• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

勘误:病例报告:遗传性心肌病患者的四例心脏结节病——两种罕见心肌病的表型重叠、共存或二次打击疾病

Corrigendum: Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy-a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease.

作者信息

Ebbinghaus Hans, Ueberham Laura, Husser-Bollmann Daniela, Bollmann Andreas, Paetsch Ingo, Jahnke Cosima, Laufs Ulrich, Dinov Borislav

机构信息

Department for Electrophysiology, Heart Center of Leipzig, Leipzig, Germany.

Klinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, Germany.

出版信息

Front Cardiovasc Med. 2024 Feb 14;11:1372782. doi: 10.3389/fcvm.2024.1372782. eCollection 2024.

DOI:10.3389/fcvm.2024.1372782
PMID:38420265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10899693/
Abstract

[This corrects the article DOI: 10.3389/fcvm.2023.1328802.].

摘要

[本文更正了文章DOI:10.3389/fcvm.2023.1328802。]

相似文献

1
Corrigendum: Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy-a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease.勘误:病例报告:遗传性心肌病患者的四例心脏结节病——两种罕见心肌病的表型重叠、共存或二次打击疾病
Front Cardiovasc Med. 2024 Feb 14;11:1372782. doi: 10.3389/fcvm.2024.1372782. eCollection 2024.
2
Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy-a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease.病例报告:遗传性心肌病患者的四例心脏结节病——两种罕见心肌病的表型重叠、共存或二次打击疾病
Front Cardiovasc Med. 2023 Dec 19;10:1328802. doi: 10.3389/fcvm.2023.1328802. eCollection 2023.
3
Different Phenotypes of Sarcomeric -Cardiomyopathy in the Same Family: Hypertrophic, Left Ventricular Noncompaction and Restrictive Phenotypes (in Association with Sarcoidosis).同一家庭中不同表型的肌节性心肌病:肥厚型、左心室致密化不全和限制型表型(与结节病相关)。
Genes (Basel). 2022 Jul 27;13(8):1344. doi: 10.3390/genes13081344.
4
Do clinical diagnoses correlate with pathological diagnoses in cardiac transplant patients? The importance of endomyocardial biopsy.心脏移植患者的临床诊断与病理诊断相关吗?心内膜心肌活检的重要性。
Can J Cardiol. 2009 Feb;25(2):e48-54. doi: 10.1016/s0828-282x(09)70484-2.
5
Corrigendum: Case Report: Family Curse: An Mutation, c.611C>A, p.A204E Associated With a Family History of Dilated Cardiomyopathy and Arrhythmia.勘误:病例报告:家族诅咒:一种与扩张型心肌病和心律失常家族史相关的突变,c.611C>A,p.A204E
Front Cardiovasc Med. 2022 Jun 15;9:944834. doi: 10.3389/fcvm.2022.944834. eCollection 2022.
6
Outcome of catheter ablation of supraventricular tachyarrhythmias in cardiac sarcoidosis.心脏结节病患者的室上性心动过速导管消融治疗结果。
Clin Cardiol. 2019 Nov;42(11):1121-1125. doi: 10.1002/clc.23263. Epub 2019 Sep 3.
7
Sarcoid heart disease: a rare cause of chest pain and malignant cardiac arrhythmia in a young Asian man. A case report.结节病性心脏病:一名年轻亚洲男性胸痛和恶性心律失常的罕见病因。病例报告。
Angiology. 1996 Sep;47(9):905-10. doi: 10.1177/000331979604700910.
8
[Patterns of delayed-enhancement in MRI of ischemic and non-ischemic cardiomyopathies].[缺血性和非缺血性心肌病的MRI延迟强化模式]
Rofo. 2007 Jan;179(1):21-30. doi: 10.1055/s-2006-927204.
9
Role of genetics in inflammatory cardiomyopathy.遗传学在炎症性心肌病中的作用。
Int J Cardiol. 2024 Apr 1;400:131777. doi: 10.1016/j.ijcard.2024.131777. Epub 2024 Jan 11.
10
Cardiac sarcoidosis and coronary artery disease: a two-hit mechanism to left ventricular dysfunction (or is it)?心脏结节病与冠状动脉疾病:左心室功能障碍的双打击机制(真的是这样吗?)
Sarcoidosis Vasc Diffuse Lung Dis. 2013 Nov 25;30(3):237-40.

引用本文的文献

1
A Unique Case of a Child with Two Rare Hereditary Diseases: Familial Dilated Cardiomyopathy and Arterial Calcification.一名患有两种罕见遗传病的儿童的独特病例:家族性扩张型心肌病和动脉钙化。
Int J Mol Sci. 2025 Jun 19;26(12):5900. doi: 10.3390/ijms26125900.