نتایج جستجو برای: methylenetetrahydrofolate reductase nadph2

تعداد نتایج: 44962  

Journal: :Journal of the Korean neurological association 2022

Decrease in the activity of methylenetetrahydrofolate reductase (MTHFR) increases level homocysteine. MTHFR C677T gene polymorphism has been reported as a well-known cause elevated homocysteine associated with cerebral venous sinus thrombosis (CVST). A 34-year-old male was admitted severe headache after generalized seizure. Brain magnetic resonance venography showed thrombus superior sagittal s...

Journal: :Blood 1999
J Chipeta Y Komeda X L Zhang M Sakurai E Azuma

important genetic-environmental interaction. Blood 91:4158, 1998 2. Jacques PF, Bostom AG, Williams RR, Ellison RC, Eckfeldt JH, Rosenberg IH, Selhub J, Rozen R: Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation 93:7, 1996 3. Verhoef P, Kok FJ, Kluijtmans LAJ, Blom HJ, Refsum H, Ueland PM, Kruyssen DACM:...

1999
I. M. H. Chalmers

important genetic-environmental interaction. Blood 91:4158, 1998 2. Jacques PF, Bostom AG, Williams RR, Ellison RC, Eckfeldt JH, Rosenberg IH, Selhub J, Rozen R: Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation 93:7, 1996 3. Verhoef P, Kok FJ, Kluijtmans LAJ, Blom HJ, Refsum H, Ueland PM, Kruyssen DACM:...

Journal: :Croatian medical journal 2009
Irena Jukic Jasna Bingulac-Popovic Vesna Dogic Ivana Babic Jelena Culej Maja Tomicic Tomislav Vuk Dorotea Sarlija Melita Balija

AIM To assess the association between ABO blood group genotypes and genetic risk factors for thrombosis (FV Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations) in the Croatian population and to determine whether genetic predisposition to thrombotic risk is higher in non-OO blood group genotypes than in OO blood group genotypes. METHODS The study included 154 ...

Farsinejad, Alireza, Ala, Fereydoun , Faranoush, Mohammad, Kazemzadeh, Shima, Mohammadi, Rezvan , Shadkam Farokhi, Fatemeh, Shafiian, Alireza,

Background: The most common polymorphisms identified in the Methylenetetrahydrofolate reductase (MTHFR) gene, C677T and A1298C lead to defective activity of this enzyme and increase the risk of venous and arterial thrombosis. There are limited investigations regarding the effects of thrombogenic polymorphisms on the clinical phenotypes of rare hereditary hemorrhagic disorders like Glanzmann's t...

Journal: :Haematologica 2004
Franca Franchi Irene Cetin Tullia Todros Patrizio Antonazzo Maria S Nobile de Santis Simona Cardaropoli Paolo Bucciarelli Eugenia Biguzzi

BACKGROUND AND OBJECTIVES Intrauterine growth restriction is an important cause of morbidity and mortality. Its pathogenesis is still a matter of debate. The aim of this study was to evaluate the association between intrauterine growth restriction (diagnosed in utero by serial ultrasound examinations and characterized by abnormal umbilical arterial Doppler velocimetry) and thrombophilic polymor...

Journal: :Proceedings of the National Academy of Sciences 2005

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