Journal Archives

Cell Therapy for Pulmonary Arterial Hypertension: Potential Efficacy of Endothelial Progenitor Cells and Mesenchymal Stem Cells
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Pulmonary arterial hypertension is a challenging disease, and our understanding of the underlying mechanisms and pathophysiology remains incomplete. However, there have been a number of important advances, which have greatly enriched our knowledge about the key mechanisms that contribute to the functional and pathological abnormalities of PAH. With each new wave of understanding come new opportunities for the rational design of therapies.

Pulmonary Hypertension in Children: New Insights Offer Opportunity to Reverse the Disease Process
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Severe, sustained pulmonary hypertension is potentially fatal. It is, however, time to adopt a more positive and aggressive approach to the management of pulmonary hypertension in children.