Pulmonary arterial hypertension (PAH) is a severe form of pulmonary hypertension that
combines multiple alterations of pulmonary arteries, including, in particular, thrombotic and …

Severe forms of pulmonary arterial hypertension (PAH) are characterized by various
degrees of remodeling of the pulmonary arterial vessels, which increases the pulmonary …

Pulmonary arterial hypertension (PAH) is a serious pathological phenomenon with poor
prognosis, which is associated with morphological as well as hemodynamic alteration of the …

Pulmonary arterial hypertension (PAH) is a syndrome characterized by pulmonary vascular
remodeling and vasoconstriction, leading to increased pulmonary vascular resistance, right …

Pulmonary arterial hypertension (PAH) is responsible for the premature death mainly
because of progressive and severe heart failure. This disease is characterized by increased …

Abstract World Health Organization category 1 pulmonary hypertension (PH) is a
heterogeneous syndrome in which PH originates in the small pulmonary arteries and is …

At present, six groups of chronic pulmonary hypertension (PH) are described. Among these,
group 1 (and 1′) comprises a group of diverse diseases termed pulmonary arterial …

Pulmonary arterial hypertension (PAH) is a disorder predominantly affecting the small
pulmonary arteries. It can occur without an identifiable cause, primary pulmonary …

Pulmonary arterial hypertension (PAH) is a debilitating and often fatal disease characterized
by a progressive increase in pulmonary vascular resistance that leads to right ventricular …

INTRODUCTION: Pulmonary arterial hypertension (PAH) is a rare syndrome of fatigue and
dyspnoea, caused by increased pulmonary vascular resistance and right heart failure …