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protein c deficiency/edema

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Combined factor VII/protein C deficiency results in intrauterine coagulopathy in mice.

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To determine whether an additional loss of the coagulation factor VII (FVII) gene influenced the coagulopathy observed in protein C gene-deficient (PC(-/-)) embryos and neonates, we crossed mice doubly heterozygous for the factor VII (FVII(+/-)) and protein C (PC(+/-)) genes to produce offspring

[The usefullness of percutaneous transluminal balloon angioplasty in the management of budd-Chiari syndrome].

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OBJECTIVE Membranous obstruction is the most common cause of Budd-Chiari syndrome in Orientals. Recently, percutaneous transluminal balloon angioplasty (PTBA) has been successfully applied as a treatment of membranous obstruction. We evaluated etiologies and clinical manifestations in our cases and

Deep venous thrombosis of lower limbs in adolescents: a study in a tertiary hospital.

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Background Venous thromboembolism (VTE) - which includes deep venous thrombosis (DVT) and pulmonary embolism (PE) - has been increasingly recognized in the pediatric population. The estimated incidence is 0.07-0.14 cases per 10,000 children. Most cases are associated with two or more risk factors.
OBJECTIVE In a preliminary pilot study of 30 treatments in 26 patients with osteonecrosis of the jaws and chronic disabling facial pain, our specific aim was to determine whether, to what degree, and how safely therapy of hypofibrinolysis and thrombophilia would ameliorate the chronic pain

Evaluating chronic venous disease with a new venous severity scoring system.

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BACKGROUND The Venous Clinical Severity Score (VCSS) has been proposed by the American Venous Forum as an objective means to clinically assess venous disease more completely than with the clinical CEAP classification. However, validation of the VCSS against an objective test is lacking. The purpose

Endothelial cell activation and hypercoagulability in ocular Behçet's disease.

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OBJECTIVE To investigate the presence of a hypercoagulable state and vascular endothelial dysfunction in patients with ocular Behçet's disease and relate the results to the activity of ocular and systemic involvement. METHODS Cross-sectional laboratory and clinical study. METHODS Prospective study
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