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Advanced interstitial lung fibrosis with emphysema and pulmonary hypertension with no evidence for interstitial lung disease on high resolution CT

The diagnosis of idiopathic pulmonary arterial hypertension (iPAH) is complex and, besides invasive hemodynamic evaluation, includes several diagnostic steps to exclude any underlying diseases. The role of a decreased diffusion capacity of the lung for carbon monoxide (DLCO) is a matter of discussio...

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Dettagli Bibliografici
Pubblicato in:Pulm Circ
Autori principali: Foris, Vasile, Brcic, Luka, Douschan, Philipp, Kovacs, Gabor, Stacher-Priehse, Elvira, Olschewski, Horst
Natura: Artigo
Lingua:Inglês
Pubblicazione: SAGE Publications 2019
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6614945/
https://ncbi.nlm.nih.gov/pubmed/30729872
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2045894019832214
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