Works matching IS 2045712X AND DT 2013 AND VI 3 AND IP 2
Results: 29
Intravenous antibiotics reduce the pressure of Aspergillus in adult CF sputum.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 63
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- Article
Ceramide mediates lung fibrosis in cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 63
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- Article
Pseudomonas aeruginoso in the paranasal sinuses and transplanted lungs have similar adaptive mutations as isolates from chronically infected CF lungs.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 62
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- Article
Pubertal height velocity and associations with prepubertal and adult heights in cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 61
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- Article
Whole-genome sequencing to identify transmission of Mlycobacterium abscessus between patients with cystic fibrosis: a retrospective cohort study.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 61
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The use of ivacaftor in an adult with severe lung disease due to cystic fibrosis (ΔF508/G551 D).
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 47
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Cystic fibrosis and fertility.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 60
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Longitudinal trends in nutritional status and the relation between lung function and BMI in cystic fibrosis: a population-based cohort study.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 59
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Loss of C1tr function exacerbates the phenotype of Na<sup>+</sup> hyperabsorption in murine airways.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 58
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Tobramycin is a suppressor of premature termination codons.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 57
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TNF gene polymorphisms in cystic fibrosis patients: contribution to the disease progression.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 57
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Effects of puberty on cystic fibrosis related pulmonary exacerbation in women versus men.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 56
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- Article
Vitamin D regulation of OX40L in immune responses to Aspergillus fumigatus.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 55
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Differences in the pattern of structural abnormalities on CT in patients with cystic fibrosis and pancreatic sufficiency or insufficiency.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 55
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- Article
Impact of bronchiectasis and trapped air on quality of life and exacerbations in cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 54
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- Article
Chronic Stenotrophomonas maltophilia infection and mortality or lung transplantation in cystic fibrosis patients.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 53
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- Article
Biofilm compared to conventional antimicrobial susceptibility for Stenotrophomonas maltophilio isolates from cystic fibrosis patients.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 53
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- Article
Distribution of early structural lung changes due to cystic fibrosis detected with chest computed tomography.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 52
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- Article
Association between Staphylococcus aureus alone or combined with Pseudomonas aeruginosa and the clinical condition of patients with cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 51
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Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 50
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Toward implementation of quorum sensing autoinducers as biomarkers for infectious disease states.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 50
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Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn screening to 5 years of age.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 49
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- Article
Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 48
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- Article
Ivacaftor treatment in patients with cystic fibrosis and the G551 D-CFTR mutation.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 48
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Long-term multicentre randomised controlled study of high frequency chest wall oscillation versus positive expiratory pressure mask in cystic fibrosis.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 47
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Saliva as a potential tool for cystic fibrosis diagnosis.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 46
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Change in sweat chloride as a clinical end point in cystic fibrosis clinical trials: the ivacaftor experience.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 45
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Advances in Cystic Fibrosis Gene Therapy.
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- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 33
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Foreword.
- Published in:
- Current Medical Literature: Cystic Fibrosis, 2013, v. 3, n. 2, p. 33
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- Article