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Akademický článek
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Autor:
Harald Kaemmerer, Matthias Gorenflo, Dörte Huscher, David Pittrow, Christian Apitz, Helmut Baumgartner, Felix Berger, Leonhard Bruch, Eva Brunnemer, Werner Budts, Martin Claussen, Gerry Coghlan, Ingo Dähnert, Michele D’Alto, Marion Delcroix, Oliver Distler, Sven Dittrich, Daniel Dumitrescu, Ralf Ewert, Martin Faehling, Ingo Germund, Hossein Ardeschir Ghofrani, Christian Grohé, Karsten Grossekreymborg, Michael Halank, Georg Hansmann, Dominik Harzheim, Attila Nemes, Kalman Havasi, Matthias Held, Marius M. Hoeper, Michael Hofbeck, Wolfgang Hohenfrost-Schmidt, Elena Jurevičienė, Lina Gumbienè, Hans-Joachim Kabitz, Hans Klose, Thomas Köhler, Stavros Konstantinides, Martin Köestenberger, Rainer Kozlik-Feldmann, Hans-Heiner Kramer, Cornelia Kropf-Sanchen, Astrid Lammers, Tobias Lange, Philipp Meyn, Oliver Miera, Katrin Milger-Kneidinger, Rhoia Neidenbach, Claus Neurohr, Christian Opitz, Christian Perings, Bjoern Andrew Remppis, Gabriele Riemekasten, Laura Scelsi, Werner Scholtz, Iveta Simkova, Dirk Skowasch, Andris Skride, Gerd Stähler, Brigitte Stiller, Iraklis Tsangaris, Carmine Dario Vizza, Anton Vonk Noordegraaf, Heinrike Wilkens, Hubert Wirtz, Gerhard-Paul Diller, Ekkehard Grünig, Stephan Rosenkranz
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 5, p 1456 (2020)
Introduction: Pulmonary hypertension (PH) is a common complication in patients with congenital heart disease (CHD), aggravating the natural, post-operative, or post-interventional course of the underlying anomaly. The various CHDs differ substantiall
Externí odkaz:
https://doaj.org/article/208b2fcce4c14f418708c42008cb333f
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Harald Kaemmerer, Christian Opitz, Juergen Behr, Marius M. Hoeper, Iraklis Tsangaris, Doerte Huscher, Hans-Jürgen Seyfarth, Andris Skride, Silvia Ulrich, Michael Halank, Henning Gall, Ralf Ewert, Christine Pausch, Carmine Dario Vizza, Katrin Milger, Matthias Held, Gerd Staehler, Oliver Distler, Martin Claussen, Stephan Rosenkranz, Karen M. Olsson, Daniel Dumitrescu, Hans Klose, Anton Vonk-Noordegraaf, H. Ardeschir Ghofrani, Tobias J. Lange, Ekkehard Grünig, Hans-Joachim Kabitz, Da-Hee Park, Heinrike Wilkens, Dirk Skowasch, David Pittrow, Marion Delcroix, J. Simon R. Gibbs
Publikováno v:
Hoeper, M M, Pausch, C, Grünig, E, Staehler, G, Huscher, D, Pittrow, D, Olsson, K M, Vizza, C D, Gall, H, Distler, O, Opitz, C, Gibbs, J S R, Delcroix, M, Ghofrani, H A, Rosenkranz, S, Park, D-H, Ewert, R, Kaemmerer, H, Lange, T J, Kabitz, H-J, Skowasch, D, Skride, A, Claussen, M, Behr, J, Milger, K, Halank, M, Wilkens, H, Seyfarth, H-J R, Held, M, Dumitrescu, D, Tsangaris, I, Vonk-Noordegraaf, A, Ulrich, S & Klose, H 2022, ' Temporal trends in pulmonary arterial hypertension : results from the COMPERA registry ', European Respiratory Journal, vol. 59, no. 6, 2102024 . https://doi.org/10.1183/13993003.02024-2021
European Respiratory Journal, 59(6):2102024. European Respiratory Society
European Respiratory Journal, 59(6):2102024. European Respiratory Society
BackgroundSince 2015, the European pulmonary hypertension guidelines recommend the use of combination therapy in most patients with pulmonary arterial hypertension (PAH). However, it is unclear to what extent this treatment strategy is adopted in cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96f663b40c819bb85ab759173ac35bfd
http://hdl.handle.net/11573/1635500
http://hdl.handle.net/11573/1635500
Akademický článek
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Autor:
Carmine Dario, Vizza, Marius M, Hoeper, Doerte, Huscher, David, Pittrow, Nicola, Benjamin, Karen M, Olsson, H Ardeschir, Ghofrani, Matthias, Held, Hans, Klose, Tobias, Lange, Stephan, Rosenkranz, Daniel, Dumitrescu, Roberto, Badagliacca, Martin, Claussen, Michael, Halank, Anton, Vonk-Noordegraaf, Dirk, Skowasch, Ralf, Ewert, J Simon R, Gibbs, Marion, Delcroix, Andris, Skride, Gerry, Coghlan, Silvia, Ulrich, Christian, Opitz, Harald, Kaemmerer, Oliver, Distler, Ekkehard, Grünig
BACKGROUND: Pulmonary hypertension (PH) in COPD is a poorly investigated clinical condition. RESEARCH QUESTION: Which factors determine the outcome of PH in COPD? STUDY DESIGN AND METHODS: We analyzed the characteristics and outcome of patients enrol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::44242e5b580a30450a1e82d2653d8c09
http://hdl.handle.net/11573/1627272
http://hdl.handle.net/11573/1627272
Autor:
Elena Jureviciene, Marion Delcroix, David Pittrow, Werner Scholtz, Oliver Distler, Hans-Joachim Kabitz, Ralf Ewert, Karen M. Olsson, Gerry Coghlan, J. Simon R. Gibbs, Harald Kaemmerer, Elena Pfeuffer-Jovic, H. Ardeschir Ghofrani, Matthias Gorenflo, Martin Claussen, Dirk Skowasch, Tobias J. Lange, Hubert Wirtz, Ekkehard Grünig, Doerte Huscher, Nicola Benjamin, Leonhard Bruch, Christine Pausch, Katrin Milger, Anton Vonk-Noordegraaf, Heinrike Wilkens, Michael Halank, Andris Skride, Henning Gall, Juergen Behr, Laura Scelsi, Stephan Rosenkranz, Carmine Dario Vizza, Christian Opitz, Claus Neurohr, Marius M. Hoeper, Egle Paleviciute, Hans Klose, Silvia Ulrich, Daniel Dumitrescu, Iraklis Tsangaris, Lars Harbaum, Matthias Held, Gerd Staehler, Skaidrius Miliauskas
Publikováno v:
Journal of Heart and Lung Transplantation, New York : Elsevier Inc., 2020, vol. 39, no. 12, p. 1435-1444
Journal of heart and lung transplantation, New York : Elsevier Inc., 2020, vol. 39, no. 12, p. 1435-1444
Journal of heart and lung transplantation, New York : Elsevier Inc., 2020, vol. 39, no. 12, p. 1435-1444
The term idiopathic pulmonary arterial hypertension (IPAH) is used to categorize patients with pre-capillary pulmonary hypertension of unknown origin. There is considerable variability in the clinical presentation of these patients. Using data from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0060ee38e05a996eb6050c598be0cac2
https://lirias.kuleuven.be/handle/123456789/662866
https://lirias.kuleuven.be/handle/123456789/662866
Autor:
Wolfgang Hohenfrost-Schmidt, Felix Berger, Hans-Heiner Kramer, Ingo Germund, Eva Brunnemer, Claus Neurohr, Kálmán Havasi, Bjoern Andrew Remppis, Michele D'Alto, Marius M. Hoeper, David Pittrow, Marion Delcroix, Michael Hofbeck, Christian Perings, Rhoia Neidenbach, Werner Scholtz, Tobias Lange, Oliver Distler, Gerhard-Paul Diller, Karsten Grossekreymborg, Christian Opitz, Heinrike Wilkens, Philipp Meyn, Rainer Kozlik-Feldmann, Sven Dittrich, Lina Gumbiene, Martin Claussen, Brigitte Stiller, Gabriele Riemekasten, Elena Jurevičienė, Helmut Baumgartner, Hubert Wirtz, Laura Scelsi, Cornelia Kropf-Sanchen, Attila Nemes, Leonhard Bruch, Ralf Ewert, Hans Klose, Iraklis Tsangaris, Dörte Huscher, Christian Grohé, Werner Budts, Katrin Milger-Kneidinger, Matthias Gorenflo, Dirk Skowasch, Gerd Stähler, Anton Vonk Noordegraaf, Michael Halank, Iveta Simkova, Oliver Miera, Andris Skride, Christian Apitz, Harald Kaemmerer, TC Köhler, Daniel Dumitrescu, Ingo Dähnert, Martin Koestenberger, Gerry Coghlan, Hossein Ardeschir Ghofrani, Stavros Konstantinides, Carmine Dario Vizza, Astrid E. Lammers, Stephan Rosenkranz, Martin Faehling, Ekkehard Grünig, Matthias Held, Dominik Harzheim, Georg Hansmann, Hans-Joachim Kabitz
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 5
Journal of Clinical Medicine, Vol 9, Iss 1456, p 1456 (2020)
Journal of clinical medicine, Basel : MDPI, 2020, vol. 9, no. 5, art. no. 1456, p. [1-21]
Kaemmerer, H, Gorenflo, M, Huscher, D R, Pittrow, D, Apitz, C, Baumgartner, H, Berger, F, Bruch, L, Brunnemer, E, Budts, W, Claussen, M, Coghlan, G, Dähnert, I, D’alto, M, Delcroix, M, Distler, O, Dittrich, S, Dumitrescu, D, Ewert, R, Faehling, M, Germund, I, Ghofrani, H A, Grohé, C, Grossekreymborg, K, Halank, M, Hansmann, G, Harzheim, D, Nemes, A, Havasi, K, Held, M, Hoeper, M M, Hofbeck, M, Hohenfrost-Schmidt, W, Jurevičienė, E, Gumbienè, L, Kabitz, H-J, Klose, H, Köhler, T, Konstantinides, S, Köestenberger, M, Kozlik-Feldmann, R, Kramer, H-H, Kropf-Sanchen, C, Lammers, A, Lange, T, Meyn, P, Miera, O, Milger-Kneidinger, K, Neidenbach, R, Neurohr, C, Opitz, C, Perings, C, Remppis, B A, Riemekasten, G, Scelsi, L, Scholtz, W, Simkova, I, Skowasch, D, Skride, A, Stähler, G, Stiller, B, Tsangaris, I, Vizza, C D, Noordegraaf, A V, Wilkens, H, Wirtz, H, Diller, G-P, Grünig, E & Rosenkranz, S 2020, ' Pulmonary hypertension in adults with congenital heart disease: Real-world data from the international compera-chd registry ', Clinical Chemistry, vol. 9, no. 5, 1456 . https://doi.org/10.3390/jcm9051456
Clinical Chemistry, 9(5):1456
Volume 9
Issue 5
Journal of Clinical Medicine, Vol 9, Iss 1456, p 1456 (2020)
Journal of clinical medicine, Basel : MDPI, 2020, vol. 9, no. 5, art. no. 1456, p. [1-21]
Kaemmerer, H, Gorenflo, M, Huscher, D R, Pittrow, D, Apitz, C, Baumgartner, H, Berger, F, Bruch, L, Brunnemer, E, Budts, W, Claussen, M, Coghlan, G, Dähnert, I, D’alto, M, Delcroix, M, Distler, O, Dittrich, S, Dumitrescu, D, Ewert, R, Faehling, M, Germund, I, Ghofrani, H A, Grohé, C, Grossekreymborg, K, Halank, M, Hansmann, G, Harzheim, D, Nemes, A, Havasi, K, Held, M, Hoeper, M M, Hofbeck, M, Hohenfrost-Schmidt, W, Jurevičienė, E, Gumbienè, L, Kabitz, H-J, Klose, H, Köhler, T, Konstantinides, S, Köestenberger, M, Kozlik-Feldmann, R, Kramer, H-H, Kropf-Sanchen, C, Lammers, A, Lange, T, Meyn, P, Miera, O, Milger-Kneidinger, K, Neidenbach, R, Neurohr, C, Opitz, C, Perings, C, Remppis, B A, Riemekasten, G, Scelsi, L, Scholtz, W, Simkova, I, Skowasch, D, Skride, A, Stähler, G, Stiller, B, Tsangaris, I, Vizza, C D, Noordegraaf, A V, Wilkens, H, Wirtz, H, Diller, G-P, Grünig, E & Rosenkranz, S 2020, ' Pulmonary hypertension in adults with congenital heart disease: Real-world data from the international compera-chd registry ', Clinical Chemistry, vol. 9, no. 5, 1456 . https://doi.org/10.3390/jcm9051456
Clinical Chemistry, 9(5):1456
Introduction: Pulmonary hypertension (PH) is a common complication in patients with congenital heart disease (CHD), aggravating the natural, post-operative, or post-interventional course of the underlying anomaly. The various CHDs differ substantiall