D'Amato N, Correale M, D'Agostino C. Aortic thrombus and acute pulmonary embolism in an individual heterozygous for the MTHFR C677T mutation, Rev Esp Cardiol ;63:1366....
Out of these 88 Tao inhabitants, including 48 p.D47E carriers and 40 non-carriers, 3 p.D47E carriers and 2 non-carriers were found to be heterozygous for the MTHFR C677T genotype. No homozygote for C677T was identified in this cohort. The frequency of T allele in Tao was around 2....
MTHFR C677T polymorphism and recurrent early pregnancy loss risk in north Indian population. The OR for heterozygous CT in the REPL versus controls is 1.9591 (95% CI = 1.0285-3.7318, P = .04). The OR for TT homozygous is 6.3009 (95% ... RR Nair,A Khanna,K Singh - 《Reproductive Sc...
Buy Now for $19.90 Payments are secure & encryptedSummaryIn homozygous self-compatible genotypes 100% of the pollen grains are potentially able to grow through their own pistil, and thus the rate of self-fertilization could be higher than in heterozygous self-compatible genotypes. To evaluate the...
After an enhanced laboratory examination, multiple inherited factors associated with thrombophilia were dis- covered in our patient: heterozygosity for FV Leiden, FII 20210A, and MTHFR C677T, together with the PAI-1 4G/4G genotype. It has been established that the presence of either FV Leiden ...
Aortic thrombus and acute pulmonary embolism in an individual heterozygous for the MTHFR C677T mutation. Rev Esp Cardiol 2010;63: 1366.D'Amato N, Correale M, D'Agostino C. Aortic thrombus and acute pulmonary embolism in an individual heterozygous for the MTHFR C677T mutation. Rev Esp ...
The article discusses two cases where the Taqman system failed to accurately genotype the MTHFR C677T polymorphism due to a rare GA heterozygous mutation at the MTHFR 679 locus. The study highlights the challenges in genotyping methodologies and emphasizes the need for adaptability in clinical ...
The MTHFR C677T polymorphism confers a high risk for stroke in both homozygous and heterozygous T allele carriers with Type 2 diabetes. M. P. Hermans,J.-L. Gala<. Diabetic Medicine . 2006Hermans, M., Gala, J., & Buysschaert, M. (2006). The MTHFR CT polymorphism confers a high ...
Retinal origin of the chief complaint was further confirmed by OCT, which showed thinning of the NFL in the corresponding region of the retina OS. Coagulopathy evaluation revealed C677T/A1298C compound heterozygous genotype for MTHFR, and plasma homocysteine level after 6 months of folate and ...
Investigation of subsequent fetal losses revealed homozygosity for the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism associated both with fetal loss and with osteoporosis (OP). Because her neonatal unilateral blindness and OP were suggestive of loss-of-function mutation(s) in the gene ...