Results 171 to 180 of about 4,856,485 (200)
Internal Jugular Vein Thrombosis as the Initial Presentation of Antiphospholipid Antibody-positive Vascular Behçet Disease: A Clinical Image. [PDF]
Katoh H, Iwata M, Terasawa T.
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Innominate artery aneurysm in behcet disease; report of one case. [PDF]
Mozafar M +4 more
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[Clinical significance of antiphospholipid antibodies in Behcet disease with thrombosis]. [PDF]
Li Y, Wang H, Luo L, Li Y, Li C.
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Serum Prolactin Levels in Behçet's Disease
Japanese Journal of Ophthalmology, 2000Evaluation of serum prolactin levels in Behçet's disease patients in Turkey.Serum prolactin levels were measured by radioimmunoassay (RIA) in 17 patients with ocular findings, and 20 patients without ocular findings of Behçet's disease, and in 17 healthy volunteers.The average prolactin levels were measured as 9.53 ng/mL in patients with ocular ...
K C, Apaydin +3 more
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Optic Nerve Involvement in Neuro-Behçet's Disease
Japanese Journal of Ophthalmology, 2002To report the ocular manifestations of neuro-Behcet's disease.A 34-year-old woman had recurrent meningitis. She developed diplopia, headache, and ataxia, and was diagnosed as having neuro-Behcet's disease.Imaging revealed two infarct foci in the transitional midbrain and pons. After treatment with prednisolone and colchicine, the diplopia resolved. Two
Toru, Nakamura +2 more
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Ciclosporin Microemulsion Preconcentrate Treatment of Patients With Behçet's Disease
Japanese Journal of Ophthalmology, 1999The new microemulsion preconcentrate (MEPC) formulation of ciclosporin has been developed to reduce problems in intestinal absorption and to stabilize fluctuations in blood levels. A multicenter, open-label clinical trial of MEPC was conducted to assess its efficacy and safety in Behçet's disease patients with ocular involvement.The patient population ...
Y, Fujino +12 more
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Strong association between plasma thrombomodulin and pathergy test in Behçet disease
Annals of the Rheumatic Diseases, 2008Behcet disease (BD) is a chronic systemic auto-inflammatory immune disorder with generalised vasculitis of the arteries and veins. It was originally described as orogenital aphthous ulcerations and uveitis but the disease can affect any organ or system. BD is characterised by recurrent crises of variable duration and intervals.
S, Menashi +6 more
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Immunology Letters, 2001
Heat shock protein (HSP, 60/65 kDa) is investigated as a candidate autoantigen in Behçet's disease (BD), a systemic vasculitis of unknown origin, and a prominent response to 'disease-specific epitopes' of mycobacterial and human HSP60/65 is described in BD patients.
G, Saruhan-Direskeneli +3 more
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Heat shock protein (HSP, 60/65 kDa) is investigated as a candidate autoantigen in Behçet's disease (BD), a systemic vasculitis of unknown origin, and a prominent response to 'disease-specific epitopes' of mycobacterial and human HSP60/65 is described in BD patients.
G, Saruhan-Direskeneli +3 more
openaire +3 more sources

