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Prediction of Mortality in Adolescents with Cystic Fibrosis

Medicine and science in sports and exercise, 2014-11, Vol.46 (11), p.2047-2052

2014

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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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A Possible Alternative Exercise Test for Youths with Cystic Fibrosis: The Steep Ramp Test

Medicine and science in sports and exercise, 2015-03, Vol.47 (3), p.485-492

2015

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Early‐life antibiotic exposure increases the risk of developing allergic symptoms later in life: A meta‐analysis

Allergy (Copenhagen), 2018-05, Vol.73 (5), p.971-986

2018

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Lung clearance index: Evidence for use in clinical trials in cystic fibrosis

Journal of cystic fibrosis, 2014-03, Vol.13 (2), p.123-138

2014

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16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients

Microbiology spectrum, 2023-06, Vol.11 (3), p.e0405722-e0405722

2023

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Is static hyperinflation a limiting factor during exercise in adolescents with cystic fibrosis?

Pediatric pulmonology, 2011-02, Vol.46 (2), p.119-124

2011

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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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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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Gene expression in CD4+ T-cells reflects heterogeneity in infant wheezing phenotypes

The European respiratory journal, 2008-11, Vol.32 (5), p.1203-1212

2008

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Open label study of inhaled aztreonam for Pseudomonas eradication in children with cystic fibrosis: The ALPINE study

Journal of cystic fibrosis, 2015-01, Vol.14 (1), p.111-119

2015

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Comparing 6 and 10 sec exhalation time in exhaled nitric oxide measurements in children

Pediatric pulmonology, 2009-04, Vol.44 (4), p.340-344

2009

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Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?

Journal of cystic fibrosis, 2016-01, Vol.15 (1), p.10-20

2016

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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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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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Serum retinol levels and pulmonary function in children and adolescents with cystic fibrosis

Journal of cystic fibrosis, 2015-05, Vol.14 (3), p.392-397

2015

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Assessment of CFTR function in homozygous R117H-7T subjects

Journal of cystic fibrosis, 2011-09, Vol.10 (5), p.326-332

2011

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What Drives Prescribing of Asthma Medication to Children? A Multilevel Population-Based Study

Annals of family medicine, 2009, Vol.7 (1), p.32-40

2009

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Bordetella species in children with cystic fibrosis: what do we know? The role in acute exacerbations and chronic course

Journal of cystic fibrosis, 2011-09, Vol.10 (5), p.307-312

2011

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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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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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Applicability of interrupter resistance measurements using the MicroRint ® in daily practice

Respiratory medicine, 2003-04, Vol.97 (4), p.366-374

2003

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Age- and height-based prediction bias in spirometry reference equations

The European respiratory journal, 2012-07, Vol.40 (1), p.190-197

2012

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Lethal encephalopathy complicating childhood shigellosis

European journal of pediatrics, 1999-07, Vol.158 (7), p.550-552

1999

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Children with mild asthma: do they benefit from inhaled corticosteroids?

The European respiratory journal, 2002-12, Vol.20 (6), p.1470-1475

2002

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Prediction of Mortality in Adolescents with Cystic Fibrosis

Chronic infection and inflammation affect exercise capacity in cystic fibrosis

A Possible Alternative Exercise Test for Youths with Cystic Fibrosis: The Steep Ramp Test

Early‐life antibiotic exposure increases the risk of developing allergic symptoms later in life: A meta‐analysis

Lung clearance index: Evidence for use in clinical trials in cystic fibrosis

16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients

Is static hyperinflation a limiting factor during exercise in adolescents with cystic fibrosis?

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

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

Gene expression in CD4+ T-cells reflects heterogeneity in infant wheezing phenotypes

Open label study of inhaled aztreonam for Pseudomonas eradication in children with cystic fibrosis: The ALPINE study

Comparing 6 and 10 sec exhalation time in exhaled nitric oxide measurements in children

Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?

Survey of clinical infant lung function testing practices

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

Serum retinol levels and pulmonary function in children and adolescents with cystic fibrosis

Assessment of CFTR function in homozygous R117H-7T subjects

What Drives Prescribing of Asthma Medication to Children? A Multilevel Population-Based Study

Bordetella species in children with cystic fibrosis: what do we know? The role in acute exacerbations and chronic course

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

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

Applicability of interrupter resistance measurements using the MicroRint ® in daily practice

Age- and height-based prediction bias in spirometry reference equations

Lethal encephalopathy complicating childhood shigellosis

Children with mild asthma: do they benefit from inhaled corticosteroids?

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