Zobrazeno 1 - 10
of 21
pro vyhledávání: '"I. E. Lundberg"'
Publikováno v:
Annals of the Rheumatic Diseases. 81:711.2-711
BackgroundLimited therapies are available for patients with idiopathic inflammatory myopathy (IIM), a heterogenous group of chronic, systemic, autoimmune inflammatory diseases characterized by progressive muscle weakness and/or distinct skin rashes.1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eec4ebb5863e18eeb843bfc79043f8f
https://doi.org/10.1136/annrheumdis-2022-eular.7
https://doi.org/10.1136/annrheumdis-2022-eular.7
Autor:
D. Demirdal, E. Van Gompel, E. Wigren, M. Dastmalchi, B. Horuluoglu, A. S. Galindo-Feria, S. Gräslund, K. Chemin, I. E. Lundberg, A. Notarnicola
Publikováno v:
Annals of the Rheumatic Diseases. 81:751.2-752
BackgroundThe association between anti-melanoma differentiation association protein 5 autoantibodies (aMDA5) and rapidly progressive interstitial lung disease (RP-ILD) in clinically amyopathic dermatomyositis is well established in Asian population c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32707683ab4365712e15dc3eb0b65329
https://doi.org/10.1136/annrheumdis-2022-eular.3789
https://doi.org/10.1136/annrheumdis-2022-eular.3789
Autor:
C. Preger, A. Notarnicola, C. Hellström, E. Wigren, I. E. Lundberg, P. J. Jakobsson, H. Persson, S. Gräslund
Publikováno v:
Annals of the Rheumatic Diseases. 81:242.2-243
BackgroundAnti-synthetase syndrome (ASSD), a sub-group of idiopathic inflammatory myopathies (IIM) is characterized by the presence of autoantibodies targeting aminoacyl tRNA synthetases (aaRS) and specific clinical manifestations such as myositis an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6a65ff64dabe06d3f834d4fcce2097b
https://doi.org/10.1136/annrheumdis-2022-eular.1980
https://doi.org/10.1136/annrheumdis-2022-eular.1980
Autor:
V. Leclair, A. S. Galindo-Feria, S. Rothwell, O. Kryštůfková, H. Mann, L. Pyndt Diederichsen, H. Andersson, M. Klein, S. Tansley, N. Mchugh, J. Lamb, J. Vencovský, H. Chinoy, M. Holmqvist, L. Padyukov, I. E. Lundberg, L. M. Diaz-Gallo
Publikováno v:
Annals of the Rheumatic Diseases. 81:104.1-105
BackgroundThere is a gap between how IIM patients are classified in practice and current validated classification criteria1. Also, different associations with genetic variations in HLA can inform about different T-cell mechanisms involved in disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a728b4e64fee764fa14ae7fe59543350
https://doi.org/10.1136/annrheumdis-2022-eular.1695
https://doi.org/10.1136/annrheumdis-2022-eular.1695
Autor:
F W, Miller, W, Chen, T P, O'Hanlon, R G, Cooper, J, Vencovsky, L G, Rider, K, Danko, L R, Wedderburn, I E, Lundberg, L M, Pachman, A M, Reed, S R, Ytterberg, L, Padyukov, A, Selva-O'Callaghan, T R, Radstake, D A, Isenberg, H, Chinoy, W E R, Ollier, P, Scheet, B, Peng, A, Lee, J, Byun, J A, Lamb, P K, Gregersen, C I, Amos, Hemlata, Varsani
Publikováno v:
Genes & Immunity. 16:470-480
Autoimmune muscle diseases (myositis) comprise a group of complex phenotypes influenced by genetic and environmental factors. To identify genetic risk factors in patients of European ancestry, we conducted a genome-wide association study (GWAS) of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0bcd9c6902e2b96ed557a87be46c59d
https://doi.org/10.1038/gene.2015.28
https://doi.org/10.1038/gene.2015.28
Autor:
G. Xu, L.-P. Li, F. Liu, D. Pei, S. Wang, D. Pang, L. Borukhson, A. Nandagudi, A. Jawad, R. C. Campbell, D. L. Scott, P. Kiely, P. A. Gordon, G. Rafferty, C. Reilly, K. Ward, P. J. Charles, E. Paterson, L. Ekholm, I. Putova, K. Danko, I. Lundberg, J. Vencovsky, H. Chinoy, I. E. Lundberg, M. Vincze, M. Lund Hetland, R. G. Cooper, M. Ohtamaa, N. Steen Krogh
Publikováno v:
Rheumatology. 50:iii67-iii69
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dfb3469e881b3882f9a12393809dde7
https://doi.org/10.1093/rheumatology/ker041
https://doi.org/10.1093/rheumatology/ker041
Akademický článek
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Publikováno v:
Journal of internal medicine. 271(6)
To investigate whether Caucasian patients with polymyositis (PM) or dermatomyositis (DM) and interstitial lung disease (ILD) have elevated serum levels of KL-6 compared with patients without ILD and whether KL-6 could be used as a marker for ILD acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a41524b0e72518630d0506e4f5ea8440
https://pubmed.ncbi.nlm.nih.gov/21950266
https://pubmed.ncbi.nlm.nih.gov/21950266
Autor:
I, Loell, I E, Lundberg
Publikováno v:
Journal of internal medicine. 269(3)
Idiopathic inflammatory myopathies (IIMs), collectively termed myositis, include three major subgroups: polymyositis, dermatomyositis and inclusion body myositis. IIMs are characterized clinically by muscle weakness and reduced muscle endurance prefe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e1ef0e32ba404854a3996584a767cc19
https://pubmed.ncbi.nlm.nih.gov/21205023
https://pubmed.ncbi.nlm.nih.gov/21205023
Autor:
I, Loell, S B, Helmers, M, Dastmalchi, H, Alexanderson, L A, Munters, I, Nennesmo, E, Lindroos, K, Borg, I E, Lundberg, M, Esbjörnsson
Publikováno v:
Clinical physiology and functional imaging. 31(1)
Polymyositis and dermatomyositis are idiopathic, inflammatory myopathies characterized by proximal muscle fatigue. Conventional immunosuppressive treatment gives a variable response. Biopsies from chronic patients display a low proportion type I and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85342a6cb234baaf35e5adc1792009f9
https://pubmed.ncbi.nlm.nih.gov/21029327
https://pubmed.ncbi.nlm.nih.gov/21029327