Search Results - "Olesen, H V"

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  1. 1

    A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome by Koppelhus, U., Tranebjærg, L., Esberg, G., Ramsing, M., Lodahl, M., Rendtorff, N. D., Olesen, H. V., Sommerlund, M.

    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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    Journal Article
  2. 2

    The relative frequency of CFTR mutation classes in European patients with cystic fibrosis by De Boeck, K, Zolin, A, Cuppens, H, Olesen, H.V, Viviani, L

    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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    Journal Article
  3. 3

    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 by Olesen, H.V., Jensenius, J.C., Steffensen, R., Thiel, S., Schiøtz, P.O.

    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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    Journal Article
  4. 4

    Co-morbidity of cystic fibrosis and celiac disease in Scandinavian cystic fibrosis patients by Fluge, G, Olesen, H.V, Gilljam, M, Meyer, P, Pressler, T, Storrösten, O.T, Karpati, F, Hjelte, L

    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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    Journal Article
  5. 5

    Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis by Wang, M, Ridderberg, W, Hansen, C.R, Høiby, N, Jensen-Fangel, S, Olesen, H.V, Skov, M, Lemming, L.E, Pressler, T, Johansen, H.K, Nørskov-Lauritsen, N

    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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    Journal Article
  6. 6

    Intravenous antibiotics given for 2 weeks do not eradicate persistent Staphylococcus aureus clones in cystic fibrosis patients by Andersen, C., Kahl, B.C., Olesen, H.V., Jensen-Fangel, S., Nørskov-Lauritsen, N.

    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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    Journal Article
  7. 7

    P1-56 Understanding the natural progression in FEV1 decline in patients with lung disease by Taylor-Robinson, D, Whitehead, M, Olesen, H V, Pressler, T, Diderichsen, F, Smyth, R, Diggle, P

    “…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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    Journal Article
  8. 8

    Childhood hypersensitivity pneumonitis probably caused by cat hair by Olesen, HV, Thelle, T, Møller, JCF

    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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    Journal Article
  9. 9

    Survival estimates in European cystic fibrosis patients and the impact of socioeconomic factors: a retrospective registry Cohort study by McKone, Edward F, Ariti, Cono, Jackson, Abaigeal, Zolin, Anna, Carr, Siobhán B, Orenti, Annalisa, van Rens, Jacqui, Lemonnier, Lydie, Macek, Jr, Milan, Keogh, Ruth H, Naehrlich, Lutz

    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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    Journal Article
  10. 10

    Differences in prevalence and treatment of Pseudomonas aeruginosa in cystic fibrosis centres in Denmark, Norway and Sweden by Knudsen, Per Kristian, Olesen, Hanne V, Høiby, Niels, Johannesson, Marie, Karpati, Ferenc, Laerum, Birger N, Meyer, Peter, Pressler, Tacjana, Lindblad, Anders

    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
  11. 11

    Contemporary N-2 and SF6 multiple breath washout in infants and toddlers with cystic fibrosis by Sandvik, R. M., Gustafsson, Per M., Lindblad, Anders, Buchvald, F., Olesen, H. V., Olsen, J. H., Skov, M., Schmidt, M. N., Thellefsen, M. R., Robinson, P. D., Rubak, S., Pressler, T., Nielsen, K. G.

    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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    Journal Article
  12. 12

    Future trends in cystic fibrosis demography in 34 European countries by Burgel, Pierre-Régis, Bellis, Gil, Olesen, Hanne V, Viviani, Laura, Zolin, Anna, Blasi, Francesco, Elborn, J Stuart

    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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    Journal Article
  13. 13

    Nationwide lung function monitoring from infancy in newborn-screened children with cystic fibrosis by Sandvik, Rikke M., Schmidt, Marika N., Voldby, Christian M., Buchvald, Frederik F., Olesen, Hanne V., Olsen, Jørgen, Kragh, Maja V., Rubak, Sune L.M., Pressler, Tacjana, Robinson, Paul D., Gustafsson, Per M., Skov, Marianne, Nielsen, Kim G.

    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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    Journal Article
  14. 14
  15. 15

    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 by Olesen, H V, Jensenius, J C, Steffensen, R, Thiel, S, Schiøtz, P O

    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…”
    Get full text
    Journal Article
  16. 16

    Good effect of IgY against Pseudomonas aeruginosa infections in cystic fibrosis patients by Nilsson, Elin, Larsson, Anders, Olesen, Hanne V., Wejåker, Per-Erik, Kollberg, Hans

    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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    Journal Article
  17. 17

    Gender differences in the Scandinavian cystic fibrosis population by Olesen, Hanne Vebert, Pressler, Tacjana, Hjelte, Lena, Mared, Lena, Lindblad, Anders, Knudsen, Per Kristian, Lærum, Birger N., Johannesson, Marie

    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
  18. 18

    Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methods by Pressler, Tacjana, Karpati, Ferenc, Granström, Marta, Knudsen, Per Kristian, Anders, Lindblad, Lena, Hjelte, Olesen, Hanne V, Meyer, Peter, Høiby, Niels

    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
  19. 19