Zobrazeno 1 - 10
of 103
pro vyhledávání: '"T. Garen"'
Autor:
T Garen, Ø Molberg, K Lerang, H Haukeland, S Reppe Moe, C Brunborg, A Botea, N Damjanic, G Wivestad, H Øvreås, T Bøe, A Orre
Publikováno v:
Lupus Science and Medicine, Vol 9, Iss Suppl 2 (2022)
Externí odkaz:
https://doaj.org/article/86d309c0c076470ca7d2b2710301d194
Autor:
H Haukeland, S Reppe Moe, C Brunborg, T Garen, A Botea, N Damjanic, G Wivestad, H Øvreås, T Bøe, A Orre, Ø Molberg, K Lerang
Publikováno v:
Thursday 06 October 2022 from 08:00 to 10:00.
Autor:
A M Hoffmann-Vold, H Fretheim, P P Diep, K Lerang, H Andersson, Ø Midtvedt, T Garen, M Durheim, T M Aaløkken, Ø Palm, Ø Molberg
Publikováno v:
12.02 - ILD/DPLD of known origin.
Akademický článek
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Autor:
J. Vikse, Ø. Midtvedt, Ø. Molberg, B. T. Svanes Fevang, Ø. Palm, T. Garen, K. B. Norheim, G. Bakland, M. Wallenius, A. M. Hoffmann-Vold
Publikováno v:
Annals of the Rheumatic Diseases. 81:1022-1023
BackgroundIgG4-related disease (IgG4-RD) is a rare, heterogenous and potentially severe disease. An open-label trial demonstrated efficacy of rituximab (RTX) in IgG4-RD [1]. Recently, four distinct phenotypes of IgG4-RD were identified [2]. There is
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
Annals of the Rheumatic Diseases. 81:1415.1-1415
BackgroundBechet’s disease (BD) is a multisystemic, inflammatory disease, characterized by variety of clinical manifestations, including mucocutaneous, ocular, vascular, neurological (CNS) and gastrointestinal (GI) involvements. The disease can be
Publikováno v:
Annals of the Rheumatic Diseases. 81:1133.1-1134
BackgroundTakayasu arteritis (TAK) is a rare vasculitis of large vessels, mainly in young women, with a point prevalence of 25.6/106 in a Norwegian population. TAK is most prevalently limited to the aortic arch and its branches (Type 1) among North E
Autor:
H. Fretheim, I. Barua, Ø. Midtvedt, T. Garen, P. P. Diep, M. Durheim, C. Brunborg, A. M. Hoffmann-Vold
Publikováno v:
Annals of the Rheumatic Diseases. 81:729.2-730
BackgroundSpirometry, in particular forced vital capacity (FVC), is a widely implemented tool in the initial diagnostic workup and monitoring of systemic sclerosis-related interstitial lung disease (SSc-ILD). In addition to ILD, several other extra-p
Autor:
A. M. Hoffmann-Vold, H. Fretheim, P. P. Diep, K. Lerang, H. Andersson, Ø. Midtvedt, T. Garen, M. Durheim, T. M. Aaløkken, Ø. Palm, Ø. Molberg
Publikováno v:
Annals of the Rheumatic Diseases. 81:249.3-249
BackgroundInterstitial lung disease (ILD) in primary Sjögren’s syndrome (pSS) has been reported to be present in 10-15% of patients, but pSS-ILD behavior over time is not well characterized.ObjectivesAssess the pattern of ILD in pSS, its disease b