Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
作者信息
Szczesna-Cordary Danuta, Morimoto Sachio, Gomes Aldrin V, Moore Jeffrey R
机构信息
Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
出版信息
Biochem Res Int. 2012;2012:870942. doi: 10.1155/2012/870942. Epub 2012 Dec 4.
Abstract
摘要
相似文献
1
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.心肌病：分类、临床特征及功能表型
Biochem Res Int. 2012;2012:870942. doi: 10.1155/2012/870942. Epub 2012 Dec 4.
2
The MOGE(S) classification for cardiomyopathies: current status and future outlook.心肌疾病的 MOGE(S)分类：现状与展望。
Heart Fail Rev. 2017 Nov;22(6):743-752. doi: 10.1007/s10741-017-9641-4.
3
[Classification of cardiomyopathy].[心肌病的分类]
Masui. 2014 Jan;63(1):5-15.
4
Defining phenotypes and disease progression in sarcomeric cardiomyopathies: contemporary role of clinical investigations.定义肌原性心肌病的表型和疾病进展：临床研究的当代作用。
Cardiovasc Res. 2015 Apr 1;105(4):409-23. doi: 10.1093/cvr/cvv024. Epub 2015 Jan 28.
5
Cardiac Magnetic Resonance in Nonischemic Cardiomyopathies.非缺血性心肌病的心脏磁共振成像
Methodist Debakey Cardiovasc J. 2020 Apr-Jun;16(2):97-105. doi: 10.14797/mdcj-16-2-97.
6
Sex differences in cardiomyopathies.心肌疾病中的性别差异。
Eur J Heart Fail. 2014 Mar;16(3):238-47. doi: 10.1002/ejhf.15. Epub 2014 Jan 16.
7
Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases.心肌病的诊断检查：弥合临床表型与最终诊断之间的差距。ESC 心肌和心包疾病工作组的立场声明。
Eur Heart J. 2013 May;34(19):1448-58. doi: 10.1093/eurheartj/ehs397. Epub 2012 Dec 4.
8
[Cardiac magnetic resonance imaging in evaluation of cardiomyopathies].[心脏磁共振成像在心肌病评估中的应用]
Ugeskr Laeger. 2018 Sep 3;180(36).
9
[Classification of cardiomyopathies and indication for endomyocardial biopsy revisited].[心肌病的分类及心内膜心肌活检指征再探讨]
Herz. 2009 Feb;34(1):55-62. doi: 10.1007/s00059-009-3195-8.
10
The MOGE(S) classification : A TNM-like classification for cardiomyopathies.MOGE(S) 分类：一种类似于TNM的心肌病分类方法。
Herz. 2016 Sep;41(6):503-6. doi: 10.1007/s00059-015-4394-0. Epub 2016 Jan 25.
引用本文的文献
1
Molecular mechanisms of cardiomyopathy phenotypes associated with myosin light chain mutations.与肌球蛋白轻链突变相关的心肌病表型的分子机制
J Muscle Res Cell Motil. 2015 Dec;36(6):433-45. doi: 10.1007/s10974-015-9423-3. Epub 2015 Sep 18.
2
Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain.肌球蛋白轻链2（MYL2）中的新型家族性扩张型心肌病突变影响肌球蛋白调节轻链的结构和功能。
FEBS J. 2015 Jun;282(12):2379-93. doi: 10.1111/febs.13286. Epub 2015 Apr 16.
3
Tropomyosin is required for cardiac morphogenesis, myofibril assembly, and formation of adherens junctions in the developing mouse embryo.原肌球蛋白对于发育中的小鼠胚胎的心脏形态发生、肌原纤维组装和黏着连接的形成是必需的。
Dev Dyn. 2014 Jun;243(6):800-17. doi: 10.1002/dvdy.24115. Epub 2014 Feb 24.
Zotero 插件