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Page 1
Alveolar inflammation in cystic fibrosis.
Ulrich M, Worlitzsch D, Viglio S, Siegmann N, Iadarola P, Shute JK, Geiser M, Pier GB, Friedel G, Barr ML, Schuster A, Meyer KC, Ratjen F, Bjarnsholt T, Gulbins E, Döring G. Ulrich M, et al. Among authors: schuster a. J Cyst Fibros. 2010 May;9(3):217-27. doi: 10.1016/j.jcf.2010.03.001. Epub 2010 Mar 29. J Cyst Fibros. 2010. PMID: 20347403 Free PMC article.
Anti-neutrophil cytoplasmic antibodies directed against the bactericidal/permeability-increasing protein (BPI) in pediatric cystic fibrosis patients do not recognize N-terminal regions important for the anti-microbial and lipopolysaccharide-binding activity of BPI.
Schultz H, Csernok E, Schuster A, Schmitz TS, Ernst M, Gross WL. Schultz H, et al. Among authors: schuster a. Pediatr Allergy Immunol. 2000 May;11(2):64-70. doi: 10.1034/j.1399-3038.2000.00069.x. Pediatr Allergy Immunol. 2000. PMID: 10893006
Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus.
Junge S, Görlich D, den Reijer M, Wiedemann B, Tümmler B, Ellemunter H, Dübbers A, Küster P, Ballmann M, Koerner-Rettberg C, Große-Onnebrink J, Heuer E, Sextro W, Mainz JG, Hammermann J, Riethmüller J, Graepler-Mainka U, Staab D, Wollschläger B, Szczepanski R, Schuster A, Tegtmeyer FK, Sutharsan S, Wald A, Nofer JR, van Wamel W, Becker K, Peters G, Kahl BC. Junge S, et al. Among authors: schuster a. PLoS One. 2016 Nov 18;11(11):e0166220. doi: 10.1371/journal.pone.0166220. eCollection 2016. PLoS One. 2016. PMID: 27861524 Free PMC article.
1,111 results