Published in Ann Allergy on April 01, 1990
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Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption. J Pediatr (1982) 1.64
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Early detection of pulmonary function abnormalities in cystic fibrosis. Pediatrics (1972) 1.29
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Effects of ultrasonically nebulized distilled water on airway dynamics in children with cystic fibrosis and asthma. J Pediatr (1972) 1.16
Sustained-release theophylline: a significant advance in the treatment of childhood asthma. J Pediatr (1982) 1.15
Corticosteroids in status asthmaticus. J Pediatr (1980) 1.15
Multiple factors limit exercise capacity in cystic fibrosis. Pediatr Pulmonol (1986) 1.14
Comparative study of histamine and exercise challenges in asthmatic children. Am Rev Respir Dis (1978) 1.14
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Nebulized albuterol in acute childhood asthma: comparison of two doses. Pediatrics (1990) 1.05
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Pseudomonas species contamination of cystic fibrosis patients' home inhalation equipment. J Pediatr (1987) 1.03
Malnutrition: a cause of elevated sweat chloride concentration. Acta Paediatr Scand (1986) 1.03
Meconium ileus in the absence of cystic fibrosis. Arch Dis Child (1992) 1.03
Normal values of maximal inspiratory and expiratory pressures with a portable apparatus in children, adolescents, and young adults. Pediatr Pulmonol (1987) 1.02
Lung mechanics in antigen-induced asthma. J Appl Physiol (1974) 1.02
The effect of a nebulized bronchodilator administered with or without intermittent positive pressure breathing on ventilatory function in children with cystic fibrosis and asthma. Am Rev Respir Dis (1972) 1.02
Response to frequent low doses of nebulized salbutamol in acute asthma. J Pediatr (1985) 1.02
Negative pressure artificial respiration: use in treatment of respiratory distress syndrome of the newborn. Can Med Assoc J (1970) 1.02
Theophylline disposition in cystic fibrosis. Am Rev Respir Dis (1983) 1.01
Randomized trial of ceftazidime versus placebo in the management of acute respiratory exacerbations in patients with cystic fibrosis. J Pediatr (1987) 1.00
The measurement of fluid deposition in humans following mist tent therapy. Pediatrics (1971) 1.00
Sputum bacteriology in patients with cystic fibrosis in a Toronto hospital during 1970-1981. J Infect Dis (1984) 0.99
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Effects of gravity on tracheal mucus transport rates in normal subjects and in patients with cystic fibrosis. Pediatrics (1977) 0.99
The correlation of radiological changes with pulmonary function in cystic fibrosis. Radiology (1971) 0.99