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Reference ranges for interrupter resistance technique: the Asthma UK Initiative

The European respiratory journal, 2010-07, Vol.36 (1), p.157-163

2010

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Allergen-specific Th2 responses in young children precede sensitization later in life

Allergy (Copenhagen), 2014-03, Vol.69 (3), p.406-410

2014

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Allergen‐specific Th2 responses in young children precede sensitization later in life

Allergy (Copenhagen), 2014-03, Vol.69 (3), p.406-410

2014

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WS07.5 Gut microbiome in healthy children and children with cystic fibrosis during the first 18 months of life

Journal of cystic fibrosis, 2016-06, Vol.15, p.S12-S12

2016

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334 What is it like to be an adolescent with cystic fibrosis? Reversing the roles of patient and health-professional

Journal of cystic fibrosis, 2013-06, Vol.12, p.S134-S134

2013

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P049 Effects of elexacaftor/tezacaftor/ivacaftor after 6 months in Dutch people with cystic fibrosis with at least 1 F508del mutation

Journal of cystic fibrosis, 2023-06, Vol.22, p.S78-S78

2023

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P173 Comparison of respiratory resistance measured with Forced Oscillation Technique and body plethysmography

Journal of cystic fibrosis, 2020-06, Vol.19, p.S105-S105

2020

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Supra-maximal verification of peak oxygen uptake in adolescents with cystic fibrosis

Journal of cystic fibrosis, 2010, Vol.9, p.S68-S68

2010

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Estimating peak oxygen uptake in adolescents with cystic fibrosis

Archives of disease in childhood, 2014-01, Vol.99 (1), p.21-25

2014

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Recombinant factor VIIa in severe uremic bleeding

Thrombosis and haemostasis, 1998-08, Vol.80 (2), p.353-353

1998

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Physical activity assessment in cystic fibrosis: A position statement

Journal of cystic fibrosis, 2015-11, Vol.14 (6), p.e25-e32

2015

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P209 Correlation between structural changes of the lungs and airways on CT scan and recovery of pulmonary function after start of CFTR modulators in cystic fibrosis patients

Journal of cystic fibrosis, 2020-06, Vol.19, p.S115-S115

2020

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P216 Sweat chloride response to lumacaftor/ivacaftor treatment in cystic fibrosis: weight correlates with magnitude of response

Journal of cystic fibrosis, 2020-06, Vol.19, p.S117-S117

2020

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Validity of the oxygen uptake efficiency slope in children with cystic fibrosis and mild-to-moderate airflow obstruction

Pediatric exercise science, 2012-02, Vol.24 (1), p.129-141

2012

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936 URINARY INCONTINENCE IN GIRLS AND FEMALE ADOLESCENTS WITH CYSTIC FIBROSIS

European urology supplements : official journal of the European Association of Urology, 2007, Vol.6 (2), p.256-256

2007

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Chest radiograph scores in preterm infants: Interobserver agreement and relation to respiratory function

Biology of the neonate, 2004-01, Vol.86 (2), p.85-91

2004

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Consensus statement for inert gas washout measurement using multiple- and single-breath tests

The European respiratory journal, 2013-03, Vol.41 (3), p.507-522

2013

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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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Pharmacogenomics in Pediatric Patients: Towards Personalized Medicine

Paediatric drugs, 2016-08, Vol.18 (4), p.251-260

2016

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Respiratory function after esophageal replacement in children

Journal of pediatric surgery, 2017-11, Vol.52 (11), p.1736-1741

2017

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Clinical effect of lumacaftor/ivacaftor in F508del homozygous CF patients with FEV1 ≥ 90% predicted at baseline

Journal of cystic fibrosis, 2020-07, Vol.19 (4), p.654-658

2020

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Survey of clinical infant lung function testing practices

Pediatric pulmonology, 2014-02, Vol.49 (2), p.126-131

2014

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Effect of long-term voluntary exercise wheel running on susceptibility to bacterial pulmonary infections in a mouse model

PloS one, 2013-12, Vol.8 (12), p.e82869-e82869

2013

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Females with cystic fibrosis have a larger decrease in sweat chloride in response to lumacaftor/ivacaftor compared to males

Journal of cystic fibrosis, 2021-01, Vol.20 (1), p.e7-e11

2021

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Chronic inflammation and infection associate with a lower exercise training response in cystic fibrosis adolescents

Respiratory medicine, 2014-03, Vol.108 (3), p.445-452

2014

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Reference ranges for interrupter resistance technique: the Asthma UK Initiative

Allergen-specific Th2 responses in young children precede sensitization later in life

Allergen‐specific Th2 responses in young children precede sensitization later in life

WS07.5 Gut microbiome in healthy children and children with cystic fibrosis during the first 18 months of life

334 What is it like to be an adolescent with cystic fibrosis? Reversing the roles of patient and health-professional

P049 Effects of elexacaftor/tezacaftor/ivacaftor after 6 months in Dutch people with cystic fibrosis with at least 1 F508del mutation

P173 Comparison of respiratory resistance measured with Forced Oscillation Technique and body plethysmography

Supra-maximal verification of peak oxygen uptake in adolescents with cystic fibrosis

Estimating peak oxygen uptake in adolescents with cystic fibrosis

Recombinant factor VIIa in severe uremic bleeding

Physical activity assessment in cystic fibrosis: A position statement

P209 Correlation between structural changes of the lungs and airways on CT scan and recovery of pulmonary function after start of CFTR modulators in cystic fibrosis patients

P216 Sweat chloride response to lumacaftor/ivacaftor treatment in cystic fibrosis: weight correlates with magnitude of response

Validity of the oxygen uptake efficiency slope in children with cystic fibrosis and mild-to-moderate airflow obstruction

936 URINARY INCONTINENCE IN GIRLS AND FEMALE ADOLESCENTS WITH CYSTIC FIBROSIS

Chest radiograph scores in preterm infants: Interobserver agreement and relation to respiratory function

Consensus statement for inert gas washout measurement using multiple- and single-breath tests

Chronic infection and inflammation affect exercise capacity in cystic fibrosis

Pharmacogenomics in Pediatric Patients: Towards Personalized Medicine

Respiratory function after esophageal replacement in children

Clinical effect of lumacaftor/ivacaftor in F508del homozygous CF patients with FEV1 ≥ 90% predicted at baseline

Survey of clinical infant lung function testing practices

Effect of long-term voluntary exercise wheel running on susceptibility to bacterial pulmonary infections in a mouse model

Females with cystic fibrosis have a larger decrease in sweat chloride in response to lumacaftor/ivacaftor compared to males

Chronic inflammation and infection associate with a lower exercise training response in cystic fibrosis adolescents

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