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Volumn 19, Issue 3, 2005, Pages 431-433
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Submucosal gland dysfunction as a primary defect in cystic fibrosis
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Author keywords
[No Author keywords available]
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Indexed keywords
ADOLESCENT;
ADULT;
AIRWAY;
ARTICLE;
CHILD;
CLINICAL ARTICLE;
CYSTIC FIBROSIS;
DISEASE COURSE;
FORCED EXPIRATORY VOLUME;
HISTOPATHOLOGY;
HUMAN;
MICROSCOPY;
MUCUS GLAND;
NASAL BIOPSY;
NOSE MUCOSA;
NOSE SECRETION;
PHOTOCHEMICAL QUENCHING;
PRIORITY JOURNAL;
SUBMUCOSA;
VISCOSITY;
ADOLESCENT;
ADULT;
BIOPSY;
CHILD;
CHILD, PRESCHOOL;
CYSTIC FIBROSIS;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
DEXTRANS;
EXOCRINE GLANDS;
FLUORESCEIN-5-ISOTHIOCYANATE;
FLUORESCENT DYES;
HUMANS;
KINETICS;
MICROSCOPY, FLUORESCENCE;
NOSE;
PHOTOBLEACHING;
PILOCARPINE;
RESPIRATORY MUCOSA;
VISCOSITY;
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EID: 14644421477
PISSN: 08926638
EISSN: None
Source Type: Journal
DOI: 10.1096/fj.04-2879fje Document Type: Article |
Times cited : (67)
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References (0)
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