Found: 138
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Serum galactomannan in cystic fibrosis patients colonized with Aspergillus species.
- Published in:
- Medical Mycology, 2012, v. 50, n. 6, p. 658, doi. 10.3109/13693786.2012.676739
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- Publication type:
- Article
Treatment response to pulmonary exacerbation in primary ciliary dyskinesia.
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 10, p. 2857, doi. 10.1002/ppul.26599
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- Publication type:
- Article
Reply to migration is not the perfect answer: Optimized methodology to assess LCI agreement between corrected legacy multiple breath nitrogen washout data and that directly collected on updated software.
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 7, p. 1861, doi. 10.1002/ppul.26430
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- Publication type:
- Article
Bronchodilator responsiveness in cystic fibrosis children treated for pulmonary exacerbations.
- Published in:
- Pediatric Pulmonology, 2021, v. 56, n. 7, p. 2036, doi. 10.1002/ppul.25409
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- Publication type:
- Article
The remaining barriers to normalcy in CF: Advances in assessment of CF lung disease.
- Published in:
- Pediatric Pulmonology, 2021, v. 56, p. S90, doi. 10.1002/ppul.24929
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- Publication type:
- Article
Evaluation of a multiple breath nitrogen washout system in children.
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 8, p. 2108, doi. 10.1002/ppul.24862
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- Publication type:
- Article
Lung compartment analysis assessed from N<sub>2</sub> multiple‐breath washout in children with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 7, p. 1671, doi. 10.1002/ppul.24773
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- Publication type:
- Article
The utility of moment ratios and abbreviated endpoints of the multiple breath washout test in preschool children with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 3, p. 649, doi. 10.1002/ppul.24618
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- Publication type:
- Article
Anti‐inflammatories and mucociliary clearance therapies in the age of CFTR modulators.
- Published in:
- Pediatric Pulmonology, 2019, v. 54, p. S46, doi. 10.1002/ppul.24364
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- Publication type:
- Article
Pharmacokinetic modelling of a once-daily dosing regimen for intravenous tobramycin in paediatric cystic fibrosis patients.
- Published in:
- Journal of Antimicrobial Chemotherapy (JAC), 2007, v. 59, n. 6, p. 1135, doi. 10.1093/jac/dkm097
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- Publication type:
- Article
The Equitable Implementation of Cystic Fibrosis Personalized Medicines in Canada.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 5, p. 382, doi. 10.3390/jpm11050382
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- Publication type:
- Article
Orkambi® and amplifier co-therapy improves function from a rare CFTR mutation in gene-edited cells and patient tissue.
- Published in:
- EMBO Molecular Medicine, 2017, v. 9, n. 9, p. 1224, doi. 10.15252/emmm.201607137
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- Publication type:
- Article
Genotype–Phenotype Correlations in Children with HHT.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 9, p. 2714, doi. 10.3390/jcm9092714
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- Publication type:
- Article
Disease Manifestations in Siblings with Primary Ciliary Dyskinesia.
- Published in:
- 2024
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- Publication type:
- Letter to the Editor
Exhaled Volatile Organic Compound Profiles Differ between Children with Primary Ciliary Dyskinesia and Cystic Fibrosis.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 11, p. 1667, doi. 10.1513/annalsats.202302-165rl
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- Publication type:
- Article
Efficacy of Antibiotic Eradication Therapy of Early Pseudomonas aeruginosa Infection in Children with Primary Ciliary Dyskinesia.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 6, p. 854, doi. 10.1513/AnnalsATS.202210-858OC
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- Publication type:
- Article
Preventing Continuous Damage in Primary Ciliary Dyskinesia: Is Airway Inflammation a Potential Target?
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 1, p. 26, doi. 10.1513/AnnalsATS.202209-782ED
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- Publication type:
- Article
Development and Validation of an Algorithm for Quality Grading of Pediatric Spirometry: A Quality Improvement Initiative.
- Published in:
- Annals of the American Thoracic Society, 2022, v. 19, n. 1, p. 74, doi. 10.1513/AnnalsATS.202103-382QI
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- Publication type:
- Article
Evaluating the Impact of Stopping Chronic Therapies after Modulator Drug Therapy in Cystic Fibrosis: The SIMPLIFY Clinical Trial Study Design.
- Published in:
- 2021
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- Publication type:
- journal article
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Clinical Outcomes Associated with Complex Infection in Patients with Cystic Fibrosis.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Non‐invasive MR imaging techniques for measuring femoral arterial flow in a pediatric and adolescent cohort.
- Published in:
- Physiological Reports, 2022, v. 10, n. 10, p. 1, doi. 10.14814/phy2.15182
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- Publication type:
- Article
Directed differentiation of human pluripotent stem cells into mature airway epithelia expressing functional CFTR protein.
- Published in:
- Nature Biotechnology, 2012, v. 30, n. 9, p. 876, doi. 10.1038/nbt.2328
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- Publication type:
- Article
Influence of Interleukin-10 on Aspergillus fumigatus Infection in Patients with Cystic Fibrosis.
- Published in:
- Journal of Infectious Diseases, 2005, v. 191, n. 11, p. 1988, doi. 10.1086/429964
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- Publication type:
- Article
Microaspiration in Infants with Laryngomalacia.
- Published in:
- Laryngoscope, 2004, v. 114, n. 9, p. 1592, doi. 10.1097/00005537-200409000-00017
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- Publication type:
- Article
Reference equations for the interpretation of forced expiratory and plethysmographic measurements in infants.
- Published in:
- Pediatric Pulmonology, 2018, v. 53, n. 7, p. 907, doi. 10.1002/ppul.24063
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- Publication type:
- Article
Changes in multiple breath washout measures after raised volume rapid thoracoabdominal compression maneuvers in infants.
- Published in:
- Pediatric Pulmonology, 2016, v. 51, n. 2, p. 183, doi. 10.1002/ppul.23220
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- Publication type:
- Article
Pulmonary exacerbations and parent-reported outcomes in children <6 years with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 3, p. 236, doi. 10.1002/ppul.23056
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- Publication type:
- Article
Novel outcome measures for clinical trials in cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 3, p. 302, doi. 10.1002/ppul.23146
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- Publication type:
- Article
Response to letter.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 1, p. 105, doi. 10.1002/ppul.23048
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- Publication type:
- Article
Physiological correlates of pulmonary function in children with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2014, v. 49, n. 9, p. 878, doi. 10.1002/ppul.22928
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- Publication type:
- Article
The cystic fibrosis gender gap: Potential roles of estrogen.
- Published in:
- Pediatric Pulmonology, 2014, v. 49, n. 4, p. 309, doi. 10.1002/ppul.22967
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- Publication type:
- Article
The prevalence of asthma in Canadian children of South Asian descent.
- Published in:
- Pediatric Pulmonology, 2014, v. 49, n. 1, p. 43, doi. 10.1002/ppul.22907
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- Publication type:
- Article
Open-label, follow-on study of azithromycin in pediatric patients with CF uninfected with Pseudomonas aeruginosa.
- Published in:
- Pediatric Pulmonology, 2012, v. 47, n. 7, p. 641, doi. 10.1002/ppul.21601
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- Publication type:
- Article
Inhaled hypertonic saline in infants and toddlers with cystic fibrosis: short-term tolerability, adherence, and safety.
- Published in:
- Pediatric Pulmonology, 2011, v. 46, n. 7, p. 666, doi. 10.1002/ppul.21425
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- Publication type:
- Article
The effect of early Pseudomonas aeruginosa treatment on lung function in pediatric cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2011, v. 46, n. 6, p. 554, doi. 10.1002/ppul.21417
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- Publication type:
- Article
Epidemiology of borderline oxacillin-resistant Staphylococcus aureus in Pediatric cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2011, v. 46, n. 5, p. 489, doi. 10.1002/ppul.21383
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- Publication type:
- Article
Plastic bronchitis as an unusual cause of mucus plugging in cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2009, v. 44, n. 9, p. 939, doi. 10.1002/ppul.21063
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- Publication type:
- Article
Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2008, v. 43, n. 12, p. 1224, doi. 10.1002/ppul.20935
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- Publication type:
- Article
Assessment of body composition in pediatric patients with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2008, v. 43, n. 10, p. 1025, doi. 10.1002/ppul.20913
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- Publication type:
- Article
Aerosol therapy in cystic fibrosis: Weighing the evidence.
- Published in:
- Pediatric Pulmonology, 2008, v. 43, n. S9, p. S3, doi. 10.1002/ppul.20861
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- Publication type:
- Article
Rapid pulmonary delivery of inhaled tobramycin for Pseudomonas infection in cystic fibrosis: A pilot project.
- Published in:
- Pediatric Pulmonology, 2008, v. 43, n. 8, p. 753, doi. 10.1002/ppul.20850
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- Publication type:
- Article
Reliability and validity of the habitual activity estimation scale (HAES) in patients with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2008, v. 43, n. 4, p. 345, doi. 10.1002/ppul.20737
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- Publication type:
- Article
Pilot study of safety and tolerability of inhaled hypertonic saline in infants with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2007, v. 42, n. 5, p. 471, doi. 10.1002/ppul.20603
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- Publication type:
- Article
Diagnostic value of serum antibodies in early Pseudomonas aeruginosa infection in cystic fibrosis patients.
- Published in:
- Pediatric Pulmonology, 2007, v. 42, n. 3, p. 249, doi. 10.1002/ppul.20562
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- Publication type:
- Article
Pediatric pulmonary pearls. By Laura S. Inselman, M.D. Philadelphia, Hanley & Belfus, Inc., 2000, 224 pp.
- Published in:
- Pediatric Pulmonology, 2001, v. 32, n. 1, p. 95, doi. 10.1002/ppul.1094
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- Publication type:
- Article
Cystic fibrosis lung disease: The role of nitric oxide.
- Published in:
- Pediatric Pulmonology, 1999, v. 28, n. 6, p. 442, doi. 10.1002/(SICI)1099-0496(199912)28:6<442::AID-PPUL10>3.0.CO;2-4
- By:
- Publication type:
- Article
Placebo-controlled, double-blind, randomized study of aerosolized tobramycin for early treatment of Pseudomonas aeruginosa colonization in cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 1998, v. 25, n. 2, p. 88, doi. 10.1002/(SICI)1099-0496(199802)25:2<88::AID-PPUL3>3.0.CO;2-J
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- Publication type:
- Article
Inter‐ and intravisit repeatability of free‐breathing MRI in pediatric cystic fibrosis lung disease.
- Published in:
- Magnetic Resonance in Medicine, 2023, v. 89, n. 5, p. 2048, doi. 10.1002/mrm.29566
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- Publication type:
- Article
A 3D stack‐of‐spirals approach for rapid hyperpolarized <sup>129</sup>Xe ventilation mapping in pediatric cystic fibrosis lung disease.
- Published in:
- Magnetic Resonance in Medicine, 2023, v. 89, n. 3, p. 1083, doi. 10.1002/mrm.29505
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- Publication type:
- Article