Results 311 to 320 of about 282,907 (338)
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Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy

Nature, 2022
M. Chaffin   +18 more
semanticscholar   +1 more source

Hypertrophic cardiomyopathy

Current Treatment Options in Cardiovascular Medicine, 1999
The degree of clinical expression of both obstructive and nonobstructive hypertrophic cardiomyopathy (HCM) is widely variable. Many patients with HCM are asymptomatic or minimally symptomatic. Most patients with mild or moderate HCM respond well to medical therapy, but medical therapy in patients with severe disease is only marginally beneficial.
openaire   +2 more sources

Hypertrophic Cardiomyopathy

Pacing and Clinical Electrophysiology, 2009
Background: Hypertrophic cardiomyopathy (HCM) is one of the most common inherited cardiac disorders, with a prevalence in young adults of one in 500 and is defined by its wall thickening. Methods: This chapter of the supplement will present major clinical impacts of this disorder in its predilection to be inherited; its ...
openaire   +2 more sources

Hypertrophic Cardiomyopathy

Anesthesia & Analgesia, 2015
Hypertrophic cardiomyopathy (HCM) is a relatively common disorder that anesthesiologists encounter among patients in the perioperative period. Fifty years ago, HCM was thought to be an obscure disease. Today, however, our understanding and ability to diagnose patients with HCM have improved dramatically.
Nadia, Hensley   +5 more
openaire   +2 more sources

Apical Hypertrophic Cardiomyopathy

Southern Medical Journal, 1996
We report the case of a patient with recurrent admissions for congestive heart failure who was subsequently diagnosed with apical hypertrophic cardiomyopathy. The major physiologic characteristic of patients with apical hypertrophic cardiomyopathy is diastolic dysfunction due to abnormal stiffness of the left ventricle during diastole, with resultant ...
J, Rivera-Diaz, A R, Moosvi
openaire   +2 more sources

Hypertrophic Cardiomyopathy

Current Heart Failure Reports
Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac condition with potential for severe complications including sudden cardiac death. Early diagnosis allows appropriate risk stratification and prompt intervention to minimise the potential for adverse outcomes.
Jason N, Dungu   +3 more
openaire   +2 more sources

Hypertrophic Cardiomyopathy-Related Sudden Cardiac Death in Young People in Ontario.

Circulation, 2019
Background: Hypertrophic cardiomyopathy (HCM) is considered a leading cause of sudden cardiac death (SCD) in younger people.
A. Weissler-Snir   +7 more
semanticscholar   +1 more source

Hypertrophic cardiomyopathy misinterpreted

European Heart Journal, 2008
A 20-year-old woman presented with increased dyspnoea and a left ventricular apical mass on echocardiogram. Cardiovascular magnetic resonance (CMR) revealed an intra-myocardial mass in the inferoapical wall, which was isointense in cine imaging. There was homogenous tissue enhancement in resting gadolinium first pass perfusion similar to the rest of ...
Ryan, Ko, Carmen, Chan, Katherine, Fan
openaire   +2 more sources

Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies

Nature Reviews Cardiology, 2021
R. Walsh   +3 more
semanticscholar   +1 more source

Hypertrophic cardiomyopathy

Disease-a-Month, 1981
M B, Leon, L S, Cohen
openaire   +2 more sources

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