• 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

相似文献

1
Editorial: Cardiovascular genetics-focus on paediatric cardiomyopathy.社论：心血管遗传学——聚焦小儿心肌病
Front Pediatr. 2023 Feb 10;11:1147527. doi: 10.3389/fped.2023.1147527. eCollection 2023.
2
Genetics of hypertrophic and dilated cardiomyopathy.肥厚型心肌病和扩张型心肌病的遗传学。
Curr Pharm Biotechnol. 2012 Oct;13(13):2467-76. doi: 10.2174/138920112804583041.
3
Epidemiology of cardiomyopathies in children and adolescents: a retrospective study over the last 10 years.儿童和青少年心肌病的流行病学：过去10年的回顾性研究
Cardiol Young. 2002 May;12(3):253-9. doi: 10.1017/s1047951102000550.
4
An Update on Pediatric Cardiomyopathy.小儿心肌病的最新进展
Curr Treat Options Cardiovasc Med. 2019 Jun 25;21(8):36. doi: 10.1007/s11936-019-0739-y.
5
[Genetics of inherited cardiomyopathies].[遗传性心肌病的遗传学]
Pathol Biol (Paris). 2010 Oct;58(5):343-52. doi: 10.1016/j.patbio.2009.10.010. Epub 2009 Nov 25.
6
Ventricular assist device support in paediatric patients with restrictive cardiomyopathy-clinical outcomes and haemodynamics.心室辅助装置在限制型心肌病儿科患者中的应用-临床结果和血液动力学。
Eur J Cardiothorac Surg. 2024 Aug 2;66(2). doi: 10.1093/ejcts/ezae277.
7
Restrictive left ventricular filling pattern in dilated cardiomyopathy assessed by Doppler echocardiography: clinical, echocardiographic and hemodynamic correlations and prognostic implications. Heart Muscle Disease Study Group.通过多普勒超声心动图评估扩张型心肌病中的限制性左心室充盈模式：临床、超声心动图及血流动力学相关性和预后意义。心肌疾病研究组
J Am Coll Cardiol. 1993 Sep;22(3):808-15. doi: 10.1016/0735-1097(93)90195-7.
8
Left Bundle Pacing for Left Bundle Branch Block and Intermittent Third-Degree Atrioventricular Block in a Mutation-Related Hypertrophic Cardiomyopathy With Restrictive Phenotype in a Child.儿童突变相关肥厚型心肌病伴限制性表型合并左束支传导阻滞和间歇性三度房室传导阻滞的左束支起搏治疗
Front Pediatr. 2020 Jun 16;8:312. doi: 10.3389/fped.2020.00312. eCollection 2020.
9
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies.肥厚型心肌病与原发性限制型心肌病：异同与表型模拟
J Clin Med. 2021 May 1;10(9):1954. doi: 10.3390/jcm10091954.
10
Desmin mutations in a St. Petersburg cohort of cardiomyopathies.圣彼得堡心肌病队列中的结蛋白突变
Acta Myol. 2006 Dec;25(3):109-15.

本文引用的文献

1
Highly malignant disease in childhood-onset arrhythmogenic right ventricular cardiomyopathy.儿童起病型心律失常性右室心肌病的高度恶性疾病。
Eur Heart J. 2022 Dec 1;43(45):4694-4703. doi: 10.1093/eurheartj/ehac485.
2
[Clinical pathway on pediatric cardiomyopathies: a genetic testing strategy proposed by the Italian Society of Pediatric Cardiology].
G Ital Cardiol (Rome). 2022 Jul;23(7):505-515. doi: 10.1714/3831.38168.
3
Diagnosis and Management of Rare Cardiomyopathies in Adult and Paediatric Patients. A Position Paper of the Italian Society of Cardiology (SIC) and Italian Society of Paediatric Cardiology (SICP).成人和儿科患者罕见心肌病的诊断和管理。意大利心脏病学会（SIC）和意大利儿科心脏病学会（SICP）的立场文件。
Int J Cardiol. 2022 Jun 15;357:55-71. doi: 10.1016/j.ijcard.2022.03.050. Epub 2022 Mar 30.
4
Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options.线粒体 DNA 疾病相关心血管表现：诊断、管理和治疗选择。
Heart Fail Clin. 2022 Jan;18(1):51-60. doi: 10.1016/j.hfc.2021.07.003. Epub 2021 Oct 26.
5
Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia.Friedreich 共济失调的心血管受累的诊断和管理。
Heart Fail Clin. 2022 Jan;18(1):31-37. doi: 10.1016/j.hfc.2021.07.001. Epub 2021 Oct 25.
6
Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management.RAS 相关疾病中的肥厚型心肌病：诊断、临床特征、预后意义和管理。
Heart Fail Clin. 2022 Jan;18(1):19-29. doi: 10.1016/j.hfc.2021.07.004. Epub 2021 Oct 25.
7
Advanced Heart Failure in Special Population-Pediatric Age.特殊人群中的心力衰竭：儿科年龄。
Heart Fail Clin. 2021 Oct;17(4):673-683. doi: 10.1016/j.hfc.2021.05.011. Epub 2021 Jul 22.
8
2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.2020年美国心脏协会/美国心脏病学会肥厚型心肌病患者诊断和治疗指南：美国心脏病学会/美国心脏协会临床实践指南联合委员会报告
Circulation. 2020 Dec 22;142(25):e558-e631. doi: 10.1161/CIR.0000000000000937. Epub 2020 Nov 20.
9
Noncoding RNAs in Cardiovascular Disease: Current Knowledge, Tools and Technologies for Investigation, and Future Directions: A Scientific Statement From the American Heart Association.非编码 RNA 在心血管疾病中的作用：当前的研究知识、工具和技术，以及未来的方向：美国心脏协会的科学声明。
Circ Genom Precis Med. 2020 Aug;13(4):e000062. doi: 10.1161/HCG.0000000000000062. Epub 2020 Jun 29.
10
Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy.肥厚型心肌病患者中“红旗”征象的流行率及临床意义。
Int J Cardiol. 2020 Jan 15;299:186-191. doi: 10.1016/j.ijcard.2019.06.073. Epub 2019 Jul 4.

Editorial: Cardiovascular genetics-focus on paediatric cardiomyopathy.

作者信息

Monda Emanuele, Kaski Juan Pablo, Limongelli Giuseppe

机构信息

Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, Naples, Italy.

Centre for Paediatric Inherited and Rare Cardiovascular Disease, Institute of Cardiovascular Science, University College London, London, United Kingdom.

出版信息

Front Pediatr. 2023 Feb 10;11:1147527. doi: 10.3389/fped.2023.1147527. eCollection 2023.

DOI:10.3389/fped.2023.1147527
PMID:36846159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9950774/
Abstract
摘要