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The influence of age and gender on sensitization to aero-allergens

Pediatric allergy and immunology, 2007-12, Vol.18 (8), p.671-678

2007

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Point-of-care CRP matters: normal CRP levels reduce immediate antibiotic prescribing for acutely ill children in primary care: a cluster randomized controlled trial

Scandinavian journal of primary health care, 2018-12, Vol.36 (4), p.423-436

2018

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Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes

Scientific reports, 2017-06, Vol.7 (1), p.3702-12, Article 3702

2017

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Allogeneic Hematopoietic Stem Cell Transplantation After Prior Lung Transplantation for Hereditary Pulmonary Alveolar Proteinosis: A Case Report

Frontiers in immunology, 2022-07, Vol.13

2022

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Is the improvement of CF patients, hospitalized for pulmonary exacerbation, correlated to a decrease in bacterial load?

PloS one, 2013-11, Vol.8 (11), p.e79010-e79010

2013

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Acceptance, well-being and goals in adolescents with chronic illness: a daily process analysis

Psychology & health, 2013-11, Vol.28 (11), p.1337-1351

2013

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Comparison of the sensitivity of culture, PCR and quantitative real-time PCR for the detection of Pseudomonas aeruginosa in sputum of cystic fibrosis patients

BMC microbiology, 2009-11, Vol.9 (1), p.244-244

2009

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When One Rare Disease Hides Another: Kartagener Syndrome Masking FMF

Clinical pediatrics, 2018-07, Vol.57 (8), p.981-985

2018

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Exercise-induced respiratory symptoms are poor predictors of bronchoconstriction

Pediatric pulmonology, 2005-04, Vol.39 (4), p.301-305

2005

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Optimizing antibiotic prescribing for acutely ill children in primary care (ERNIE2 study protocol, part B): a cluster randomized, factorial controlled trial evaluating the effect of a point-of-care C-reactive protein test and a brief intervention combined with written safety net advice

BMC pediatrics, 2014-10, Vol.14 (1), p.246-246, Article 246

2014

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Shared Genotypes of Achromobacter xylosoxidans Strains Isolated from Patients at a Cystic Fibrosis Rehabilitation Center

Journal of Clinical Microbiology, 2005-06, Vol.43 (6), p.2998-3002

2005

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Disseminated Mycobacterium avium Infection in a Patient with a Novel Mutation in the Interleukin-12 Receptor-β1 Chain

The Journal of pediatrics, 2008-11, Vol.153 (5), p.721-722

2008

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Comparison of culture and qPCR for the detection of Pseudomonas aeruginosa in not chronically infected cystic fibrosis patients

BMC microbiology, 2010-09, Vol.10 (1), p.245-245

2010

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Cystic fibrosis sputum : A barrier to the transport of nanospheres

American journal of respiratory and critical care medicine, 2000-11, Vol.162 (5), p.1905-1911

2000

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PCR and the detection of Pseudomonas aeruginosa in respiratory samples of CF patients. A literature review

Journal of cystic fibrosis, 2011-09, Vol.10 (5), p.293-297

2011

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Recurrent spontaneous pneumomediastinum in a child with tracheomalacia

Pediatric pulmonology, 2017-06, Vol.52 (6), p.E29-E31

2017

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A novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B-cell maturation defects

Journal of allergy and clinical immunology, 2018-01, Vol.141 (1), p.432-435.e7

2018

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Transport of nanoparticles in cystic fibrosis sputum and bacterial biofilms by single-particle tracking microscopy

Nanomedicine (London, England), 2013-06, Vol.8 (6), p.935-949

2013

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Severe Exacerbations and Decline in Lung Function in Asthma

American journal of respiratory and critical care medicine, 2009-01, Vol.179 (1), p.19-24

2009

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Establishing the diagnosis of chronic colonization with Pseudomonas aeruginosa of cystic fibrosis patients: Comparison of the European consensus criteria with genotyping of P. aeruginosa isolates

Journal of cystic fibrosis, 2018-11, Vol.17 (6), p.729-735

2018

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Eradication therapy for Pseudomonas aeruginosa colonization episodes in cystic fibrosis patients not chronically colonized by P. aeruginosa

Journal of cystic fibrosis, 2013-01, Vol.12 (1), p.1-8

2013

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Epidemic Achromobacter xylosoxidans strain among Belgian cystic fibrosis patients and review of literature

BMC microbiology, 2016-06, Vol.16 (1), p.122-122, Article 122

2016

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Exercise performance and quality of life in children with cystic fibrosis and mildly impaired lung function: relation with antibiotic treatments and hospitalization

European journal of pediatrics, 2017-12, Vol.176 (12), p.1689-1696

2017

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A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosis

Journal of cystic fibrosis, 2014-03, Vol.13 (2), p.148-155

2014

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The effect of enteral tube feeding in cystic fibrosis: A registry based study

Journal of cystic fibrosis, 2018-03, Vol.17 (2), p.264-270

2018

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The influence of age and gender on sensitization to aero-allergens

Point-of-care CRP matters: normal CRP levels reduce immediate antibiotic prescribing for acutely ill children in primary care: a cluster randomized controlled trial

Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes

Allogeneic Hematopoietic Stem Cell Transplantation After Prior Lung Transplantation for Hereditary Pulmonary Alveolar Proteinosis: A Case Report

Is the improvement of CF patients, hospitalized for pulmonary exacerbation, correlated to a decrease in bacterial load?

Acceptance, well-being and goals in adolescents with chronic illness: a daily process analysis

Comparison of the sensitivity of culture, PCR and quantitative real-time PCR for the detection of Pseudomonas aeruginosa in sputum of cystic fibrosis patients

When One Rare Disease Hides Another: Kartagener Syndrome Masking FMF

Exercise-induced respiratory symptoms are poor predictors of bronchoconstriction

Optimizing antibiotic prescribing for acutely ill children in primary care (ERNIE2 study protocol, part B): a cluster randomized, factorial controlled trial evaluating the effect of a point-of-care C-reactive protein test and a brief intervention combined with written safety net advice

Shared Genotypes of Achromobacter xylosoxidans Strains Isolated from Patients at a Cystic Fibrosis Rehabilitation Center

Disseminated Mycobacterium avium Infection in a Patient with a Novel Mutation in the Interleukin-12 Receptor-β1 Chain

Comparison of culture and qPCR for the detection of Pseudomonas aeruginosa in not chronically infected cystic fibrosis patients

Cystic fibrosis sputum : A barrier to the transport of nanospheres

PCR and the detection of Pseudomonas aeruginosa in respiratory samples of CF patients. A literature review

Recurrent spontaneous pneumomediastinum in a child with tracheomalacia

A novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B-cell maturation defects

Transport of nanoparticles in cystic fibrosis sputum and bacterial biofilms by single-particle tracking microscopy

Severe Exacerbations and Decline in Lung Function in Asthma

Establishing the diagnosis of chronic colonization with Pseudomonas aeruginosa of cystic fibrosis patients: Comparison of the European consensus criteria with genotyping of P. aeruginosa isolates

Eradication therapy for Pseudomonas aeruginosa colonization episodes in cystic fibrosis patients not chronically colonized by P. aeruginosa

Epidemic Achromobacter xylosoxidans strain among Belgian cystic fibrosis patients and review of literature

Exercise performance and quality of life in children with cystic fibrosis and mildly impaired lung function: relation with antibiotic treatments and hospitalization

A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosis

The effect of enteral tube feeding in cystic fibrosis: A registry based study

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