e-learning
resources
Madrid 2019
Wednesday, 02.10.2019
Rare and ultra-rare diseases and the lungs: updates and new perspectives
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
Development of Pulmonary Arteriovenous Malformations and Occurrence of Neurological Complications in patients with Hereditary Haemorrhagic Telangiectasia with isolated micronodules and/or intrapulmonary shunt at first screening
V. Margelidon-Cozzolino (Bron, France), C. Khouatra (Bron, France), J. Traclet (Bron, France), K. Ahmad (Bron, France), S. Dupuis-Girod (Bron, France), V. Cottin (Bron, France)
Source:
International Congress 2019 – Rare and ultra-rare diseases and the lungs: updates and new perspectives
Session:
Rare and ultra-rare diseases and the lungs: updates and new perspectives
Session type:
Oral Presentation
Number:
5326
Disease area:
Pulmonary vascular diseases
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
V. Margelidon-Cozzolino (Bron, France), C. Khouatra (Bron, France), J. Traclet (Bron, France), K. Ahmad (Bron, France), S. Dupuis-Girod (Bron, France), V. Cottin (Bron, France). Development of Pulmonary Arteriovenous Malformations and Occurrence of Neurological Complications in patients with Hereditary Haemorrhagic Telangiectasia with isolated micronodules and/or intrapulmonary shunt at first screening. 5326
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:
Optimizing invasive ventilation for SMA type 1 children who are receiving the gene therapy
Middle-long term pulmonary abnormalities after severe COVID-19 pneumonia which required invasive ventilation
N3 hilar sampling decision in the staging of mediastinal lung cancer
Related content which might interest you:
Pulmonary arteriovenous malformations: isolated anomaly and hereditary hemorrhagic telengectasia
Source: Eur Respir J 2005; 26: Suppl. 49, 316s
Year: 2005
Outcomes in embolisations of pulmonary arterio-venous malformations
Source: International Congress 2014 – Chronic thromboembolic pulmonary hypertension
Year: 2014
Association between Pulmonary Infections and the Prognosis in Patients with Idiopathic Pulmonary Fibrosis
Source: Virtual Congress 2021 – Interstitial lung disease around the world
Year: 2021
Architecture and spatial distribution of pulmonary arteriovenous shunts in patients with hereditary haemorrhagic teleangiectasia
Source: Eur Respir J 2001; 18: Suppl. 33, 492s
Year: 2001
Warfarin-associated intracranial hemorrhage during anticoagulation therapy
Source: International Congress 2014 – Acute pulmonary embolism
Year: 2014
Rare case of extensive systemic to pulmonary arteriovenous malformation presenting with recurrent headaches
Source: International Congress 2015 – Pulmonary hypertension: management
Year: 2015
Screening for pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia in the French national reference centre
Source: International Congress 2018 – Pulmonary hypertension in lung diseases and the role of the right ventricle
Year: 2018
Management of spontaneous pneumothorax in patients with or without Birt-Hogg-Dubé syndrome
Source: International Congress 2014 – ILDs 1
Year: 2014
Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia
Source: Eur Respir J 2009; 34: 875-881
Year: 2009
Clinical and Epidemiological Features of Tumor and Non-tumor Patients Complicated with Pulmonary Embolism
Source: International Congress 2017 – Prognostic factors and outcomes in pulmonary embolism
Year: 2017
Recurrent massive pulmonary hemorrhage in the course of hereditary hemorrhagic teleangiectasia (HHT) with diffuse pulmonary arteriovenous malformations
Source: Annual Congress 2009 - Interesting case reports and case series
Year: 2009
Management of pulmonary artery-venous malformations
Source: Annual Congress 2008 - Congenital lung lesions and emphysema; lung cancer surgery
Year: 2008
Do persistent perfusion defects predict late recurrences in pulmonary embolism?
Source: International Congress 2014 – Acute pulmonary embolism
Year: 2014
Treatment of Idiopathic Pulmonary Fibrosis
Source: Guideline 2015
Year: 2015
Is Pulmonary Rehabilitation A Savior In Idiopathic Pulmonary Fibrosis?
Source: Virtual Congress 2020 – News on diagnosis and therapy of idiopathic pulmonary fibrosis
Year: 2020
Genetic epidemiology of hereditary hemorrhagic telangiectasia complicated with pulmonary arteriovenous malformation
Source: Annual Congress 2011 - Genetics of airway diseases and treatment
Year: 2011
Platelet activation indices in patients with Idiopathic Pulmonary Fibrosis
Source: International Congress 2014 – ILDs 5
Year: 2014
Embolisation of pulmonary arteriovenous malformations improves nosebleeds in people with hereditary haemorrhagic telangiectasia
Source: International Congress 2016 – Pulmonary hypertension: the clinic II
Year: 2016
Clinical Features and Prognosis of Acute exacerbation of Connective Tissue Diseases Associated Pulmonary Fibrosis------ Comparision with Idiopathic Pulmonary Fibrosis
Source: International Congress 2017 – The spectrum of CTDs: from pathogenesis to treatment
Year: 2017
Unusual cause of pulmonary haemorrhage in adolescent
Source: Annual Congress 2013 –Paediatric bronchology
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