H. Olesen

发表

Low socioeconomic status is associated with worse lung function in the Danish cystic fibrosis population

P. Diggle, M. Whitehead, D. Taylor-Robinson, 2014, European Respiratory Journal.

Incidence of SARS-CoV-2 in people with cystic fibrosis in Europe between February and June 2020

M. Mei-Zahav, P. Yiallouros, P. Burgel, 2021, Journal of Cystic Fibrosis.

Future trends in cystic fibrosis demography in 34 European countries

P. Burgel, F. Blasi, J. Elborn, 2015, European Respiratory Journal.

Report of the European Respiratory Society/European Cystic Fibrosis Society task force on the care of adults with cystic fibrosis

T. Welte, P. Burgel, C. Castellani, 2015, European Respiratory Journal.

Atopic dermatitis and birth factors: historical follow up by record linkage

A. Olesen, K. thestrup-pedersen, S. Juul, 1997, BMJ.

Comparative demographics of the European cystic fibrosis population: a cross-sectional database analysis

M. Macek, L. Viviani, J. McCormick, 2010, The Lancet.

Marked increase in incidence of Achromobacter xylosoxidans infections caused by sporadic acquisition from the environment.

K. E. Bendstrup, S. Jensen-Fangel, N. nørskov-lauritsen, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Unusual Distribution of Burkholderia cepacia Complex Species in Danish Cystic Fibrosis Clinics May Stem from Restricted Transmission between Patients

N. Høiby, N. nørskov-lauritsen, H. Johansen, 2010, Journal of Clinical Microbiology.

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

K. De Boeck, H. Cuppens, L. Viviani, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS Patient Registry

E. Kerem, P. Dřevínek, V. Gulmans, 2013, European Respiratory Journal.

Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis-data from the European cystic fibrosis society patient registry.

M. Mei-Zahav, M. Macek, P. Dřevínek, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Serum-surfactant SP-D correlates inversely to lung function in cystic fibrosis.

U. Holmskov, G. Sorensen, H. Olesen, 2010, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Being affiliated to a cystic fibrosis centre is important for parents' everyday life

H. Olesen, C. S. Jensen, P. B. Nielsen, 2022, Acta paediatrica.

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

T. Pressler, M. Gilljam, H. Olesen, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Disease severity of people with cystic fibrosis carrying residual function mutations: Data from the ECFS Patient Registry.

E. Kerem, A. Jung, A. Orenti, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Late diagnosis and poor nutrition in cystic fibrosis diagnosed before implementation of newborn screening

M. Skov, T. Pressler, H. Olesen, 2019, Acta paediatrica.

Reference percentiles for FEV1 and BMI in European children and adults with cystic fibrosis

M. Mei-Zahav, J. Vibert, P. Böelle, 2012, Orphanet Journal of Rare Diseases.

Validation of nasal tracheal aspiration in children with lung disease

S. Rubak, A. H. Spannow, H. Olesen, 2022, BMC Pulmonary Medicine.

Good effect of IgY against Pseudomonas aeruginosa infections in cystic fibrosis patients

A. Larsson, H. Kollberg, P. Wejåker, 2008, Pediatric pulmonology.

Differences in prevalence and treatment of Pseudomonas aeruginosa in cystic fibrosis centres in Denmark, Norway and Sweden.

N. Høiby, A. Lindblad, M. Johannesson, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Contemporary N2 and SF6 multiple breath washout in infants and toddlers with cystic fibrosis

M. Skov, S. Rubak, P. Gustafsson, 2022, Pediatric pulmonology.

Atopic dermatitis and birth factors: historical follow up by record linkage

A. Olesen, K. thestrup-pedersen, S. Juul, 1997, BMJ.

Gender differences in the Scandinavian cystic fibrosis population

A. Lindblad, M. Johannesson, P. K. Knudsen, 2010, Pediatric pulmonology.

Viral and atypical bacterial infections in the outpatient pediatric cystic fibrosis clinic

L. Nielsen, H. Olesen, P. O. Schiøtz, 2006, Pediatric pulmonology.

Intravenous antibiotics given for 2 weeks do not eradicate persistent Staphylococcus aureus clones in cystic fibrosis patients.

S. Jensen-Fangel, N. nørskov-lauritsen, C. Andersen, 2014, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome

U. Koppelhus, L. Tranebjærg, M. Sommerlund, 2011, Clinical and experimental dermatology.

Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methods.

M. Granström, N. Høiby, A. Lindblad, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Low occurrence of 'non-haemolytic Haemophilus haemolyticus' misidentified as Haemophilus influenzae in cystic fibrosis respiratory specimens, and frequent recurrence of persistent H. influenzae clones despite antimicrobial treatment.

H. Olesen, W. Ridderberg, M. Fenger, 2012, International journal of medical microbiology : IJMM.

Patients with cystic fibrosis and advanced lung disease benefit from lumacaftor/ivacaftor treatment

M. Skov, S. Jensen-Fangel, I. Mathiesen, 2020, Pediatric pulmonology.

Cystic fibrosis related diabetes in Europe: Prevalence, risk factors and outcome; Olesen et al.

M. Mei-Zahav, P. Dřevínek, V. Gulmans, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years

D. Hougaard, M. Baekvad-Hansen, M. Duno, 2020, Pediatric pulmonology.

Oral administration of specific yolk antibodies (IgY) may prevent Pseudomonas aeruginosa infections in patients with cystic fibrosis: A phase I feasibility study

D. Carlander, A. Larsson, H. Kollberg, 2003, Pediatric pulmonology.

Factors for severe outcomes following SARS-CoV-2 infection in people with cystic fibrosis in Europe

M. Mei-Zahav, P. Yiallouros, P. Dřevínek, 2021, ERJ Open Research.

Evaluation of Home Monitoring for Patients with Cystic Fibrosis: A Feasibility Study

M. Jeppesen, H. Olesen, Haugen Ss, 2020 .

Change in exercise capacity measured by Cardio-pulmonary Exercise Testing (CPET) in Danish people with cystic fibrosis after initiation of treatment with Lumacaftor/Ivacaftor and Tezacaftor/Ivacaftor.

H. Olesen, C. Leo-Hansen, J. H. Jensen, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The European Cystic Fibrosis Society Patient Registry: valuable lessons learned on how to sustain a disease registry

Anil Mehta, Laura Viviani, Hanne Vebert Olesen, 2014, Orphanet Journal of Rare Diseases.

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

S. Jensen-Fangel, H. T. Maindal, M. Jeppesen, 2017 .

Exercise and quality of life in patients with cystic fibrosis: A 12-week intervention study

T. Ingemann-Hansen, M. Thastum, H. Olesen, 2011, Physiotherapy theory and practice.

Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study

Peter Diggle, Margaret Whitehead, David Taylor-Robinson, 2012, Thorax.

Author's response: understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study

P. Diggle, M. Whitehead, D. Taylor-Robinson, 2012, Thorax.

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

M. Skov, S. Jensen-Fangel, N. Høiby, 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Comparing the harmful effects of nontuberculous mycobacteria and Gram negative bacteria on lung function in patients with cystic fibrosis☆

Peter J. Diggle, Elisabeth Waldmann, Rosalind L. Smyth, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Clinical profile of children experiencing in-hospital clinical deterioration requiring transfer to a higher level of care

H. Kirkegaard, H. Aagaard, H. Olesen, 2018, Journal of child health care : for professionals working with children in the hospital and community.

A multicentre, randomised intervention study of the Paediatric Early Warning Score: study protocol for a randomised controlled trial

H. Kirkegaard, H. Aagaard, H. Olesen, 2017, Trials.

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

S. Jensen-Fangel, Mikala Wang, H. Olesen, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The mannan-binding lectin pathway and lung disease in cystic fibrosis--disfunction of mannan-binding lectin-associated serine protease 2 (MASP-2) may be a major modifier.

S. Thiel, R. Steffensen, J. Jensenius, 2006, Clinical immunology.

Characteristics of cystic fibrosis‐related diabetes: Data from two different sources the European cystic fibrosis society patient registry and German/Austrian diabetes prospective follow‐up registry

R. Holl, T. Frischer, A. Jung, 2019, Pediatric diabetes.

Low socioeconomic status and lung function

P. Diggle, D. Taylor-Robinson, K. Thielen, 2015, European Respiratory Journal.

University of Dundee The European Cystic Fibrosis Society Patient Registry

L. Viviani, A. Mehta, A. Zolin, 2014 .

Gastrointestinal transit times and motility in patients with cystic fibrosis

T. Gregersen, K. Krogh, H. Olesen, 2012, Scandinavian journal of gastroenterology.

Pediatric Early Warning Score Systems, Nurses Perspective – A Focus Group Study

H. Kirkegaard, H. Aagaard, H. Olesen, 2018, Journal of pediatric nursing.

Inter-rater reliability of two paediatric early warning score tools

H. Kirkegaard, H. Aagaard, H. Olesen, 2017, European journal of emergency medicine : official journal of the European Society for Emergency Medicine.

Comparison of Two Pediatric Early Warning Systems: A Randomized Trial

H. Kirkegaard, H. Aagaard, M. L. Svendsen, 2019, Journal of pediatric nursing.

Nationwide lung function monitoring from infancy in newborn-screened children with cystic fibrosis

M. Skov, S. Rubak, K. Nielsen, 2023, ERJ Open Research.

Consensus on patient cases for hospitalised children with a high paediatric track and trigger tool score that raises no mounting concern: a Delphi process study

H. Kirkegaard, M. Lisby, H. Olesen, 2022, BMJ Paediatrics Open.