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[Calculated pulmonary vascular resistance, is definitively a worthless variable. Current methods for a better definition].
Arch Cardiol Mex. 2008 Jan-Mar;78(1):95-113.
Arch Cardiol Mex. 2008.
PMID: 18581718
Review.
Spanish.
[Clinical-hemodynamic correlation of the NYHA/WHO system in idiopathic pulmonary artery hypertension. Clinical, therapeutic and long-term prognosis implications].
Herrera EL, Zárate JS, Solano JF, Martínez LE, Zamudio TR, Bautista EG.
Herrera EL, et al. Among authors: zamudio tr.
Arch Cardiol Mex. 2008 Apr-Jun;78(2):148-61.
Arch Cardiol Mex. 2008.
PMID: 18754406
Spanish.
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Macitentan for the treatment of inoperable chronic thromboembolic pulmonary hypertension (MERIT-1): results from the multicentre, phase 2, randomised, double-blind, placebo-controlled study.
Ghofrani HA, Simonneau G, D'Armini AM, Fedullo P, Howard LS, Jaïs X, Jenkins DP, Jing ZC, Madani MM, Martin N, Mayer E, Papadakis K, Richard D, Kim NH; MERIT study investigators.
Ghofrani HA, et al.
Lancet Respir Med. 2017 Oct;5(10):785-794. doi: 10.1016/S2213-2600(17)30305-3. Epub 2017 Sep 11.
Lancet Respir Med. 2017.
PMID: 28919201
Retracted and republished. Retracted.
Clinical Trial.
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Selexipag for the Treatment of Pulmonary Arterial Hypertension.
Sitbon O, Channick R, Chin KM, Frey A, Gaine S, Galiè N, Ghofrani HA, Hoeper MM, Lang IM, Preiss R, Rubin LJ, Di Scala L, Tapson V, Adzerikho I, Liu J, Moiseeva O, Zeng X, Simonneau G, McLaughlin VV; GRIPHON Investigators.
Sitbon O, et al.
N Engl J Med. 2015 Dec 24;373(26):2522-33. doi: 10.1056/NEJMoa1503184.
N Engl J Med. 2015.
PMID: 26699168
Free article.
Clinical Trial.
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