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Toplam kayıt 10, listelenen: 1-10
Development Of Calciphylaxis After Long-Term Steroid And Methotroxate Use In A Patient With Rheumatoid Arthritis
(Japan Soc Internal Medicine, 2005)
Calciphylaxis may be considered a small vessel vasculopathy which is generaly associated with end-stage renal disease and hyperparathyroidism. The precise pathogenesis of the disease is not known. It needs sensitizers and ...
Is Visual Loss Due to Giant Cell Arteritis Reversible?
(Yonsei Univ Coll Medicine, 2003)
Giant cell arteritis (GCA) is a common systemic vasculitis with an unknown etiology. It mainly affects people older than 50 years of age and often presents with symptoms such as headache, jaw claudication, visual loss, ...
Skewed X Chromosome Inactivation in Blood Cells of Women with Scleroderma
(Wiley, 2005)
Objective. Scleroderma (SSc) is an autoimmune disease of unknown etiology. The disease is 3-8 times more frequent in women than in men. The role of X chromosome inactivation (XCI) in the predisposition of women to autoinimunity ...
Interferon Alfa in Protracted Arthritis of Familial Mediterranean Fever: A Robust Alternative for Synovectomy
(B M J Publishing Group, 2004)
Effects Of Oral Cyclophosphamide And Prednisolone Therapy On The Endothelial Functions And Clinical Findings In Patients With Early Diffuse Systemic Sclerosis
(Wiley-Liss, 2003)
Objective. The endothelial damage of microvascular structures in systemic sclerosis (SSc; scleroderma) is associated with increased levels of endothelial adhesion molecules and endothelium-associated cytokines, including ...
Myocardial Infarction And Deep Venous Thrombosis In A Young Patient With Behcet Disease
(Sage Publications Inc, 2006)
Behcet disease (BD) is a chronic relapsing systemic vasculitic disorder affecting the arteries, veins, and vessels of any size. Vascular lesions in BD usually represent an occlusive nature suggesting a hypercoagulable/ ...
The Efficacy of Interferon-Alpha in a Patient with Resistant Familial Mediterranean Fever Complicated by Polyarteritis Nodosa
(Japan Soc Internal Medicine, 2004)
Familial Mediterranean fever (IMF) is a recurrent self-limiting polyserositis. Polyarteritis nodosa (PAN) complicating IMF is very rare. Here, we present a 17-year-old male patient with IMF who subsequently developed PAN ...
Changes In The Concentration And Distribution Of Tissue Factor Pathway Inhibitor In Behcet'S Disease And Systemic Lupus Erythematosus: Effect On The Prethrombotic State
(British Med Journal Publ Group, 2001)
Background-Tissue factor pathway inhibitor (TFPI) is an anticoagulant which modulates the tissue factor (TF) dependent pathway, acting on the factor VIIa/TF complex, factor Xa, and thrombin. Although most TFPI is found in ...
Effects Of Interferon Alpha Treatment On The Clinical Course Of Refractory Behcet'S Disease: An Open Study
(British Med Journal Publ Group, 2003)
Qt Dispersion As A Predictor of Arrhythmic Events in Patients with Ankylosing Spondylitis
(Oxford Univ Press, 2000)
Objective. The aim of the study was to evaluate QT dispersion (QTd), an indicator of repolarization heterogeneity, and its relation to ventricular arrhythmias in patients with ankylosing spondylitis (AS). Methods. A full ...