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The neutrophil-recruiting chemokine GCP-2/CXCL6 is expressed in cystic fibrosis airways and retains its functional properties after binding to extracellular DNA

Mucosal immunology, 2016, Vol.9 (1), p.112-123

2016

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Guidelines for the management of pregnancy in women with cystic fibrosis

Journal of cystic fibrosis, 2008-01, Vol.7, p.S2-S32

2008

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WS21.2.2 Effects of individual tailored physiotherapy on physical capacity and lung function

Journal of cystic fibrosis, 2016-06, Vol.15, p.S33-S33

2016

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WS21.2.1 Results of long term optimized physiotherapy on quality of life and activity hours

Journal of cystic fibrosis, 2016-06, Vol.15, p.S33-S33

2016

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European respiratory society guidelines on the use of nebulizers

The European respiratory journal, 2001-07, Vol.18 (1), p.228-242

2001

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EPS8.08 Musculoskeletal pain and regional interdependence in cystic fibrosis

Journal of cystic fibrosis, 2024-06, Vol.23, p.S59-S59

2024

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Demographic transition of the Swedish cystic fibrosis community—results of modern care

Respiratory medicine, 2002-09, Vol.96 (9), p.681-685

2002

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P313 Experiences of the Nuvoair home spirometry, a pilot study

Journal of cystic fibrosis, 2020-06, Vol.19, p.S143-S143

2020

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Only a few osteoporotic adult CF patients and no vertebral fractures

Journal of cystic fibrosis, 2008-06, Vol.7, p.S72-S72

2008

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P431 Factors related to higher level of physical activity in Swedish cystic fibrosis-patients – a registry-based cross sectional study

Journal of cystic fibrosis, 2023-06, Vol.22, p.S195-S195

2023

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Patients with cystic fibrosis can preserve peak working capacity, even if lung function is substantially impaired

Journal of cystic fibrosis, 2010, Vol.9, p.S67-S67

2010

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Long-term effects from individualized and continuously optimized physiotherapy in cystic fibrosis

Physiotherapy Research and Reports, 2018, Vol.1 (3)

2018

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WS16.6 Decreased performance of airway clearance and physical exercise with age in the Swedish cystic fibrosis population - what’s the solution?

Journal of cystic fibrosis, 2020-06, Vol.19, p.S28-S28

2020

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Mucus clearance with three chest physiotherapy regimes in cystic fibrosis: a comparison between postural drainage, PEP and physical exercise

The European respiratory journal, 1992-06, Vol.5 (6), p.748-753

1992

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Physical activity assessment in cystic fibrosis: A position statement

Journal of cystic fibrosis, 2015-11, Vol.14 (6), p.e25-e32

2015

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French implementation of the ERS guidelines on the use of guidelines

Revue des maladies respiratoires, 2004-11, Vol.21 (5), p.1033

2004

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Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions

Biochemical journal, 1999-12, Vol.344 Pt 2 (2), p.321-330

1999

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Physiotherapy in infants and young children with cystic fibrosis: current practice and future developments

Journal of the Royal Society of Medicine, 2004, Vol.97 Suppl 44 (Suppl 44), p.8-25

2004

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Adaptations des recommandations de l’European Respiratory Society (ERS) sur l’aérosolthérapie par nébulisation par le Groupe Aérosolthérapie (GAT) de la Société de Pneumologie de Langue Française (SPLF)

Revue des maladies respiratoires, 2004-11, Vol.21 (5), p.1033-1038

2004

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Lung function in the aging Swedish cystic fibrosis population

Respiratory medicine, 2009, Vol.103 (7), p.1076-1082

2009

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Adaptations des recommandations de l’ European Respiratory Society (ERS) sur l’aérosolthérapie par nébulisation par le Groupe Aérosolthérapie (GAT) de la Société de Pneumologie de Langue Française (SPLF)

Revue des maladies respiratoires, 2004, Vol.21 (5), p.1033-1038

2004

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Mild cystic fibrosis mutations in Southern Sweden with special reference to S549I and T338I

Clinical genetics, 1998-05, Vol.53 (5), p.383-386

1998

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S24.5. Guidelines for inhalation, practical aspects

Netherlands journal of medicine, 1999-06, Vol.54, p.S20

LANNEFORS, L

1999

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233 Survival and physical capacity among lung transplanted CF patients in Lund

Journal of cystic fibrosis, 2006, Vol.5, p.S55-S55

2006

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European Respiratory Society Guidelines on the use of nebulizers: Guidelines prepared by a European Respiratory Society Task Force on the use of nebulizers

The European respiratory journal, 2001-07, Vol.18 (1), p.228-242

2001

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The neutrophil-recruiting chemokine GCP-2/CXCL6 is expressed in cystic fibrosis airways and retains its functional properties after binding to extracellular DNA

Guidelines for the management of pregnancy in women with cystic fibrosis

WS21.2.2 Effects of individual tailored physiotherapy on physical capacity and lung function

WS21.2.1 Results of long term optimized physiotherapy on quality of life and activity hours

European respiratory society guidelines on the use of nebulizers

EPS8.08 Musculoskeletal pain and regional interdependence in cystic fibrosis

Demographic transition of the Swedish cystic fibrosis community—results of modern care

P313 Experiences of the Nuvoair home spirometry, a pilot study

Only a few osteoporotic adult CF patients and no vertebral fractures

P431 Factors related to higher level of physical activity in Swedish cystic fibrosis-patients – a registry-based cross sectional study

Patients with cystic fibrosis can preserve peak working capacity, even if lung function is substantially impaired

Long-term effects from individualized and continuously optimized physiotherapy in cystic fibrosis

WS16.6 Decreased performance of airway clearance and physical exercise with age in the Swedish cystic fibrosis population - what’s the solution?

Mucus clearance with three chest physiotherapy regimes in cystic fibrosis: a comparison between postural drainage, PEP and physical exercise

Physical activity assessment in cystic fibrosis: A position statement

French implementation of the ERS guidelines on the use of guidelines

Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions

Physiotherapy in infants and young children with cystic fibrosis: current practice and future developments

Adaptations des recommandations de l’European Respiratory Society (ERS) sur l’aérosolthérapie par nébulisation par le Groupe Aérosolthérapie (GAT) de la Société de Pneumologie de Langue Française (SPLF)

Lung function in the aging Swedish cystic fibrosis population

Adaptations des recommandations de l’ European Respiratory Society (ERS) sur l’aérosolthérapie par nébulisation par le Groupe Aérosolthérapie (GAT) de la Société de Pneumologie de Langue Française (SPLF)

Mild cystic fibrosis mutations in Southern Sweden with special reference to S549I and T338I

S24.5. Guidelines for inhalation, practical aspects

233 Survival and physical capacity among lung transplanted CF patients in Lund

European Respiratory Society Guidelines on the use of nebulizers: Guidelines prepared by a European Respiratory Society Task Force on the use of nebulizers

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