Int J Physiol Pathophysiol Pharmacol
November 2017
[This corrects the article on p. 112 in vol. 9, PMID: 28951773.
View Article and Find Full Text PDFInt J Physiol Pathophysiol Pharmacol
September 2017
Background: Pulmonary Arterial Hypertension (PAH) is a deadly and disabling disease for which there is no marketed drug that addresses the underlying disease mechanism and targets to cure patients. The lack of understanding of the disease mechanism represents the main challenges in developing curative therapies. We here report, for the first time, that mice lacking natriuretic peptides clearance receptor develop PAH.
View Article and Find Full Text PDFBiomed Pharmacother
September 2017
Background: In patients with left ventricular heart failure (HF), the development of pulmonary hypertension (PH) is common and represents a strong predictor of death. Despite recent advances in the pathophysiological understanding there is as yet no prospect of cure of this deadly clinical entity and the majority of patients continue to progress to right ventricular failure and die. Furthermore, there is no single medical treatment currently approved for PH related to HF.
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