نتایج جستجو برای: g20210a

تعداد نتایج: 673  

Journal: :Mediterranean Journal of Hematology and Infectious Diseases 2011

Journal: :فیض 0
بتول پورقیصری batool pourgheysari pathology and hematology department, shahrekord university of medical sciences, shahrekord, i. r. iran.شهرکرد، دانشگاه علوم پزشکی شهرکرد، گروه پاتولوژی عفت فرخی efat farrokhi مجتبی ساعدی mojtaba saedi

background: inherited thrombophilic gene polymorphisms have been related to the pathogenesis of venous thromboembolism and its outcomes. considering the scarcity of data on the frequency of the thrombophilic gene polymorphisms in iranian populations, the aim of this study was to assess such polymorphisms in healthy individuals. materials and methods: this cross-sectional study was performed on ...

Journal: :Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva 2013
José Andrés García-Marín Ramón Lirón-Ruiz Jose Antonio Torralba-Martínez Juan Gervasio Martín-Lorenzo José Luis Aguayo-Albasini

Venous intestinal ischemia is a relatively rare disease, which has some predisposing factor up to 80 % of cases. These factors may be temporary or permanent. Cancer, immobilization, trauma, intraabdominal infections, or oral contraceptives are temporary factors. Paroxysmal nocturnal hemoglobinuria and hypercoagulability states as factor V Leiden, G20210A mutation in prothrombin gene, C677T meth...

2000
Valeria Genoud Mercedes Castañon Joyce Annichino-Bizzacchi Jorge Korin

ORIGINAL ARTICLE Prevalence of Three Prothrombotic Polymorphisms: Factor V G1691A, Factor II G20210A and Methylenetetrahydrofolate Reductase (MTHFR) C 677T in Argentina Valeria Genoud1, Mercedes Castañon1, Joyce Annichino-Bizzacchi2, Jorge Korin1 and Lucı́a Kordich1 on behalf of the Grupo Cooperativo Argentino de Hemostasia y Trombosis 1Facultad de Ciencias Exactas y Naturales. Dpto. Quı́mica Bio...

Journal: :Acta clinica Croatica 2014
Nikolina Ivica Irena Pintarić Marina Titlić

A 55-year-old, previously healthy woman, presented with frequent headaches. She had no neurological disturbances, but had a positive family history; her father died from stroke. Magnetic resonance imaging showed brain infarction; therefore detailed diagnostic evaluation of thrombophilia markers and genetic testing were performed. The patient was found to be homozy- gous for the C677T mutation o...

Journal: :Neurology India 2009
Maria Thomas Jeyaraj D Pandian

Ischemic stroke is a heterogeneous multifactorial disease that is affected by several genetic mutations and environmental factors. Various polymorphisms and mutations have been described as risk factors for stroke and they include angiotensin-converting enzyme (ACE) genotype, factor V Leiden, prothrombin G20210A, methylene tetrahydrofolate reductase (MTHFR), human platelet antigen type 1, facto...

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