Search Results - "Olesen, H V"
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A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome
Published in Clinical and experimental dermatology (01-03-2011)“…Summary Background. Keratitis–ichthyosis–deafness (KID) syndrome is a rare congenital ectodermal disorder, caused by heterozygous missense mutation in GJB2,…”
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The relative frequency of CFTR mutation classes in European patients with cystic fibrosis
Published in Journal of cystic fibrosis (01-07-2014)“…Abstract More than 1900 different mutations in the CFTR gene have been reported. These are grouped into classes according to their effect on the synthesis…”
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The mannan-binding lectin pathway and lung disease in cystic fibrosis—dysfunction of mannan-binding lectin-associated serine protease 2 (MASP-2) may be a major modifier
Published in Clinical Immunology (01-12-2006)“…The lectin pathway of complement activation is initiated by mannan-binding lectin (MBL) or the ficolins through the common MBL-associated serine protease-2…”
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Co-morbidity of cystic fibrosis and celiac disease in Scandinavian cystic fibrosis patients
Published in Journal of cystic fibrosis (2009)“…Abstract Background The co-morbidity of cystic fibrosis (CF) and celiac disease (CD) has been reported sporadically since the 1960s. To our knowledge, this is…”
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Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis
Published in Journal of cystic fibrosis (01-12-2013)“…Abstract Objectives In this nationwide retrospective study, we analysed species distribution, antimicrobial susceptibility and time to next occurrence of…”
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Intravenous antibiotics given for 2 weeks do not eradicate persistent Staphylococcus aureus clones in cystic fibrosis patients
Published in Clinical microbiology and infection (01-05-2014)“…Staphylococcus aureus is the most commonly isolated pathogen in respiratory tract secretions from young patients with cystic fibrosis (CF), and several…”
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P1-56 Understanding the natural progression in FEV1 decline in patients with lung disease
Published in Journal of epidemiology and community health (1979) (01-08-2011)“…IntroductionWe outline a novel approach for longitudinal modelling of lung function with long-term follow-up in which within-patient variation over time is…”
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Childhood hypersensitivity pneumonitis probably caused by cat hair
Published in Acta Paediatrica (01-07-1998)“…A case is reported of a 10‐y‐old boy with hypersensitivity pneumonitis probably caused by his cat. Hypersensitivity pneumonitis caused by animal hairs is…”
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Survival estimates in European cystic fibrosis patients and the impact of socioeconomic factors: a retrospective registry Cohort study
Published in The European respiratory journal (01-09-2021)“…Median survival for cystic fibrosis (CF) patients in Europe is unknown and is likely to be influenced by socioeconomic factors. Using the European Cystic…”
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Differences in prevalence and treatment of Pseudomonas aeruginosa in cystic fibrosis centres in Denmark, Norway and Sweden
Published in Journal of cystic fibrosis (01-03-2009)“…Abstract Background Chronic Pseudomonas aeruginosa (PA) infection causes increased morbidity and mortality in cystic fibrosis (CF). This study aimed to answer…”
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Journal Article Conference Proceeding -
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Contemporary N-2 and SF6 multiple breath washout in infants and toddlers with cystic fibrosis
Published in Pediatric pulmonology (25-01-2022)“…Introduction Multiple breath washout (MBW) is used for early detection of cystic fibrosis (CF) lung disease, with SF6MBW commonly viewed as the reference…”
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Future trends in cystic fibrosis demography in 34 European countries
Published in The European respiratory journal (01-07-2015)“…Median survival has increased in people with cystic fibrosis (CF) during the past six decades, which has led to an increased number of adults with CF. The…”
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Nationwide lung function monitoring from infancy in newborn-screened children with cystic fibrosis
Published in ERJ open research (01-09-2023)“…BackgroundCystic fibrosis (CF) lung disease starts in infancy and can be assessed for structural lung abnormalities using computed tomography or magnetic…”
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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
Published in Clinical immunology (Orlando, Fla.) (01-12-2006)“…The lectin pathway of complement activation is initiated by mannan-binding lectin (MBL) or the ficolins through the common MBL-associated serine protease-2…”
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Journal Article -
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Good effect of IgY against Pseudomonas aeruginosa infections in cystic fibrosis patients
Published in Pediatric pulmonology (01-09-2008)“…This is an extended open study of oral prophylactic treatment with egg yolk antibodies against Pseudomonas aeruginosa, Anti‐Pseudomonas IgY, of 17 Swedish…”
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Gender differences in the Scandinavian cystic fibrosis population
Published in Pediatric pulmonology (01-10-2010)“…Aims To explore whether gender differences in the Scandinavian Cystic Fibrosis (CF) patients exist in the areas of key clinical parameters, complications, and…”
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Journal Article -
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Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methods
Published in Journal of cystic fibrosis (01-01-2009)“…Abstract The aim of the study was to evaluate three serological methods for their ability to identify CF patients in different infection status especially…”
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Journal Article -
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Childhood hypersensitivity pneumonitis probably caused by cat hair
Published in Acta Pædiatrica (01-07-1998)Get full text
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