Source: Annual Congress 2013 –The burden of respiratory infections in children
Disease area: Paediatric lung diseases, Respiratory infections



Rating:

Share or cite this content

Citations should be made in the following way:
V. Giubergia, M. Salim, F. Jesica, C. Nicolas, S. Luisa, M. Andrea, C. Claudio (Buenos Aires, Argentina). Mannose-binding lectin (MBL) polymorphisms in children with post-infectious obliterant bronchiolitis (PIBO). Eur Respir J 2013; 42: Suppl. 57, 1201

Member's Comments

No comment yet.

Related content which might interest you: Mannose-binding lectin (MBL) insufficiency in children with chronic obstructive pulmonary disease post-adenovirus infection (COPDadv) Source: Eur Respir J 2006; 28: Suppl. 50, 585s Year: 2006 Mannose-binding lectin promoter polymorphisms and gene variants in pulmonary tuberculosis patients from Cantabria (Northern Spain) Source: Annual Congress 2013 –Tuberculosis susceptibility: genetic polymorphism and vitamin D deficiency Year: 2013 Relevance of mannose-binding lectin (MBL) polymorphism in repeated respiratory infections Source: Eur Respir J 2001; 18: Suppl. 33, 465s Year: 2001 Polymorphisms of the vitamin D-binding protein (DBP) gene in Japanese patients with aspirin-exacerbated respiratory disease (AERD) Source: International Congress 2014 – Allergy and asthma: novel findings based on human cell biology Year: 2014 Mannose binding lectin polymorphisms in children with acute bronchiolitis Source: Annual Congress 2007 - Bronchiolitis - genetics and immunity Year: 2007 Interleukin 33 (IL33) polymorphisms associate with incident adult-onset asthma Source: International Congress 2015 – Genetics, genomics and exposures in asthma and COPD Year: 2015 Mannose binding lectin - HYPD allele is associated with frequent exacerbation in COPD patients Source: International Congress 2015 – Monitoring and phenotyping COPD Year: 2015 Selective IgA deficiency and the risk of asthma Source: Annual Congress 2013 –Studies of asthma in man Year: 2013 Impaired neutrophil function in patients with common variable immunodeficiency (CVID) Source: International Congress 2015 – Bronchiectasis and NTM infections: clinical and functional characterisation Year: 2015 Severe acute viral bronchiolitis: A genetic entity Source: International Congress 2016 – Paediatric respiratory infection Year: 2016 Influence of single nucleotide polymorphisms in post-bronchiolitis wheezing Source: International Congress 2016 – Paediatric respiratory infection Year: 2016 Prevalence of mannose-binding lectin variant alleles among cystic fibrosis patients in Italy Source: Eur Respir J 2002; 20: Suppl. 38, 339s Year: 2002 Childhood asthma and hay fever are heritable, but specific high-risk genetic variants are not shared between diseases Source: International Congress 2015 – Understanding paediatric asthma and allergy: genetics and environment Year: 2015 Prevalence and impact of Diabetes mellitus (DM) among hospitalized community-acquired pneumonia (CAP) patients Source: International Congress 2015 – Risk factors and co-morbidities in asthma and COPD Year: 2015 LATE-BREAKING ABSTRACT: Pneumococcal serotypes causing community-acquired pneumonia (CAP) among hospitalized adults in Spain using a new urinary antigen detection (UAD) test. The CAPA study Source: International Congress 2014 – New technologies and biomarkers in lung disease Year: 2014 LATE-BREAKING ABSTRACT: Viral etiology, disease severity and treatment effect in acute bronchiolitis in South-Eastern Norway Source: Annual Congress 2013 –New molecular and cell biology mechanisms Year: 2013 Antimicrobial peptides cathelicidin (LL-37) ve human beta2 defensin levels of pediatric patients with bronchiolitis obliterans Source: International Congress 2014 – Respiratory infections in children Year: 2014 The incidence of alpha-1-antitrypsin (A1AT) deficiency alleles in Polish population - results from large scale newborn screening Source: International Congress 2014 – Molecular pathogenesis of pulmonary inflammatory diseases (COPD, asthma and ILD) Year: 2014 ALOX15 gene polymorphisms in Japanese patients with aspirin-exacerbated respiratory disease (AERD) Source: International Congress 2016 – Role of genetics and exposures in COPD and asthma Year: 2016 Respiratory syncytial virus (RSV) hospitalization in infants with congenital airway anomalies (CAA) in the canadian registry of palivizumab (CARESS) after prophylaxis (2005-2012) Source: International Congress 2014 – Paediatric epidemiology: new insights into primary ciliary dyskinesia, prematurity and bronchiolitis Year: 2014