e-learning
resources
Amsterdam 2015
Sunday, 27.09.2015
Cystic fibrosis: microbiology, immunology and assessment
Login
Search all ERS
e-learning
resources
Disease Areas
Airways Diseases
Interstitial Lung Diseases
Respiratory Critical Care
Respiratory Infections
Paediatric Respiratory Diseases
Pulmonary Vascular Diseases
Sleep and Breathing Disorders
Thoracic Oncology
Events
International Congress
Courses
Webinars
Conferences
Research Seminars
Journal Clubs
Publications
Breathe
Monograph
ERJ
ERJ Open Research
ERR
European Lung White Book
Handbook Series
Guidelines
All ERS guidelines
e-learning
CME Online
Case reports
Short Videos
SpirXpert
Procedure Videos
CME tests
Reference Database of Respiratory Sounds
Radiology Image Challenge
Brief tobacco interventions
EU Projects
VALUE-Dx
ERN-LUNG
ECRAID
UNITE4TB
Disease Areas
Events
Publications
Guidelines
e-learning
EU Projects
Login
Search
Statistical properties of clinical trial outcome measures in pre-school aged children with cystic fibrosis
Lidija Turkovic (Perth, Australia), Lidija Turkovic, Tim Rosenow, Marc Padros, Kathryn Ramsey, Stephen Stick
Source:
International Congress 2015 – Cystic fibrosis: microbiology, immunology and assessment
Session:
Cystic fibrosis: microbiology, immunology and assessment
Session type:
Thematic Poster Session
Number:
1306
Disease area:
Paediatric lung diseases
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
Lidija Turkovic (Perth, Australia), Lidija Turkovic, Tim Rosenow, Marc Padros, Kathryn Ramsey, Stephen Stick. Statistical properties of clinical trial outcome measures in pre-school aged children with cystic fibrosis. Eur Respir J 2015; 46: Suppl. 59, 1306
You must
login
to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.
Member's Comments
No comment yet.
You must
Login
to comment this presentation.
Related content which might interest you:
Late Breaking Abstract - Implications of treatable traits and treatment choices on exacerbation risk in moderate-severe asthma
Impact of Dexamethasone on pathogen profile of COVID-19 patients requiring intensive care: a multicentre retrospective study
Muscle energy techniques for COPD patients: Effects on pulmonary function and activities of daily living
Related content which might interest you:
Multi-center validation study on feasibility of multiple-breath washout technique in infants and toddlers with cystic fibrosis
Source: International Congress 2016 – Cystic fibrosis: various aspects
Year: 2016
Development of lung radiological findings of cystic fibrosis patients under 6 years old
Source: Annual Congress 2013 –Cystic fibrosis: clinical problems, genetics and microbiology in children
Year: 2013
Longitudinal lung function in school-age children born very preterm
Source: International Congress 2015 – New findings in paediatric respiratory physiology
Year: 2015
Structural lung disease, pulmonary infection and inflammation in infancy is associated with reduced spirometry at school-age in children with cystic fibrosis (CF)
Source: Annual Congress 2013 –Cystic fibrosis: lung function and change of lung function in infants and children before and after treatment
Year: 2013
Respiratory infections in young children with cystic fibrosis: A community-based longitudinal study
Source: Annual Congress 2012 - Epidemiology: risk factors and prognosis in respiratory infections
Year: 2012
Longitudinal study of lung function in infants with cystic fibrosis diagnosed by newborn screening: Preliminary results
Source: Annual Congress 2010 - Advances in lung function from infancy to adolescence
Year: 2010
Longitudinal study of lung function in very prematurely born infants
Source: Annual Congress 2013 –Neonatal and paediatric intensive care
Year: 2013
Impact of sedation on interpretation of longitudinal lung function growth
Source: International Congress 2015 – Respiratory physiology in children: technical and clinical aspects
Year: 2015
Interim results for INSPIRE-CF: A 24-month RCT evaluating effects of weekly supervised exercise in children with CF
Source: International Congress 2016 – Cystic fibrosis: monitoring and management
Year: 2016
LATE-BREAKING ABSTRACT: Predictors of lung function decline in a cohort of subjects with severe asthma
Source: International Congress 2015 – Monitoring airway diseases with lung function tests
Year: 2015
Multidimensional severity assessment in bronchiectasis - An analysis of 7 European cohorts
Source: International Congress 2016 – Clinical update on bronchiectasis
Year: 2016
The effect of occupational farming on lung function development in young adults: A 15 year follow-up study
Source: International Congress 2015 – Occupational factors in COPD and bronchitis
Year: 2015
Assessment of NuvoAir platform use on clinical outcomes in adults with cystic fibrosis: a first Italian experience
Source: Virtual Congress 2021 – Cystic fibrosis
Year: 2021
CF-ABLE-UK score: Modification and validation of a clinical prediction rule for prognosis in cystic fibrosis on data from UK CF registry
Source: International Congress 2015 – Cystic fibrosis: physiology, biomarkers, microbiology and miscellaneous
Year: 2015
Physical activity levels of children with cystic fibrosis and their parents: Pilot study
Source: International Congress 2018 – Chronic respiratory disease : determinants of physical activity in patients
Year: 2018
Longitudinal assessment of Lung Clearance Index as a marker of disease progression in a cohort of children with cystic fibrosis and normal spirometry
Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology
Year: 2020
Dietary fat is not associated with lung function in middle-age: Cross-sectional results from a cohort study
Source: International Congress 2015 – Epidemiology of respiratory disease
Year: 2015
Clinical presentation and characteristics of 25 adult cases of pulmonary sequestration, a retrospective study
Source: International Congress 2016 – Special issues in thoracic surgery
Year: 2016
LATE-BREAKING ABSTRACT: Socio-economic status does not influence lung function decline in children with cystic fibrosis in Australia
Source: Annual Congress 2013 –Cystic fibrosis: clinical problems, genetics and microbiology in children
Year: 2013
We use cookies on our website to give you the most relevant experience by remembering your preferences and repeat visits. By clicking "Accept", you consent to the use of the cookies.
Accept