Cargando…
Anticipated classes of new medications and molecular targets for pulmonary arterial hypertension
Pulmonary arterial hypertension (PAH) remains a life-limiting condition with a major impact on the ability to lead a normal life. Although existing therapies may improve the outlook in some patients there remains a major unmet need to develop more effective therapies in this condition. There have be...
Autores principales: | Morrell, Nicholas W., Archer, Stephen L., DeFelice, Albert, Evans, Steven, Fiszman, Monica, Martin, Thomas, Saulnier, Muriel, Rabinovitch, Marlene, Schermuly, Ralph, Stewart, Duncan, Truebel, Hubert, Walker, Gennyne, Stenmark, Kurt R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641734/ https://www.ncbi.nlm.nih.gov/pubmed/23662201 http://dx.doi.org/10.4103/2045-8932.109940 |
Ejemplares similares
-
The pulmonary hypertension academic research consortium
por: Rich, Stuart
Publicado: (2013) -
Clinical trials in neonates and children: Report of the pulmonary hypertension academic research consortium pediatric advisory committee
por: Adatia, Ian, et al.
Publicado: (2013) -
Clinical trials in pulmonary hypertension: Time for a consortium
por: Newman, John H., et al.
Publicado: (2013) -
Real-World Switching to Riociguat: Management and Practicalities in Patients with PAH and CTEPH
por: Gall, Henning, et al.
Publicado: (2018) -
Initial Riociguat Monotherapy and Transition from Sildenafil to Riociguat in Patients with Idiopathic Pulmonary Arterial Hypertension: Influence on Right Heart Remodeling and Right Ventricular–Pulmonary Arterial Coupling
por: Taran, Irina N., et al.
Publicado: (2018)