Hyperhomocysteinemia in patients with Behçet’s disease: is it due to inflammation or therapy?

Author:

Yesilova Zeki,Pay Salih,Oktenli Cagatay,Musabak Ugur,Saglam Kenan,Sanisoglu S. Yavuz,Dagalp Kemal,Erbil M. Kemal,Kocar Ismail H.

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy,Rheumatology

Reference65 articles.

1. Behçet H (1937) Ueber rezidivierende Aphtoese, durch ein Virus verursachte Geschwuere am Mund, am Auge, und an den Genitalien. Dermatol Wochenschr 105:1152

2. Sahin S, Akoglu T, Direskeneli H, Sen LS, Lawrence R (1996) Neutrophil adhesion to endothelial cells and factors affecting adhesion in patients with Behçet’s disease. Ann Rheum Dis 55:128–133

3. O’Duffy JD (1990) Vasculitis in Behçet’s disease. Rheum Dis Clin North Am 16:423–431

4. Koc Y, Gullu I, Akpek G, Akpolat T, Kansu E, Kiraz S, Batman F, Kansu T, Balkanci F, Akkaya S (1992) Vascular involvement in Behçet’s disease. J Rheumatol 19:402–410

5. Gul A, Ozbek U, Ozturk C, Inanc M, Konice M, Ozcelik T (1996) Coagulation factor V mutation increases the risk of venous thrombosis in Behçet’s disease. Br J Rheumatol 35:1178–1180

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