Results 11 to 20 of about 29,955 (251)

PB1834: ACQUIRED FACTOR VII DEFICIENCY ASSOCIATED WITH ACUTE MYELOID LEUKEMIA [PDF]

open access: yesHemaSphere, 2023
Haifa Hafsa   +6 more
doaj   +2 more sources

Factor VII Deficiency [PDF]

open access: yesSeminars 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
openaire   +4 more sources

Congenital Factor VII Deficiency Presenting with Isolated Recurrent Hematuria: A Case Report

open access: yesActa 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
doaj   +1 more source

A case-report of the unprovoked thrombotic event in a patient with thymoma and severe FVII deficiency

open access: yesThrombosis 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
doaj   +1 more source

Factor VII deficiency [PDF]

open access: yesBlood Coagulation & Fibrinolysis, 2002
As yet, there have been neither systematic reviews nor reports of randomized, controlled trials involving factor VII (FVII) deficiency. Hence, a picture of this disorder can only be drawn by reviewing and summarizing the data that is available. This article provides an overview of the understanding of this rare, inherited disorder of coagulation.
openaire   +3 more sources

Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER)

open access: yesHaematologica, 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
doaj   +1 more source

A case of intracranial hemorrhage in a neonate with congenital factor VII deficiency [PDF]

open access: yesKorean Journal of Pediatrics, 2010
Congenital factor VII deficiency is a rare autosomal-recessive bleeding disorder. Bleeding manifestations and clinical findings vary widely, ranging from asymptomatic subjects to patients with hemorrhages that may cause significant handicaps.
Won Seok Lee, Young Sil Park
doaj   +1 more source

Inhibitors to factor VII in congenital factor VII deficiency [PDF]

open access: yesHaemophilia, 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
openaire   +3 more sources

Congenital factor VII deficiency presenting first time as isolated recurrent hematuria at late age

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2019
Hematological conditions rarely present as isolated hematuria. Factor VII deficiency is a rare congenital coagulopathy inherited as autosomal recessive pattern. It usually presents a severe life-threatening bleeding at an early age.
Suman Sethi   +5 more
doaj   +1 more source

Generation of a human induced pluripotent stem cell line, YCMi002-A, from a Factor VII deficiency patient carrying F7 mutations

open access: yesStem Cell Research, 2020
Factor VII (FVII) deficiency is the most common among the rare bleeding disorders, which is caused by mutations in coagulation factor VII. Clinical features caused by FVII deficiency vary from mild or asymptomatic to fatal cerebral hemorrhage.
Do-Hun Kim   +3 more
doaj   +1 more source

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