Results 11 to 20 of about 13,117,018 (331)

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, Pavithra M. Rallapalli, S. Perkins, G. Kemball-Cook, D. Hampshire, K. Gomez, C. Ludlam, J. McVey   +7 more
semanticscholar   +1 more source

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

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, Xi Wu, Wenman Wu, Qiulan Ding, Xuefeng Wang   +4 more
doaj   +1 more source

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, V. N. Maksimov, Ya. V. Polonskaya, I. S. Murashov, A. M. Volkov, A. V. Kurguzov, A. M. Chernyavsky, E. V. Kashtanova   +7 more
doaj   +1 more source

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, Maryam Shamspour, Neda Ashayery, Milad Ahmadi Marzaleh   +3 more
doaj   +1 more source

Case Report: Factor VII Deficiency Presented With Cephalohematoma After Birth

Frontiers in Pediatrics, 2021
Introduction: Factor VII deficiency is a rare inherited autosomal recessive bleeding disorder with a global prevalence of 1/500,000. Most cases remain asymptomatic, and cases with severe clinical presentation are rarely reported.Case Presentation: A ...
Yuan-Chun Lo, Ching-Tien Peng, Ching-Tien Peng, Yin-Ting Chen   +3 more
doaj   +1 more source

Factor VII deficiency [PDF]

Blood 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

Olive oil and haemostasis

Grasas y Aceites, 2004
Olive oil is a key component of the traditional Mediterranean diet; a diet that may explain the low rate of cardiovascular disease (CVD) in Southern European.
Colette N.M. Kelly, George J. Miller, Christine M. Williams   +2 more
doaj   +1 more source

A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.

Blood, 2019
Factor VII (FVII) is an important component of the coagulation cascade. Few genetic loci regulating FVII activity and/or levels have been discovered to date.
P. D. de Vries, M. Sabater-Lleal, J. Huffman, J. Marten, Ci Song, N. Pankratz, Traci M. Bartz, H. D. de Haan, G. Delgado, J. Eicher, A. Martinez-Perez, C. Ward‐Caviness, J. Brody, Ming-Huei Chen, M. D. de Maat, Mattias Frånberg, D. Gill, M. Kleber, F. Rivadeneira, J. Soria, Weihong Tang, G. Tofler, A. Uitterlinden, A. van Hylckama Vlieg, S. Seshadri, E. Boerwinkle, N. Davies, A. Giese, M. Ikram, S. Kittner, B. McKnight, B. Psaty, A. Reiner, M. Sargurupremraj, Kent D Taylor, M. Fornage, A. Hamsten, W. März, F. Rosendaal, J. Souto, A. Dehghan, A. Johnson, A. Morrison, Christopher J. O'Donnell, N. Smith   +44 more
semanticscholar   +1 more source

Factor VII Deficiency: Clinical Phenotype, Genotype and Therapy

Journal of Clinical Medicine, 2017
Factor VII deficiency is the most common among rare inherited autosomal recessive bleeding disorders, and is a chameleon disease due to the lack of a direct correlation between plasma levels of coagulation Factor VII and bleeding manifestations. Clinical
M. Napolitano, S. Siragusa, G. Mariani
semanticscholar   +1 more source

Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII

The Turkish Journal of Pediatrics, 2018
Intracranial hemorrhage is considered the most common cause of death in newborns with congenital factor VII (FVII) deficiency. Recombinant activated FVII (rFVIIa) provides specific replacement therapy, however there is limited experience with its ...
Zeynep İnce, Özgül Bulut, Melike Tuğrul-Aksakal, Ayşegül Ünüvar, Ömer Devecioğlu, Asuman Çoban   +5 more
doaj   +1 more source