Results 61 to 70 of about 20,708 (216)
Background and Purpose Novel heart failure (HF) pharmacotherapies, including angiotensin receptor‐neprilysin inhibitor (ARNI) and sodium‐glucose cotransporter 2 inhibitors (SGLT2is), may confer cardiovascular benefits by attenuating myocardial fibrosis. However, direct evidence from human failing myocardial samples is limited.
Dávid Nagy +10 more
wiley +1 more source
Post-transplant rejection surveillance remains a cornerstone of heart transplant care. Although endomyocardial biopsy has long been the gold standard for monitoring rejection, its invasiveness and limitations have driven innovations in noninvasive ...
Hatem Alansari, Janardhana R. Gorthi
doaj +1 more source
Is arrhythmogenic right ventricular cardiomyopathy a paediatric problem too? [PDF]
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that is often familial, characterized by arrhythmias of right ventricular origin, due to transmural fatty or fibrofatty replacement of atrophic myocardium. ARVC is usually
Basso, Cristina +4 more
core
Abnormal Myocardial Blood Flow Reserve Observed in Cardiac Amyloidosis [PDF]
We performed real-time myocardial contrast echocardiography on a patient with cardiac amyloidosis and previous normal coronary angiography presenting with atypical chest pain to assess myocardial blood flow reserve (MBFR).
Greaves, K, Nam, MC, Nel, K, Senior, R
core +1 more source
Baseline heart‐type fatty acid binding protein (H‐FABP) independently predicts all‐cause mortality in patients with light chain cardiac amyloidosis (AL‐CA). Elevated H‐FABP levels (> 9.5 ng/mL) are associated with significantly worse survival and provide incremental prognostic value beyond established staging systems, improving risk stratification as ...
Xinqing Li +10 more
wiley +1 more source
A positive nuclear scintigraphy with hydroxy bisphosphonate bone tracer (99mTc‐HPD) is believed to have high sensitivity (>99%) and specificity (91%) for the diagnosis of transthyretin amyloid cardiomyopathy. We report the case of an 85‐year‐old man with
Cristina Chimenti +7 more
doaj +1 more source
This study compared T1 time and ECV in cardiac and thoracic skeletal muscle using CMR in 267 CA patients and 1709 non‐CA controls. Representative T1‐maps (central panel) illustrate regions of interest placed in the cardiac and thoracic skeletal muscle.
Christina Kronberger +20 more
wiley +1 more source
Endomyocardial biopsy in Chagas' heart disease: pathogenetic contributions
Endomyocardial biopsy procedure has been performed in many centers around the world, allowing a better treatment and follow up of the patients with myocardial disease.
Maria de Lourdes Higuchi
doaj +1 more source
Case Report: Diagnosis of Dual-Biopsy Negative Severe Cardiac Amyloidosis [PDF]
INTRODUCTION Amyloidosis is a rare disorder that involves the deposition of misfolded protein in extracellular tissue. Disease manifestations vary depending on the affected organs.
Kasprowicz, MD, Eric, Lohr, MD, Kristin
core +2 more sources
ESC Heart Failure, Volume 12, Issue 2, Page 1514-1522, April 2025.
Takamasa Iwai +4 more
wiley +1 more source

