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The relative frequency of CFTR mutation classes in European patients with cystic fibrosis

Journal of cystic fibrosis, 2014-07, Vol.13 (4), p.403-409

2014

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331 The nutritional status in cystic fibrosis patients with PEG tube and the long-term effects on BMI and pulmonary functions

Journal of cystic fibrosis, 2017-06, Vol.16, p.S147-S147

2017

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P363 Socio-economic choices in the cystic fibrosis family with a child with cystic fibrosis in primary school

Journal of cystic fibrosis, 2023-06, Vol.22, p.S175-S175

2023

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WS12.6 How does transferral from CF doctors to endocrinologists affect blood glucose control in patients with CFRD

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

2016

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166 Characterization of airway microbiota in 63 children with early-stage cystic fibrosis using deep sequencing – a Danish cohort study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S109-S109

2017

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Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis

Journal of cystic fibrosis, 2013-12, Vol.12 (6), p.638-643

2013

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P002: Growth, lung microbiology and structure after implementation of newborn screening in Danish cystic fibrosis patients

Journal of cystic fibrosis, 2022-06, Vol.21, p.S61

2022

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129 Colistin resistance in Achromobacter sp. and Pseudomonas aeruginosa isolated from Danish cystic fibrosis patients is not related to plasmid-mediated expression of mcr-1

Journal of cystic fibrosis, 2017-06, Vol.16, p.S98-S98

2017

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346 Evaluation of home monitoring for patients with cystic fibrosis a feasibility study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S151-S152

2017

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EPS6.9 Validation of lung monitor for home monitoring of patients with cystic fibrosis. A feasibility study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S52-S52

2017

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WS9.1 Can lung function predict exercise capacity in patients with CF?

Journal of cystic fibrosis, 2014-06, Vol.13, p.S19-S19

2014

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414 Demographic and clinical aspects of cystic fibrosis-related diabetes (CFRD) – a registry comparison between the European CF Society Patient Registry (ECFSPR) and the German/Austrian/Luxembourg diabetes patient follow-up registry DPV

Journal of cystic fibrosis, 2017-06, Vol.16, p.S168-S168

2017

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WS09-1 Breastfeeding and growth in infants with cystic fibrosis diagnosed through newborn screening

Journal of cystic fibrosis, 2019-06, Vol.18, p.S16-S16

2019

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WS17.5 Patients with cystic fibrosis and the R117H mutation: The European experience

Journal of cystic fibrosis, 2015-06, Vol.14, p.S32-S32

2015

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WS11.5 The consequences of no newborn cystic fibrosis screening in a well-developed country

Journal of cystic fibrosis, 2015-06, Vol.14, p.S23-S23

2015

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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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54 Limited transmission of non-tuberculous mycobacteria among Danish cystic fibrosis patients

Journal of cystic fibrosis, 2015-06, Vol.14, p.S71-S71

2015

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P374 Effect of CFTR-modulators on cystic fibrosis related school absenteeism in children attending primary school

Journal of cystic fibrosis, 2024-06, Vol.23, p.S182-S183

2024

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298 Vitamin deficiency in children with cystic fibrosis

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

2011

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WS10.6 How does airway infection with chronic Gram-negative and nontuberculous mycobacteria affect lung function? A longitudinal study

Journal of cystic fibrosis, 2015-06, Vol.14, p.S21-S21

2015

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ePS06.6 Full reversibility of lung function decline following clearance of Mycobacterium abscessus complex infection

Journal of cystic fibrosis, 2015-06, Vol.14, p.S54-S54

2015

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P368 Parents’ experiences when their child is diagnosed with cystic fibrosis in the newborn screening program

Journal of cystic fibrosis, 2020-06, Vol.19, p.S159-S159

2020

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Increased incidence of Achromobacter xylosoxidans infections in a Danish CF centre is not caused by cross infections

Journal of cystic fibrosis, 2010, Vol.9, p.S34-S34

2010

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92 Early treatment with inhaled antibiotics postpones recurrence of Achromobacter species in cystic fibrosis

Journal of cystic fibrosis, 2013-06, Vol.12, p.S72-S72

2013

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63 Time to recurrence and antimicrobial susceptibility of first-time detected Achromobacter xylosoxidans in respiratory tract specimens from patients with cystic fibrosis

Journal of cystic fibrosis, 2012-06, Vol.11, p.S72-S72

2012

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The relative frequency of CFTR mutation classes in European patients with cystic fibrosis

331 The nutritional status in cystic fibrosis patients with PEG tube and the long-term effects on BMI and pulmonary functions

P363 Socio-economic choices in the cystic fibrosis family with a child with cystic fibrosis in primary school

WS12.6 How does transferral from CF doctors to endocrinologists affect blood glucose control in patients with CFRD

166 Characterization of airway microbiota in 63 children with early-stage cystic fibrosis using deep sequencing – a Danish cohort study

Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis

P002: Growth, lung microbiology and structure after implementation of newborn screening in Danish cystic fibrosis patients

129 Colistin resistance in Achromobacter sp. and Pseudomonas aeruginosa isolated from Danish cystic fibrosis patients is not related to plasmid-mediated expression of mcr-1

346 Evaluation of home monitoring for patients with cystic fibrosis a feasibility study

EPS6.9 Validation of lung monitor for home monitoring of patients with cystic fibrosis. A feasibility study

WS9.1 Can lung function predict exercise capacity in patients with CF?

414 Demographic and clinical aspects of cystic fibrosis-related diabetes (CFRD) – a registry comparison between the European CF Society Patient Registry (ECFSPR) and the German/Austrian/Luxembourg diabetes patient follow-up registry DPV

WS09-1 Breastfeeding and growth in infants with cystic fibrosis diagnosed through newborn screening

WS17.5 Patients with cystic fibrosis and the R117H mutation: The European experience

WS11.5 The consequences of no newborn cystic fibrosis screening in a well-developed country

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

54 Limited transmission of non-tuberculous mycobacteria among Danish cystic fibrosis patients

P374 Effect of CFTR-modulators on cystic fibrosis related school absenteeism in children attending primary school

298 Vitamin deficiency in children with cystic fibrosis

WS10.6 How does airway infection with chronic Gram-negative and nontuberculous mycobacteria affect lung function? A longitudinal study

ePS06.6 Full reversibility of lung function decline following clearance of Mycobacterium abscessus complex infection

P368 Parents’ experiences when their child is diagnosed with cystic fibrosis in the newborn screening program

Increased incidence of Achromobacter xylosoxidans infections in a Danish CF centre is not caused by cross infections

92 Early treatment with inhaled antibiotics postpones recurrence of Achromobacter species in cystic fibrosis

63 Time to recurrence and antimicrobial susceptibility of first-time detected Achromobacter xylosoxidans in respiratory tract specimens from patients with cystic fibrosis

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