e-learning
resources
Amsterdam 2015
Tuesday, 29.09.2015
Respiratory physiology in children: technical and clinical aspects
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
Respiratory and neurobehavioural characteristics of a murine model of congenital myotonic dystrophy type 1
Helène Prigent (Garches, France), Helene Prigent, Maud Ringot, Nelina Ramanantsoa, Lise Michel, Thomas Bourgeois, Boris Matrot, Genevieve Gourdon, Jorge Gallego
Source:
International Congress 2015 – Respiratory physiology in children: technical and clinical aspects
Session:
Respiratory physiology in children: technical and clinical aspects
Session type:
Thematic Poster Session
Number:
4151
Disease area:
Paediatric lung diseases, Sleep and breathing disorders
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
Helène Prigent (Garches, France), Helene Prigent, Maud Ringot, Nelina Ramanantsoa, Lise Michel, Thomas Bourgeois, Boris Matrot, Genevieve Gourdon, Jorge Gallego. Respiratory and neurobehavioural characteristics of a murine model of congenital myotonic dystrophy type 1. Eur Respir J 2015; 46: Suppl. 59, 4151
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:
From pulmonary gas exchange to the interpretation of arterial blood gases
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
Related content which might interest you:
Hypercapnic ventilatory response in patients with Steinert's myotonic dystrophy type 1
Source: Annual Congress 2013 –Clinical respiratory physiology in different diseases
Year: 2013
Respiratory function and sleep respiratory disorders in facio-scapulo-humeral dystrophy (FSHD)
Source: Annual Congress 2008 - Weight control and comorbidity in obstructive sleep apnoea
Year: 2008
Paradoxical motion time as an early indicator of nocturnal desaturation in adolescents with Duchenne muscular distrophy (DMD)
Source: Annual Congress 2013 –Clinical applications of respiratory physiology in children
Year: 2013
Noninvasive assessment of respiratory muscle strenght and activity in myotonic dystrophy
Source: International Congress 2016 – From cardiopulmonary interaction to locomotor muscles and dyspnoea in health and disease
Year: 2016
Longitudinal assessment of respiratory function in Duchenne muscular dystrophy (DMD): The effect of steroid therapy
Source: International Congress 2014 – New aspects of lung function testing in children
Year: 2014
Lack of relationship between reduction in the ventilatory response to CO2 and lung function impairment in myotonic dystrophy patients
Source: International Congress 2014 – Of mice and men: physiology and biology of sleep disordered breathing
Year: 2014
Lung function quality in patients with myotonic dystrophia type 1
Source: International Congress 2014 – Alterations of exercise and lung function in different diseases
Year: 2014
Chronic respiratory failure in myotonic dystrophy type 1 (DM1): Incidence & risk factors
Source: International Congress 2017 – Clinical and physiological challenges in noninvasive ventilation
Year: 2017
Sleep disordered breathing and lung function in myotonic dystrophy
Source: Eur Respir J 2007; 30: Suppl. 51, 595s
Year: 2007
Respiratory function, scoliosis and arthrodesis in Duchenne muscular dystrophy
Source: International Congress 2015 – Respiratory physiology in children: technical and clinical aspects
Year: 2015
Assesment for Sleep in Myotonic Dystrophy type 1(MD-1) patients
Source: International Congress 2018 – Obesity: comorbidities
Year: 2018
Respiratory involvement in myotonic dystrophy type 1: Experience of pulmonology consultation in a pediatric hospital
Source: Annual Congress 2013 –Long-term NIV: children, neuromuscular patients and technical aspects
Year: 2013
Relationships between inspiratory muscle function and daytime or nocturnal hypoventilation in myotonic dystrophy (MD)
Source: Eur Respir J 2005; 26: Suppl. 49, 687s
Year: 2005
Scoliosis and spinal fusion (SF) correlate with spirometry but not with breathing pattern at rest in Duchenne muscular dystrophy (DMD)
Source: International Congress 2015 – Respiratory physiology in children: technical and clinical aspects
Year: 2015
Template-operated quantitative motor unit potential analysis in diaphragm of patients with myotonic dystrophy
Source: International Congress 2014 – Pathophysiological mechanisms at different scales
Year: 2014
Assessment of diaphragmatic function by ultrasonography (US) and opto-electronic plethysmography (OEP) in patients with Duchenne muscular dystrophy (DMD)
Source: Annual Congress 2013 –Functional imaging of the lung, airways and diaphragm
Year: 2013
Physiology of respiratory disturbances in muscular dystrophies
Source: Breathe 2016; 12: 318-327
Year: 2016
Evaluation of the respiratory function in a population with mild/moderate Parkinson's disease
Source: International Congress 2014 – Sleep disordered breathing 5
Year: 2014
Nocturnal efficacy of servo-adaptative ventilation in patient with Type 1 myotonic dystrophy (MD1)
Source: Annual Congress 2010 - Long-term noninvasive ventilation in the chronic patient: outcome and pathophysiology
Year: 2010
Oximetry screening alone is not sufficient to identify nocturnal hypoventilation in Duchenne muscular dystrophy
Source: International Congress 2016 – Latest advances in paediatric sleep medicine
Year: 2016
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