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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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Biological variability of the sweat chloride in diagnostic sweat tests: A retrospective analysis

Journal of cystic fibrosis, 2017-01, Vol.16 (1), p.30-35

2017

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Lung clearance index in cystic fibrosis

Revue des maladies respiratoires, 2019-03, Vol.36 (3), p.377

2019

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Hesperidin inhibits ovariectomized-induced osteopenia and shows differential effects on bone mass and strength in young and adult intact rats

Journal of applied physiology (1985), 2008-03, Vol.104 (3), p.648-654

2008

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Inhaled phosphodiesterase type 5 inhibitors restore chloride transport in cystic fibrosis mice

The European respiratory journal, 2011, Vol.37 (1), p.72-78

2011

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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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ABPA in adulthood: a CFTR-related disorder

Thorax, 2011-06, Vol.66 (6), p.540-541

2011

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Modulation of soy isoflavones bioavailability and subsequent effects on bone health in ovariectomized rats : the case for equol

Osteoporosis international, 2007-05, Vol.18 (5), p.671-679

2007

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ePS01.6 Biological variability of the sweat chloride in diagnostic sweat tests: a retrospective analysis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S38-S38

2016

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326 DRESS syndrome should be included in the differential diagnosis of life-threatening systemic symptoms in patients with cystic fibrosis

Journal of cystic fibrosis, 2015-06, Vol.14, p.S142-S142

2015

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313 Serum 25-hydroxyvitamin D does not correlate with pancreatic status, FEV1, BMI, IgG nor prescribed doses of oral supplementation in patients with cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S142-S142

2017

Volltextzugriff (PDF)

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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Olive oil and its main phenolic micronutrient (oleuropein) prevent inflammation-induced bone loss in the ovariectomised rat

British journal of nutrition, 2004-07, Vol.92 (1), p.119-127

2004

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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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WS21.4 Multiple breath nitrogen washout: The Exhalyzer D (Ecomedics) is more sensitive than the EasyOne Pro (NDD) in detecting ventilation inhomogeneities in children with CF and normal FEV1

Journal of cystic fibrosis, 2015-06, Vol.14, p.S39-S39

2015

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132 Improving the feasibility of multiple-breath nitrogen washout in cystic fibrosis adults

Journal of cystic fibrosis, 2014-06, Vol.13, p.S80-S80

2014

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128 Multiple breath nitrogen washout in adults with cystic fibrosis: a comparison of two commercially available devices

Journal of cystic fibrosis, 2014-06, Vol.13, p.S79-S79

2014

Volltextzugriff (PDF)

131 Multiple breath nitrogen washout in healthy children and adults: a comparison of two commercially available devices

Journal of cystic fibrosis, 2014-06, Vol.13, p.S80-S80

2014

Volltextzugriff (PDF)

107 RGM medium versus MGIT™ for isolation of nontuberculous mycobacteria from sputum of patients with cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S92-S92

2017

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Prevention of bone loss by phloridzin, an apple polyphenol, in ovariectomized rats under inflammation conditions

Calcified tissue international, 2005-11, Vol.77 (5), p.311-318

2005

Volltextzugriff (PDF)

Cystic fibrosis prognosis in Europa : chronicle of an announced dilemma

Revue médicale de Liège, 2021-03, Vol.76 (3), p.202

2021

Volltextzugriff (PDF)

19 Performing the Stanford beta-sweat test using non-invasive drug delivery

Journal of cystic fibrosis, 2016-06, Vol.15, p.S56-S56

2016

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

WS15.3 Failure rate of sweat testing in different Belgium CF centers in the light of preparing CF-newborn screening (NBS)

Journal of cystic fibrosis, 2017-06, Vol.16, p.S27-S27

2017

Volltextzugriff (PDF)

L’indice de clairance pulmonaire dans la mucoviscidose

Revue des maladies respiratoires, 2019-03, Vol.36 (3), p.377-395

2019

Volltextzugriff (PDF)

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

Biological variability of the sweat chloride in diagnostic sweat tests: A retrospective analysis

Lung clearance index in cystic fibrosis

Hesperidin inhibits ovariectomized-induced osteopenia and shows differential effects on bone mass and strength in young and adult intact rats

Inhaled phosphodiesterase type 5 inhibitors restore chloride transport in cystic fibrosis mice

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

ABPA in adulthood: a CFTR-related disorder

Modulation of soy isoflavones bioavailability and subsequent effects on bone health in ovariectomized rats : the case for equol

ePS01.6 Biological variability of the sweat chloride in diagnostic sweat tests: a retrospective analysis

326 DRESS syndrome should be included in the differential diagnosis of life-threatening systemic symptoms in patients with cystic fibrosis

313 Serum 25-hydroxyvitamin D does not correlate with pancreatic status, FEV1, BMI, IgG nor prescribed doses of oral supplementation in patients with cystic fibrosis

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

Olive oil and its main phenolic micronutrient (oleuropein) prevent inflammation-induced bone loss in the ovariectomised rat

Early referral to cystic fibrosis specialist centre impacts on respiratory outcome

WS21.4 Multiple breath nitrogen washout: The Exhalyzer D (Ecomedics) is more sensitive than the EasyOne Pro (NDD) in detecting ventilation inhomogeneities in children with CF and normal FEV1

132 Improving the feasibility of multiple-breath nitrogen washout in cystic fibrosis adults

128 Multiple breath nitrogen washout in adults with cystic fibrosis: a comparison of two commercially available devices

131 Multiple breath nitrogen washout in healthy children and adults: a comparison of two commercially available devices

107 RGM medium versus MGIT™ for isolation of nontuberculous mycobacteria from sputum of patients with cystic fibrosis

Prevention of bone loss by phloridzin, an apple polyphenol, in ovariectomized rats under inflammation conditions

Cystic fibrosis prognosis in Europa : chronicle of an announced dilemma

19 Performing the Stanford beta-sweat test using non-invasive drug delivery

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

WS15.3 Failure rate of sweat testing in different Belgium CF centers in the light of preparing CF-newborn screening (NBS)

L’indice de clairance pulmonaire dans la mucoviscidose

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