Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Anne, Mehl"'
Autor:
Stephanie Thee, Mirjam Völler, Anne Mehl, Doris Staab, Christian Meisel, Horst Bernuth von, Cornelia Feiterna-Sperling, Renate Krüger
Publikováno v:
Klinische Pädiatrie. 234:314-316
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe5e5fff9a93cadf05799182cd385a23
https://doi.org/10.1055/a-1696-1861
https://doi.org/10.1055/a-1696-1861
Autor:
Stephanie, Thee, Mirjam, Völler, Anne, Mehl, Doris, Staab, Christian, Meisel, Horst, Bernuth von, Cornelia, Feiterna-Sperling, Renate, Krüger
Publikováno v:
Klinische Padiatrie. 234(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cbc175802fc481b1bf76f22bcffde2d8
https://pubmed.ncbi.nlm.nih.gov/34979580
https://pubmed.ncbi.nlm.nih.gov/34979580
Autor:
Hartmut Grasemann, Thomas Jaecklin, Anne Mehl, Hailu Huang, Mahroukh Rafii, Paul Pencharz, Felix Ratjen
Publikováno v:
Mediators of Inflammation, Vol 2014 (2014)
Externí odkaz:
https://doaj.org/article/9d4c552e63404cbaaa3e2f913d19a139
Autor:
Anne Mehl, Peyman Ghorbani, David Douda, Hailu Huang, Nades Palaniyar, Felix Ratjen, Hartmut Grasemann
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e90232 (2014)
Infection of the lung with Pseudomonas aeruginosa results in upregulation of nitric oxide synthases (NOS) and arginase expression, and both enzymes compete for L-arginine as substrate. Nitric oxide (NO) production may be regulated by arginase as it c
Externí odkaz:
https://doaj.org/article/19cc393f78904581948a252ca2d6ac1e
Autor:
Martin H. Maurer, Joachim Böttcher, Bernd Hamm, H-J Mentzel, Alexander Huppertz, Anne Mehl, Timm Denecke, Florian Streitparth, Alexander Pfeil, O Scholz, Diane M. Renz, Doris Staab, Carsten Schwarz
Publikováno v:
Clinical Radiology. 72:754-763
Aim To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary manifestations of cystic fibrosis (CF) in comparison to chest computed tomography (CT), including an extended outcome analysis. Materials and Methods Twen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a2c01a47f175c8b833a9005bc4112e1
https://doi.org/10.1016/j.crad.2017.03.017
https://doi.org/10.1016/j.crad.2017.03.017
Autor:
Mahroukh Rafii, Hailu Huang, Hartmut Grasemann, Paul B. Pencharz, Felix Ratjen, Anne Mehl, Thomas Jaecklin
Publikováno v:
Mediators of Inflammation, Vol 2014 (2014)
Mediators of Inflammation
Mediators of Inflammation
Cystic fibrosis airways are deficient for L-arginine, a substrate for nitric oxide synthases (NOSs) and arginases. The rationale for this study was to quantify NOS and arginase activity in the mouse lung. Anesthetized unventilated mice received a pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::788d706aafdfc7dc2f55b12a8d368de9
https://doi.org/10.1155/2014/323526
https://doi.org/10.1155/2014/323526
Autor:
Jaques Belik, Suhail Al-Saleh, Jeremy A. Scott, Reshma Amin, Hartmut Grasemann, Mahroukh Rafii, Felix Ratjen, Darakhshanda Shehnaz, Paul B. Pencharz, Anne Mehl
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 183:1363-1368
Rationale: Airway nitric oxide is reduced in cystic fibrosis airways. Asymmetric dimethylarginine is an endogenous nitric oxide synthase inhibitor that may contribute to nitric oxide deficiency in cystic fibrosis.Objectives: To test the hypothesis th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8cfb19bc869010e8624c811e7853645
https://doi.org/10.1164/rccm.201012-1995oc
https://doi.org/10.1164/rccm.201012-1995oc
Autor:
Hartmut Grasemann, Anne Mehl
Publikováno v:
The Open Nitric Oxide Journal. 2:55-63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7247d534a8bd56a9a23f192f4fb122e
https://doi.org/10.2174/1875042701002020055
https://doi.org/10.2174/1875042701002020055
Autor:
Rosaria Casciaro, Philippe Reix, Adria Perez-Rovira, M. H. Smet, Desmond Cox, Anne Mehl, Pilar Garcia Peña, Torkel B. Brismar, Annmarie Jeanes, G Lucigrai, Silvia Gartner, Veronika Skalická, Marleen de Bruijne, Jacqueline Payen De La Garanderie, Marco Di Maurizio, Lena Hjelte, Marianne Nuijsink, I. Sermet, Kris De Boeck, David Rea, Mariëtte van de Corput, Herma C. Holscher, Cesare Braggion, Marcel van Straten, Harm A.W.M. Tiddens, Laureline Berteloot, Wieying Kuo, Jane C. Davies, David M. Hansell, C. Kors van der Ent, Pim A. de Jong, Nanko de Graaf, Ahmed Kheniche, Anne Munck, Isabelle Fajac, Tim W.R. Lee, Hana Vitouskova, Florian Streitparth
Publikováno v:
European Respiratory Journal, 47(6), 1706. European Respiratory Society
Progressive cystic fibrosis (CF) lung disease is the main cause of mortality in CF patients. CF lung disease starts in early childhood. With current standards of care, respiratory function remains largely normal in children and more sensitive outcome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b0a13d1214ce3bab9713e8b7bba4b4c
https://pubmed.ncbi.nlm.nih.gov/27076593
https://pubmed.ncbi.nlm.nih.gov/27076593
Publikováno v:
Clinical and Translational Allergy
Background Hypersensitivity reactions to parenteral administered antibiotics (HRPA) are a substantial problem in managing pulmonary disease in Cystic Fibrosis (CF), especially in advanced CF. This group of patients requires a life long antibiotic tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a9bca9f4b345070623b8b0f1c31bd1d
https://doi.org/10.1186/2045-7022-4-s3-p66
https://doi.org/10.1186/2045-7022-4-s3-p66