e-learning
resources
London 2016
Tuesday, 06.09.2016
Orphan diseases I
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
Family history of pneumothorax leading to Birt-Hogg-Dubé syndrome diagnosis
Agisilaos Dervas (Athens, Greece), Agisilaos Dervas, Dimosthenis Papapetrou, Amerini Dimitrakopoulou, Dimitri Tchernitchko, Caroline Kannengiesser, Raphael Borie, Demosthenes Bouros, Spyros Papiris, Effrosyni Manali
Source:
International Congress 2016 – Orphan diseases I
Session:
Orphan diseases I
Session type:
Thematic Poster
Number:
3879
Disease area:
Interstitial lung diseases
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
Agisilaos Dervas (Athens, Greece), Agisilaos Dervas, Dimosthenis Papapetrou, Amerini Dimitrakopoulou, Dimitri Tchernitchko, Caroline Kannengiesser, Raphael Borie, Demosthenes Bouros, Spyros Papiris, Effrosyni Manali. Family history of pneumothorax leading to Birt-Hogg-Dubé syndrome diagnosis. Eur Respir J 2016; 48: Suppl. 60, 3879
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: ANCA associated vasculitis and lung disease
Panel discussion on genetics in pulmonary fibrosis
Observational cohort study of pulmonary exacerbations in alpha-1 antitrypsin deficiency
Related content which might interest you:
Genetic testing in idiopathic interstitial pneumonia
Source: International Congress 2015 – New insights into IIPs
Year: 2015
Childhood interstitial lung disease: A diagnostic challenge
Source: International Congress 2015 – Connective tissue disorders
Year: 2015
Does the HLA-DRB1-genotype influence the course of disease in Danish sarcoidosis patients?
Source: Annual Congress 2013 –Sarcoidosis
Year: 2013
Hughes-Stovin syndrome: A case report
Source: International Congress 2015 – Pulmonary circulation: pulmonary embolism and chronic thromboembolic pulmonary hypertension
Year: 2015
Early pulmonary phenotype in Hermansky-Pudlak syndrome: Analysis of the chILD-EU registry
Source: International Congress 2016 – Paediatric bronchology I
Year: 2016
Childhood diffuse parenchymal lung diseases: Diagnosis, treatment and outcome
Source: Annual Congress 2013 –Diffuse parenchymal lung disease I
Year: 2013
Rare cause of interstitiel lung disease in children: Pleuroparanchymal fibroelastosis
Source: International Congress 2016 – Orphan diseases I
Year: 2016
Interstitial lung disease caused by filamin A gene mutations: Clinical course of three paediatric cases
Source: International Congress 2016 – Orphan diseases II
Year: 2016
Genetic basis of familial spontaneous pneumothorax and lung cysts in an Indian family
Source: International Congress 2015 – Translational research in respiratory care: new findings
Year: 2015
Erdheim-Chester disease: Patterns and pulmonary involvement
Source: International Congress 2016 – Epidemiological and clinical data regarding the modern management of chronic lung diseases
Year: 2016
Pulmonary manifestations in adult patients with chronic granulomatous disease
Source: Annual Congress 2013 –Clinical management of orphan lung diseases
Year: 2013
Clues in interstitial lung disease in children (chILD)
Source: International Congress 2016 – Paediatric bronchology II
Year: 2016
Genetic analysis of ethnicity of sarcoidosis patients in the Netherlands
Source: Annual Congress 2013 –Sarcoidosis and other granulomatosis
Year: 2013
Chronic lung disease in two patients with new integrin alfa3 gene mutations
Source: International Congress 2016 – Orphan diseases II
Year: 2016
Clinical study of pediatric interstitial lung diseases in China
Source: Annual Congress 2013 –Diffuse parenchymal lung disease II
Year: 2013
Aetiological panorama in the diagnosis of interstitial lung diseases
Source: International Congress 2014 – ILDs 5
Year: 2014
Clinical features and prognosis of 108 patients with lymphangioleiomyomatosis
Source: International Congress 2014 – ILDs: diagnostic and prognostic investigations
Year: 2014
Relevance of the expert ILD clinical-radiological evaluation of referred cases to the MDT
Source: International Congress 2016 – Clinical aspects of ILD
Year: 2016
Establishment of the consecutive registration system for pulmonary alveolar proteinosis in Japan: Updated incidence, prevalence and surveillance for intractable cases
Source: International Congress 2016 – Orphan diseases I
Year: 2016
Phenotype heterogeneity in a familial "brain lung thyroid syndrome" related to a novel NKX-2.1 mutation
Source: International Congress 2016 – ILD: from the bench to the bedside
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