- ►bmj.com DH Verity, GR Wallace, RW Vaughan, MR … - British Medical Journal, 2003 - bjo.bmj.com 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, ... Cited by 73 - Related articles - BL Direct - All 8 versions
DH Verity, GR Wallace, RW Vaughan, MR … - The British Journal of Ophthalmology, 2003 - ukpmc.ac.uk 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, ... Related articles
- ►bmj.com A Gul, M Inanc, L Ocal, O Aral, M Konice - British Medical Journal, 2000 - ard.bmj.com Subsequently (second step), we used the method described by Sun-Wei Guo to
calculate the recurrence rate in siblings. 17 To avoid an ascertainment bias we
defined the immediately older sibling, or if an older sibling was not ... Cited by 69 - Related articles - BL Direct - All 5 versions
DH Verity, JE Marr, S Ohno, GR Wallace, MR … - Tissue Antigens, 1999 - interscience.wiley.com Behçet's disease (BD), also known as the Silk Road disease, is a blinding
inflammatory disorder of young adults found predominantly between the
Mediterranean basin and the Orient, and is strongly associated with the ... Cited by 104 - Related articles - BL Direct - All 3 versions
T Ahmad, GR Wallace, T James, M Neville, M … - Arthritis Care & Research - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 78 - Related articles - BL Direct - All 3 versions
- ►bmj.com H Direskeneli - British Medical Journal, 2001 - ard.bmj.com Although BD does not have the features of a classical autoimmune disorder, such
as female dominance, hypergammaglobulinaemia, Sjögren's syndrome, and
antinuclear antibodies, 18 some B cell activity, such as increased ... Cited by 125 - Related articles - BL Direct - All 6 versions
A Akman, N Sallakci, M Coskun, A Bacanli, U … - Br J Dermatol, 2006 - interscience.wiley.com Background Genetic factors that predispose individuals to Behçet's disease (BD)
are considered to play an important role in development of the disease. The
tumour necrosis factor (TNF)-α gene, which is closely linked to the ... Cited by 20 - Related articles - BL Direct - All 4 versions
C Evereklioglu - Survey of ophthalmology, 2005 - Elsevier Behçet disease is an idiopathic, multisystem, chronic, and recurrent disease
characterized by exacerbations alternating with phases of quiescence, episodic
panuveitis, and aggressive non-granulomatous occlusive vasculitis of the ... Cited by 111 - Related articles - All 22 versions
G Azizlerli, A Akdag Kose, R Sarica, A Gul, IT … - International journal of dermatology, 2003 - interscience.wiley.com Patients and methods This study investigated the cross-sectional prevalence of
BD in individuals aged > 12 years in Istanbul, Turkey, in two stages. The first
stage aimed to identify individuals with recurrent oral ulcers (ROUs) by ... Cited by 69 - Related articles - BL Direct - All 4 versions
M Zierhut, N Mizuki, S Ohno, H Inoko, A Gül, … - Cellular and Molecular Life Sciences, 2003 - Springer Abstract. Behçet's disease (BD) is a multisystemic in- flammatory disorder.
Although the cause and pathogene- sis of BD are still unclear, there is evidence
for genetic, immunologic and infectious factors at the onset or in the ... Cited by 46 - Related articles - BL Direct - All 4 versions
