Results 11 to 20 of about 14,512,458 (287)

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

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

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, T. 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

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

The international, prospective Glanzmann Thrombasthenia Registry: treatment modalities and outcomes of non-surgical bleeding episodes in patients with Glanzmann thrombasthenia

Haematologica, 2015
Standard treatment for Glanzmann thrombasthenia is platelet transfusion. Recombinant activated factor VII has been shown to be successful in patients with Glanzmann thrombasthenia with platelet antibodies or who are refractory to platelet transfusions ...
Giovanni Di Minno, Rainer B Zotz, Roseline d’Oiron, Niels Bindslev, Matteo Nicola Dario Di Minno, Man-Chiu Poon   +5 more
doaj   +1 more source

Evaluation of Clinical Features, Laboratory Findings and Treatment of Patients with Rare Factor Deficiency: A Retrospective Single Center Experience

Çocuk Dergisi, 2023
Objective: Patients with a rare factor deficiency (RFD) may be asymptomatic or present with life-threatening bleeding. Studies have shown no direct relationship between factor activity level and bleeding severity, with difficulties being experienced in ...
Işık Odaman Al, Tuba Hilkay Karapınar, Salih Gözmen, Yeşim Oymak   +3 more
doaj   +1 more source

Identification of two different coagulation phenotypes in people living with HIV with undetectable viral replication

Scientific Reports, 2021
Altered coagulation has been reported in people living with HIV (PLWH) with ongoing viral replication and may predispose to cardiovascular diseases. However, less is known about coagulation in PLWH with undetectable viral replication.
Asbjørn Fink, Andreas Dehlbæk Knudsen, Rebekka Faber Thudium, Jakob Hjorth Von Stemann, Shoaib Afzal, Jens Lundgren, Ditte Marie Kirkegaard-Klitbo, Sisse Rye Ostrowski, Børge G. Nordestgaard, Susanne Dam Nielsen   +9 more
doaj   +1 more source

Factor VII verona coagulation disorder: double heterozygosis with an abnormal factor VII and heterozygous factor VII deficiency [PDF]

Blood, 1977
A family with a peculiar defect of factor VII is described. The propositi, a brother and sister, were born of a nonconsanguineous marriage and presented a mild to moderate bleeding tendency since childhood (epistaxis, excessive bleeding after tooth extraction).
A, Girolami, G, Falezza, G, Patrassi, M, Stenico, L, Vettore   +4 more
openaire   +3 more sources