Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Jan C Kamp"'
Publikováno v:
PLoS ONE, Vol 16, Iss 10, p e0257807 (2021)
Patients after lung transplantation are at risk for life-threatening infections. Recently, several publications on COVID-19 outcomes in this patient population appeared, but knowledge on optimal treatment, mortality, outcomes, and appropriate risk pr
Externí odkaz:
https://doaj.org/article/531082291f1e43ec82709b3dd4e2f569
Autor:
Athiththan Yogeswaran, Jan Grimminger, Khodr Tello, Lukas Becker, Werner Seeger, Friedrich Grimminger, Natascha Sommer, Hossein A. Ghofrani, Tobias J. Lange, Stefan Stadler, Karen Olsson, Jan C. Kamp, Stephan Rosenkranz, Felix Gerhardt, Katrin Milger, Michaela Barnikel, Silvia Ulrich, Stéphanie Saxer, Ekkehard Grünig, Satenik Harutynova, Christian Opitz, Hans Klose, Heinrike Wilkens, Michael Halank, Melanie Heberling, Henning Gall, Manuel J. Richter
Publikováno v:
Pulmonary Circulation, Vol 14, Iss 3, Pp n/a-n/a (2024)
Abstract The PEGASUS study is the first multicentric and prospective assessment of the safety of air travel flying in pulmonary hypertension (PH) (NCT03051763). Data of air travel from 60 patients with PH was available. No severe adverse events occur
Externí odkaz:
https://doaj.org/article/819d8ab294854ca5b1895bc7859bab93
Autor:
Maximilian Ackermann, Jan C. Kamp, Christopher Werlein, Claire L. Walsh, Helge Stark, Verena Prade, Rambabu Surabattula, Willi L. Wagner, Catherine Disney, Andrew J. Bodey, Thomas Illig, Diana J. Leeming, Morten A. Karsdal, Alexandar Tzankov, Peter Boor, Mark P. Kühnel, Florian P. Länger, Stijn E. Verleden, Hans M. Kvasnicka, Hans H. Kreipe, Axel Haverich, Stephen M. Black, Axel Walch, Paul Tafforeau, Peter D. Lee, Marius M. Hoeper, Tobias Welte, Benjamin Seeliger, Sascha David, Detlef Schuppan, Steven J. Mentzer, Danny D. Jonigk
Publikováno v:
EBioMedicine, Vol 85, Iss , Pp 104296- (2022)
Summary: Background: COVID-19 is characterized by a heterogeneous clinical presentation, ranging from mild symptoms to severe courses of disease. 9–20% of hospitalized patients with severe lung disease die from COVID-19 and a substantial number of
Externí odkaz:
https://doaj.org/article/b4f5f451eaf04dc4b18d8490c6c059a3
Autor:
Athiththan Yogeswaran, Henning Gall, Khodr Tello, Ekkehard Grünig, Panagiota Xanthouli, Ralf Ewert, Jan C. Kamp, Karen M. Olsson, Max Wißmüller, Stephan Rosenkranz, Hans Klose, Lars Harbaum, Tobias J. Lange, Christian F. Opitz, Andrea Waelde, Katrin Milger, Natascha Sommer, Werner Seeger, Hossein Ardeschir Ghofrani, Manuel J. Richter
Publikováno v:
Pulmonary Circulation, Vol 10 (2020)
Pulmonary hypertension is frequently underdiagnosed, and referral is delayed with subsequent impact on outcomes. During the SARS-CoV-2 pandemic, restrictions on daily life and changes in hospitals' daily routine care were introduced in Germany. This
Externí odkaz:
https://doaj.org/article/2ce90324372040b69edf3662435943c0
Autor:
Katharina Schuetz, Axel Schmidt, Nicolaus Schwerk, Diane Renz, Benedicte Gerard, Elise Schaefer, Maria Cristina Antal, Sophia Peters, Matthias Griese, Christina Katharina Rapp, Hartmut Engels, Kirsten Cremer, Anke Katharina Bergmann, Gunnar Schmidt, Bernd Auber, Jan C. Kamp, Florian Laenger, Sandra von Hardenberg
Fibroblast growth factor 10 (FGF10) is a signaling molecule with a well-established role for lung branching morphogenesis. Rare heterozygous, deleterious variants in the FGF10 gene are known causes of the lacrimo-auriculo-dento-digital (LADD) syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78dbf67c778c2221c5a9bb0a65ae45d9
https://doi.org/10.22541/au.168480547.77927589/v1
https://doi.org/10.22541/au.168480547.77927589/v1
Autor:
Jakob Reichmann, Stijn E Verleden, Mark Kühnel, Jan C Kamp, Christopher Werlein, Lavinia Neubert, Jan-Hendrik Müller, Thanh Quynh Bui, Maximilian Ackermann, Danny Jonigk, Tim Salditt
Publikováno v:
Physics in medicine & biology
As the central organ of the respiratory system, the human lung is responsible for supplying oxygen to the blood, which reaches the erythrocytes by diffusion through the alveolar walls and is then distributed throughout the body. By exploiting the dif
Autor:
Jan C. Kamp, Naomi N. Kappe, Carlos Fernández Moro, Jan Fuge, Mark P. Kuehnel, Sabine Wrenger, Tobias Welte, Bart van Hoek, Danny D. Jonigk, Padmini P. S. J. Khedoe, Pavel Strnad, Mikael Björnstedt, Jan Stolk, Sabina Janciauskiene, Antal Nemeth
Publikováno v:
International Journal of Molecular Sciences, 24(3). MDPI
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2485
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2485
PiZZ (Glu342Lys) α1-antitrypsin deficiency (AATD) is characterized by intrahepatic AAT polymerization and is a risk factor for liver disease development in children. The majority of PiZZ children are disease free, hence this mutation alone is not su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86e175275b92ababc9fc315d1d2cb23d
http://hdl.handle.net/1887/3590817
http://hdl.handle.net/1887/3590817
Autor:
Marius M. Hoeper, Da-Hee Park, Jan C. Kamp, Susanne Greve, Karen M. Olsson, Christian Kühn, Constantin von Kaisenberg, Jan Fuge, Lotta Winter
Publikováno v:
The Journal of Heart and Lung Transplantation. 40:229-233
Current guidelines recommend that patients with pulmonary arterial hypertension (PAH) avoid pregnancy because of a high mortality risk for the patients and their offspring. Still, some PAH patients become pregnant. We herein report the mid-term mater
Autor:
Flora Caldarone, Philippa Gebhardt, Marius M. Hoeper, Karen M. Olsson, Jan Fuge, Da-Hee Park, Tanja Meltendorf, Jan C. Kamp, Britta Stapel, Manuel J. Richter, Henning Gall, Hossein A. Ghofrani, Kai G. Kahl, Ivo Heitland
Publikováno v:
Frontiers in Psychiatry. 13
BackgroundThe prevalence of mental disorders, particularly adjustment disorder (AD), major depressive disorder (MDD) and panic disorder (PD) is increased in patients with pulmonary arterial hypertension (PAH). However, it is unclear which pathogenic
Autor:
Madelaine-Rachel Dering, Nicole Lepsy, Jan Fuge, Tanja Meltendorf, Marius M. Hoeper, Ivo Heitland, Jan C. Kamp, Da-Hee Park, Manuel J. Richter, Henning Gall, Hossein A. Ghofrani, Dietmar Ellermeier, Hans-Dieter Kulla, Kai G. Kahl, Karen M. Olsson
Publikováno v:
Frontiers in Psychiatry. 13
ObjectivePulmonary hypertension (PH) is a chronic and progressive pulmonary vascular disease resulting in symptoms such as shortness of breath and fatigue and leading to death from right heart failure if not adequately treated. Chronic thromboembolic