Matches in SemOpenAlex for { <https://semopenalex.org/work/W2023462472> ?p ?o ?g. }
Showing items 1 to 76 of
76
with 100 items per page.
- W2023462472 endingPage "1515" @default.
- W2023462472 startingPage "1513" @default.
- W2023462472 abstract "To the Editor: Idiopathic pulmonary arterial hypertension (IPAH) is a rare, chronically progressive disease associated with high mortality. Despite remarkable achievements in treatment, prognosis remains poor with a survival rate of ∼60% 3 years after diagnosis [1]. The clinical course of the disease (short survival and no cure), as well as its pathophysiological aspects, reveals analogies between IPAH and neoplastic diseases [2]. Abnormalities of pulmonary vasomotor tone only partly explain the mechanism of IPAH and more irrevocable changes, such as resistance to apoptotic signals of pulmonary arterial endothelial cells, may lead to abnormal angioproliferation and an increase in pulmonary vascular resistance [3].We report on a 37-year-old female who presented to our pulmonary arterial hypertension (PAH) referral centre (University Medical Centre Hamburg-Eppendorf, Hamburg, Germany) with severe exercise intolerance in 2000. Her past medical history, drug history and laboratory examinations, including serology for HIV and autoimmune diseases, were unremarkable. Parenchymal lung disease, hepato-splenomegaly or adenopathy were not present on the computed tomography (CT) scan at this time. Right heart catheterisation demonstrated severe pre-capillary pulmonary hypertension, with a mean pulmonary artery pressure (mPAP) of 65 mmHg, right atrial pressure of 8 mmHg, pulmonary arterial wedge pressure of 6 mmHg, pulmonary vascular resistance of 863 dyn·s−1·cm−5, cardiac index of 3.01 L·min−1·m−2 and pulmonary arterial oxygen saturation of 70%. The patient did not respond to an inhaled vasodilatator during diagnostic catheterisation. A full diagnostic work-up, including ventilation/perfusion scanning and pulmonary angiography, ruled out other aetiologies, such as chronic thromboembolic disease, pulmonary veno-occlusive disease (PVOD) or polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder and skin …" @default.
- W2023462472 created "2016-06-24" @default.
- W2023462472 creator A5058582407 @default.
- W2023462472 creator A5061453029 @default.
- W2023462472 creator A5070150190 @default.
- W2023462472 creator A5074139045 @default.
- W2023462472 creator A5077836810 @default.
- W2023462472 creator A5078383767 @default.
- W2023462472 date "2014-04-30" @default.
- W2023462472 modified "2023-09-24" @default.
- W2023462472 title "Complete resolution of idiopathic pulmonary arterial hypertension following chemotherapy" @default.
- W2023462472 cites W10297047 @default.
- W2023462472 cites W1969602301 @default.
- W2023462472 cites W2003880651 @default.
- W2023462472 cites W2014217144 @default.
- W2023462472 cites W2019982202 @default.
- W2023462472 cites W2029754093 @default.
- W2023462472 cites W2033521825 @default.
- W2023462472 cites W2060017024 @default.
- W2023462472 cites W2098368231 @default.
- W2023462472 cites W2101882672 @default.
- W2023462472 cites W2117339256 @default.
- W2023462472 cites W2139960813 @default.
- W2023462472 cites W2168552292 @default.
- W2023462472 cites W2183644045 @default.
- W2023462472 cites W2403335107 @default.
- W2023462472 doi "https://doi.org/10.1183/09031936.00185713" @default.
- W2023462472 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24789952" @default.
- W2023462472 hasPublicationYear "2014" @default.
- W2023462472 type Work @default.
- W2023462472 sameAs 2023462472 @default.
- W2023462472 citedByCount "4" @default.
- W2023462472 countsByYear W20234624722015 @default.
- W2023462472 countsByYear W20234624722017 @default.
- W2023462472 countsByYear W20234624722019 @default.
- W2023462472 countsByYear W20234624722020 @default.
- W2023462472 crossrefType "journal-article" @default.
- W2023462472 hasAuthorship W2023462472A5058582407 @default.
- W2023462472 hasAuthorship W2023462472A5061453029 @default.
- W2023462472 hasAuthorship W2023462472A5070150190 @default.
- W2023462472 hasAuthorship W2023462472A5074139045 @default.
- W2023462472 hasAuthorship W2023462472A5077836810 @default.
- W2023462472 hasAuthorship W2023462472A5078383767 @default.
- W2023462472 hasBestOaLocation W20234624721 @default.
- W2023462472 hasConcept C126322002 @default.
- W2023462472 hasConcept C164705383 @default.
- W2023462472 hasConcept C2776694085 @default.
- W2023462472 hasConcept C2780930700 @default.
- W2023462472 hasConcept C71924100 @default.
- W2023462472 hasConceptScore W2023462472C126322002 @default.
- W2023462472 hasConceptScore W2023462472C164705383 @default.
- W2023462472 hasConceptScore W2023462472C2776694085 @default.
- W2023462472 hasConceptScore W2023462472C2780930700 @default.
- W2023462472 hasConceptScore W2023462472C71924100 @default.
- W2023462472 hasIssue "5" @default.
- W2023462472 hasLocation W20234624721 @default.
- W2023462472 hasLocation W20234624722 @default.
- W2023462472 hasOpenAccess W2023462472 @default.
- W2023462472 hasPrimaryLocation W20234624721 @default.
- W2023462472 hasRelatedWork W2046069863 @default.
- W2023462472 hasRelatedWork W2048862592 @default.
- W2023462472 hasRelatedWork W2333145688 @default.
- W2023462472 hasRelatedWork W2410314862 @default.
- W2023462472 hasRelatedWork W2412645198 @default.
- W2023462472 hasRelatedWork W2595673966 @default.
- W2023462472 hasRelatedWork W2790232384 @default.
- W2023462472 hasRelatedWork W2990595088 @default.
- W2023462472 hasRelatedWork W2999964781 @default.
- W2023462472 hasRelatedWork W584255262 @default.
- W2023462472 hasVolume "43" @default.
- W2023462472 isParatext "false" @default.
- W2023462472 isRetracted "false" @default.
- W2023462472 magId "2023462472" @default.
- W2023462472 workType "article" @default.