Results 11 to 20 of about 26,229 (182)
В статье рассматриваются вопросы классификации, этиологии, патогенеза, клиники, диагностики и лечения рестриктивной кардиомиопатии (РКМП) как широкого спектра заболеваний, объединенных одним патофизиологическим механизмом рестриктивной диастолической дисфункции вследствие распространенного фиброза или инфильтрации стенок желудочков различными ...
E. A. Butko, K. Yu. Kinoshenko
exaly +6 more sources
Restrictive Cardiomyopathy [PDF]
S S, Kushwaha, J T, Fallon, V, Fuster
exaly +7 more sources
Unusual case of restrictive cardiomyopathy in young
Restrictive cardiomyopathy (RCM) is an uncommon form of cardiomyopathy and is characterized by impaired ventricular filling due to increased myocardial stiffness.
Archit Dahiya +4 more
doaj +1 more source
Restrictive cardiomyopathy: definition and diagnosis. [PDF]
Rapezzi C +8 more
europepmc +2 more sources
NON ISCHEMIC CARDIOMYOPATHY – A CASE REPORT
Cardiomyopathies are a group of diseases characterized by the structural and functional abnormalities of the heart muscles in the absence of other illnesses that might be responsible for the observed myocardial anomaly.
Anny Ashiq Ali Anny Ashiq Ali +1 more
doaj +1 more source
Outcomes after heart transplantation in patients with cardiac sarcoidosis
Background The number of patients with sarcoidosis requiring heart transplantation (HT) is increasing. The aim of this study was to evaluate outcomes of isolated HT in patients with sarcoid cardiomyopathy and compare them to recipients with non‐ischaemic
Rabea Asleh +8 more
doaj +1 more source
Background Cardiomyopathy is a common cause of atrial fibrillation (AF) and may also present as a complication of AF. However, there is a scarcity of evidence of clinical outcomes for people with cardiomyopathy and concomittant AF. The aim of the present
Benjamin J. R. Buckley +5 more
doaj +1 more source
Time spent with cats is never wasted: Lessons learned from feline acromegalic cardiomyopathy, a naturally occurring animal model of the human disease [PDF]
BackgroundIn humans, acromegaly due to a pituitary somatotrophic adenoma is a recognized cause of increased left ventricular (LV) mass. Acromegalic cardiomyopathy is incompletely understood, and represents a major cause of morbidity and mortality.
A Colao +80 more
core +2 more sources
Absence of Myocardial Thyroid Hormone Inactivating Deiodinase Results in Restrictive Cardiomyopathy in Mice [PDF]
Cardiac injury induces myocardial expression of the thyroid hormone inactivating type 3 deiodinase (D3), which in turn dampens local thyroid hormone signaling.
Antonio C. Bianco +35 more
core +1 more source
Significance of myocardial tenascin-C expression in left ventricular remodelling and long-term outcome in patients with dilated cardiomyopathy [PDF]
Aim Dilated cardiomyopathy (DCM) has a variety of causes, and no useful approach to predict left ventricular (LV) remodelling and long-term outcome has yet been established.
Anzai, T +12 more
core +1 more source

