Works matching IS 2045712X AND DT 2011 AND VI 1 AND IP 4
Results: 29
Recommendations for the classification of diseases as CFTR-related disorders.
- Published in:
- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 130
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Nebulized hypertonic saline via positive expiratory pressure versus via jet nebulizer in patients with severe cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 122
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Frequent body CT scanning of young adults: indications, outcomes, and risk for radiation-induced cancer.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 130
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Azithromycin blocks autophagy and may predispose cystic fibrosis patients to mycobacterial infection.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 124
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Mannitol-guided delivery of ciprofloxacin in artificial cystic fibrosis mucus model.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 124
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Targeting airway inflammation in cystic fibrosis in children: past, present, and future.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 123
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Clinical use of dornase alpha is associated with a slower rate of FEV1 decline in cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 122
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Guideline on the design and conduct of cystic fibrosis clinical trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN).
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 129
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The implementation of standards of care in Europe: state of the art.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 129
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European cystic fibrosis bone mineralisation guidelines.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 128
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Hyperglycemia and death in cystic fibrosis-related diabetes.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 128
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Nocturnal saturation and glucose tolerance in children with cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 127
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- Article
Intestinal obstruction syndromes in cystic fibrosis: meconium ileus, distal intestinal obstruction syndrome, and constipation.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 126
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Topical nasal steroids for treating nasal polyposis in people with cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 126
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Effects of ginseng on Pseudomonas aeruginosa motility and biofilm formation.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 125
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Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 125
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Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 121
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- Article
Development of an inhaled dry-powder formulation of tobramycin using PulmoSphere<sup>TM</sup> technology.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 120
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Pneumothorax in cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 120
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Bronchoscopy in cystic fibrosis infants diagnosed by newborn screening.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 119
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The airway microbiome in cystic fibrosis and implications for treatment.
- Published in:
- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 119
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Pulmonary exacerbation: towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 118
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Elevated vascular endothelial growth factor is correlated with elevated erythropoietin in stable, young cystic fibrosis patients.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 118
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Achromobacter xylosoxidans respiratory tract infection in cystic fibrosis patients.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 117
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Serine proteases degrade airway mucins in cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 116
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Foreword.
- Published in:
- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 97
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Infection, inflammation, and lung function decline in infants with cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 116
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Multidrug-Resistant Pseudomonas aeruginosa in Cystic Fibrosis. Part 2: Management Considerations.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 97
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Lung clearance index and HRCT are complementary markers of lung abnormalities in young children with CF.
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- Current Medical Literature: Cystic Fibrosis, 2011, v. 1, n. 4, p. 115
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- Article