UB Paderborn / Katalog / Suche / in CDI

Pseudomonas aeruginosa: resistance and therapeutic options at the turn of the new millennium

Clinical microbiology and infection, 2007-06, Vol.13 (6), p.560-578

2007

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Influence of lung transplantation on the essential fatty acid profile in cystic fibrosis

Prostaglandins, leukotrienes and essential fatty acids, 2020-07, Vol.158, p.102060-102060, Article 102060

2020

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Gastro-oesophageal reflux and aspiration of gastric contents in adult patients with cystic fibrosis

Gut, 2008-08, Vol.57 (8), p.1049-1055

2008

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What can the CF registry tell us about rare CFTR-mutations? A Belgian study

Orphanet journal of rare diseases, 2017-08, Vol.12 (1), p.142-142, Article 142

2017

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The clinical benefits of long-term supplementation with omega-3 fatty acids in cystic fibrosis patients – A pilot study

Prostaglandins, leukotrienes and essential fatty acids, 2016-05, Vol.108, p.45-50

2016

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Inhaled dry powder mannitol in children with cystic fibrosis: A randomised efficacy and safety trial

Journal of cystic fibrosis, 2017-05, Vol.16 (3), p.380-387

2017

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Emergence of livestock-associated MRSA isolated from cystic fibrosis patients: Result of a Belgian national survey

Journal of cystic fibrosis, 2019-01, Vol.18 (1), p.86-93

2019

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Pseudomonas aeruginosa in the home environment of newly infected cystic fibrosis patients

The European respiratory journal, 2008-04, Vol.31 (4), p.822-829

2008

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The relationship between gastroesophageal reflux and cough in children with chronic unexplained cough using combined impedance-pH-manometry recordings

Pediatric pulmonology, 2011-03, Vol.46 (3), p.286-294

2011

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Characteristics of Gastroesophageal Reflux and Potential Risk of Gastric Content Aspiration in Children With Cystic Fibrosis

Journal of pediatric gastroenterology and nutrition, 2010-02, Vol.50 (2), p.161-166

2010

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Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptoms

The European respiratory journal, 2012-02, Vol.39 (2), p.392-395

2012

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ePS04.3 CF patients' pain experience with different sampling methods for bacterial culture

Journal of cystic fibrosis, 2016-06, Vol.15, p.S44-S44

2016

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A semi-blinded study comparing 2 methods of measuring nasal potential difference: Subcutaneous needle versus dermal abrasion

Journal of cystic fibrosis, 2016-01, Vol.15 (1), p.60-66

2016

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Early referral to cystic fibrosis specialist centre impacts on respiratory outcome

Journal of cystic fibrosis, 2009-01, Vol.8 (1), p.26-30

2009

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WS23.2 Characterizing Belgian CF-registry (BCFR)-patients with a rare CFTR-mutation (RM): towards better identification of the role of RM in disease liability

Journal of cystic fibrosis, 2016-06, Vol.15, p.S35-S35

2016

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342 Handgrip force in CF children and adolescents: impact of nutritional and pulmonary status

Journal of cystic fibrosis, 2017-06, Vol.16, p.S150-S150

2017

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Immunogenicity and safety of a measles–mumps–rubella–varicella vaccine following a 4-week or a 12-month interval between two doses

Vaccine, 2011-05, Vol.29 (22), p.3842-3849

2011

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ePS06.5 Burkholderia cepacia complex acquisition: A threat in all CF patients?

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

2015

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67 CF patients with a declining FEV1 : At risk for acquisition of Burkholderia cepacia complex infection?

Journal of cystic fibrosis, 2015-06, Vol.14, p.S74-S74

2015

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304 Children with typical CF have better spirometric data than children with non CF bronchiectasis (BE) – a Belgian multicentric study

Journal of cystic fibrosis, 2015-06, Vol.14, p.S136-S136

2015

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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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WS9.3 Bronchial hyperreactivity related to 4 commonly used inhalation drugs in cystic fibrosis

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

2013

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Efficacy and safety of lumacaftor and ivacaftor in patients aged 6–11 years with cystic fibrosis homozygous for F508del-CFTR : a randomised, placebo-controlled phase 3 trial

The lancet respiratory medicine, 2017-07, Vol.5 (7), p.557-567

2017

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Genome sequence analysis of a Belgian epidemic cystic fibrosis Pseudomonas aeruginosa isolate

International journal of infectious diseases, 2014-04, Vol.21 (S1), p.351-351

2014

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Siblings of children with cystic fibrosis: quality of life and the impact of illness

Child : care, health & development, 2011-03, Vol.37 (2), p.252-260

2011

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Pseudomonas aeruginosa: resistance and therapeutic options at the turn of the new millennium

Influence of lung transplantation on the essential fatty acid profile in cystic fibrosis

Gastro-oesophageal reflux and aspiration of gastric contents in adult patients with cystic fibrosis

What can the CF registry tell us about rare CFTR-mutations? A Belgian study

The clinical benefits of long-term supplementation with omega-3 fatty acids in cystic fibrosis patients – A pilot study

Inhaled dry powder mannitol in children with cystic fibrosis: A randomised efficacy and safety trial

Emergence of livestock-associated MRSA isolated from cystic fibrosis patients: Result of a Belgian national survey

Pseudomonas aeruginosa in the home environment of newly infected cystic fibrosis patients

The relationship between gastroesophageal reflux and cough in children with chronic unexplained cough using combined impedance-pH-manometry recordings

Characteristics of Gastroesophageal Reflux and Potential Risk of Gastric Content Aspiration in Children With Cystic Fibrosis

Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptoms

ePS04.3 CF patients' pain experience with different sampling methods for bacterial culture

A semi-blinded study comparing 2 methods of measuring nasal potential difference: Subcutaneous needle versus dermal abrasion

Early referral to cystic fibrosis specialist centre impacts on respiratory outcome

WS23.2 Characterizing Belgian CF-registry (BCFR)-patients with a rare CFTR-mutation (RM): towards better identification of the role of RM in disease liability

342 Handgrip force in CF children and adolescents: impact of nutritional and pulmonary status

Immunogenicity and safety of a measles–mumps–rubella–varicella vaccine following a 4-week or a 12-month interval between two doses

ePS06.5 Burkholderia cepacia complex acquisition: A threat in all CF patients?

67 CF patients with a declining FEV1 : At risk for acquisition of Burkholderia cepacia complex infection?

304 Children with typical CF have better spirometric data than children with non CF bronchiectasis (BE) – a Belgian multicentric study

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

WS9.3 Bronchial hyperreactivity related to 4 commonly used inhalation drugs in cystic fibrosis

Efficacy and safety of lumacaftor and ivacaftor in patients aged 6–11 years with cystic fibrosis homozygous for F508del-CFTR : a randomised, placebo-controlled phase 3 trial

Genome sequence analysis of a Belgian epidemic cystic fibrosis Pseudomonas aeruginosa isolate

Siblings of children with cystic fibrosis: quality of life and the impact of illness

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