Zobrazeno 1 - 10
of 144
pro vyhledávání: '"O. F. Wagner"'
Autor:
Helge Hebestreit, Cornelia Zeidler, Christopher Schippers, Martina de Zwaan, Jürgen Deckert, Peter Heuschmann, Christian Krauth, Monika Bullinger, Alexandra Berger, Mark Berneburg, Lilly Brandstetter, Anna Deibele, Jan Dieris-Hirche, Holm Graessner, Harald Gündel, Stephan Herpertz, Gereon Heuft, Anne-Marie Lapstich, Thomas Lücke, Tim Maisch, Christine Mundlos, Andrea Petermann-Meyer, Susanne Müller, Stephan Ott, Lisa Pfister, Julia Quitmann, Marcel Romanos, Frank Rutsch, Kristina Schaubert, Katharina Schubert, Jörg B. Schulz, Susann Schweiger, Oliver Tüscher, Kathrin Ungethüm, Thomas O. F. Wagner, Kirsten Haas, ZSE-DUO working group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background In individuals suffering from a rare disease the diagnostic process and the confirmation of a final diagnosis often extends over many years. Factors contributing to delayed diagnosis include health care professionals' limited know
Externí odkaz:
https://doaj.org/article/e133f2dc7c254cdaa0e70f98011f467c
Autor:
Alexandra Berger, Anne-Kathrin Rustemeier, Jens Göbel, Dennis Kadioglu, Vanessa Britz, Katharina Schubert, Klaus Mohnike, Holger Storf, Thomas O. F. Wagner
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Abstract Background About 30 million people in the EU and USA, respectively, suffer from a rare disease. Driven by European legislative requirements, national strategies for the improvement of care in rare diseases are being developed. To improve tim
Externí odkaz:
https://doaj.org/article/1d574d5518b242cb9bc721747a472dc6
Autor:
Tabea Horn, Michael Ludwig, Olaf Eickmeier, Anne H. Neerinex, Anke H. Maitland-van der Zee, Christina Smaczny, Thomas O. F. Wagner, Ralf Schubert, Stefan Zielen, Christof Majoor, Lieuwe D. Bos, Sabina Schmitt-Grohé
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundLung disease phenotype varies widely even in the F508del (homozygous) genotype. Leukocyte-driven inflammation is important for pulmonary disease pathogenesis in cystic fibrosis (CF). Blood cytokines correlate negatively with pulmonary funct
Externí odkaz:
https://doaj.org/article/2ab698d1b93c4ae189b24ff5e33b561e
Autor:
Ana Babac, Martin Frank, Frédéric Pauer, Svenja Litzkendorf, Daniel Rosenfeldt, Verena Lührs, Lisa Biehl, Tobias Hartz, Holger Storf, Franziska Schauer, Thomas O. F. Wagner, J-Matthias Graf von der Schulenburg
Publikováno v:
BMC Health Services Research, Vol 18, Iss 1, Pp 1-14 (2018)
Abstract Background Rare diseases are, by definition, very serious and chronic diseases with a high negative impact on quality of life. Approximately 350 million people worldwide live with rare diseases. The resulting high disease burden triggers hea
Externí odkaz:
https://doaj.org/article/b75454208e5643aa8a23af54ee966039
Autor:
Manuela Till, Christine Mundlos, Michaela Neff, Niels Tegtbauer, Holger Storf, Thomas O. F. Wagner, Johanna Schäfer, Holm Graeßner, Jannik Schaaf
Publikováno v:
Der Internist
In the European Union a disease is classified as rare if it affects no more than 5 out of 10,000 people. Currently, there are more than 6000 rare diseases, consisting of a large and heterogeneous number of different diseases that are complex in their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2e09590c96d6dda0dd35c04727316b9
https://doi.org/10.1007/s00108-021-01085-y
https://doi.org/10.1007/s00108-021-01085-y
Autor:
Helge, Hebestreit, Cornelia, Zeidler, Christopher, Schippers, Martina, de Zwaan, Jürgen, Deckert, Peter, Heuschmann, Christian, Krauth, Monika, Bullinger, Alexandra, Berger, Mark, Berneburg, Lilly, Brandstetter, Anna, Deibele, Jan, Dieris-Hirche, Holm, Graessner, Harald, Gündel, Stephan, Herpertz, Gereon, Heuft, Anne-Marie, Lapstich, Thomas, Lücke, Tim, Maisch, Christine, Mundlos, Andrea, Petermann-Meyer, Susanne, Müller, Stephan, Ott, Lisa, Pfister, Julia, Quitmann, Marcel, Romanos, Frank, Rutsch, Kristina, Schaubert, Katharina, Schubert, Jörg B, Schulz, Susann, Schweiger, Oliver, Tüscher, Kathrin, Ungethüm, Thomas O F, Wagner, Kirsten, Haas, Stephan, Zipfel
Publikováno v:
Orphanet journal of rare diseases : OJRD 17(1), 47 (2022). doi:10.1186/s13023-022-02176-1
Orphanet journal of rare diseases : OJRD 17(1), 47 (2022). doi:10.1186/s13023-022-02176-1
Published by BioMed Central, London
Published by BioMed Central, London
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba62672e4580218d7990ff2cc43937a5
https://doi.org/10.21203/rs.3.rs-936612/v1
https://doi.org/10.21203/rs.3.rs-936612/v1
Autor:
T. O. Hirche, C. Knoop, H. Hebestreit, D. Shimmin, A. Solé, J. S. Elborn, H. Ellemunter, P. Aurora, M. Hogardt, T. O. F. Wagner, ECORN-CF Study Group
Publikováno v:
Pulmonary Medicine, Vol 2015 (2015)
Externí odkaz:
https://doaj.org/article/6a06bf85fdab493fb4878109ae3422ae
Autor:
T. O. Hirche, C. Knoop, H. Hebestreit, D. Shimmin, A. Solé, J. S. Elborn, H. Ellemunter, P. Aurora, M. Hogardt, T. O. F. Wagner, ECORN-CF Study Group
Publikováno v:
Pulmonary Medicine, Vol 2014 (2014)
There are no European recommendations on issues specifically related to lung transplantation (LTX) in cystic fibrosis (CF). The main goal of this paper is to provide CF care team members with clinically relevant CF-specific information on all aspects
Externí odkaz:
https://doaj.org/article/eafe8101dd75494586102ee7f6ed57ec
Autor:
Jannik, Schaaf, James, Chalmers, Heymut, Omran, Petra, Pennekamp, Olivier, Sitbon, Thomas O F, Wagner, Abilio, Reis, Dennis, Kadioglu, Holger, Storf
Publikováno v:
Studies in health technology and informatics. 278
Rare lung diseases affect 1.5-3 million people in Europe while causing bad prognosis or early deaths for patients. The European Reference Network for Respiratory Diseases (ERN-Lung) is a patient centric network, funded by the European Union (EU). The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::10bdbcdfe0efc9d106860cf9d00b0f41
https://pubmed.ncbi.nlm.nih.gov/34042874
https://pubmed.ncbi.nlm.nih.gov/34042874
Autor:
Abílio Reis, James D. Chalmers, Petra Pennekamp, Jannik Schaaf, Heymut Omran, Dennis Kadioglu, Olivier Sitbon, Thomas O. F. Wagner, Holger Storf
Publikováno v:
GMDS
Studies in Health Technology and Informatics
Studies in Health Technology and Informatics-German Medical Data Sciences: Bringing Data to Life
Studies in Health Technology and Informatics
Studies in Health Technology and Informatics-German Medical Data Sciences: Bringing Data to Life
Rare lung diseases affect 1.5–3 million people in Europe while causing bad prognosis or early deaths for patients. The European Reference Network for Respiratory Diseases (ERN-Lung) is a patient centric network, funded by the European Union (EU). T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f3eb708f3a40b62c29916ecc5fbb854
https://doi.org/10.3233/shti210049
https://doi.org/10.3233/shti210049