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Comment
. 2022 Oct;10(10):e89.
doi: 10.1016/S2213-2600(22)00308-3.

Phenotypes of idiopathic pulmonary arterial hypertension

Affiliations
Comment

Phenotypes of idiopathic pulmonary arterial hypertension

Roberto Badagliacca et al. Lancet Respir Med. 2022 Oct.
No abstract available

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Conflict of interest statement

RB reports personal fees from UT, Dompè, Ferrer, Bayer, MSD, AOP, and Orphan Pharmaceuticals, outside of the submitted work. RLB reports grants from Actelion, Bayer, Bellerophon, Eiger, and Abbott. GM declares no competing interests. KT has received speaking fees from Actelion and Bayer, outside of the submitted work. RN reports relationships including consultancies, speaker's fees, and membership of advisory boards with AOP, Orphan Pharmaceuticals, Johnson & Johnson, Lung Biotechnology Corporation, and United Therapeutics. All authors contributed to writing of this Correspondence and approved the manuscript for submission.

Comment in

Comment on

  • Phenotyping of idiopathic pulmonary arterial hypertension: a registry analysis.
    Hoeper MM, Dwivedi K, Pausch C, Lewis RA, Olsson KM, Huscher D, Pittrow D, Grünig E, Staehler G, Vizza CD, Gall H, Distler O, Opitz C, Gibbs JSR, Delcroix M, Park DH, Ghofrani HA, Ewert R, Kaemmerer H, Kabitz HJ, Skowasch D, Behr J, Milger K, Lange TJ, Wilkens H, Seyfarth HJ, Held M, Dumitrescu D, Tsangaris I, Vonk-Noordegraaf A, Ulrich S, Klose H, Claussen M, Eisenmann S, Schmidt KH, Swift AJ, Thompson AAR, Elliot CA, Rosenkranz S, Condliffe R, Kiely DG, Halank M. Hoeper MM, et al. Lancet Respir Med. 2022 Oct;10(10):937-948. doi: 10.1016/S2213-2600(22)00097-2. Epub 2022 Jun 28. Lancet Respir Med. 2022. PMID: 35777416 Free PMC article.

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