Zobrazeno 1 - 10
of 27
pro vyhledávání: '"G R, Wallace"'
Objective Behçet’s disease (BD) is a multisystem autoinflammatory disease characterised by mucosal ulceration, ocular, neural, joint and skin inflammation. The cause of BD is not known but there is a strong genetic association with HLA-B*51, IL10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8158435907f9eabfb650b0b467d5de7d
https://doi.org/10.21203/rs.3.rs-481837/v1
https://doi.org/10.21203/rs.3.rs-481837/v1
Publikováno v:
British Journal of Ophthalmology. 87:1175-1183
Behçet’s disease (BD) is characterised by recurrent episodes of orogenital aphthae, systemic vasculitis, and systemic and retinal venous thrombosis. An association between HLA-B51 and BD was first identified over 20 years ago, but recently identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17e221b652a11dfbda8261fbdb3c20b
https://doi.org/10.1136/bjo.87.9.1175
https://doi.org/10.1136/bjo.87.9.1175
Autor:
Miles Stanford, J. E. Marr, G R Wallace, Wafa Madanat, D H Verity, Faisal Fayyad, C A Kanawati, Robert Vaughan, H Zureikat, E. Kondeatis
Publikováno v:
Tissue Antigens. 54:264-272
The role of HLA-B*51 and other major histocompatibility complex (MHC) genes in Behcet's disease (BD) remains unknown. We have performed HLA and tumour necrosis factor (TNF) polymorphism analysis in BD and evaluated their contribution to ocular diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::825ab40dfaab92326584250cd83405f2
https://doi.org/10.1034/j.1399-0039.1999.540307.x
https://doi.org/10.1034/j.1399-0039.1999.540307.x
Publikováno v:
European Journal of Clinical Investigation. 26:686-691
Increased levels of soluble intercellular adhesion molecule 1 (sICAM-1) in serum have been demonstrated in several human disease conditions. We have previously shown, in a point-prevalence study, a positive correlation between sICAM-1 levels and dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df6a6d0841aca9305bc2850e4afc12d7
https://doi.org/10.1111/j.1365-2362.1996.tb02154.x
https://doi.org/10.1111/j.1365-2362.1996.tb02154.x
Autor:
J A M van Laar, R.A.M. Quax, Marwen Ghabra, J W Koper, R van Heerebeek, S W J Lamberts, Jasper H Kappen, J M W Hazes, R A Feelders, K Greiner, G R Wallace, Farida Fortune, M Stanford, P. M. van Hagen, M Soylu, Eldad Ben-Chetrit
Publikováno v:
Endocrine Connections
ObjectiveGlucocorticoid (GC) sensitivity is highly variable among individuals and has been associated with susceptibility to develop (auto-)inflammatory disorders. The purpose of the study was to assess GC sensitivity in Behçet's disease (BD) by stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5a54cde4edcd0a6acf651fa0ed72596
https://hdl.handle.net/20.500.12605/8686
https://hdl.handle.net/20.500.12605/8686
Autor:
Farida Fortune, Marion G. Macey, Penelope Shirlaw, Eleni Hagi-Pavli, Miles Stanford, J. Stewart, G R Wallace
Publikováno v:
Rheumatology (Oxford, England). 50(10)
Behçet's disease (BD) is more severe among young males and disease severity decreases with age. Therefore, the effect of disease activity, gender and age on platelet and neutrophil activation in whole blood taken from patients with BD was investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cf9c52d70ac319948d492124850e85b
https://pubmed.ncbi.nlm.nih.gov/21719422
https://pubmed.ncbi.nlm.nih.gov/21719422
Autor:
Omar M. Durrani, John Hamburger, Laura McBride, Katherine Banahan, Miles Stanford, Farida Fortune, Robert Vaughan, Philip I. Murray, Eldad Ben-Chetrit, Kathryn Greiner, E. Kondeatis, Frederick J. Sheedy, G R Wallace, Luke A. J. O'Neill
Publikováno v:
Rheumatology (Oxford, England). 50(10)
Objectives. The initiating cause of Behcet's disease (BD) is unknown, but an aberrant response to infection has been suggested. In this study, single nucleotide polymorphisms in Toll-like receptors (TLRs) and associated molecules that have a sentinel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cd9975da88a2763970a5942591293fa
https://pubmed.ncbi.nlm.nih.gov/21705416
https://pubmed.ncbi.nlm.nih.gov/21705416
Autor:
Goitze Seerp Baarsma, Wafa Madanat, Miles R. Stanford, Jan A. M. van Laar, Jasper H. Kappen, Farida Fortune, André G. Uitterlinden, Paul L. A. van Daele, Petrus Martin van Hagen, F. Rivadeneira, Robert W. A. M. Kuijpers, Jon D. Laman, G R Wallace, Lisette Stolk
Publikováno v:
Rheumatology (Oxford, England). 48(11)
Objective. It has been shown previously that three nucleotide-binding oligomerization domain containing 2 (NOD2) variants (Arg702Trp, Gly908Arg and Lue1007fs) are associated with Crohn's disease (CD), a disorder clinically resembling Behcet's disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffaeb53b4bde2bf7ace377ff8d43a399
https://pubmed.ncbi.nlm.nih.gov/19748964
https://pubmed.ncbi.nlm.nih.gov/19748964
Autor:
G R Wallace
Publikováno v:
Journal of special operations medicine : a peer reviewed journal for SOF medical professionals. 9(3)
The North Atlantic Treaty Organization (NATO) Special Operations Forces (SOF) Coordination Center (NSCC) is a new NATO memorandum of understanding (MOU) organization that is effecting rapid advancement in NATO's ability to efficiently utilize SOF at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a621de31e76700b38d5d85a5d8f01fa
https://pubmed.ncbi.nlm.nih.gov/19739471
https://pubmed.ncbi.nlm.nih.gov/19739471
Publikováno v:
British Journal of Ophthalmology. 83:1393-1395
AIMS—To determine whether patients with idiopathic retinal vasculitis have altered production of cortisol and dehydroepiandrosterone sulphate (DHEA-S), and whether differences in these variables occur between those who are sensitive (SS) and resist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66239bffd80f22a35255b472fbc35e7f
https://doi.org/10.1136/bjo.83.12.1393
https://doi.org/10.1136/bjo.83.12.1393