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See Latest ArticlesProtein-energy malnutrition as the first manifestation of cystic fibrosis in infancy
Pediatrics International, 10/01/09
Fustik S et al. – PEM is a common manifestation of CF in infancy. Early infant age, breast–feeding, impaired liver function and the presence of severe cystic fibrosis transmembrane conductance regulator mutations are predisposing factors for the development of PEM.
Today in Cystic Fibrosis...keeping you current
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Long-term pulmonary outcome after meconium ileus in cystic fibrosis
Pediatric Pulmonology, 11/17/09
Growth in children with cystic fibrosis-related diabetes
Pediatric Pulmonology, 11/09/09
Aminoglycoside therapy against Pseudomonas aeruginosa in cystic fibrosis: A review
Journal of Cystic Fibrosis , 11/24/09
Today in Pediatric Pulmonology...keeping you current
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Anti-inflammatory drug therapy in asthma
Paediatric Respiratory Reviews, 11/02/09
A Randomized, Double-Blind Study Examining the Comparative Efficacies and Safety of Inhaled Epinephrine and Nasal Decongestant in Hospitalized Infants With Acute Bronchiolitis
The Pediatric Infectious Disease Journal, 11/17/09
A Randomized Trial of Nebulized 3% Hypertonic Saline With Epinephrine in the Treatment of Acute Bronchiolitis in the Emergency Department
Archives of Pediatrics and Adolescent Medicine, 11/23/09
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