Results 311 to 320 of about 282,907 (338)
Some of the next articles are maybe not open access.
Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy
Nature, 2022M. Chaffin +18 more
semanticscholar +1 more source
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
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
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
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
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
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, 1996We 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
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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
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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, 2019Background: 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, 2008A 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
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Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
Nature Reviews Cardiology, 2021R. Walsh +3 more
semanticscholar +1 more source

