Zobrazeno 1 - 10
of 542
pro vyhledávání: '"O, Førre"'
Publikováno v:
Arthritis & Rheumatism. 54:3573-3582
Objective To compare the clinical, functional, and radiographic outcomes in patients with enthesitis-related arthritis (ERA) with those in patients with other subtypes of juvenile idiopathic arthritis (JIA) and healthy controls, and to determine gene
This book incorporates the latest advances in immunopharmacological treatment. One objective has been to provide appropriate bridges between the basic sciences of immunology and pharmacology on the one hand and clinical medicine on the other. A furth
Publikováno v:
The Journal of Immunology. 150:5466-5475
This article describes the characterization of a mouse monoclonal anti-idiotypic antibody (1H7B) prepared against a human monoclonal rheumatoid factor (RFSJ2) whose L chain utilized a V lambda I subgroup gene. The mAb 1H7B reacted with 6 of the teste
Autor:
I Randen, D Brown, K M Thompson, N Hughes-Jones, V Pascual, K Victor, J D Capra, O Førre, J B Natvig
Publikováno v:
The Journal of Immunology. 148:3296-3301
Using hybridoma technology we established a panel of human monoclonal rheumatoid factors (RF) from the synovial tissues of two patients with rheumatoid arthritis (RA), and one patient with polyarticular juvenile RA. Nucleotide sequence analysis of th
Autor:
Erik Thorsby, Marte K. Viken, Siri Tennebø Flåm, Marita Olsson, O Førre, Benedicte A. Lie, Tore K Kvien
Publikováno v:
Tissue antigens. 70(3)
The protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene has, during the last 2 years, been recognized as a susceptibility gene for numerous autoimmune diseases, including rheumatoid arthritis (RA) and type 1 diabetes. An association between the
Autor:
Ewald Lindner, Anne Marit Selvaag, Gry B. N. Nordang, Berit Flatø, O Førre, Tore K Kvien, E. Melum, Erik Thorsby, Benedicte A. Lie
Publikováno v:
BMC Medical Genetics, Vol 8, Iss 1, p 33 (2007)
BMC Medical Genetics
BMC Medical Genetics
Background The chemokine receptor CCR5 has been detected at elevated levels on synovial T cells, and a 32 bp deletion in the CCR5 gene leads to a non-functional receptor. A negative association between the CCR5Δ32 and rheumatoid arthritis (RA) has b
Autor:
Anne Marit Selvaag, Erik Thorsby, Kjersti S. Rønningen, Tore K Kvien, Berit Flatø, Knut Dahl-Jørgensen, Dag E. Undlien, Geir Joner, Hege Dahlen Sollid, Arthur Melms, Benedicte A. Lie, Eva Tolosa, Marte K. Viken, O Førre
Publikováno v:
Human immunology. 68(9)
Type 1 diabetes (T1D) is an autoimmune disease characterized by loss of beta cells in the pancreas. The CTSL2 gene encodes the cysteine protease cathepsin V involved in antigen presentation in human cortical thymic epithelial cells, and involvement o
Publikováno v:
Clinical and experimental rheumatology. 23(2)
To investigate the frequency of organ damage in childhood-onset systemic lupus erythematosus (SLE) and to identify disease variables and patient characteristics related to organ damage.A cohort of 71 patients was examined in a cross-sectional study a
Autor:
J. Pazdur, E Kubasiewicz, A Venalis, E Kaminska, A Smerdel, Rafał Płoski, P Sliwinska, K Valiukiene, O Førre, Vaidutis Kučinskas, I Butrimiene, E. Jastrzebska, J Jaworski, A Kozakiewicz
Publikováno v:
Annals of the rheumatic diseases. 64(1)
A recognised feature of rheumatoid arthritis (RA) is its clinical heterogeneity, which may be caused by HLA factors. This theory is supported by observations that relatively severe and mild RA are associated with, respectively, DRB1*041 and DRB1*01.2
Publikováno v:
Speaker abstracts 2001.
Background Centre for Rheumatic Diseases is a National Centre for children with JIA and Connective Idiopathic Arthritis. In 1999 we established a registry to increase the knowledge about JIA and Connective Idiopathic Arthritis in addition to insure d