Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Claudia Wojnarowski"'
Autor:
Ernst Mayerhofer, Franz Ratzinger, Nina Elvira Kienreich, Annika Stiel, Nadine Witzeneder, Eva Schrefl, Georg Greiner, Christoph Wegscheider, Irene Graf, Klaus Schmetterer, Rodrig Marculescu, Thomas Szekeres, Thomas Perkmann, Martina Fondi, Oswald Wagner, Harald Esterbauer, Matthias Mayerhofer, Stefana Holocher-Ertl, Claudia Wojnarowski, Gregor Hoermann
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Childhood obesity is an increasing health care problem associated with insulin resistance and low-level systemic inflammation, which can ultimately lead to diabetes. Evidence for efficacy of therapeutic intervention programs on the early development
Externí odkaz:
https://doaj.org/article/cffa419098c14a47b31378d11cd327cd
Autor:
Anna Maria Cavini, Doris Ehringer-Schetitska, Dieter Furthner, Susanne Greber-Platzer, Adrian Kamper, Roman Metzger, Katharina Mörwald, Sabine Scholl-Bürgi, André van Egmond-Fröhlich, Daniel Weghuber, Kurt Widhalm, Claudia Wojnarowski
Publikováno v:
Pädiatrie & Pädologie. 57:2-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a93a8b9315b7e6a27de75c9791d7f3c4
https://doi.org/10.1007/s00608-022-00967-0
https://doi.org/10.1007/s00608-022-00967-0
Autor:
Regina Rath, G. Halmerbauer, Thomas Frischer, I Eichler, C. Gartner, Claudia Wojnarowski, Manfred Götz, E. Tauber
Publikováno v:
Pediatric Pulmonology. 33:263-268
Improved care for patients with cystic fibrosis (CF) has led to their improved survival. We analyzed retrospectively whether improvements in lung function (LF) could be detected in our CF patients over the decade 1980–1990. In 72 patients, 153 LF m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cedd3521eba02a312536a6a05921d6d8
https://doi.org/10.1002/ppul.10076
https://doi.org/10.1002/ppul.10076
Autor:
Christian J. Herold, Gertraud Heinz-Peer, Patrick Wunderbaldinger, Claudia Wojnarowski, Irmgard Eichler, Robert C. Brasch, Manfred Götz, Thomas H. Helbich
Publikováno v:
Radiology. 213:537-544
To compare a computed tomographic (CT)-based scoring system with nonimaging indexes of pulmonary status in patients with cystic fibrosis.Pulmonary CT findings were assessed in 117 patients with cystic fibrosis, with cases classified according to thre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::160a65991b0051a4ed479d36312bd21c
https://doi.org/10.1148/radiology.213.2.r99nv04537
https://doi.org/10.1148/radiology.213.2.r99nv04537
Autor:
Irmgard Eichler, Dominik Fleischmann, Sabine Huber, Christian J. Herold, Claudia Wojnarowski, Thomas H. Helbich, Gertraud Heinz-Peer, Patrick Wunderbaldinger
Publikováno v:
American Journal of Roentgenology. 173:81-88
The aim of our study was to assess the evolution of pulmonary CT findings in cystic fibrosis patients.Serial CT examinations were performed in four different follow-up periods on 107 patients with cystic fibrosis. Lung images of the initial and follo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27c6c3f4ee398fd7560cff79526864a4
https://doi.org/10.2214/ajr.173.1.10397104
https://doi.org/10.2214/ajr.173.1.10397104
Autor:
Thomas Frischer, I Eichler, Kurt Herkner, Georg Weinländer, D. Y. Koller, Claudia Wojnarowski, Markus Raderer
Publikováno v:
Journal of Allergy and Clinical Immunology. 99:752-756
In association with respiratory tract infections, infants may have episodes of wheezing, which represent the onset of asthma in some of them. Activated eosinophils play a central part in asthmatic inflammation.We investigated whether, in infants expe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b28dbdfe49023d7f4096179078d4086
https://doi.org/10.1016/s0091-6749(97)80007-3
https://doi.org/10.1016/s0091-6749(97)80007-3
Autor:
Erich, Tauber, Irmgard, Eichler, Christian, Gartner, Gerhard, Halmerbauer, Manfred, Götz, Regina, Rath, Claudia, Wojnarowski, Thomas, Frischer
Publikováno v:
Pediatric pulmonology. 33(4)
Improved care for patients with cystic fibrosis (CF) has led to their improved survival. We analyzed retrospectively whether improvements in lung function (LF) could be detected in our CF patients over the decade 1980-1990. In 72 patients, 153 LF mea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc0c7f48c4d0cbd4d3ed0642458f2bb1
https://pubmed.ncbi.nlm.nih.gov/11921455
https://pubmed.ncbi.nlm.nih.gov/11921455
Autor:
Johannes Forster, G. Halmerbauer, Joachim Kuehr, Claudia Wojnarowski, Thomas Frischer, C. Gartner, E. Mayatepek
Publikováno v:
Allergy. 56(9)
Background: Eosinophilic airways inflammation forms the pathophysiologic basis for a proportion of children at risk of developing recurrent wheezing. Early preventive measures and/or anti-inflammatory treatment may be guided by the identification of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cfaa4ef99a46b5fb5bb2ff67b5697cd
https://pubmed.ncbi.nlm.nih.gov/11551254
https://pubmed.ncbi.nlm.nih.gov/11551254
Publikováno v:
Transplantation. 64(5)
Twenty-one to 63% of patients with cystic fibrosis (CF) accepted for lung and heart-lung transplantation die on the waiting list. A significant delay between referral and assessment may present an unrecognized hazard toward mortality.All parents of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff29b79ce79716667b469c3ad143d070
https://pubmed.ncbi.nlm.nih.gov/9311713
https://pubmed.ncbi.nlm.nih.gov/9311713