Background: Natural progression of CHD often results in the development of pulmonary arterial hypertension (PAH), which is a leading cause of death and disability. Aim: The goal of this work is to clarify the prognostic and diagnostic usefulness of OPN in children with PAH-CHD, a...
Open access
Research Article10.9734/jammr/2022/v34i224824
Background: Pulmonary arterial hypertension (PAH) is a frequent complication of congenital heart disease (CHD) with left-to-right shunt. Increased pulmonary pressure leads to vascular remodeling and RV dysfunction. Objectives: To analyze the role of high-sensitive cardiac tropo...
Open access
Research Article10.9734/jammr/2020/v32i2330728
Objectives: Assessment of plasma level of connective tissue growth factor in congestive heart failure children, assessment of its diagnostic and prognostic role and correlate its level with clinical and echocardiographic assessment of congestive heart failure. Methods: Connective...
Open access
Research Article10.9734/jammr/2020/v32i130358