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ERS International Congress, Milan 2017

Browse by day: Saturday, 09.09.2017 Sunday, 10.09.2017 Monday, 11.09.2017 Tuesday, 12.09.2017 Wednesday, 13.09.2017		Sponsored symposia: Industry Evening Symposium at ERS 2017: “Evolving Concepts in Asthma with Type 2 Inflammation: the Role of Biologics”

Citations should be made in the following way: Authors. Title. Eur Respir J 2017; 50: Suppl. 61, abstract number.

Rare and common genetic variants of common and rare airway diseases

Poster Discussion
Chairs: M. Dahl (Køge, Denmark), T. Sigsgaard (Århus, Denmark)

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Late Breaking Abstract - SERPINA1 methylation and lung function: Results from SAPALDIA, the Swiss population-based cohort study A. Beckmeyer-Borowko (Basel, Switzerland)
Alpha-1 antitrypsin deficiency and spontaneous pneumothorax: just a coincidence? G. Menga (Ciudad Autónoma Buenos Aires, Argentina)
A rare genetic mutation in primary ciliary dyskinesia S. Diakova (Moscow, Russian Federation)
Alpha-1 antitrypsin deficiency – a potentially fatal disease C. da Costa Dias de Sousa (Lordelo, Portugal)
Screening for a1-antitrypsin deficiency in the pneumologist’s office using a dried blood spots kit: promising first results. c. chapuis cellier (Pierre Benite, France)
Exploring the relationship between alpha-1-antitrypsin deficiency and persistent airflow limitation in severe asthma. G. Menga (Ciudad Autónoma Buenos Aires, Argentina)
Molecular diagnosis of Alpha-1 antitrypsin deficiency: a new method based on Luminex Technology S. Ottaviani (Pavia, Italy)
Preliminary Results of Whole Exome Sequencing in Turkish Primary Ciliary Dyskinesia Patients - Hacettepe University Experience: “Three candidate genes, five novel and two known mutations” H. Özçelik (ANKARA, Turkey)
Rare genetic variants in genes with ciliary function underlie non-smoking related COPD M. de Vries (Groningen, Netherlands)
Unraveling effects of lung function GWAS candidates using airway epithelial eQTLs A. Faiz (Groningen, Netherlands)
A nasal gene expression profile differentiates individuals with and without COPD and overlaps bronchial gene expression I. Boudewijn (Groningen, Netherlands)
Lung function and telomere shortening in blood leukocytes in clean-up workers of Chornobyl NPP suffered of COPD K. Bazyka (Kyiv, Ukraine)
Relationship with Loss of SIGLEC14 and the Risk of COPD Exacerbation M. Çalikoglu (Mersin, Turkey)
Genetic polymorphisms of the adrenergic ß2-receptor in COPD: systematic review and meta-analyses of disease risk and treatment response A. Nielsen (Køge, Denmark)
Gene variants and clinical course of pulmonary sarcoidosis in a Slavic population A. Kishore (Olomouc, Czech Republic)
A genome-wide SNP-by-NO2 interaction study on lung function in the LifeLines study. A. De Faria Coimbra Lichtenfels (Groningen, Netherlands)

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