e-learning
resources
Barcelona 2010
Sunday, 19.09.2010
High-priority questions on airway infections in diseases seen in children and adults
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
Treatment strategies for cystic fibrosis: what's in the pipeline?
A. Smyth (Notthingham, United Kingdom)
Source:
Annual Congress 2010 - High-priority questions on airway infections in diseases seen in children and adults
Session:
High-priority questions on airway infections in diseases seen in children and adults
Session type:
Symposium
Number:
154
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:
A. Smyth (Notthingham, United Kingdom). Treatment strategies for cystic fibrosis: what's in the pipeline?. Annual Congress 2010 - High-priority questions on airway infections in diseases seen in children and adults
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:
The Relationship Between Functional Status and Fatigue After COVID-19 Infection
Late Breaking Abstract - Implications of treatable traits and treatment choices on exacerbation risk in moderate-severe asthma
Observational cohort study of pulmonary exacerbations in alpha-1 antitrypsin deficiency
Related content which might interest you:
Tezacaftor-ivacaftor for the treatment of cystic fibrosis: what’s next?
Source: International Congress 2018 – Therapeutic breakthroughs Year in Review
Year: 2018
End-stage cystic fibrosis: what to measure and what to try?
Source: Annual Congress 2011 - End-stage lung disease in children
Year: 2011
What’s new in cystic fibrosis?
Source: International Congress 2018 – Paediatric Year in Review
Year: 2018
The use of telehealth system in improving adherence to nebulised treatment in children with cystic fibrosis: Benefits and pitfalls
Source: International Congress 2014 – Cystic fibrosis: basic science, physiology and clinical aspects
Year: 2014
Is newborn screening for cystic fibrosis cost-effective?
Source: Annual Congress 2010 - Does cost-effectiveness go together with best quality of treatment? New drivers in medicine
Year: 2010
Re-imagining cystic fibrosis care: next generation thinking
Source: Eur Respir J, 55 (5) 1902443; 10.1183/13993003.02443-2019
Year: 2020
Revisiting α1-antitrypsin therapy in cystic fibrosis: can it still offer promise?
Source: Eur Respir J 2007; 29: 229-230
Year: 2007
What's it like to live with idiopathic pulmonary fibrosis? Ask the experts
Source: Eur Respir J 2016; 47:1324-1326
Year: 2016
Modelling and simulation of experimental designs to find the best design of randomized clinical trials in a rare disease: Cystic fibrosis
Source: International Congress 2014 – Cystic fibrosis: clinical assessment and treatment
Year: 2014
Monitoring early lung disease in cystic fibrosis: where are we now?
Source: Breathe 2014; 10: 34-47
Year: 2014
A new paradigm for the management of children with cystic fibrosis at home: experiences from a Dutch cystic fibrosis clinic
Source: Virtual Congress 2021 – New technologies for the management of children with respiratory diseases
Year: 2021
Idiopathic pulmonary fibrosis: time for greater expectations?
Source: Eur Respir J, 52 (2) 1801312; 10.1183/13993003.01312-2018
Year: 2018
Intervention trials and ventilation distribution in mild cystic fibrosis lung disease: will it all come out in the wash?
Source: Eur Respir J 2011; 37: 757-759
Year: 2011
Does this patient have cystic fibrosis?
Source: International Congress 2017 – GR6 Paediatric Ground Round: an interactive session
Year: 2017
Combination therapy in idiopathic pulmonary fibrosis: the way ahead will be hard
Source: Eur Respir J 2015; 45: 1208-1210
Year: 2015
Trying to find a cure for cystic fibrosis: CFTR biomarkers as outcomes
Source: Eur Respir J 2013; 42: 1155
Year: 2013
Trying to find a cure for cystic fibrosis: CFTR biomarkers as outcomes
Source: Eur Respir J 2013; 42: 1156-1157
Year: 2013
Cystic fibrosis: prospects for therapy of some class 1 mutations
Source: Annual Congress 2007 - Cystic fibrosis: will the new biology deliver?
Year: 2007
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