نتایج جستجو برای: methylenetetrahydrofolate reductase gene

تعداد نتایج: 1173819  

Journal: :International Journal of Technology: IJ Tech 2022

Hypertension has relatively large morbidity and mortality rates throughout the world, including in Indonesia. The prevalence of hypertension tends to be greater patients with a family history hypertension. This is thought influenced by polymorphisms

بارگاهی, نسرین , طباطبائی, سید محمود , منفردان, امیر, نیکانفر , مسعود,

 Background & Aims: Brain infractions with Ischemic strokes are the most common and important causes of death in human communities. Studying genetic factors as prognostic factors has an important role in the control and reduction of irreversible ischemic brain damages. This study aimed to investigate methylenetetrahydrofolate reductase (MTHFR) gene mutation with a frequency greater than expecte...

Journal: :Hypertension 1999
K M O'Shaughnessy B Fu F Ferraro I Lewis S Downing N H Morris

Preeclampsia is a heritable condition that develops as a result of widespread vascular endothelial dysfunction. The thrombotic tendency in this condition has suggested a number of candidate genes, and there have been recent reports of positive association with the Leiden variant of factor V and the thermolabile variant of methylenetetrahydrofolate reductase. We attempted to reproduce these resu...

Journal: :Pediatric neurology 2003
Sameiro Barreirinho Anabela Ferro Manuela Santos E lísio Costa Jorge Pinto-Basto Alda Sousa Jorge Sequeiros Patricia Maciel Clara Barbot José Barbot

The aim of this study was to identify hereditary and acquired risk-factors as they are related to the occurrence of stroke in children. We identified 21 children with stroke. A search of the Factor V Leiden mutation, the Factor II G20210A variant, and the thermolabile variant of methylenetetrahydrofolate reductase was performed in patients and in a control group (n = 115). We identified risk fa...

Journal: :Archives of disease in childhood 1989
E Holme B Kjellman E Ronge

A 24 day old girl with homocystinuria and hypomethioninaemia caused by methylenetetrahydrofolate reductase deficiency presented with rapidly progressing encephalopathy and myopathy. An almost complete recovery was achieved by treatment with betaine.

Journal: :Journal of the American College of Cardiology 1998

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