e-learning
resources
Copenhagen 2005
Tuesday 20.09.2005
Novel physiotherapeutic interventions in medical, surgical and neurological conditions
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
Evolution of pulmonary function in children with Duchenne muscular dystrophy: implication of expiratory muscles
C. R. Carvalho, A. C. Lunardi, C. C. Berto, M. Rojo, M. B. D. Rezende, U. C. Reed, M. S. Carvalho, S. K. Marie (Sao Paulo, Brazil)
Source:
Annual Congress 2005 - Novel physiotherapeutic interventions in medical, surgical and neurological conditions
Session:
Novel physiotherapeutic interventions in medical, surgical and neurological conditions
Session type:
Poster Discussion
Number:
3267
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
C. R. Carvalho, A. C. Lunardi, C. C. Berto, M. Rojo, M. B. D. Rezende, U. C. Reed, M. S. Carvalho, S. K. Marie (Sao Paulo, Brazil). Evolution of pulmonary function in children with Duchenne muscular dystrophy: implication of expiratory muscles. Eur Respir J 2005; 26: Suppl. 49, 3267
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:
Panel discussion: respiratory care for newborns in resource-limited settings
Optimizing invasive ventilation for SMA type 1 children who are receiving the gene therapy
Muscle energy techniques for COPD patients: Effects on pulmonary function and activities of daily living
Related content which might interest you:
Implication of regular pulmonary function evaluation in Duchenne muscular dystrophy
Source: Virtual Congress 2020 – Pulmonary function and rehabilitation in non-respiratory disease
Year: 2020
Pulmonary function in Duchenne muscular dystrophy patients before and after noninvasive ventilation
Source: Eur Respir J 2005; 26: Suppl. 49, 85s
Year: 2005
Inspiratory and expiratory muscle weakness in facioscapulohumeral muscular dystrophy
Source: International Congress 2019 – Lung function and respiratory muscle testing
Year: 2019
Long term efficacy: Idebenone reduces the rate of both inspiratory and expiratory functional loss in Duchenne muscular dystrophy (DMD)
Source: International Congress 2019 – Rare and ultra-rare diseases and the lungs: updates and new perspectives
Year: 2019
Effects of posture on peak cough flow and respiratory muscle activation in Duchenne muscular dystrophy
Source: International Congress 2018 – New insights in testing lung and respiratory muscle functions
Year: 2018
Sniff nasal inspiratory pressure in the longitudinal assessment of young Duchenne muscular dystrophy children
Source: Eur Respir J 2013; 42: 671-680
Year: 2013
Evolution of respiratory function in Duchenne muscular dystrophy from childhood to adulthood
Source: Eur Respir J, 51 (2) 1701418; 10.1183/13993003.01418-2017
Year: 2018
Ventilatory assistance in patients with Duchenne muscular dystrophy
Source: Eur Respir J 2006; 28: 468-469
Year: 2006
Respiratory kinematics in Duchenne muscular dystrophy (DMD)
Source: Eur Respir J 2007; 30: Suppl. 51, 376s
Year: 2007
Abdominal volume contribution to tidal volume as an early indicator of respiratory impairment in Duchenne muscular dystrophy
Source: Eur Respir J 2010; 35: 1118-1125
Year: 2010
Respiratory muscle testing: a valuable tool for young patients with Duchenne muscular dystrophy
Source: Eur Respir J 2006; 28: Suppl. 50, 357s
Year: 2006
Which are the most informative parameters to follow the respiratory decline in Duchenne muscular dystrophy?
Source: Annual Congress 2012 - Physiological monitoring during sleep and in neuromuscular disease in children
Year: 2012
Assessment of diaphragm thickness variations by ultrasonography in patients with Duchenne muscular dystrophy (DMD)
Source: Annual Congress 2012 - Physiological monitoring during sleep and in neuromuscular disease in children
Year: 2012
Effects of idebenone on pulmonary morbidity in Duchenne muscular dystrophy (DMD)
Source: International Congress 2017 – New ideas for the management of chronic lung diseases
Year: 2017
Gastrointestinal dysfunction in ventilated patients with Duchenne muscular dystrophy
Source: Annual Congress 2012 - Current trends in home mechanical ventilation
Year: 2012
Sleep in patients with Duchenne muscular dystrophy (DMD) and spinal muscular atrophy (SMA): is there a difference?
Source: Eur Respir J 2001; 18: Suppl. 33, 88s
Year: 2001
Inefficient cough in Duchenne muscular dystrophy (DMD)
Source: Annual Congress 2012 - Physiological monitoring during sleep and in neuromuscular disease in children
Year: 2012
Characterization and survival in Duchenne muscular dystrophy with non-invasive ventilation in Chile
Source: International Congress 2017 – Noninvasive ventilation for chronic respiratory failure
Year: 2017
The natural course of lung volumes in Duchenne Muscular Dystrophy (DMD)
Source: International Congress 2017 – Assessing the impact of respiratory and sleep problems in children
Year: 2017
Home-based versus hospital monitoring of respiratory function changes in Duchenne muscular dystrophy (DMD)
Source: International Congress 2018 – Management of chronic cough and respiratory muscle dysfunction
Year: 2018
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