只需一步,快速開(kāi)始

掃一掃,訪問(wèn)微社區(qū)

打印 上一主題 下一主題

Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Textbook 2020Latest edition Springer Nature Switzerland AG 202

[復(fù)制鏈接]
查看: 47336|回復(fù): 58
樓主
發(fā)表于 2025-3-21 18:34:29 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Clinical Cardiogenetics
編輯Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete
視頻videohttp://file.papertrans.cn/228/227837/227837.mp4
概述Represents 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
圖書(shū)封面Titlebook: Clinical Cardiogenetics;  Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Textbook 2020Latest edition Springer Nature Switzerland AG 202
描述.This thoroughly revised third edition provides a comprehensive grounding on hereditary heart diseases with special emphasis on the genetic aspects of 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 cardiomyopathies, the primary arrhythmia syndromes and the hereditary thoracic aortic disorders. In addition other topics such as cardiac involvement in hereditary neuromuscular diseases, the clinical policy for sudden cardiac death and the possibilities of pre-implantation genetic diagnosis are included to extend the discussion.?.Clinical Cardiogenetics. compiles current knowledge on the topic in an easy to understand reference. It provides a practical clinical primer for cardiologists, clinical geneticists, trainees and other physicians involved in the management of these patients..
出版日期Textbook 2020Latest edition
關(guān)鍵詞Hypertrophic cardiomyopathy; Short QT-syndrome; Brugada syndrome; Sudden cardiac death; Congenital heart
版次3
doihttps://doi.org/10.1007/978-3-030-45457-9
isbn_softcover978-3-030-45459-3
isbn_ebook978-3-030-45457-9
copyrightSpringer Nature Switzerland AG 2020
The information of publication is updating

書(shū)目名稱(chēng)Clinical Cardiogenetics影響因子(影響力)




書(shū)目名稱(chēng)Clinical Cardiogenetics影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Clinical Cardiogenetics網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)Clinical Cardiogenetics網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)Clinical Cardiogenetics被引頻次




書(shū)目名稱(chēng)Clinical Cardiogenetics被引頻次學(xué)科排名




書(shū)目名稱(chēng)Clinical Cardiogenetics年度引用




書(shū)目名稱(chēng)Clinical Cardiogenetics年度引用學(xué)科排名




書(shū)目名稱(chēng)Clinical Cardiogenetics讀者反饋




書(shū)目名稱(chēng)Clinical Cardiogenetics讀者反饋學(xué)科排名




單選投票, 共有 0 人參與投票
 

0票 0%

Perfect with Aesthetics

 

0票 0%

Better Implies Difficulty

 

0票 0%

Good and Satisfactory

 

0票 0%

Adverse Performance

 

0票 0%

Disdainful Garbage

您所在的用戶組沒(méi)有投票權(quán)限
沙發(fā)
發(fā)表于 2025-3-21 20:13:22 | 只看該作者
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
板凳
發(fā)表于 2025-3-22 00:44:09 | 只看該作者
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
地板
發(fā)表于 2025-3-22 06:56:24 | 只看該作者
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
5#
發(fā)表于 2025-3-22 10:32:44 | 只看該作者
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
6#
發(fā)表于 2025-3-22 14:50:46 | 只看該作者
7#
發(fā)表于 2025-3-22 19:49:11 | 只看該作者
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
8#
發(fā)表于 2025-3-22 22:16:25 | 只看該作者
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
9#
發(fā)表于 2025-3-23 03:50:36 | 只看該作者
10#
發(fā)表于 2025-3-23 06:08:57 | 只看該作者
 關(guān)于派博傳思  派博傳思旗下網(wǎng)站  友情鏈接
派博傳思介紹 公司地理位置 論文服務(wù)流程 影響因子官網(wǎng) 吾愛(ài)論文網(wǎng) 大講堂 北京大學(xué) Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點(diǎn)評(píng) 投稿經(jīng)驗(yàn)總結(jié) SCIENCEGARD IMPACTFACTOR 派博系數(shù) 清華大學(xué) Yale Uni. Stanford Uni.
QQ|Archiver|手機(jī)版|小黑屋| 派博傳思國(guó)際 ( 京公網(wǎng)安備110108008328) GMT+8, 2025-10-16 05:00
Copyright © 2001-2015 派博傳思   京公網(wǎng)安備110108008328 版權(quán)所有 All rights reserved
快速回復(fù) 返回頂部 返回列表
昌黎县| 神农架林区| 昭平县| 资溪县| 高平市| 安义县| 兴业县| 邹城市| 英山县| 涿鹿县| 临西县| 航空| 通州区| 苏州市| 伊金霍洛旗| 灌云县| 黔东| 西畴县| 鹿邑县| 寻甸| 泰宁县| 出国| 乐至县| 土默特左旗| 紫金县| 措勤县| 武邑县| 大埔县| 鄂尔多斯市| 宁波市| 察隅县| 汉源县| 镇雄县| 巴马| 凌海市| 灌南县| 晋江市| 阿拉善右旗| 浦东新区| 杭州市| 阿克|