نتایج جستجو برای: g20210a

تعداد نتایج: 673  

Journal: :Haematologica 2000
P Sivera S Bosio M T Bertero M Demaestri U Mazza C Camaschella

2. Morse B, Giuliani D, Nussbaum M. Quantitation of platelet-associated IgG by radial immunodiffusion. Blood 1981; 57:809-11. 3. George JN. Platelet immunoglobulin G: its significance for the evaluation of thrombocytopenia and for understanding the origin of alpha-granule proteins. Blood 1990; 76:859-70. 4. Robinson MSC, Mackie IJ, Machin SJ, Savidge GF, Harrison P. Dense granules non-specifica...

ژورنال: :مجله دانشگاه علوم پزشکی مازندران 0
سیدمحمدباقر هاشمی سوته m.b hashemi soteh çellular and molecular biology research çenter, faculty of medicine, mazandaran üniversity of medical sciences, sari, ïran.ساری: کیلومتر 18 جاده خزر آباد، مجتمع دانشگاهی پیامبر اعظم، دانشکده پزشکی آیلی علی اصغریان a âliasgharian حسین جلالی h jalali سیده نرگس نجاتی فرد s.n nejati fard مهرنوش کوثریان m kosarian حسین کرمی h karami

سابقه و هدف: جهش در ژن فاکتورv لیدن (g1691a)، جهش در پروموتور پروترومبین (g20210a) و جهش c667t در ژن سازنده آنزیم متیلن تتراهیدروفولات ردوکتاز (mthfr) از تغییرات ژنتیکی هستند که خطر ترومبوز را افزایش می دهند. هدف از این مطالعه تعیین فراوانی سه ریسک فاکتور فوق در بیماران مبتلا به تالاسمی ماژور، تالاسمی اینترمدیا و مقایسه آن با افراد سالم می باشد.مواد و روش ها: در این مطالعه 164 نفر شامل 59 بیمار...

Journal: :Annals of neurology 2004
Otfried M Debus Andrea Kosch Ronald Sträter Rainer Rossi Ulrike Nowak-Göttl

This study was initiated to investigate prothrombotic risk factors in children with porencephaly. 76 porencephalic and 76 healthy infants were investigated for factor V (FV) G1691A mutation, factor II G20210A variant, methylenetetrahydrofolate reductase (MTHFR) C677T genotype, lipoprotein (a), protein C, protein S, and antithrombin. Only the FV mutation (p = 0.005) and combinations of two or th...

Journal: :Blood 2012
Aisha Bruce M Patricia Massicotte

In this issue of Blood, Holzhauer et al have determined a novel method of identifying patients with protein C, protein S, and antithrombin deficiency who are at increased risk of developing venous thromboembolism (VTE; see figure). Children with VTE and their relatives were screened for inherited thrombophilia including proteins C and S and antithrombin deficiency; and Factor (F)V G1691A and FI...

2012
Waheed Gul Khurram Abbass Arif M. Qazi Ronald J. Markert Christopher J. Barde

Laparoscopic cholecystectomy is now the gold standard for the treatment of symptomatic cholelithiasis. Portal venous thrombosis after laparoscopic cholecystectomy is rare. We report a case of thrombosis of the portal venous system after laparoscopic cholecystectomy in a patient with a latent prothrombin gene mutation. An abdominal computed tomography and magnetic resonance angiogram of the abd...

Journal: :Clinical chemistry and laboratory medicine 2014
Emmanuel J Favaloro

There has been increasing recognition of various laboratory markers of thrombophilia that are associated with increased risk of thrombosis either through hereditary (especially Factor V Leiden, prothrombin G20210A mutation, and protein C, S and antithrombin deficiencies) and/or acquired means (e.g., antiphospholipid antibodies) over past decades. This has led to an explosion of clinical request...

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