Zobrazeno 1 - 10
of 90
pro vyhledávání: '"K. Michl"'
Autor:
J. Englert, A. Claude, A. Demichelis, S. Persijn, A. Baldan, J. Li, C. Plass-Duelmer, K. Michl, E. Tensing, R. Wortman, Y. Ghorafi, M. Lecuna, G. Sassi, M. P. Sassi, D. Kubistin
Publikováno v:
Atmospheric Measurement Techniques, Vol 11, Pp 3197-3203 (2018)
Air quality observations are performed globally to monitor the status of the atmosphere and its level of pollution and to assess mitigation strategies. Regulations of air quality monitoring programmes in various countries demand high-precision mea
Externí odkaz:
https://doaj.org/article/dc2fd0cbdf824683ac175e026bf48cde
Autor:
C. C. Hoerger, A. Claude, C. Plass-Duelmer, S. Reimann, E. Eckart, R. Steinbrecher, J. Aalto, J. Arduini, N. Bonnaire, J. N. Cape, A. Colomb, R. Connolly, J. Diskova, P. Dumitrean, C. Ehlers, V. Gros, H. Hakola, M. Hill, J. R. Hopkins, J. Jäger, R. Junek, M. K. Kajos, D. Klemp, M. Leuchner, A. C. Lewis, N. Locoge, M. Maione, D. Martin, K. Michl, E. Nemitz, S. O'Doherty, P. Pérez Ballesta, T. M. Ruuskanen, S. Sauvage, N. Schmidbauer, T. G. Spain, E. Straube, M. Vana, M. K. Vollmer, R. Wegener, A. Wenger
Publikováno v:
Atmospheric Measurement Techniques, Vol 8, Iss 7, Pp 2715-2736 (2015)
The performance of 18 European institutions involved in long-term non-methane hydrocarbon (NMHC) measurements in ambient air within the framework of the Global Atmosphere Watch (GAW) and the European Monitoring and Evaluation Programme (EMEP) was ass
Externí odkaz:
https://doaj.org/article/f8029415a03245218820ac4e375d6c5e
Akademický článek
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Autor:
Ruth K. Michl, Anke Jaudszus, Michael Lorenz, Elena Pfeifer, Christin Arnold, Tatjana Jans, Harold Tabori, Elisa Zeman, N. Beiersdorf, Jochen G. Mainz
Publikováno v:
The Patient - Patient-Centered Outcomes Research. 12:419-428
For people with cystic fibrosis, validated patient-reported outcome measures for the assessment of the complex abdominal involvement are lacking. The objective of this study was to examine whether the CFAbd-Score, a novel questionnaire consisting of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df0c65a91b8c0297b589545f66f97fe7
https://doi.org/10.1007/s40271-019-00361-2
https://doi.org/10.1007/s40271-019-00361-2
Autor:
Jochen G. Mainz, N. Beiersdorf, Tanja Groten, Ruth K. Michl, Uwe Schneider, Anke Jaudszus, Michael Lorenz
Publikováno v:
Klinische Pädiatrie. 231:271-273
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7050b092357427a4a43f6f45c3710adc
https://doi.org/10.1055/a-0973-8565
https://doi.org/10.1055/a-0973-8565
Autor:
Ruth K. Michl, Diane M. Renz, Thomas Lehmann, Anke Jaudszus, Jochen G. Mainz, Harold Tabori, Hans-Joachim Mentzel, Michael Lorenz, Christin Arnold
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports
Scientific Reports
Abdominal symptoms are a hallmark of Cystic fibrosis (CF). Yet, their association with morphological abnormalities of different abdominal organs is still poorly understood. Aim was therefore to relate these symptoms, assessed with a questionnaire, to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c23efd55133363f26f0154b8dc12c34
http://link.springer.com/article/10.1038/s41598-017-17302-4
http://link.springer.com/article/10.1038/s41598-017-17302-4
Publikováno v:
Frauenheilkunde up2date. 10:380-387
Die Lebenserwartung von Mukoviszidose-Patienten stieg dank intensiver Forschung und Therapie in den letzten 4 Jahrzehnten vom Vorschulalter auf heute uber 40 Jahre. Entsprechend nimmt auch die Anzahl von Schwangerschaften an Mukoviszidose erkrankter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::746d30c8d663620bf75199aebbe620bf
https://doi.org/10.1055/s-0042-113794
https://doi.org/10.1055/s-0042-113794
Publikováno v:
Expert Review of Respiratory Medicine. 10:1177-1186
Cystic fibrosis (CF) is the most frequent life-shortening autosomal recessive disorder in Caucasians. Defects or absence of the CF-transmembrane conductance regulator impair ion transport in apical membranes of exocrine glands. Leading symptoms of ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::361d93c03734fa99e298941e8350cb59
https://doi.org/10.1080/17476348.2016.1240032
https://doi.org/10.1080/17476348.2016.1240032
Autor:
Mathias W. Pletz, Ruth K. Michl, Jochen G. Mainz, Michael Lorenz, A. Gerber, Andreas H. Mueller, James F. Beck, Anika Nader, Julia Hentschel
Publikováno v:
Case Reports in Infectious Diseases
Case Reports in Infectious Diseases, Vol 2015 (2015)
Case Reports in Infectious Diseases, Vol 2015 (2015)
Introduction. P. aeruginosais the primary cause for pulmonary destruction and premature death in cystic fibrosis (CF). Therefore, prevention of airway colonization with the pathogen, ubiquitously present in water, is essential. Infection of CF patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1227c7f3e83a6f000a198b18fbced5e
https://doi.org/10.1155/2015/438517
https://doi.org/10.1155/2015/438517
Publikováno v:
Klinische Padiatrie. 229(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a69866f3ce7b17779ac66273f37e8181
https://pubmed.ncbi.nlm.nih.gov/28558414
https://pubmed.ncbi.nlm.nih.gov/28558414