Results 111 to 120 of about 286,742 (224)

Neurocardiology: Brain–Heart Interactions in the Heart

open access: yesMedComm, Volume 7, Issue 9, September 2026.
The heart and brain maintain systemic homeostasis through bidirectional communication involving neural, biochemical, and mechanical pathways. Dysregulation of these pathways contributes to a spectrum of conditions involving heart–brain interactions, including Takotsubo syndrome, the epileptic heart, stroke–heart syndrome, heart failure, cardiac ...
Wentao Wang   +3 more
wiley   +1 more source

Sex disparities in the use and outcomes of septal reduction therapies for obstructive hypertrophic cardiomyopathy

open access: yes
Background There is limited data examining potential sex-based disparities in the utilization and complications of septal reduction therapy (SRT) in patients with obstructive hypertrophic cardiomyopathy (HCM).
Hernandez, Adrian V.   +8 more
core   +1 more source

Acute myocardial infarction with diminutive right coronary artery and obstructive hypertrophic cardiomyopathy without significant coronary stenoses

open access: yes, 2009
Focal tissue abnormalities consistent with regional ischemia have been reported in patients with hypertrophic cardiomyopathy (HCM). Coronary microvascular dysfunction has been also reported to be present in patients with HCM despite normal epicardial ...
Marte, Filippo   +3 more
core   +1 more source

Hot Tub Lung: Misdiagnosed Hypersensitivity Pneumonitis Revealing a Mycobacterial Aetiology—A Case Report and Literature Review

open access: yesRespirology Case Reports, Volume 14, Issue 9, September 2026.
Our case describes chronic daily exposure with histologic detection of rare MAC organisms, illustrating the spectrum and possible coexistence between hypersensitivity and infection, emphasising the diagnostic and therapeutic complexity of this uncommon disease.
Fadi Abualhommos   +5 more
wiley   +1 more source

Surgical treatment of hypertrophic obstructive cardiomyopathy

open access: yes, 2001
The rationale for surgical treatment of hypertrophic obstructive cardiomyopathy is based on the assumption that dynamical obstruction is mainly caused by a reduction in the left ventricular outflow tract cross-sectional area due to bulging septal ...
Schoendube, Friedrich Albert
core   +1 more source

Efficacy and Safety of a Single‐Pill Triple Combination of Valsartan, Amlodipine, and Chlorthalidone in Patients With Essential Hypertension Inadequately Controlled on Dual Therapy With Valsartan and Amlodipine: A Randomized, Double‐Blind, Multicenter, Phase 3 Trial

open access: yesThe Journal of Clinical Hypertension, Volume 28, Issue 9, September 2026.
ABSTRACT Many hypertensive patients require three or more antihypertensive agents to achieve target blood pressure. This randomized, double‐blind, multicenter phase 3 trial conducted in South Korea evaluated the efficacy and safety of a single‐pill triple combination therapy with valsartan (Val), amlodipine (Aml), and chlorthalidone (CTD) in patients ...
In‐Jeong Cho   +10 more
wiley   +1 more source

Clinical Course and Predictors of Heart Failure in Asymptomatic Obstructive Hypertrophic Cardiomyopathy

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Left ventricular outflow tract obstruction is a major contributor to morbidity in hypertrophic cardiomyopathy and an established therapeutic target.
Alexander Schulz   +10 more
doaj   +1 more source

Septal Ablation for Hypertrophic Obstructive Cardiomyopathy: Transcoronary and Endocardial Approach

open access: yes, 2016
Septal reduction therapy is the gold standard treatment method for symptomatic, hypertrophic obstructive cardiomyopathy. Although surgical myectomy is a well-established and effective technique with decades of experience in its application, use of ...
Yalin, Kıvanç   +4 more
core   +1 more source

Attenuated Cardiac–Ocular Phenotype of Sanfilippo Syndrome (MPS IIIA) Presenting With Hypertrophic Cardiomyopathy and Cone-Rod Dystrophy

open access: yesAnnals of Internal Medicine: Clinical Cases
We describe a 39-year-old woman with cone-rod dystrophy and hypertrophic obstructive cardiomyopathy complicated by an apical aneurysm, ventricular tachycardia, and ischemic stroke, ultimately requiring heart transplantation.
Marc Vanderheyden   +2 more
doaj   +1 more source

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation [PDF]

open access: yes, 2011
Genetic causes for autosomal recessive forms of dilated cardiomyopathy (DCM) are only rarely identified, although they are thought to contribute considerably to sudden cardiac death and heart failure, especially in young children.
Steenbergen, Gerry   +20 more
core  

Home - About - Disclaimer - Privacy