Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Matthias Wiebel"'
Autor:
Mark O Wielpütz, Oliver Weinheimer, Monika Eichinger, Matthias Wiebel, Jürgen Biederer, Hans-Ulrich Kauczor, Claus P Heußel, Marcus A Mall, Michael Puderbach
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e73142 (2013)
BackgroundHistopathological studies on lung specimens from patients with cystic fibrosis (CF) and recent results from a mouse model indicate that emphysema may contribute to CF lung disease. However, little is known about the relevance of emphysema i
Externí odkaz:
https://doaj.org/article/c3bd6750fc2b491ea236c096d4990ed1
Autor:
Marie-Christine Vantyghem, Dominique Hubert, Andreas Claaß, Anne Munck, Doris Staab, Ute Staden, Helmut Teschler, Klaus-Michael Keller, Laurence Kessler, Horst Generlich, Guy-André Loeuille, Helen Mosnier-Pudar, Gabriela H. Thalhammer, Tanja Nickolay, Matthias V. Kopp, Nicole Prinz, Gérard Lenoir, Jürgen Hautz, Irmgard Eichler, Rüdiger Szczepanski, R Serreau, Jean-Jacques Robert, Hans-Georg Bresser, Birgit Schilling, Baroukh M. Assael, Martin Stern, Manfred Ballmann, Christina Smaczny, Egbert Herting, Matthias Wiebel, Lutz Naehrlich, Uwe Mellies, Hans-Georg Posselt, Ernst Rietschel, Thomas Biedermann, Thomas Köhnlein, Ernst-Hinrich Ballke, Wolfgang Kamin, Antje Schuster, Gerd Dockter, Holger Köster, Nathalie Wizla, Wolfram Wiebicke, Hans-Joachim Feickert, Manfred Götz, Sylvie Leroy, Marcus A Mall, Fawzia Aissat, Helge Hebestreit, Vera Wienhausen-Wilke, H.-E. Heuer, Isidor Huttegger, Alexandra Hebestreit, Raphaële Nove-Josserand, Laurence Weiss, Martin Claßen, Marguerite Honer, Reinhard W. Holl, Friedrich-Karl Tegtmeyer, Egbert Meyer, Peter Küster
Publikováno v:
The Lancet Diabetes & Endocrinology. 6:114-121
Summary Background As survival among patients with cystic fibrosis has improved in recent decades, complications have become increasingly relevant. The most frequent complication is cystic-fibrosis-related diabetes. The recommended treatment is injec
Publikováno v:
Seltene Lungenerkrankungen ISBN: 9783662484180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45c5cbf8853238b6eca208e3764fcebb
https://doi.org/10.1007/978-3-662-48419-7_20
https://doi.org/10.1007/978-3-662-48419-7_20
Publikováno v:
Medizinische Klinik. 101:148-152
Autor:
Bernd Schucher, Klaus Freidel, Matthias Wiebel, Hansjörg Baumann, Heinrich Matthys, Franz Petermann, Wolfram Windisch
Publikováno v:
Journal of Clinical Epidemiology. 56:752-759
The objective of this study was to develop a specific instrument for measuring health-related quality of life (HRQL) in patients receiving home mechanical ventilation (HMV).The Severe Respiratory Insufficiency (SRI) Questionnaire was developed and te
Autor:
Klaus Freidel, Bernd Schucher, Hansjörg Baumann, Matthias Wiebel, Franz Petermann, Heinrich Matthys, Wolfram Windisch
Publikováno v:
Intensive Care Medicine. 29:615-621
To collect benchmark data on the MOS 36-Item Short-Form Health Status Survey (SF-36) in patients receiving noninvasive positive pressure ventilation and to examine whether health-related quality of life is influenced by the underlying disease or by p
Publikováno v:
Lecture Notes in Computer Science ISBN: 9783642216510
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc64bd8a13d643ed86327a9b4e02cb0e
https://doi.org/10.1007/978-3-642-21652-7_4
https://doi.org/10.1007/978-3-642-21652-7_4
Autor:
Michael, Kreuter, Ralf, Eberhardt, Matthias, Wiebel, Martin R, Schulz, Klaus-Michael, Mueller, Felix Jf, Herth
Publikováno v:
Respiratory care. 55(7)
We present a case of a 65-year-old man with recurrent hemoptysis and weight loss for 6 months. Thirty-two years earlier, lobectomy of the right lower lobe had been performed for abcessing pneumonia. Due to recurrent pulmonary infections after lobecto
Autor:
Heidi Rossmann, Matthias Wiebel, Carolin Neukirch, Wolfgang Kamin, Jürgen J. Wenzel, Manfred Stuhrmann, Julia K. Bickmann, Friederike Häuser, Karl J. Lackner
Publikováno v:
Clinical chemistry. 55(6)
Background: Cystic fibrosis (CF) is a common autosomal recessive genetic disorder caused by a variety of sequence alterations in the CFTR gene [cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)]. Becaus
Autor:
Holger, Hein, Kurt, Rasche, Matthias, Wiebel, Martin, Winterholler, Gerhard, Laier-Groeneveld
Publikováno v:
Medizinische Klinik (Munich, Germany : 1983). 101(2)