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Pulmonary arterial hypertension: future directions: report of a National Heart, Lung and Blood Institute/Office of Rare Diseases workshop.
Newman JH, Fanburg BL, Archer SL, Badesch DB, Barst RJ, Garcia JG, Kao PN, Knowles JA, Loyd JE, McGoon MD, Morse JH, Nichols WC, Rabinovitch M, Rodman DM, Stevens T, Tuder RM, Voelkel NF, Gail DB; National Heart, Lung and Blood Institute/Office of Rare Diseases. Newman JH, et al. Among authors: loyd je. Circulation. 2004 Jun 22;109(24):2947-52. doi: 10.1161/01.CIR.0000132476.87231.6F. Circulation. 2004. PMID: 15210611 No abstract available.
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF.
Lawson WE, Grant SW, Ambrosini V, Womble KE, Dawson EP, Lane KB, Markin C, Renzoni E, Lympany P, Thomas AQ, Roldan J, Scott TA, Blackwell TS, Phillips JA 3rd, Loyd JE, du Bois RM. Lawson WE, et al. Among authors: loyd je. Thorax. 2004 Nov;59(11):977-80. doi: 10.1136/thx.2004.026336. Thorax. 2004. PMID: 15516475 Free PMC article.
Genetics and mediators in pulmonary arterial hypertension.
Austin ED, Loyd JE. Austin ED, et al. Among authors: loyd je. Clin Chest Med. 2007 Mar;28(1):43-57, vii-viii. doi: 10.1016/j.ccm.2006.11.007. Clin Chest Med. 2007. PMID: 17338927 Free PMC article. Review.
249 results