immunopathologia The importance of aeroallergen sensitivity in children with cystic fibrosis

Background : Cystic fibrosis (CF) is an inherited autosomal recessive disorder that causes chronic airway disease. In addition to genetic factors, environmental factors may affect the clinical phenotype of CF. In this study,

[1]  A. Kılınç,et al.  Evaluation of the health‐related quality of life in Turkish cystic fibrosis patients , 2020, Pediatrics international : official journal of the Japan Pediatric Society.

[2]  A. Jan,et al.  BMI Classification Percentile And Cut Off Points , 2019 .

[3]  Patrizia Calella,et al.  Association between body composition and pulmonary function in children and young people with cystic fibrosis. , 2017, Nutrition.

[4]  M. Moustaki,et al.  The Role of Sensitization to Allergen in Asthma Prediction and Prevention , 2017, Front. Pediatr..

[5]  A. Aggarwal,et al.  Developments in the diagnosis and treatment of allergic bronchopulmonary aspergillosis , 2016, Expert review of respiratory medicine.

[6]  H. Mussaffi,et al.  Reversible airway obstruction in cystic fibrosis: Common, but not associated with characteristics of asthma. , 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

[7]  I. Panse,et al.  Natural history of allergic sensitization in infants with early‐onset atopic dermatitis: results from ORCA Study , 2014, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

[8]  R. Pabary.  Severe pulmonary exacerbation in cystic fibrosis caused by cat allergy. , 2014, Paediatric respiratory reviews.

[9]  T. Craig.  Asthma Epidemiology and Risk Factors , 2014 .

[10]  H. Tiddens,et al.  Asthma and cystic fibrosis: A tangled web , 2014, Pediatric pulmonology.

[11]  H. Tsai,et al.  Total Serum IgE in a Population-Based Study of Asian Children in Taiwan: Reference Value and Significance in the Diagnosis of Allergy , 2013, PloS one.

[12]  G. Cutting,et al.  Environmental allergies and respiratory morbidities in cystic fibrosis , 2013, Pediatric pulmonology.

[13]  C. Riedi,et al.  Cystic fibrosis and atopy. , 2013, Allergologia et immunopathologia.

[14]  G. Cutting,et al.  Quantification of the relative contribution of environmental and genetic factors to variation in cystic fibrosis lung function. , 2010, The Journal of pediatrics.

[15]  G. Cutting,et al.  Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients , 2010, Respiratory research.

[16]  P. Leiria-Pinto,et al.  Cystic fibrosis, atopy, asthma and ABPA. , 2010, Allergologia et immunopathologia.

[17]  W. Morgan,et al.  Relationship between inhaled corticosteroid therapy and rate of lung function decline in children with cystic fibrosis. , 2008, The Journal of pediatrics.

[18]  Vicky A Legrys,et al.  Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. , 2008, The Journal of pediatrics.

[19]  B. Yawn,et al.  Allergic Rhinitis and its Impact on Asthma (ARIA) 2008 update , 2008 .

[20]  N. Uzuner,et al.  The determination of asthma, rhinitis, eczema, and atopy prevalence in 9- to 11-year-old children in the city of Izmir. , 2006, Allergy and asthma proceedings.

[21]  W. Henderson,et al.  The role of allergy in manifestations of respiratory disease in adult cystic fibrosis. , 2004, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[22]  J. Elborn,et al.  “CF asthma”: what is it and what do we do about it? , 2002, Thorax.

[23]  C. Dezateux,et al.  Inhaled corticosteroids for cystic fibrosis. , 2016, The Cochrane database of systematic reviews.

[24]  P. Brand.  Bronchodilators in cystic fibrosis. , 2000, Journal of the Royal Society of Medicine.

[25]  J L Hankinson,et al.  Spirometric reference values from a sample of the general U.S. population. , 1999, American journal of respiratory and critical care medicine.

[26]  M. Hodson,et al.  International practice patterns by age and severity of lung disease in cystic fibrosis: Data from the epidemiologic registry of cystic fibrosis (ERCF) , 1997, Pediatric pulmonology.

[27]  J. Warner,et al.  Cystic fibrosis and allergy , 1996, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

[28]  J. Warner,et al.  Identification of allergic bronchopulmonary aspergillosis in cystic fibrosis patients by recombinant Aspergillus fumigatus I/a-specific serology. , 1995, American journal of respiratory and critical care medicine.

[29]  A. Spock,et al.  Allergic bronchopulmonary aspergillosis in patients with cystic fibrosis. , 1994, Chest.

[30]  D. Dockery,et al.  Pulmonary function growth velocity in children 6 to 18 years of age. , 1993, The American review of respiratory disease.

[31]  R. Wilmott.  The relationship between atopy and cystic fibrosis , 1991, Clinical reviews in allergy.

[32]  R. Levinsky,et al.  Pseudomonas infection, allergy, and cystic fibrosis. , 1982, Archives of disease in childhood.

[33]  F. Hobbs,et al.  Cystic fibrosis, atopy, and airways lability. , 1978, Archives of disease in childhood.