NSTL国家科技图书文献中心

1. Standardizing Histopathological Evaluation of Resected Myocardium in Obstructive Hypertrophic Cardiomyopathy NSTL国家科技图书文献中心

Ahmad Masri - 《JACC..Heart failure.》 - 2025,13(4) - 641～643 - 共3页

摘要：The modern description of hypertrophic | cardiomyopathy (HCM) was prompted by histopathological | evaluation of a series of patients who died suddenly.1 In | 1958, Donald Teare1 published his seminal paper on 8 | patients who had sudden death and severe asymmetric

关键词： histology; hypertrophic cardiomyopathy; myectomy; myocytes

2. Apical Hypertrophic Cardiomyopathy: Diagnosis, Natural History, and Management NSTL国家科技图书文献中心

Rouskas, Pavlos | Katranas, Sotiris ... - 《Cardiology in review.》 - 2025,33(1) - 58～63 - 共6页

摘要：Apical hypertrophic* cardiomyopathy (ApHCM* | ) represents a rare variant of hypertrophic cardiomyopathy | (HCM) with distinct phenotypic characteristics. The | prevalence of this variant varies according to each study's | geographic region. The leading imaging modality for the

关键词： apical | diagnosis | hypertrophic cardiomyopathy | natural history | prognosis

3. Medical, Surgical, and Interventional Management of Hypertrophic Cardiomyopathy NSTL国家科技图书文献中心

Massera, Daniele | Sherrid, Mark V.... - 《Circulation..Cardiovascular interventions.》 - 2025,18(3) - e014023～e014023 - 共11页

摘要：Hypertrophic cardiomyopathy is a common but | arrhythmia. Hypertrophic* cardiomyopathy is often heritable* | hypertrophic cardiomyopathy with negative inotropic therapy | practical overview of important topics in hypertrophic | cardiomyopathy, including evaluation of differential diagnosis

关键词： adults | cardiac surgery | humans | hypertrophic cardiomyopathy | ventricular outflow obstruction

4. Endpoint Selection in Randomized Clinical Trials for Hypertrophic Cardiomyopathy NSTL国家科技图书文献中心

Aimo, Alberto | Olivotto, Iacopo ... - 《JACC..Heart failure.》 - 2025,13(2) - 200～212 - 共13页

摘要： hypertrophic cardiomyopathy (HCM) have long been challenging | Randomized clinical trials (RCTs) for | caused by the condition's rarity, low event rates, and | diverse clinical presentations. However, recent advances | in targeted therapies have sparked increased

关键词： endpoint | HCM | hypertrophic cardiomyopathy | study design | trial

5. Hypertrophic cardiomyopathy overview: Genetics, screening, and treatment NSTL国家科技图书文献中心

Smania, Mary Alison - 《Journal of the American Association of Nurse Practitioners.》 - 2025,37(3) - 142～144 - 共3页

摘要：Hypertrophic cardiomyopathy (HCM) is a common | obstruction. Hypertrophic* cardiomyopathy results from* | genetic cardiac disorder marked by unexplained | asymmetrical left ventricular wall thickening. This condition | exhibits histopathological hallmarks including enlarged

关键词： Cardiomyopathy | genetic | hypertrophic | sudden cardiac death

6. Beyond hypertrophic cardiomyopathy: unmasking alternative causes of LVOT obstruction on CMR NSTL国家科技图书文献中心

Tanushree,Banerjee | Avanti,Gulhane ... - 《The international journal of cardiovascular imaging.》 - 2025,41(2) - 387～388 - 共2页

摘要： mimic hypertrophic* cardiomyopathy (HCM). We describe a* | Abstract Stress/Takotsubo cardiomyopathy* (TCM* | ) is a transient regional left ventricular (LV | ) systolic dysfunction, often mimicking acute myocardial | infarction with normal coronary arteries. Rarely TCM can

关键词： Takotsubo cardiomyopathy | Hypertrophic cardiomyopathy | Cardiac magnetic resonance

7. Association between cardiovascular risk factors and dilated and hypertrophic cardiomyopathy: Mendelian randomization analysis NSTL国家科技图书文献中心

Zou, Chenchao | Zou, Huaxi ... - 《Nutrition, metabolism, and cardiovascular diseases》 - 2025,35(1) - Article 103752～Article 103752 - 共6页 - 被引量：1

摘要： cardiomyopathy data on 355,318 samples and hypertrophic | hypertrophic cardiomyopathies. Independent genetic variants | Background and aim: Dilated cardiomyopathy is | a major cause of heart failure, and hypertrophic | cardiomyopathy is a common cause of sudden cardiac death in

关键词： Dilated cardiomyopathy | Hypertrophic cardiomyopathy | Smoking | Alcohol | Obesity | Mendelian randomization analysis

8. Diagnosis and management of hypertrophic cardiomyopathy: European vs. American guidelines NSTL国家科技图书文献中心

Aimo, Alberto | Todiere, Giancarlo ... - 《Heart failure reviews》 - 2025,30(2) - 315～325 - 共11页

摘要：Hypertrophic cardiomyopathy (HCM) is the most | common genetic heart disease, affecting 1:200 to 1:500 | individuals worldwide. Guidelines on the diagnosis and | management of HCM have been recently published by the | European Society of Cardiology (ESC) and American

关键词： Hypertrophic cardiomyopathy | HCM | Guidelines | Recommendations | Diagnosis | Management | Therapy

9. The Psychometric Performance of the Kansas City Cardiomyopathy Questionnaire-12 in Symptomatic Obstructive Hypertrophic Cardiomyopathy NSTL国家科技图书文献中心

ANDREW J. SAUER | CHARLES F. SHERROD ... - 《Journal of cardiac failure》 - 2025,31(5) - 813～820 - 共8页

摘要： patients with obstructive hypertrophic cardiomyopathy | Hypertrophic Cardiomyopathy Symptom Questionnaire [HCMSQ | the 23-item Kansas City Cardiomyopathy* Questionnaire* | Background: A primary goal of treating | (oHCM) is to improve their symptoms, function and

关键词： Hypertrophic cardiomyopathy; Kansas City Cardiomyopathy Questionnaire; patient-reported

10. The clinical utility of cardiac myosin inhibitors for the management of hypertrophic cardiomyopathy: a scoping review NSTL国家科技图书文献中心

Leen,Othman | Lida,Koskina ... - 《Heart failure reviews》 - 2025,30(2) - 453～467 - 共15页

摘要：Abstract Hypertrophic* cardiomyopathy (HCM) is* | an inherited condition characterized by left | ventricular, non-dilated hypertrophy in the absence of | another secondary underlying cause. There has been an | ongoing increase in the diagnosis of HCM over the past

摘要：The modern description of hypertrophic | cardiomyopathy (HCM) was prompted by histopathological | evaluation of a series of patients who died suddenly.1 In | 1958, Donald Teare1 published his seminal paper on 8 | patients who had sudden death and severe asymmetric

关键词： histology; hypertrophic cardiomyopathy; myectomy; myocytes

摘要：Apical hypertrophic* cardiomyopathy (ApHCM* | ) represents a rare variant of hypertrophic cardiomyopathy | (HCM) with distinct phenotypic characteristics. The | prevalence of this variant varies according to each study's | geographic region. The leading imaging modality for the

关键词： apical | diagnosis | hypertrophic cardiomyopathy | natural history | prognosis

摘要：Hypertrophic cardiomyopathy is a common but | arrhythmia. Hypertrophic* cardiomyopathy is often heritable* | hypertrophic cardiomyopathy with negative inotropic therapy | practical overview of important topics in hypertrophic | cardiomyopathy, including evaluation of differential diagnosis

关键词： adults | cardiac surgery | humans | hypertrophic cardiomyopathy | ventricular outflow obstruction

摘要： hypertrophic cardiomyopathy (HCM) have long been challenging | Randomized clinical trials (RCTs) for | caused by the condition's rarity, low event rates, and | diverse clinical presentations. However, recent advances | in targeted therapies have sparked increased

关键词： endpoint | HCM | hypertrophic cardiomyopathy | study design | trial

摘要：Hypertrophic cardiomyopathy (HCM) is a common | obstruction. Hypertrophic* cardiomyopathy results from* | genetic cardiac disorder marked by unexplained | asymmetrical left ventricular wall thickening. This condition | exhibits histopathological hallmarks including enlarged

关键词： Cardiomyopathy | genetic | hypertrophic | sudden cardiac death

摘要： mimic hypertrophic* cardiomyopathy (HCM). We describe a* | Abstract Stress/Takotsubo cardiomyopathy* (TCM* | ) is a transient regional left ventricular (LV | ) systolic dysfunction, often mimicking acute myocardial | infarction with normal coronary arteries. Rarely TCM can

关键词： Takotsubo cardiomyopathy | Hypertrophic cardiomyopathy | Cardiac magnetic resonance

摘要： cardiomyopathy data on 355,318 samples and hypertrophic | hypertrophic cardiomyopathies. Independent genetic variants | Background and aim: Dilated cardiomyopathy is | a major cause of heart failure, and hypertrophic | cardiomyopathy is a common cause of sudden cardiac death in

关键词： Dilated cardiomyopathy | Hypertrophic cardiomyopathy | Smoking | Alcohol | Obesity | Mendelian randomization analysis

摘要：Hypertrophic cardiomyopathy (HCM) is the most | common genetic heart disease, affecting 1:200 to 1:500 | individuals worldwide. Guidelines on the diagnosis and | management of HCM have been recently published by the | European Society of Cardiology (ESC) and American

关键词： Hypertrophic cardiomyopathy | HCM | Guidelines | Recommendations | Diagnosis | Management | Therapy

摘要： patients with obstructive hypertrophic cardiomyopathy | Hypertrophic Cardiomyopathy Symptom Questionnaire [HCMSQ | the 23-item Kansas City Cardiomyopathy* Questionnaire* | Background: A primary goal of treating | (oHCM) is to improve their symptoms, function and

关键词： Hypertrophic cardiomyopathy; Kansas City Cardiomyopathy Questionnaire; patient-reported

摘要：Abstract Hypertrophic* cardiomyopathy (HCM) is* | an inherited condition characterized by left | ventricular, non-dilated hypertrophy in the absence of | another secondary underlying cause. There has been an | ongoing increase in the diagnosis of HCM over the past

关键词： Cardiac myosin inhibitor | Hypertrophic cardiomyopathy | Hypertrophic obstructive cardiomyopathy | Aficamten | Mavacamten

4008-161-200 800-990-8900

国家科技图书文献中心

摘要：The modern description of hypertrophic | cardiomyopathy (HCM) was prompted by histopathological | evaluation of a series of patients who died suddenly.1 In | 1958, Donald Teare1 published his seminal paper on 8 | patients who had sudden death and severe asymmetric

关键词： histology; hypertrophic cardiomyopathy; myectomy; myocytes

摘要：Apical hypertrophic cardiomyopathy (ApHCM | ) represents a rare variant of hypertrophic cardiomyopathy | (HCM) with distinct phenotypic characteristics. The | prevalence of this variant varies according to each study's | geographic region. The leading imaging modality for the

关键词： apical | diagnosis | hypertrophic cardiomyopathy | natural history | prognosis

摘要：Hypertrophic cardiomyopathy is a common but | arrhythmia. Hypertrophic cardiomyopathy is often heritable | hypertrophic cardiomyopathy with negative inotropic therapy | practical overview of important topics in hypertrophic | cardiomyopathy, including evaluation of differential diagnosis

关键词： adults | cardiac surgery | humans | hypertrophic cardiomyopathy | ventricular outflow obstruction

摘要： hypertrophic cardiomyopathy (HCM) have long been challenging | Randomized clinical trials (RCTs) for | caused by the condition's rarity, low event rates, and | diverse clinical presentations. However, recent advances | in targeted therapies have sparked increased

关键词： endpoint | HCM | hypertrophic cardiomyopathy | study design | trial

摘要：Hypertrophic cardiomyopathy (HCM) is a common | obstruction. Hypertrophic cardiomyopathy results from | genetic cardiac disorder marked by unexplained | asymmetrical left ventricular wall thickening. This condition | exhibits histopathological hallmarks including enlarged

关键词： Cardiomyopathy | genetic | hypertrophic | sudden cardiac death

摘要： mimic hypertrophic cardiomyopathy (HCM). We describe a | Abstract Stress/Takotsubo cardiomyopathy (TCM | ) is a transient regional left ventricular (LV | ) systolic dysfunction, often mimicking acute myocardial | infarction with normal coronary arteries. Rarely TCM can

关键词： Takotsubo cardiomyopathy | Hypertrophic cardiomyopathy | Cardiac magnetic resonance

摘要： cardiomyopathy data on 355,318 samples and hypertrophic | hypertrophic cardiomyopathies. Independent genetic variants | Background and aim: Dilated cardiomyopathy is | a major cause of heart failure, and hypertrophic | cardiomyopathy is a common cause of sudden cardiac death in

关键词： Dilated cardiomyopathy | Hypertrophic cardiomyopathy | Smoking | Alcohol | Obesity | Mendelian randomization analysis

摘要：Hypertrophic cardiomyopathy (HCM) is the most | common genetic heart disease, affecting 1:200 to 1:500 | individuals worldwide. Guidelines on the diagnosis and | management of HCM have been recently published by the | European Society of Cardiology (ESC) and American

关键词： Hypertrophic cardiomyopathy | HCM | Guidelines | Recommendations | Diagnosis | Management | Therapy

摘要： patients with obstructive hypertrophic cardiomyopathy | Hypertrophic Cardiomyopathy Symptom Questionnaire [HCMSQ | the 23-item Kansas City Cardiomyopathy Questionnaire | Background: A primary goal of treating | (oHCM) is to improve their symptoms, function and

关键词： Hypertrophic cardiomyopathy; Kansas City Cardiomyopathy Questionnaire; patient-reported

摘要：Abstract Hypertrophic cardiomyopathy (HCM) is | an inherited condition characterized by left | ventricular, non-dilated hypertrophy in the absence of | another secondary underlying cause. There has been an | ongoing increase in the diagnosis of HCM over the past

关键词： Cardiac myosin inhibitor | Hypertrophic cardiomyopathy | Hypertrophic obstructive cardiomyopathy | Aficamten | Mavacamten

4008-161-200 800-990-8900

国家科技图书文献中心

摘要：Apical hypertrophic* cardiomyopathy (ApHCM* | ) represents a rare variant of hypertrophic cardiomyopathy | (HCM) with distinct phenotypic characteristics. The | prevalence of this variant varies according to each study's | geographic region. The leading imaging modality for the

摘要：Hypertrophic cardiomyopathy is a common but | arrhythmia. Hypertrophic* cardiomyopathy is often heritable* | hypertrophic cardiomyopathy with negative inotropic therapy | practical overview of important topics in hypertrophic | cardiomyopathy, including evaluation of differential diagnosis

摘要：Hypertrophic cardiomyopathy (HCM) is a common | obstruction. Hypertrophic* cardiomyopathy results from* | genetic cardiac disorder marked by unexplained | asymmetrical left ventricular wall thickening. This condition | exhibits histopathological hallmarks including enlarged

摘要： mimic hypertrophic* cardiomyopathy (HCM). We describe a* | Abstract Stress/Takotsubo cardiomyopathy* (TCM* | ) is a transient regional left ventricular (LV | ) systolic dysfunction, often mimicking acute myocardial | infarction with normal coronary arteries. Rarely TCM can

摘要： patients with obstructive hypertrophic cardiomyopathy | Hypertrophic Cardiomyopathy Symptom Questionnaire [HCMSQ | the 23-item Kansas City Cardiomyopathy* Questionnaire* | Background: A primary goal of treating | (oHCM) is to improve their symptoms, function and

摘要：Abstract Hypertrophic* cardiomyopathy (HCM) is* | an inherited condition characterized by left | ventricular, non-dilated hypertrophy in the absence of | another secondary underlying cause. There has been an | ongoing increase in the diagnosis of HCM over the past