Results 11 to 20 of about 306,427 (234)
MYOCARDIAL REMODELLING TYPES IN HYPERTROPHIC NON-OBSTRUCTIVE CARDIOMYOPATHY [PDF]
Российский кардиологический журнал, 2015 Aim. To evaluate the prevalence of the left ventricle remodeling types in hypertrophic non-obstructive cardiomyopathy, and their relation to clinical and instrumental data. Material and methods.
D. V. Bogdanov
doaj +2 more sources
Педиатрическая фармакология, 2007 The article is dedicated to the issue of curing children with obstructive form of hypertrophic cardiomyopathy. It presents a complex evaluation of adrenergic blockers influence on the clinical finding, heart rate disorder and vegetative regulation of ...
E.A. Tikhomirova +3 more
doaj +3 more sources
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY
Alʹmanah Kliničeskoj Mediciny, 2016 Hypertrophic cardiomyopathy (HCMP) is a relatively common disease with genetic predisposition, that is widely spread irrespective of gender, race or ethnicity. The cause of this pathology are mutations of genes encoding synthesis of contracting proteins.
A. G. Osiev +4 more
doaj +3 more sources
LEOPARD syndrome and hypertrophic obstructive cardiomyopathy: a case report [PDF]
The Turkish Journal of Pediatrics, 2004 The LEOPARD syndrome is a rare, autosomal dominant multisystemic disorder characterized by lentiginosis, ocular hypertelorism, abnormal genitalia, growth retardation, sensorineural deafness, and cardiac and electrocardiographic abnormalities ...
Ergun Cetinkaya +6 more
doaj +2 more sources
Hypertrophic cardiomyopathy with mid-ventricular obstruction and apical aneurysm [PDF]
Кардіохірургія та інтервенційна кардіологія, 2016 A case report of apical left ventricular aneurysm in patient with hypertrophic cardiomyopathy with mid-ventricular obstruction (diagnosis and surgical treatment) is presented.
N.D. Oryshchyn +6 more
doaj +1 more source
Hypertrophic obstructive cardiomyopathy [PDF]
The Lancet, 2017 Hypertrophic obstructive cardiomyopathy is an inherited myocardial disease defined by cardiac hypertrophy (wall thickness ≥15 mm) that is not explained by abnormal loading conditions, and left ventricular obstruction greater than or equal to 30 mm Hg. Typical symptoms include dyspnoea, chest pain, palpitations, and syncope.
Veselka, Josef +2 more
openaire +4 more sources
Hypertrophic Obstructive Cardiomyopathy [PDF]
Deutsches Ärzteblatt international, 2019 Hypertrophic cardiomyopathy (HCM) is caused by mutations in a number of genes. Its prevalence is 0.2% to 0.6%.This review is based on publications retrieved by a selective literature search and on the authors' clinical experi- ence.70% of patients with HCM suffer from the obstructive type of the condition, clinically characterized by highly dynamic and
Angelika, Batzner +3 more
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Symptomatic Obstructive Hypertrophic Cardiomyopathy [PDF]
Circulation: Cardiovascular Interventions, 2013 Hypertrophic cardiomyopathy (HCM) is a common, yet challenging condition for clinical management. The majority of these patients have evidence of left ventricular outflow tract (LVOT) obstruction that may be asymptomatic or associated with debilitating symptoms of heart failure.
Paul, Sorajja +2 more
openaire +2 more sources
Quality first in obstructive hypertrophic cardiomyopathy
, 2021 Increasing clinician awareness, earlier diagnosis, and implantable cardioverter-defibrillators have allowed hypertrophic cardiomyopathy to transition from being a relatively common cause of sudden death in young people to a chronic disease affecting ...
Prasad, Sandhir B +3 more
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Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy [PDF]
, 2023 Left ventricular outflow obstruction (LVOTO) and diastolic dysfunction are the main pathophysiological characteristics of hypertrophic cardiomyopathy (HCM)LVOTO, may be identified in more than half of HCM patients and represents an important determinant ...
Errico Federico Perillo +6 more
core +2 more sources