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Autor:
M Lopez Ramon, M.J. del Cerro Marín, S Villagra Albert, G Inigo Martin, L M Caicedo Cuenca, T Segura De La Cal, A Sabate Rotes, I Guillen Rodriguez, C Labrandero, J Playan Escribano, L Conejo Munoz, S. Escriba Bori, P Escribano Subias, M.A Izquierdo Riezu, A Mendoza Soto
Publikováno v:
European Heart Journal. 41
Introduction Pulmonary arterial hypertension (PAH) is a rare disease that affects the small pulmonary arteries, producing gradual obliteration of arterial lumen leading to the progressive increase in pulmonary vascular resistance and, ultimately, rig