The role of ACE insertion/deletion polymorphism in RDS development in neonates from Russia Source: Eur Respir J 2005; 26: Suppl. 49, 393s Year: 2005
VEGF gene polymorphisms are associated with post-natal lung function development Source: Annual Congress 2011 - Genetics of airway diseases and treatment Year: 2011
The role of ASC signalling in preterm infants at risk of chronic lung disease of prematurity Source: International Congress 2018 – Prematurity and lung disease Year: 2018
The role of C/T polymorphism of NOS1 gene in COPD pathogenesis Source: Eur Respir J 2005; 26: Suppl. 49, 96s Year: 2005
The role of CD14 polymorphisms in the pathogenesis of RSV infection in infants Source: Annual Congress 2010 - Genetics of obstruction 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
The association of NQO1 C609 T polymorphism and the susceptibility of bronchopulmonary dysplasia in preterm neonates Source: Annual Congress 2012 - Issues in neonatal and paediatric intensive care Year: 2012
ß2-adrenergic receptor polymorphisms and risk of COPD Source: International Congress 2018 – Role of omics in population studies Year: 2018
The role of genes coding Glutation-S-Transferase M1 and T1 as risk factors for the development of bronchial asthma Source: Eur Respir J 2001; 18: Suppl. 33, 502s Year: 2001
A BTNL2 gene variant confers to sarcoidosis susceptibility by an increased risk towards the chronic form of the disease Source: Eur Respir J 2006; 28: Suppl. 50, 148s Year: 2006
Polymorphism T3801C of CYP1A1 influence the RDS development in neonates Source: Annual Congress 2010 - Genetics of obstruction Year: 2010
Interleukin-10 polymorphisms influence the neonatal immune response and may be a risk factor for childhood allergic disease and wheeze Source: Annual Congress 2011 - Inflammation and genes in childhood asthma Year: 2011
The role of IL-18 level and genetic polymorphism in patients with bronchial asthma and its relation to disease severity Source: Annual Congress 2012 - Gene-environment treatment and asthma Year: 2012
A genome-wide association study on the risk variations for susceptibility to early COPD Source: International Congress 2019 – New molecular signatures in COPD, lung cancer and a1-antitrypsin deficiency Year: 2019
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 effect of a few genetic polymorphism on childhood asthma Source: Eur Respir J 2004; 24: Suppl. 48, 161s Year: 2004
NOS3 786C/T polymorphism associated with plasma nitric oxide level and risk of development essential hypertension in patients with asthma Source: International Congress 2019 – Novel methods, diagnostics and biomarkers in chronic lung diseases Year: 2019
Role of genome integrity genes polymorphism in risk of lung cancer of middle-aged men Source: Eur Respir J 2007; 30: Suppl. 51, 132s Year: 2007
The role of LTA4H and ALOX5AP polymorphisms in asthma susceptibility Source: Eur Respir J 2007; 30: Suppl. 51, 130s Year: 2007
Maternal genetic asthma predisposition affects signaling networks in lungs of neonatal offspring Source: Annual Congress 2012 - Predicting and observing paediatric allergic disease Year: 2012