Study of pulmonary function in children with homozygous beta thalassemia Source: Eur Respir J 2002; 20: Suppl. 38, 140s Year: 2002
Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertension Source: Eur Respir J, 54 (2) 1801965; 10.1183/13993003.01965-2018 Year: 2019
Pulmonary function in children with transfusion-dependent thalassemia and its relation to serum ferritin Source: Virtual Congress 2021 – New insights into lung function testing Year: 2021
Pulmonary function abnormalities in Egyptian sickle cell disease patients Source: Annual Congress 2011 - Paediatric epidemiology: bronchiolitis, pneumonia, asthma and spirometry in non-respiratory conditions Year: 2011
Cardiopulmonary functions in children with severe beta-thalassemia before and after transfusion Source: Eur Respir J 2006; 28: Suppl. 50, 405s Year: 2006
Echocardiography of pulmonary vascular function in asymptomatic carriers of BMPR2 mutations Source: Eur Respir J 2012; 40: 1287-1289 Year: 2012
Clinical phenotypes and outcomes of pulmonary veno-occlusive disease in carriers of bi-allelic EIF2AK4 mutations Source: International Congress 2016 – The nature of pulmonary hypertension Year: 2016
Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis Source: Eur Respir J 2015; 46: 474-485 Year: 2015
Screening of pulmonary arterial hypertension in BMPR2 mutation carriers Source: Virtual Congress 2020 – Genetics and genomics of pulmonary arterial hypertension Year: 2020
Evaluation of pulmonary function in children with Cooley’s anemia Source: Eur Respir J 2004; 24: Suppl. 48, 400s Year: 2004
Pulmonary disease in intermediate alpha1-antitrypsin deficient patients Source: International Congress 2017 – Clinical challenges in chronic lung diseases Year: 2017
Telomere-Related Gene mutations in a Greek cohort of suspected monogenic pulmonary fibrosis patients Source: Virtual Congress 2020 – Idiopathic pulmonary fibrosis and interstitial lung disease: progression, genes and more Year: 2020
Pulmonary dysfunction and diffusing capacity in patients with thalassemia major Source: Annual Congress 2009 - Paediatric respiratory epidemiology: respiratory infections and rare diseases Year: 2009
Young adult with inherited PiMZ alpha-1-antitrypsin deficiency (A1ATD)-related bronchiectasis: characteristic of blood neutrophils and A1AT protein Source: International Congress 2016 – Translational studies in lung disease Year: 2016
Is pulmonary hypertension in intermedia beta-thalassemia patients related to pulmonary ventilatory dysfunction? Source: Annual Congress 2009 - Impact on respiratory function of pulmonary and extrapulmonary diseases Year: 2009
First heterozygous NOP10 mutation in familial pulmonary fibrosis Source: Eur Respir J, 55 (6) 1902465; 10.1183/13993003.02465-2019 Year: 2020
Phenotype and outcome of pulmonary arterial hypertension patients carrying a TBX4 mutation Source: Eur Respir J, 55 (5) 1902340; 10.1183/13993003.02340-2019 Year: 2020
Lung function and disease severity in cystic fibrosis patients heterozygous for p.Arg117His Source: ERJ Open Res, 3 (1) 00056-2016; 10.1183/23120541.00056-2016 Year: 2017
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
Pulmonary function in Thai children and adolescents with obesity Source: Annual Congress 2011 - New insights in paediatric respiratory physiology Year: 2011