نتایج جستجو برای: thrombophilic markers

تعداد نتایج: 223187  

2014
Petr Kolar

Retinal vein occlusion (RVO) is a major cause of vision loss. Of the two main types of RVO, branch retinal vein occlusion (BRVO) is 4 to 6 times more prevalent than central retinal vein occlusion (CRVO). A basic risk factor for RVO is advancing age. Further risk factors include systemic conditions like hypertension, arteriosclerosis, diabetes mellitus, hyperlipidemia, vascular cerebral stroke, ...

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...

2008
JD Cavenagh BT Colvin

JD Cavenagh, BT Colvin Summary Although there are numerous risk factors for venous thromboembolic disease, the term 'thrombophilia' refers only to those familial or acquired disorders of the haemostatic system that result in an increased risk of thrombosis. The inherited thrombophilias include antithrombin III deficiency, resistance to activated protein C (factor V Leiden), protein C and protei...

Journal: :Blood 2006
Francesco Dentali Mark Crowther Walter Ageno

Recent studies suggest that thrombophilic abnormalities and the use of oral contraceptives (OCs) are the leading causes of cerebral vein thrombosis (CVT). The purpose of this study was to assess the association between CVT and thrombophilic states, OCs, and their interaction. For data sources, we used the MEDLINE, EMBASE, and Cochrane Library databases (January 1994 to March 2005), reference li...

2009
Dimitrios Brouzas Antonios Charakidas Ioannis Ladas Michael Apostolopoulos

INTRODUCTION We report on three cases of visual loss due to nonarteritic anterior ischemic optic neuropathy that developed during the course of refractory anemia, a subtype of myelodysplastic syndrome. PATIENTS AND METHODS Patients underwent fundus, visual field examination, and fluorescein angiography. A thrombophilic tendency investigation including prothrombin time, partial thromboplastin ...

Journal: :Blood 1994
X Sun B Evatt J H Griffin

A coagulation test abnormality, termed activated protein C (APC) resistance, involving poor anticoagulant response to APC is currently the most common laboratory finding among venous thrombophilic patients. Because the anticoagulant activity of APC involves inactivation of factors Va and VIIIa, studies were made to assess the presence of abnormal factors V or VIII. Diluted aliquots of plasma fr...

Journal: :Fertility and sterility 1999
Z Blumenfeld B Brenner

OBJECTIVE To critically review the literature regarding inherited thrombophilia and recurrent fetal loss. DESIGN English-language literature review. PATIENT(S) Women who experienced repeated pregnancy wastage. INTERVENTION(S) Aspirin, glucocorticoids, heparin, and IV immunoglobulin for the prevention of miscarriage. MAIN OUTCOME MEASURE(S) Live birth, miscarriage, preeclampsia, and preg...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2005
Carla Y Vossen Isobel D Walker Peter Svensson Juan C Souto Inge Scharrer F Eric Preston Gualtiero Palareti Ingrid Pabinger Felix J M van der Meer Mike Makris Jordi Fontcuberta Jacqueline Conard Frits R Rosendaal

OBJECTIVE Few comprehensive data are available on the recurrence rate of venous thrombosis in carriers of thrombophilic defects from thrombophilic families. We prospectively determined the recurrence rate after a first venous thrombotic event in patients with familial thrombophilia attributable to factor V Leiden or deficiencies of protein C, S, or antithrombin. METHODS AND RESULTS Data were ...

2012
Khalid K Alharbi Imran Ali Khan Rabbani Syed

We performed a study to evaluate the role of three single nucleotide polymorphisms (SNPs), factor V Leiden G1691A (FVL), prothrombin gene mutation G20210A (PRT or FII-G20210A) and methylenotetrahydrofolate reductase variant C677T (MTHFRC677T), as risk factors for G6PD in Saudi populations. Our results did not show any association with the three Thrombophilic genes with FVL gene, no statistical ...

Journal: :Reproductive biomedicine online 2006
Carolyn B Coulam R S Jeyendran Laurence A Fishel Roumen Roussev

While the role of inherited thrombophilia has been accepted as a cause of recurrent late pregnancy complications, the contribution of mutated thrombophilic genes to implantation failure has not been studied. Proteins involved in fibrinolysis are necessary for trophoblast invasion into the endometrium. This study compared the prevalence of 10 thrombophilic gene mutations among 42 women with a hi...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید