Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kasper Aanaes"'
Autor:
Carlos Emílio Levy, Niels Høiby, Anton Barucha, Renan Marrichi Mauch, Jochen G. Mainz, Kasper Aanaes, Julia Hentschel, Marcos Tadeu Nolasco da Silva
Publikováno v:
Pediatric Pulmonology. 55:959-967
Background The upper airways (UAW) are a niche and a reservoir of Pseudomonas aeruginosa strains that cause chronic infection of the lower airways (LAW) in cystic fibrosis (CF). Here, we assessed the role of anti-P. aeruginosa immunoglobulin A (IgA)
Autor:
Kim G. Nielsen, Niels Høiby, Kasper Aanaes, Elisabeth Arndal, Tania Pressler, Christian von Buchwald
Most patients with cystic fibrosis have the risk of pathogenic bacteria being exchanged between their sinuses and lungs. A method for topical application of antibiotics where the antibiotics persist for a long period of time is needed. Ten patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db75117cf909f50375a4bdb4de9303f1
Publikováno v:
Rasmussen, E R, Aanæs, K, Jakobsen, M A & Bygum, A 2019, ' Acquired complement C1 esterase inhibitor deficiency in a patient with a rare SERPING1 variant with unknown significance ', BMJ Case Reports, vol. 12, no. 9, e231122 . https://doi.org/10.1136/bcr-2019-231122
Angioedema (AE) is caused by a wide range of diseases and pharmaceuticals; it can become life-threatening when located to the airways. Patients with deficiency or malfunction of complement C1 esterase inhibitor (hereditary or acquired) experience rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::780251b80f2a2d7aa5b4fba93b5ab70e
https://findresearcher.sdu.dk:8443/ws/files/155303331/Acquired_complement_C1esterase_inhibitor_deficiency_in_a_patient_with_a_rare_SERPING1_variant_with_unknown_significance.pdf
https://findresearcher.sdu.dk:8443/ws/files/155303331/Acquired_complement_C1esterase_inhibitor_deficiency_in_a_patient_with_a_rare_SERPING1_variant_with_unknown_significance.pdf
Autor:
Helle Krogh Johansen, Tine Yding Wolff, Trine Rolighed Thomsen, Kasper Aanaes, Vibeke Børsholt Rudkjøbing, Christian von Buchwald
Publikováno v:
Rudkjøbing, V B, Aanaes, K, Wolff, T Y, von Buchwald, C, Johansen, H K & Thomsen, T R 2014, ' An exploratory study of microbial diversity in sinus infections of cystic fibrosis patients by molecular methods ', Journal of Cystic Fibrosis, vol. 13, no. 6, pp. 645-652 . https://doi.org/10.1016/j.jcf.2014.02.008
Background: For the first time microorganisms in CF sinuses are investigated by molecular methods in response to an absence of anaerobes in CF sinus samples during a two-year period at the Copenhagen CF center. Methods: Endoscopic sinus surgery was p
Autor:
Helle Krogh Johansen, Christian von Buchwald, Kasper Aanaes, Marianne Nielsine Skov, Mikkel Christian Alanin, Thomas Hjuler
Publikováno v:
American Journal of Rhinology & Allergy. 27:e1-e4
Background Most patients with cystic fibrosis (CF) have chronic rhinosinusitis; their sinuses are often colonized with bacteria that can initiate and maintain deleterious pulmonary infections. Theoretically, eradication of the sinus bacteria should r
Autor:
Jacob Fisker, Tania Pressler, Helle Krogh Johansen, Kasper Aanaes, Christian von Buchwald, Marianne Nielsine Skov, Niels Høiby, Kim Gjerrum Nielsen
Publikováno v:
Journal of Cystic Fibrosis. 11:525-531
Background We studied whether the sinuses might be foci for Pseudomonas aeruginosa lung infection. Methods Endoscopic Sinus Surgery was performed in 78 CF patients; PFGE was used for bacterial genotyping. Material from sinuses and lungs were Gram-sta
Autor:
Lei Yang, Helle Krogh Johansen, Oana Ciofu, Søren Molin, Susse Kirkelund Hansen, Niels Høiby, Christian von Buchwald, Hanne Østergaard Jarmer, Martin Holm Rau, Kasper Aanaes, Lars Jelsbak, Anders Folkesson
Publikováno v:
The ISME Journal. 6:31-45
The opportunistic pathogen Pseudomonas aeruginosa is a frequent colonizer of the airways of patients suffering from cystic fibrosis (CF). Depending on early treatment regimens, the colonization will, with high probability, develop into chronic infect
Autor:
Peter Østrup Jensen, Niels Høiby, Kasper Aanaes, Lars Fledelius Rickelt, Tacjana Pressler, Helle Krogh Johansen, Christian von Buchwald
Publikováno v:
Journal of Cystic Fibrosis. 10:114-120
Background Pseudomonas aeruginosa in the sinuses plays a role in the lungs in cystic fibrosis (CF) patients, but little is known about the sinus environment where the bacteria adapt. Anoxic areas are found in the lower respiratory airways but it is u
Autor:
C. von Buchwald, Kim G. Nielsen, Helle Krogh Johansen, Mikkel Christian Alanin, Marianne Skov, Niels Høiby, Kasper Aanaes
Publikováno v:
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases. 21(12)
In patients with primary ciliary dyskinesia (PCD), impaired mucociliary clearance leads to an accumulation of secretions in the airways and susceptibility to repeated bacterial infections. The primary aim of this study was to investigate the bacteria
Autor:
Trine Markussen, Helle Krogh Johansen, Alexandra E. Burleigh, Rasmus L. Marvig, Kasper Aanaes, Lars Jelsbak, Niels Høiby, María Gómez-Lozano, Søren Molin
Publikováno v:
mBio
mBio, Vol 5, Iss 5 (2014)
mBio, Vol 5, Iss 5 (2014)
Microbial population polymorphisms are commonly observed in natural environments, including long-term infected hosts. However, the underlying processes promoting and stabilizing diversity are difficult to unravel and are not well understood. Here, we