Zobrazeno 1 - 10
of 688
pro vyhledávání: '"Douschan, P."'
Autor:
Katarina Zeder, Teresa Sassmann, Vasile Foris, Philipp Douschan, Horst Olschewski, Gabor Kovacs
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 17, Iss , Pp 100519- (2024)
Rationale: Severe pulmonary hypertension (PH) in chronic obstructive pulmonary disease (COPD) is currently defined by an elevated mean pulmonary arterial pressure and strongly elevated pulmonary vascular resistance >5 wood units. Clinically, these pa
Externí odkaz:
https://doaj.org/article/86d84c02f6d14a54bbe3bbfdaac2b777
Autor:
Manuel J. Richter, Philipp Douschan, Federico Fortuni, Henning Gall, Hossein A. Ghofrani, Stanislav Keranov, Nils Kremer, Steffen D. Kriechbaum, Zvonimir A. Rako, Andreas J. Rieth, Bruno Brito daRocha, Werner Seeger, Daniel Zedler, Selin Yildiz, Athiththan Yogeswaran, Khodr Tello
Publikováno v:
ESC Heart Failure, Vol 10, Iss 5, Pp 3209-3215 (2023)
Abstract Aims Commercially available integrated software for echocardiographic measurement of stroke work (SW) is increasingly used for the right ventricle, despite a lack of validation. We sought to assess the validity of this method [echo‐based m
Externí odkaz:
https://doaj.org/article/f4b68dc31882487bb4e6ff94fa1cddd3
Autor:
Florian Posch, Luka Brčić, Gudrun Absenger, Verena Schlintl, Nikolaus John, Robert Wurm, Philipp J Jost, Angelika Terbuch, Teresa Sassmann, Jörg Lindenmann, Melanie Fediuk, Philipp Douschan, Martin Zacharias, Lipika Kalson
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 12, Iss 4 (2024)
Background The use and approval of immune checkpoint inhibitors for the treatment of non-small cell lung cancer (NSCLC) depends on PD-L1 expression in the tumor tissue. Nevertheless, PD-L1 often fails to predict response to treatment. One possible ex
Externí odkaz:
https://doaj.org/article/7b357905ef25400b8600961cad6d9dc2
Akademický článek
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Autor:
Zeder K; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz.; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.; Division of Cardiovascular Medicine, University of Maryland School of Medicine, Baltimore.; University of Maryland-Institute for Health Computing, Bethesda, Maryland, USA., Douschan P; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz.; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria., Foris V; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz.; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA., Sassmann T; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz.; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria., Maron BA; Division of Cardiovascular Medicine, University of Maryland School of Medicine, Baltimore.; University of Maryland-Institute for Health Computing, Bethesda, Maryland, USA., Olschewski H; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz.; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria., Kovacs G; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz.; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.
Publikováno v:
Current opinion in pulmonary medicine [Curr Opin Pulm Med] 2024 Sep 01; Vol. 30 (5), pp. 451-458. Date of Electronic Publication: 2024 Jul 03.
Autor:
Teresa Sassmann, Philipp Douschan, Vasile Foris, Natascha Tröster, Katarina Zeder, Luka Brcic, Adrienn Tornyos, Gerhard Bachmaier, Michael Fuchsjäger, Horst Olschewski, Gabor Kovacs
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Pulmonary hypertension (PH) is a frequent complication in COPD and it is associated with decreased exercise capacity and poor prognosis. We hypothesized that even in COPD patients without significant PH at rest, abnormal pulmonary
Externí odkaz:
https://doaj.org/article/714192d0a4f34031b2fd0d93de53f2cc
Autor:
Athiththan Yogeswaran, Zvonimir A. Rako, Selin Yildiz, Hossein Ardeschir Ghofrani, Werner Seeger, Bruno Brito da Rocha, Henning Gall, Nils C. Kremer, Philipp Douschan, Silvia Papa, Carmine Dario Vizza, Domenico Filomena, Ryan J. Tedford, Robert Naeije, Manuel J. Richter, Roberto Badagliacca, Khodr Tello
Publikováno v:
ERJ Open Research, Vol 9, Iss 5 (2023)
Background Right ventricular (RV) diastolic dysfunction may be prognostic in pulmonary hypertension (PH). However, its assessment is complex and relies on conductance catheterisation. We aimed to evaluate echocardiography-based parameters as surrogat
Externí odkaz:
https://doaj.org/article/c85bc48591ed407c9f3a3d167f8b3a72
Akademický článek
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Autor:
Vasile Foris, Gabor Kovacs, Alexander Avian, Zoltán Bálint, Philipp Douschan, Bahil Ghanim, Walter Klepetko, Andrea Olschewski, Horst Olschewski
Publikováno v:
Frontiers in Physiology, Vol 13 (2023)
Background: NT-proBNP and GDF-15 are established blood-derived biomarkers for risk assessment in pulmonary hypertension (PH), despite limited sensitivity and specificity. Apelin has a crucial function in endothelial homeostasis, thus it might represe
Externí odkaz:
https://doaj.org/article/9b4ebb590a874cb0a61e6b956be28d58
Akademický článek
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