Results 181 to 190 of about 592,769 (337)

Arrhythmogenic cardiomyopathy mimicking cardiac amyloidosis with Waldenström macroglobulinaemia: A diagnostic challenge

open access: yes
ESC Heart Failure, EarlyView.
Lianyue Ma   +7 more
wiley   +1 more source

Clinical and echocardiographic phenotype of cardiac wasting in patients with advanced cancer

open access: yesEuropean Journal of Heart Failure, EarlyView.
Cardiac wasting‐associated cardiomyopathy in cancer patients. E/e', early diastolic filling velocity (E) over mitral annulus early diastolic tissue velocity (e'); GLS, global longitudinal strain; LV, left ventricular; LVEF, left ventricular ejection fraction; TAPSE, tricuspid annular plane systolic excursion.
Markus S. Anker   +27 more
wiley   +1 more source

Mendelian Randomization Study on the Associations Between Genetically Predicted Cardiovascular Disease Subtypes and the Risk of Developing Cardiomyopathies

open access: yesClinical and Applied Thrombosis/Hemostasis
Cardiomyopathies are commonly believed to have genetic origins; however, the connection between cardiomyopathies and cardiovascular diseases remains uncertain.
Qiaolin Tang MD   +3 more
doaj   +1 more source

Effects of sodium‐glucose cotransporter 2 inhibitors on pulmonary artery pressure in patients with chronic heart failure

open access: yes
ESC Heart Failure, EarlyView.
Judith Rovira‐Solé   +5 more
wiley   +1 more source

Computational modelling of myocardial metabolism in patients with advanced heart failure

open access: yesEuropean Journal of Heart Failure, EarlyView.
LV, left ventricular; LVAD, left ventricular assist device; LVEF, left ventricular ejection fraction. Abstract Aims Perturbations of myocardial metabolism and energy depletion are well‐established hallmarks of heart failure (HF), yet methods for their systematic assessment remain limited in humans.
Niklas Beyhoff   +17 more
wiley   +1 more source

An Unusual Case of 11αB‐Crystallin (CRYAB) Mutation as a Cause of Dilated Cardiomyopathy With Restrictive Physiology: A Case Report and Focused Review of the Literature

open access: yesClinical Case Reports
Several diseases have been linked to αB‐crystallin (CRYAB) mutation. However, this mutation is an uncommon cause that has been associated in recent years with the development of dilated cardiomyopathy.
Porras Bueno Cristian Orlando   +5 more
doaj   +1 more source

Clustering in dilated cardiomyopathy at initial evaluation: An effective tool for clinical stratification

open access: yesEuropean Journal of Heart Failure, EarlyView.
Visual description of study design and main results. BBB, bundle branch block; ECG, electrocardiogram; MVA, major ventricular arrhythmia; SCD, sudden cardiac death. Abstract Aims Dilated cardiomyopathy (DCM) has a highly variable presentation and disease course. Current stratification strategies are complex and require multimodality evaluation.
Ilaria Gandin   +16 more
wiley   +1 more source

Mechanical Dyssynchrony Precedes QRS Widening in ATP‐Sensitive K + Channel–Deficient Dilated Cardiomyopathy [PDF]

open access: gold, 2013
Satsuki Yamada   +9 more
openalex   +1 more source

Atrial cardiomyopathy: From healthy atria to atrial failure. A clinical consensus statement of the Heart Failure Association of the ESC

open access: yesEuropean Journal of Heart Failure, EarlyView.
The diagnosis of atrial cardiomyopathy (AtCM) requires electrical atrial dysfunction, with evidence of either mechanical atrial dysfunction, atrial enlargement, or excessive atrial fibrosis. The diagnostic cut‐points presented are for standard electrocardiogram and echocardiogram studies (see Figure 1 for further detail).
Jerremy Weerts   +26 more
wiley   +1 more source

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