نتایج جستجو برای: g20210a

تعداد نتایج: 673  

Journal: :CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2013
Birgitte F Sode Kristine H Allin Morten Dahl Finn Gyntelberg Børge G Nordestgaard

BACKGROUND ABO blood type locus has been reported to be an important genetic determinant of venous and arterial thrombosis in genome-wide association studies. We tested the hypothesis that ABO blood type alone and in combination with mutations in factor V Leiden R506Q and prothrombin G20210A is associated with the risk of venous thromboembolism and myocardial infarction in the general populatio...

Journal: :Blood 1998
A Zivelin N Rosenberg S Faier N Kornbrot H Peretz C Mannhalter M H Horellou U Seligsohn

The polymorphism G20210A in the 3' untranslated region of the prothrombin gene is associated with an increased level of factor II activity and confers a twofold to fivefold increase in the risk for venous thromboembolism. Among Caucasian populations, the prevalence of factor II G20210A heterozygotes is 1% to 6%, whereas in non-Caucasian populations it is very rare or absent. The aim of the pres...

Journal: :The European respiratory journal 2003
E Nizankowska-Mogilnicka L Adamek P Grzanka T B Domagala M Sanak M Krzanowski A Szczeklik

Frequently an inherited predisposition to thrombosis remains clinically silent until an additional environmental factor intervenes. The present study aimed to assess distribution of inherited risk factors of venous thrombosis in patients with venous thromboembolism (VTE). The prevalences of factor V Leiden (FV Leiden), prothrombin factor II G20210A (FII G20210A), C677T and A1298C of methylenete...

2012
Nahid Ashjazadeh Maryam Poursadeghfard Shirin Farjadian

Objective: Cerebral venous thrombosis (CVT) is an important cause of stroke, especially in young adults, that has many predisposing factors. G20210A mutation in prothrombin gene (Factor II) and G1691A mutation in Factor V Leiden (FVL) are two common hereditary causes of CVT. This study aimed to study the rate of these mutations in patients with CVT from Fars Province in southern Iran. Methods: ...

امینی, نصرت, جان بابایی, قاسم, شکرریز, رامین, قائمیان, علی, مهدوی, محمدرضا, هاشمی سوته, سید محمدباقر, هاشمی پطرودی, سید محمد جواد,

Background and purpose: Beside the environmental determinants there are major genetic factors that could cause Myocardial Infarction (MI). The aim of this study was to clarify the relationship between factor V Leiden and prothrombin G20210A with acute MI in patients younger than 50 years of age. Materials and methods: In this case-control study we recruited 101 MI patients and 101 healthy ...

2016
Joaquín V. Gonzalez Andrés G. Barboza Fernando J. Vazquez Esteban Gándara

OBJECTIVES To compare the prevalence of prothrombin G20210A in patients with objectively confirmed cerebral vein or cortical vein thrombosis against healthy controls, and evaluate geographical variations. DESIGN Systematic review and meta-analysis of case control studies. METHODS We conducted a systematic review of electronic databases including MEDLINE and EMBASE. The main outcome was the ...

Journal: :Pathophysiology of haemostasis and thrombosis 2002
Gregorios A Paspatis Aikaterini Sfyridaki Nikolaos Papanikolaou Kostantinos Triantafyllou Aikaterini Livadiotaki Andreas Kapsoritakis Niki Lydataki

OBJECTIVE The aim of our study was to determine the frequency of resistance to activated protein C (APC), factor V Leiden (FVL) and the prothrombin G20210A variant in patients with colorectal cancer. METHODS 74 patients with colorectal cancer and 192 colonoscopically selected controls were prospectively investigated for the presence of APC resistance, FVL and the prothrombin G20210A variant. ...

2015
Tarek Hamed Attia Hisham Ahmed Fawzi Ibrahim Shahat Desouki

Prothrombin gene G20210A mutation is a risk factor for the development of deep vein thrombosis. We present a 6-year-old Egyptian boy who had vomiting associated with headache and dizziness. His conscious level was normal, with neither focal neurological signs nor papilledema. Brain computed tomographic scan, magnetic resonance imaging and magnetic resonance venography (MRV) revealed thrombosis ...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2006
Andreas L Serra Maja Klein Dorothea Nitsch Daniel Dürr Bendicht Wermuth Felix J Frey

kidney disease who started peritoneal dialysis in 2000. Four years later, the patient received a cadaver donor transplant from a 52-year-old woman. Surgery was performed without technical difficulties and good initial graft perfusion was observed. An immunosuppressive regimen consisting of tacrolimus, mycophenolate mofetil and steroids was initiated. The post-operative course showed persistent ...

ژورنال: :genetics in the 3rd millennium 0
حسین نجم آبادی hossein najmabadi prof of human genetics, welfare & rehabilitation university of medical sciences, tehran, iranتهران، اوین، بلوار دانشجو،خیابان کودکیار، دانشگاه علوم بهزیستی و توانبخشی، مرکز تحقیقات ژنتیک/ مرکز پاتولوژی و ژنتیک کریمی نژاد- نجم آبادی مریم رستمی maryam rostami واله هادوی valeh hadavi آریانا کریمی نژاد ariana kariminejad فریبا افروزان fariba afroozan هاشم ایمانیان hashem imanian کریستین آبرکانینز

در این بررسی 208 فرد بدون علائم بالینی بیماریهای قلبی-عروقی و سابقه ترومبوز وریدی از نقاط مختلف ایران با نژادهای متفاوت مورد مطالعه قرار گرفتند. جهت ارزیابی توزیع پلی مرفیسم پروترومبین g20210a، عامل ژنتیکی ایجاد بیماری های قلبی عروقی (cvd)، در جمعیت ایران از روش هیبریداسیون معکوس برای تشخیص سریع و دقیق استفاده شد. اساس تست بروش multiplex pcr و هیبریداسیون برروی نوار تست است که این نوار شامل خطو...

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