Background Prognosis of hypertrophic cardiomyopathy (HCM) is particularly heterogeneous. Patients with nonobstructive HCM (NOCM) are thought to be at relatively low-risk as compared with obstructive HCM (HOCM) with no need of major treatment options. However, available evidence of NOCM comes mainly from tertiary centers where a referral bias is likely to occur. Aim of this study was to perform a systematic review and meta-analysis of the published literature on hypertrophic cardiomyopathy (HCM) in order to outline differences in presenting features and long-term outcome between NOCM and HOCM. Methods MEDLINE/Pubmed, EMBASE and Cochrane databases up to December 31, 2016, and reviewed cited references to identify relevant studies were used. T...
Aim. Based on the results of a long-term follow-up, to determine the clinical variants of hype...
Background-\u2014Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disease characteriz...
Patients with hypertrophic cardiomyopathy (HC) are reported to have a mortality rate of about 1.0% p...
Background Prognosis of hypertrophic cardiomyopathy (HCM) is particularly heterogeneous. Patients wi...
BACKGROUND: Prognosis of hypertrophic cardiomyopathy (HCM) is particularly heterogeneous. Patients w...
ObjectivesThe purpose of this study was to characterize the prognosis of minimally symptomatic patie...
Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disease characterized by varying deg...
Patients with nonobstructive hypertrophic cardiomyopathy (HC) are considered low risk, generally not...
textabstractOverall annual cardiac mortality in hypertrophic cardiomyopathy (HC) has been reported t...
AbstractObjectivesThis study was designed to clarify and resolve the clinical profile of older patie...
Abstract Aims We aim to clarify the prognosis on patients with hypertrophic cardiomyopathy (HCM) for...
Background: Patients with hypertrophic cardiomyopathy (HCM) are generally regarded as having increas...
ObjectivesThe aim of this study was to compare the survival of patients with hypertrophic cardiomyop...
Background: Despite hypertrophic cardiomyopathy (HCM) being the most common inherited heart disease ...
AbstractBackgroundHypertrophic cardiomyopathy (HCM) has been prominently associated with adverse dis...
Aim. Based on the results of a long-term follow-up, to determine the clinical variants of hype...
Background-\u2014Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disease characteriz...
Patients with hypertrophic cardiomyopathy (HC) are reported to have a mortality rate of about 1.0% p...
Background Prognosis of hypertrophic cardiomyopathy (HCM) is particularly heterogeneous. Patients wi...
BACKGROUND: Prognosis of hypertrophic cardiomyopathy (HCM) is particularly heterogeneous. Patients w...
ObjectivesThe purpose of this study was to characterize the prognosis of minimally symptomatic patie...
Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disease characterized by varying deg...
Patients with nonobstructive hypertrophic cardiomyopathy (HC) are considered low risk, generally not...
textabstractOverall annual cardiac mortality in hypertrophic cardiomyopathy (HC) has been reported t...
AbstractObjectivesThis study was designed to clarify and resolve the clinical profile of older patie...
Abstract Aims We aim to clarify the prognosis on patients with hypertrophic cardiomyopathy (HCM) for...
Background: Patients with hypertrophic cardiomyopathy (HCM) are generally regarded as having increas...
ObjectivesThe aim of this study was to compare the survival of patients with hypertrophic cardiomyop...
Background: Despite hypertrophic cardiomyopathy (HCM) being the most common inherited heart disease ...
AbstractBackgroundHypertrophic cardiomyopathy (HCM) has been prominently associated with adverse dis...
Aim. Based on the results of a long-term follow-up, to determine the clinical variants of hype...
Background-\u2014Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disease characteriz...
Patients with hypertrophic cardiomyopathy (HC) are reported to have a mortality rate of about 1.0% p...