Massive pulmonary embolism as the first manifestation in a patient with double heterozygocity for MTHFR and prothrombin 20210 G/A Source: Eur Respir J 2003; 22: Suppl. 45, 443s Year: 2003
The G20210A polymorphism of the prothrombin gene is the strong genetic risk factor for the pulmonary embolism development in young patients Source: Eur Respir J 2004; 24: Suppl. 48, 556s Year: 2004
The relationship between polymorphisms of fibrinogen beta gene and pulmonary thromboembolism in Chinese Han population Source: Eur Respir J 2006; 28: Suppl. 50, 400s Year: 2006
PLA2 polymorphism of platelet glycoprotein IIb/IIIa but not Factor V Leiden and prothrombin G20210A polymorphisms is associated with venous thromboembolism and more recurrent events Source: Annual Congress 2012 - Pulmonary circulation: clinical diagnosis, treatment, end-points and animal models Year: 2012
ACE gene I/D polymorphism in sarcoidosis Source: Annual Congress 2010 - Sarcoidosis: from the bench to the bedside Year: 2010
Genetic polymorphisms associated with acute pulmonary embolism and deep venous thrombosis Source: Eur Respir J 2003; 21: 25-30 Year: 2003
Late-breaking abstract: Significant association between protein C promoter region polymorphism and susceptibility to pulmonary thromboembolism in a Chinese Han population Source: Annual Congress 2011 - Prediction of pulmonary thromboembolism Year: 2011
Association of IL-1β (-511 C>T) and IL1RN 86-bp VNTR polymorphism suspectibility with chronic obstrutive pulomary disease between male and female patients in northern Indian population Source: Annual Congress 2011 - Genetics of airway diseases and treatment Year: 2011
ACE gene I/D polymorphism and initial disease presentation in sarcoidosis Source: Eur Respir J 2003; 22: Suppl. 45, 75s Year: 2003
Analysis of the association between protein C gene single nucleotide polymorphism and pulmonary thromboembolism in Chinese population Source: Annual Congress 2012 - Pulmonary circulation: acute and chronic pulmonary embolism Year: 2012
Rare SERPINA1 allele Mwhitstable in patients with Alpha1-antitrypsin deficiency Source: International Congress 2019 – New molecular signatures in COPD, lung cancer and a1-antitrypsin deficiency Year: 2019
Risk of venous thromboembolism (VTE) in first degree relatives (FDRS) of patients with unprovoked VTE who do not have factor V Leiden (FVL) or the G20210A prothrombin gene mutation (PGM) Source: Annual Congress 2008 - Pulmonary venous thromboembolic disease Year: 2008
Prothrombin gene variant (20210A) as cause of thromboembolic events in a young pregnant woman Source: Eur Respir J 2001; 18: Suppl. 33, 382s Year: 2001
Genetic association between COPD and polymorphisms in TNF, ADRB2 and EPHX1 Source: Eur Respir J 2006; 27: 682-688 Year: 2006
Angiotensin-converting enzyme insertion/deletion gene polymorphism and interstitial pulmonary fibrosis in Iranian population Source: Eur Respir J 2005; 26: Suppl. 49, 542s Year: 2005
Alpha1 -antitrypsin deficiency-related PI*Z and PI*S alleles in a random sample of Polish population Source: Eur Respir J 2006; 28: Suppl. 50, 453s Year: 2006
Association of C3435T polymorphism of MDR1 gene and T1808A polymorphism of NR3C1 gene with bronchial obstruction in severe asthmatics and COPD patients Source: Annual Congress 2010 - Recent developments of molecular pathology and functional genomics in chronic and acute airway diseases Year: 2010
The role of 774C/T, -691C/T and 894G/T polymorphisms of NOS3 gene in development of COPD Source: Eur Respir J 2004; 24: Suppl. 48, 316s Year: 2004
GSTP1 polymorphisms in patients with COPD and alpha-1 antitrypsin deficiency Source: Eur Respir J 2003; 22: Suppl. 45, 384s Year: 2003
ACE I/D but not AGT (-6)A/G polymorphism is a risk factor for mortality in ARDS Source: Eur Respir J 2007; 29: 482-488 Year: 2007