Results 1 to 10 of about 14,512,458 (287)
Haematologica, 2013 Because of the very short half-life of factor VII, prophylaxis in factor VII deficiency is considered a difficult endeavor. The clinical efficacy and safety of prophylactic regimens, and indications for their use, were evaluated in factor VII-deficient ...
Mariasanta Napolitano +13 more
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Inhibitors to factor
Haemophilia, 2014 We performed a prospective study of FVII inhibitor occurrence in a large number of patients with FVII deficiency who had received replacement therapy for spontaneous or traumatic bleeding episodes, major or minor surgical interventions or prophylaxis.Inhibitor development was detected in 2.6% (3/115) of patients, but the incidence of de novo inhibitors
Batorova A +11 more
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A 5-year-old Chinese boy with mild symptoms despite severe congenital factor VII deficiency: A case report [PDF]
Journal of International Medical ResearchCongenital factor VII deficiency is a rare autosomal recessive bleeding disorder characterized by markedly heterogeneous clinical phenotypes and reduced plasma factor VII activity.
Wei Luo +3 more
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Seminars in Thrombosis and Hemostasis, 2009 The complex formed between the procoagulant serine protease activated factor VII (FVII) and the membrane protein tissue factor, exposed on the vascular lumen upon injury, triggers the initiation of blood clotting. This review describes the clinical picture of FVII deficiency and provides information on diagnosis and management of the disease.
G. Mariani, BERNARDI, Francesco
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Hereditary Factor VII Deficiency
Definitions, 2020 rare autosomal recessive inherited blood ...
semanticscholar +1 more source
The EAHAD blood coagulation factor VII variant database
Human Mutation, 2020 Hereditary blood coagulation factor VII (FVII) deficiency is a rare autosomal recessive bleeding disorder resulting from variants in the gene encoding FVII (F7).
M. Giansily-Blaizot +7 more
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Polymorphisms in F2, F7, and PAI1 genes in men with coronary atherosclerosis
Российский кардиологический журнал, 2020 Aim. To study the associations of polymorphisms in F2, F7, and PAI1 genes with the presence of vulnerable plaque in coronary arteries (CA) and the blood concentration of proteins encoded by these genes.Material and methods.
E. V. Stryukova +7 more
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Thrombosis Journal, 2023 Background Factor VII deficiency is a rare bleeding disorder caused by a deficiency of clotting factor VII. However, there have been some case reports of venous thrombosis in patients with factor VII deficiency, especially underlying the prothrombotic ...
Lei Li +4 more
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Congenital Factor VII Deficiency Presenting with Isolated Recurrent Hematuria: A Case Report
Acta Medica Iranica, 2021 Introduction: Factor VII deficiency is a rare congenital coagulopathy disorder. In most cases this disorder is diagnosed in childhood. Common symptoms of congenital factor VII deficiency are different and consist of mucosal cutaneous hemorrhage ...
Shahla Ansary Damavandi +3 more
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