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

Nico Derichs,Frauke Mekus,Inez Bronsveld,J. Bijman,Henk J. Veeze,Horst von der Hardt,Burkhard Tümmler,Manfred Ballmann

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

2004

Nico Derichs
Frauke Mekus
Inez Bronsveld
J. Bijman
Henk J. Veeze
Horst von der Hardt
Burkhard Tümmler
Manfred Ballmann

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

Keywords:

Respiratory disease
Pancreatic disease
Cystic fibrosis
Secretion
Chloride
Endocrinology
Cystic fibrosis transmembrane conductance regulator
Internal medicine
Medicine
Pseudomonas aeruginosa
Pseudomonadaceae
Diabetes mellitus

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