نتایج جستجو برای: thrombophilic gene

تعداد نتایج: 1141932  

Journal: :Haematologica 2001
I Tirado J Mateo J M Soria A Oliver M Borrell I Coll C Vallvé J C Souto E Martínez-Sánchez J Fontcuberta

BACKGROUND AND OBJECTIVES The aims of this study were to compare the lifetime probability of developing thrombosis in 722 relatives of 132 thrombophilic families of symptomatic probands with recognized thrombophilic defects and to determine the prevalence of the factor V Leiden (FVL) mutation and the 20210A allele of the prothrombin gene (PT20210A) in these families. DESIGN AND METHODS The st...

2009
Filip Konecny

Pulmonary embolism (PE) and deep vein thrombosis (DVT) are associated with considerable morbidity and mortality, mostly, in case of PE for its lack of sensitivity of its early detection. For as much as twenty-five percent of PE patients the primary clinical appearance is unexpected death. While PE is one of the most avertable causes of hospital associated deaths, its diagnostics can be extremel...

Journal: :Ophthalmology 2005
Martin Weger Wilfried Renner Iris Steinbrugger Lisa Cichocki Werner Temmel Olaf Stanger Yosuf El-Shabrawi Helga Lechner Otto Schmut Anton Haas

OBJECTIVE Branch retinal vein occlusion (BRVO) is a common cause of severe visual loss. Numerous risk factors, including arterial hypertension, diabetes mellitus, and arteriosclerosis, have been identified. Gene polymorphisms affecting hemostasis may also play a role in the pathogenesis of BRVO. The present study was therefore done to determine the prevalence of genetic polymorphisms in factors...

2008
Valeria Nagy Lili Takacs Zita Steiber György Pfliegler Andras Berta

BACKGROUND Retinal artery occlusion (RAO) is an ischemic vascular damage of the retina, which frequently leads to sudden, mostly irreversible loss of vision. In this study, blood thrombophilic factors as well as cardiovascular risk factors were investigated for their relevance to this pathology. Thrombophilic risk factors so far not evaluated were included in the study. PATIENTS AND METHODS 2...

2013
Flávio Luís Garcia Edvaldo Luiz Ramalli Celso Hermínio Ferraz Picado

OBJECTIVE To compare the occurrence of thrombophilic disorders in patients with idiopathic osteonecrosis of the femoral head and patients with secondary osteonecrosis of the femoral head. METHODS Twenty-four consecutive patients were enrolled, with eight of them presenting idiopathic osteonecrosis and 16 presenting secondary osteonecrosis. The tests for detection of thrombophilic disorders we...

Journal: :Menopause 2011
Margaret J Nachtigall Rebecca H Jessel Robert Flaumenhaft Richard Nachtigall Israel Yoles Frederick Naftolin Lila E Nachtigall

OBJECTIVE The purpose of this study was to assess the effect of DT56a (Femarelle), a selective estrogen receptor modulator, on platelet function in normal and thrombophilic women being treated for severe menopausal symptoms. METHODS The Platelet Function Analyzer-100 (PFA-100) was used to asses platelet reactivity at baseline and after 8 weeks of treatment with Femarelle (644 mg/d in divided ...

Journal: :the journal of tehran university heart center 0
seyed mohsen mirhosseini chronic respiratory disease research center, national research institute of tuberculosis and lung diseases, shahid beheshti university of medical sciences, tehran, iran. ali sanjari moghaddam school of medicine, shahid beheshti university of medical sciences, tehran, iran.

major complications of heart transplantation include graft rejection, infection, graft arteriosclerosis, malignancy, and drug toxicity. among these complications, infections and thrombophilic disorders are of particular interest owing to their major contribution to morbidity and mortality among heart transplantation patients. thrombophilic disorders are caused by imbalance between hypercoagulat...

Journal: :Advanced pharmaceutical bulletin 2012
Kobra Hamdi Maryam Vaezi Behrooz Dagigazar Mahzad Mehrzad Sadagiani Laya Farzadi Maryam Pashaei-Asl

PURPOSE This study was performed to investigate the incidence of thrombophilic gene mutations in repeated assisted reproductive technology (ART) failures. METHODS The prevalence of mutated genes in the patients with a history of three or more previous ART failures was compared with the patients with a history of successful pregnancy following ARTs. The study group included 70 patients, 34 wit...

Journal: :Neurology India 2009
Fahri Yakaryilmaz Sefa Guliter Bulent Degertekin Candan Tuncer Selahattin Unal

Inflammatory bowel diseases are associated with increased risk for thrombotic complications, In patients with ulcerative colitis (UC) cerebral sinus venous thrombosis (CSVT) is an extremely rare complication. We report a patient with active UC and CSVT. The patient was heterozygous for Factor V Leiden and G20210A prothrombin gene mutations without other identifiable precipitating factors. This ...

Journal: :Frontiers in Neurology 2014

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید