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Page 1
Infections with Pseudomonas aeruginosa in patients with cystic fibrosis.
Tümmler B, Bosshammer J, Breitenstein S, Brockhausen I, Gudowius P, Herrmann C, Herrmann S, Heuer T, Kubesch P, Mekus F, Römling U, Schmidt KD, Spangenberg C, Walter S. Tümmler B, et al. Among authors: mekus f. Behring Inst Mitt. 1997 Feb;(98):249-55. Behring Inst Mitt. 1997. PMID: 9382747 Review.
Cystic fibrosis transmembrane conductance regulator (CFTR)-mediated residual chloride secretion does not protect against early chronic Pseudomonas aeruginosa infection in F508del homozygous cystic fibrosis patients.
Derichs N, Mekus F, Bronsveld I, Bijman J, Veeze HJ, von der Hardt H, Tummler B, Ballmann M. Derichs N, et al. Among authors: mekus f. Pediatr Res. 2004 Jan;55(1):69-75. doi: 10.1203/01.PDR.0000100758.66805.CE. Epub 2003 Nov 6. Pediatr Res. 2004. PMID: 14605249
Cystic fibrosis and NOS3.
Mekus F, Tümmler B. Mekus F, et al. Am J Respir Crit Care Med. 2004 Jan 15;169(2):319-20; author reply 320. doi: 10.1164/ajrccm.169.2.957. Am J Respir Crit Care Med. 2004. PMID: 14718247 No abstract available.
Genes, environment, ion transport, and cystic fibrosis.
Mekus F, Tümmler B. Mekus F, et al. Am J Respir Crit Care Med. 2004 Mar 15;169(6):770; author reply 770. doi: 10.1164/ajrccm.169.6.950. Am J Respir Crit Care Med. 2004. PMID: 15003951 No abstract available.
13 results