Mucociliary transport in trachea of patients with cystic fibrosis.
نویسندگان
چکیده
منابع مشابه
Mucociliary transport in trachea of patients with cystic fibrosis.
Mucociliary tracheal transport rates were measured in 20 patients with cystic fibrosis, in whom these rates ranged from 0 to 12.8 mm/min. The patients were divided into 3 roughly equal groups on the basis of their transport rates. (1) Those in whom no abnormality in mucociliary transport was detected in the trachea; (2) those in whom normal transport rates were measured but in whom abnormalitie...
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Introduction: Bronchiectasis is a common problem in children especially under 5 years. Early diagnosis of disease and its causes could be useful in early treatment and preventing probable complications. This study aimed at evaluating the cystic fibrosis (CF) in patients with bronchiectasis. Methods: In a cross-sectional study, 374 children with bronchiectasis were studied. The diagnosis was ma...
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متن کاملEffect of increasing doses of hypertonic saline on mucociliary clearance in patients with cystic fibrosis.
BACKGROUND Patients with cystic fibrosis are known to have decreased mucociliary clearance. It has previously been shown that inhalation of a 7.0% solution of hypertonic saline significantly improved mucociliary clearance in a group of adult patients with cystic fibrosis. The aim of this study was to measure the response to increasing concentrations of inhaled hypertonic saline. METHODS Ten p...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1976
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.51.1.28