THE FAMILIAL CARDIOMYOPATHY REGISTRY

家族性心肌病登记处

• 批准号: 7719539
• 负责人: Luisa Mestroni
• 金额: $ 0.05万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-04-01 至 2008-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7719539
• 关键词: Cardiomyopathies; Clinical; Clinical Management; Computer Retrieval of Information on Scientific Projects Database; Defect; Dilated Cardiomyopathy; Disease; Evolution; Funding; Genes; Genetic; Genetic Counseling; Goals; Grant; Heart failure; Institution; Prevention; Registries; Research; Research Personnel; Resources; Source; Sudden Death; United States National Institutes of Health; Ventricular; genetic risk factor; human disease; improved

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The broad, long-term goal of this study is to study and understand the genetic (inherited) factors that can cause heart failure and sudden death. The specific human diseases studied are familial cardiomyopathies. We will analyze the clinical features, the evolution and gene defects causing familial cardiomyopathies (dilated, hypertrophic and right ventricular) to improve the clinical management, prevention and genetic counseling of this diseases.

该副本是利用众多研究子项目之一 由NIH/NCRR资助的中心赠款提供的资源。子弹和 调查员（PI）可能已经从其他NIH来源获得了主要资金， 因此可以在其他清晰的条目中代表。列出的机构是 对于中心，这不一定是调查员的机构。 这项研究的广泛长期目标是研究和了解可能导致心力衰竭和猝死的遗传（遗传）因素。研究的特定人类疾病是家族性心肌病。我们将分析引起家族性心肌病（扩张，肥厚和右心室）的临床特征，进化和基因缺陷，以改善这种疾病的临床管理，预防和遗传咨询。