e-learning
resources
Amsterdam 2015
Wednesday, 30.09.2015
New insights into IIPs
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
Classification of different ABCA3 mutations causing interstitial lung disease
Thomas Wittmann (Munich, Germany), Thomas Wittmann, Ulrike Schindlbeck, Stefanie Höppner, Susanna Kinting, Gerhard Liebisch, Ralf Zarbock, Matthias Griese
Source:
International Congress 2015 – New insights into IIPs
Session:
New insights into IIPs
Session type:
Poster Discussion
Number:
4851
Disease area:
Interstitial lung diseases, Paediatric lung diseases
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
Thomas Wittmann (Munich, Germany), Thomas Wittmann, Ulrike Schindlbeck, Stefanie Höppner, Susanna Kinting, Gerhard Liebisch, Ralf Zarbock, Matthias Griese. Classification of different ABCA3 mutations causing interstitial lung disease. Eur Respir J 2015; 46: Suppl. 59, 4851
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: respiratory care for newborns in resource-limited settings
Panel discussion on genetics in pulmonary fibrosis
Related content which might interest you:
Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer
Source: International Congress 2016 – IPF pathogenesis
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
Chronic lung disease in two patients with new integrin alfa3 gene mutations
Source: International Congress 2016 – Orphan diseases II
Year: 2016
Familial interstitial lung disease and ABCA3 gene Gly964Asp mutation
Source: Annual Congress 2010 - Pathogenesis of diffuse parenchymal lung disease
Year: 2010
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
Mitochondrial tRNA gene mutations in patients with idiopathic pulmonary fibrosis (IPF) and sarcoidosis
Source: International Congress 2014 – Basic and translational research in lung cancer and non-neoplastic pulmonary diseases
Year: 2014
Pediatric interstitial lung disease caused by a novel ABCA3 mutation: ABCA3
G964A
Source: Annual Congress 2009 - Cell biology of lung disease
Year: 2009
SP-C deficiency: Three different phenotypes for the same mutation
Source: International Congress 2015 – Paediatric bronchology
Year: 2015
Loss of PTEN induced lung fibroblasts exhibiting similar pathogenic features to cancer cells in idiopathic pulmonary fibrosis
Source: International Congress 2014 – ILDs 2
Year: 2014
Novel lung function tests in patients with interstitial lung disease (ILD)
Source: International Congress 2016 – Clinical aspects of ILD
Year: 2016
Hermansky-Pudlak syndrome type 4 with interstitial pneumonia
Source: Annual Congress 2013 –Diffuse parenchymal lung disease I
Year: 2013
Distinct gene expression profiles of cultured stromal cells from the patients with idiopathic pulmonary fibrosis and lung adenocarcinoma
Source: International Congress 2015 – Translational studies in airway cell biology
Year: 2015
Regulation and localization of the telomerase enzyme-complex and the shelterin-telosom-complex in sporadic idiopathic pulmonary fibrosis (IPF)
Source: Annual Congress 2013 –Idiopathic pulmonary fibrosis: pathogenesis
Year: 2013
Strong reversal of the lung fibrosis disease signature by autotaxin inhibitor GLPG1690 in a mouse model for IPF
Source: International Congress 2016 – Therapeutic horizons: novel targets and pharmacological models
Year: 2016
The role of detection of myositis specific and associated antibodies in Japanese patient with interstitial lung disease
Source: International Congress 2014 – ILDs: connective tissue disease
Year: 2014
An insight of lung cysts with filamin A mutation
Source: International Congress 2015 – Interstitial lung diseases II
Year: 2015
Mutation alone does not predict the clinical course of surfactant protein C deficiency in children
Source: International Congress 2014 – ILDs: pathogenesis and clinical features
Year: 2014
Functional assessment and phenotypic heterogeneity of
SFTPA1
and
SFTPA2
mutations in interstitial lung diseases and lung cancer
Source: Eur Respir J, 56 (6) 2002806; 10.1183/13993003.02806-2020
Year: 2020
Genetic testing in idiopathic interstitial pneumonia
Source: International Congress 2015 – New insights into IIPs
Year: 2015
Comparative proteome analysis of lung tissue from patients with idiopathic pulmonary fibrosis (IPF) and non-specific interstitial pneumonia (NSIP)
Source: Annual Congress 2013 –Connective tissue disease and interstitial lung disease
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