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1.
Kröner, C.* et al.: Lung disease in STAT3 hyper-IgE syndrome requires intense therapy. Allergy, accepted (2019)
2.
Griese, M.* et al.: International management platform for children's interstitial lung disease (chILD-EU). Thorax 73, 231-239 (2018)
3.
Xu, Z.* et al.: Bi-allelic mutations in Phe-tRNA synthetase associated with a multi-system pulmonary disease support non-translational function. Am. J. Hum. Genet. 103, 100-114 (2018)
4.
Griese, M.* et al.: Inhalation treatment with glutathione in patients with cystic fibrosis. A randomized clinical trial. Am. J. Respir. Crit. Care Med. 188, 83-89 (2013)
5.
Hector, A.* et al.: Expression and regulation of interferon-related development regulator-1 in cystic fibrosis neutrophils. Am. J. Respir. Cell Mol. Biol. 48, 71-77 (2013)
6.
Kormann, M.S.* et al.: CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease. Eur. Respir. J. 39, 1385-1390 (2012)
7.
Hector, A.* et al.: The chitinase-like protein YKL-40 modulates cystic fibrosis lung disease. PLoS ONE 6:e24399 (2011)
8.
Hartl, D.* et al.: Pulmonary Th2 response in Pseudomonas aeruginosa-infected patients with cystic fibrosis. J. Allergy Clin. Immunol. 117, 204-211 (2006)
9.
Kappler, M.* ; Krauss-Etschmann, S. ; Diehl, V.* ; Zeilhofer, H.* & Koletzko, S.*: Detection of secretory IgA antibodies against gliadin and human tissue transglutaminase in stool to screen for coeliac disease in children: Validation study. BMJ:Br. Med. J. 332, 213-214 (2006)
10.
Muntau, A.C.* et al.: Age-related Reference Values for Serum Selenium Concentrations in Infants and Children. Clin. Chem. 48, 555-560 (2002)