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Clinical impact of vitamin D treatment in cystic fibrosis: a pilot randomized, controlled trial

European journal of clinical nutrition, 2017-02, Vol.71 (2), p.203-205

2017

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Vitamin D treatment modulates immune activation in cystic fibrosis

Clinical and experimental immunology, 2017-09, Vol.189 (3), p.359-371

2017

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Pulmonary exacerbation: Towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials

Journal of cystic fibrosis, 2011-06, Vol.10, p.S79-S81

2011

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Chronic Pseudomonas aeruginosa infection definition: EuroCareCF Working Group report

Journal of cystic fibrosis, 2011-06, Vol.10, p.S75-S78

2011

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Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations

Journal of cystic fibrosis, 2011-05, Vol.10 (3), p.187-192

2011

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WS9.4 Non invasive ventilation as airway clearance technique compared to PEP in adult patients with cystic fibrosis

Journal of cystic fibrosis, 2013-06, Vol.12, p.S18-S18

2013

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393 Anxiety and depression can predict the development in lung function in adults with cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S162-S162

2017

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Inverse relation between vitamin D and serum total immunoglobulin G in the Scandinavian Cystic Fibrosis Nutritional Study

European journal of clinical nutrition, 2011-01, Vol.65 (1), p.102-109

2011

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264 Natural history of patients with cystic fibrosis carrying nonsense mutations: an analysis of placebo-treated patients from the 009 study

Journal of cystic fibrosis, 2016-06, Vol.15, p.S118-S119

2016

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84 Unexpectedly severe infection susceptibility in a CF patient defective in MAIT cells

Journal of cystic fibrosis, 2017-06, Vol.16, p.S86-S86

2017

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Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

Thorax, 2009-08, Vol.64 (8), p.683-691

2009

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Vitamin D deficiency as a risk factor for cystic fibrosis-related diabetes in the Scandinavian Cystic Fibrosis Nutritional Study

Diabetologia, 2011-12, Vol.54 (12), p.3007-3015

2011

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WS02.2 Gastrostomy tubes in patients with cystic fibrosis in Sweden

Journal of cystic fibrosis, 2016-06, Vol.15, p.S3-S3

2016

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WS15.4 Cystic fibrosis bronchial epithelial cells have impaired ability to activate vitamin D

Journal of cystic fibrosis, 2014-06, Vol.13, p.S32-S32

2014

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187 The need for bronchodilators before airway clearance therapy sessions in CF

Journal of cystic fibrosis, 2012-06, Vol.11, p.S104-S104

2012

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232 Gastrointestinal cancer survey at the Stockholm CF Center

Journal of cystic fibrosis, 2012-06, Vol.11, p.S116-S116

2012

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WS13.1.1 Ataluren in nonsense mutation cystic fibrosis patients not receiving tobramycin: significant lung function benefits in the paediatric age range

Journal of cystic fibrosis, 2016-06, Vol.15, p.S21-S21

2016

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317 Depression, anxiety and quality of life in adolescents with cystic fibrosis

Journal of cystic fibrosis, 2013-06, Vol.12, p.S130-S130

2013

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WS16.3 Vitamin D supplementation in patients with cystic fibrosis: A pilot randomized controlled trial

Journal of cystic fibrosis, 2013-06, Vol.12, p.S32-S32

2013

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234 Physical activity level in thirteen children with CF, at Stockholm CF-center

Journal of cystic fibrosis, 2013-06, Vol.12, p.S108-S108

2013

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Predictors of deterioration of lung function in cystic fibrosis

Pediatric pulmonology, 2002-06, Vol.33 (6), p.483-491

2002

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WS13.1 Ataluren significantly reduces exacerbations in nonsense mutation cystic fibrosis patients not receiving tobramycin

Journal of cystic fibrosis, 2016-06, Vol.15, p.S20-S21

2016

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Co-morbidity of cystic fibrosis and celiac disease in Scandinavian cystic fibrosis patients

Journal of cystic fibrosis, 2009-05, Vol.8 (3), p.198-202

2009

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Vitamin D status in Stockholm cystic fibrosis patients in 2007–2009

Journal of cystic fibrosis, 2010, Vol.9, p.S91-S91

2010

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Clinical impact of vitamin D treatment in cystic fibrosis: a pilot randomized, controlled trial

Vitamin D treatment modulates immune activation in cystic fibrosis

Pulmonary exacerbation: Towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials

Chronic Pseudomonas aeruginosa infection definition: EuroCareCF Working Group report

Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations

WS9.4 Non invasive ventilation as airway clearance technique compared to PEP in adult patients with cystic fibrosis

393 Anxiety and depression can predict the development in lung function in adults with cystic fibrosis

Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease

Inverse relation between vitamin D and serum total immunoglobulin G in the Scandinavian Cystic Fibrosis Nutritional Study

264 Natural history of patients with cystic fibrosis carrying nonsense mutations: an analysis of placebo-treated patients from the 009 study

84 Unexpectedly severe infection susceptibility in a CF patient defective in MAIT cells

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

Vitamin D deficiency as a risk factor for cystic fibrosis-related diabetes in the Scandinavian Cystic Fibrosis Nutritional Study

WS02.2 Gastrostomy tubes in patients with cystic fibrosis in Sweden

WS15.4 Cystic fibrosis bronchial epithelial cells have impaired ability to activate vitamin D

187 The need for bronchodilators before airway clearance therapy sessions in CF

232 Gastrointestinal cancer survey at the Stockholm CF Center

WS13.1.1 Ataluren in nonsense mutation cystic fibrosis patients not receiving tobramycin: significant lung function benefits in the paediatric age range

317 Depression, anxiety and quality of life in adolescents with cystic fibrosis

WS16.3 Vitamin D supplementation in patients with cystic fibrosis: A pilot randomized controlled trial

234 Physical activity level in thirteen children with CF, at Stockholm CF-center

Predictors of deterioration of lung function in cystic fibrosis

WS13.1 Ataluren significantly reduces exacerbations in nonsense mutation cystic fibrosis patients not receiving tobramycin

Co-morbidity of cystic fibrosis and celiac disease in Scandinavian cystic fibrosis patients

Vitamin D status in Stockholm cystic fibrosis patients in 2007–2009

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