Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Dimitrios Kalafatis"'
Autor:
Jing Gao, Dimitrios Kalafatis, Lisa Carlson, Ida H. A. Pesonen, Chuan-Xing Li, Åsa Wheelock, Jesper M. Magnusson, C. Magnus Sköld
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-13 (2021)
Abstract Background Observational data under real-life conditions in idiopathic pulmonary fibrosis (IPF) is scarce. We explored anti-fibrotic treatment, disease severity and phenotypes in patients with IPF from the Swedish IPF Registry (SIPFR). Metho
Externí odkaz:
https://doaj.org/article/69f748c5acc24d39ab251984584f4766
Publikováno v:
BMC Pulmonary Medicine, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a disease with poor prognosis mainly affecting males. Differences in clinical presentation between genders may be important both for the diagnostic work-up and for follow-up. In the present s
Externí odkaz:
https://doaj.org/article/ca3c7af037f64bfc9f978d567cccc835
Autor:
C. Magnus Sköld, Jesper Magnusson, Jing Gao, Åsa M. Wheelock, Lisa Carlson, Dimitrios Kalafatis, Chuanxing Li, Ida Pesonen
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-13 (2021)
Respiratory Research
Respiratory Research
Background Observational data under real-life conditions in idiopathic pulmonary fibrosis (IPF) is scarce. We explored anti-fibrotic treatment, disease severity and phenotypes in patients with IPF from the Swedish IPF Registry (SIPFR). Methods Patien
Autor:
Dimitrios Kalafatis, Anna Löfdahl, Per Näsman, Göran Dellgren, Åsa M. Wheelock, Linda Elowsson Rendin, Magnus Sköld, Gunilla Westergren-Thorsson
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 13421, p 13421 (2021)
International Journal of Molecular Sciences; Volume 22; Issue 24; Pages: 13421
International Journal of Molecular Sciences, Vol 22, Iss 13421, p 13421 (2021)
International Journal of Molecular Sciences; Volume 22; Issue 24; Pages: 13421
Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with an unmet need of biomarkers that can aid in the diagnostic and prognostic assessment of the disease and response to treatment. In this two-part explorative proteomic stud
Autor:
Michael T. Durheim, Tone Sjåheim, Charlotte Hyldgaard, Elisabeth Bendstrup, Marjukka Myllärniemi, Dimitrios Kalafatis, Lisa Carlson, Eva Sutinen, C. Magnus Sköld
Publikováno v:
Durheim, M T, Bendstrup, E, Carlson, L, Sutinen, E M, Hyldgaard, C, Kalafatis, D, Myllärniemi, M, Sköld, C M & Sjåheim, T 2021, ' Outcomes of patients with advanced idiopathic pulmonary fibrosis treated with nintedanib or pirfenidone in a real-world multicentre cohort ', Respirology, vol. 26, no. 10, pp. 982-988 . https://doi.org/10.1111/resp.14116
Background and objective: Antifibrotic therapy with nintedanib or pirfenidone slows disease progression and reduces mortality in patients with idiopathic pulmonary fibrosis (IPF). However, patients with advanced IPF, as defined by forced vital capaci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe986efb391d30ca7852dd64120de55
https://pure.au.dk/portal/da/publications/outcomes-of-patients-with-advanced-idiopathic-pulmonary-fibrosis-treated-with-nintedanib-or-pirfenidone-in-a-realworld-multicentre-cohort(06f0874b-070a-4c34-99cf-bfd164a23607).html
https://pure.au.dk/portal/da/publications/outcomes-of-patients-with-advanced-idiopathic-pulmonary-fibrosis-treated-with-nintedanib-or-pirfenidone-in-a-realworld-multicentre-cohort(06f0874b-070a-4c34-99cf-bfd164a23607).html
Autor:
Magnus Sköld, Ida Pesonen, Lisa Carlson, Hiroki Tanahashi, Dimitrios Kalafatis, Kakuhiro Yamaguchi, Noboru Hattori, Jing Gao, Hiroshi Iwamoto, Yasushi Horimasu
Publikováno v:
Idiopathic interstitial pneumonias.
Publikováno v:
Idiopathic interstitial pneumonias.
Publikováno v:
Idiopathic interstitial pneumonias.
Background: Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal fibrosing lung disease of unknown aetiology. The Swedish IPF-registry (SIPFR) was established in 2014. Aim: To explore patient characteristics, the effect of anti-fibrotic tre
Publikováno v:
Idiopathic interstitial pneumonias.
Background: Presence of autoantibodies is a hallmark of connective tissue diseases (CTD). Exclusion of CTD is required for diagnosis of idiopathic pulmonary fibrosis (IPF). We studied the prevalence of autoantibodies in IPF-patients in Sweden. Method
Publikováno v:
Idiopathic interstitial pneumonias.
Background: Six-minute walk test (6MWT) is commonly performed in patients with idiopathic pulmonary fibrosis (IPF). We investigated whether a change in 6MWT during 1 year are associated with a worse outcome. Aim: To assess the 1-year change in 6-minu