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Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics

PloS one, 2015-09, Vol.10 (9), p.e0137681-e0137681

2015

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Intestinal microbiota composition after antibiotic treatment in early life: the INCA study

BMC pediatrics, 2015-12, Vol.15 (1), p.204-204, Article 204

2015

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Prevalence and Predictors of Uncontrolled Asthma in Children Referred for Asthma and Other Atopic Diseases

Journal of asthma and allergy, 2020-01, Vol.13, p.67-75

2020

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Aspergillus fumigatus colonization in cystic fibrosis: implications for lung function?

Clinical microbiology and infection, 2011-09, Vol.17 (9), p.1381-1386

2011

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Chronic infection and inflammation affect exercise capacity in cystic fibrosis

The European respiratory journal, 2012-04, Vol.39 (4), p.893-898

2012

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Long‐term effects of ivacaftor on nonpulmonary outcomes in individuals with cystic fibrosis, heterozygous for a S1251N mutation

Pediatric pulmonology, 2020-06, Vol.55 (6), p.1400-1405

2020

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Initial Pseudomonas aeruginosa infection in patients with cystic fibrosis: characteristics of eradicated and persistent isolates

Clinical microbiology and infection, 2012-06, Vol.18 (6), p.567-574

2012

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Biomarkers of therapy responsiveness in asthma: pitfalls and promises

Clinical and experimental allergy, 2011-05, Vol.41 (5), p.615-629

2011

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Clinical impact of a highly prevalent Pseudomonas aeruginosa clone in Dutch cystic fibrosis patients

Clinical microbiology and infection, 2011-03, Vol.17 (3), p.382-385

2011

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Association of the CLCA1 p.S357N Variant With Meconium Ileus in European Patients With Cystic Fibrosis

Journal of pediatric gastroenterology and nutrition, 2010-03, Vol.50 (3), p.347-349

2010

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Rapid early weight gain is associated with wheeze and reduced lung function in childhood

The European respiratory journal, 2012-02, Vol.39 (2), p.403-410

2012

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Preventive effects of selected probiotic strains on the development of asthma and allergic rhinitis in childhood. The Panda study

Clinical and experimental allergy, 2014-11, Vol.44 (11), p.1431-1433

2014

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Forced expiratory manoeuvres in children: do they meet ATS and ERS criteria for spirometry?

The European respiratory journal, 2001-10, Vol.18 (4), p.655-660

2001

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Dietary intake in children and adolescents with cystic fibrosis

Clinical nutrition (Edinburgh, Scotland), 2014-06, Vol.33 (3), p.528-532

2014

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The Wheezing Illnesses Study Leidsche Rijn (WHISTLER): Rationale and Design

European journal of epidemiology, 2004-09, Vol.19 (9), p.895-903

2004

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Radiological and functional changes over 3 years in young children with cystic fibrosis

The European respiratory journal, 2007-08, Vol.30 (2), p.279-285

2007

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Systemic eosinophil response induced by respiratory syncytial virus

Clinical and experimental immunology, 2006-06, Vol.144 (3), p.409-417

2006

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Pseudomonas aeruginosa diversity in distinct paediatric patient groups

Clinical microbiology and infection, 2008-10, Vol.14 (10), p.935-941

2008

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Excess early postnatal weight gain and blood pressure in healthy young children

Journal of developmental origins of health and disease, 2019-10, Vol.10 (5), p.563-569

2019

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Are inhaled corticosteroids safe and effective in infants with asthma-like symptoms?

Pediatrics (Evanston), 2004-07, Vol.114 (1), p.325-325

2004

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Functional Restoration of CFTR Nonsense Mutations in Intestinal Organoids

Journal of cystic fibrosis, 2022-03, Vol.21 (2), p.246-253

2022

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Using Component-Resolved Diagnostics in the Management of Peanut-Allergic Patients

Current treatment options in allergy, 2016, Vol.3 (2), p.169-180

2016

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Spirometry in young children: should computer-animation programs be used during testing?

The European respiratory journal, 2003-05, Vol.21 (5), p.872-875

2003

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Measurements of interrupter resistance: reference values for children 3-13 yrs of age

The European respiratory journal, 2002-10, Vol.20 (4), p.907-911

2002

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Forskolin induced swelling (FIS) assay in intestinal organoids to guide eligibility for compassionate use treatment in a CF patient with a rare genotype

Journal of cystic fibrosis, 2022-03, Vol.21 (2), p.254-257

2022

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Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics

Intestinal microbiota composition after antibiotic treatment in early life: the INCA study

Prevalence and Predictors of Uncontrolled Asthma in Children Referred for Asthma and Other Atopic Diseases

Aspergillus fumigatus colonization in cystic fibrosis: implications for lung function?

Chronic infection and inflammation affect exercise capacity in cystic fibrosis

Long‐term effects of ivacaftor on nonpulmonary outcomes in individuals with cystic fibrosis, heterozygous for a S1251N mutation

Initial Pseudomonas aeruginosa infection in patients with cystic fibrosis: characteristics of eradicated and persistent isolates

Biomarkers of therapy responsiveness in asthma: pitfalls and promises

Clinical impact of a highly prevalent Pseudomonas aeruginosa clone in Dutch cystic fibrosis patients

Association of the CLCA1 p.S357N Variant With Meconium Ileus in European Patients With Cystic Fibrosis

Rapid early weight gain is associated with wheeze and reduced lung function in childhood

Preventive effects of selected probiotic strains on the development of asthma and allergic rhinitis in childhood. The Panda study

Forced expiratory manoeuvres in children: do they meet ATS and ERS criteria for spirometry?

Dietary intake in children and adolescents with cystic fibrosis

The Wheezing Illnesses Study Leidsche Rijn (WHISTLER): Rationale and Design

Radiological and functional changes over 3 years in young children with cystic fibrosis

Systemic eosinophil response induced by respiratory syncytial virus

Pseudomonas aeruginosa diversity in distinct paediatric patient groups

Excess early postnatal weight gain and blood pressure in healthy young children

Are inhaled corticosteroids safe and effective in infants with asthma-like symptoms?

Functional Restoration of CFTR Nonsense Mutations in Intestinal Organoids

Using Component-Resolved Diagnostics in the Management of Peanut-Allergic Patients

Spirometry in young children: should computer-animation programs be used during testing?

Measurements of interrupter resistance: reference values for children 3-13 yrs of age

Forskolin induced swelling (FIS) assay in intestinal organoids to guide eligibility for compassionate use treatment in a CF patient with a rare genotype

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