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

N Derichs; F Mekus; I (Inez) Bronsveld; J Bijman; HJ  Veeze; H von der Hardt; B Tümmler; M Ballmann

doi:10.1203/01.PDR.0000100758.66805.CE

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

N Derichs, F Mekus, I (Inez) Bronsveld, J Bijman, HJ Veeze, H von der Hardt, B Tümmler, M Ballmann

Research output: Contribution to journal › Article › Academic › peer-review

14 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	69-75
Number of pages	7
Journal	Pediatric Research
Volume	55
Issue number	1
DOIs	https://doi.org/10.1203/01.PDR.0000100758.66805.CE
Publication status	Published - 2004

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10.1203/01.PDR.0000100758.66805.CE

http://hdl.handle.net/1765/56991

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Derichs, N., Mekus, F., Bronsveld, I., Bijman, J., Veeze, HJ., von der Hardt, H., Tümmler, B., & Ballmann, M. (2004). 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. Pediatric Research, 55(1), 69-75. https://doi.org/10.1203/01.PDR.0000100758.66805.CE

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Derichs, N, Mekus, F, Bronsveld, I, Bijman, J, Veeze, HJ, von der Hardt, H, Tümmler, B & Ballmann, M 2004, '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', Pediatric Research, vol. 55, no. 1, pp. 69-75. https://doi.org/10.1203/01.PDR.0000100758.66805.CE

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 (Inez) et al.

In: Pediatric Research, Vol. 55, No. 1, 2004, p. 69-75.

Research output: Contribution to journal › Article › Academic › peer-review

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AU - Derichs, N

AU - Mekus, F

AU - Bronsveld, I (Inez)

AU - Bijman, J

AU - Veeze, HJ

AU - von der Hardt, H

AU - Tümmler, B

AU - Ballmann, M

PY - 2004

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Derichs N, Mekus F, Bronsveld I, Bijman J, Veeze HJ, von der Hardt H et al. 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. Pediatric Research. 2004;55(1):69-75. doi: 10.1203/01.PDR.0000100758.66805.CE