Cardiology patient pages. Homocysteine and MTHFR mutations: relation to thrombosis and coronary artery disease.
about
Migraine in the era of precision medicineBudd-Chiari syndromeGenetic epidemiology of coronary artery disease: an Asian Indian perspectiveHeterogenous Distribution of MTHFR Gene Variants among Mestizos and Diverse Amerindian Groups from MexicoAssociations of MTHFR C677T polymorphism with insulin resistance, results of NURSE Study (Nursing Unacquainted Related Stress Etiologies)Successful conservative treatment of myocardial infarction in a teenager with MTHFR mutationPaget-Schroetter syndrome forerunning the diagnoses of thoracic outlet syndrome and thrombophilia.Homocysteine, methylenetetrahydrofolate reductase C677T polymorphism, and risk of retinal vein occlusion: an updated meta-analysis.Folic acid mitigates angiotensin-II-induced blood pressure and renal remodeling.The application of a chemical determination of N-homocysteinylation levels in developing mouse embryos: implication for folate responsive birth defects.In silico analyses of metagenomes from human atherosclerotic plaque samples.Association between methylenetetrahydrofolate reductase (MTHFR) polymorphism and carotid intima medial thickness progression in post ischaemic stroke patientChallenges in the diagnosis and treatment of pediatric stroke.Association study of methylenetetrahydrofolate reductase A1298C mutation with cerebral venous thrombosis risk in an Iranian population.Recurrent unprovoked venous thromboembolism in a young female patient with high levels of homocysteine.Are centenarians genetically predisposed to lower disease risk?Anxiety and Methylenetetrahydrofolate Reductase Mutation Treated With S-Adenosyl Methionine and Methylated B Vitamins.Intracardiac Thrombosis Involving All Four Cardiac Chambers after Extracardiac Membranous Oxygenation Associated with MTHFR MutationsHemolysis and hyperhomocysteinemia caused by cobalamin deficiency: three case reports and review of the literature.Mendelian randomization analysis of the effect of maternal homocysteine during pregnancy, as represented by maternal MTHFR C677T genotype, on birth weightThrombotic genetic risk factors and warfarin pharmacogenetic variants in São Miguel's healthy population (Azores)The MTHFR 677T allele may influence the severity and biochemical risk factors of Alzheimer's disease in an Egyptian populationInherited metabolic disorders and cerebral infarction.Laboratory informatics based evaluation of methylene tetrahydrofolate reductase C677T genetic test overutilization.Papilloedema associated with dural venous sinus thrombosis.The role of micronutrients in the response to ambient air pollutants: Potential mechanisms and suggestions for research design.Evaluation of homocysteine levels in individuals having nonsyndromic cleft lip with or without palate.Subdural Hematoma Associated With Labor Epidural Analgesia: A Case Series.A plasma proteomics method reveals links between ischemic stroke and MTHFR C677T genotype.The association between plasma homocysteine and coronary heart disease is modified by the MTHFR 677C>T polymorphism.Livedoid vasculopathy in a patient with lupus anticoagulant and MTHFR mutation: treatment with low-molecular-weight heparin.Congenital MTHFR deficiency causing early-onset cerebral stroke in a case homozygous for MTHFR thermolabile variant.Severe Hyperhomocysteinemia Decreases Creatine Kinase Activity and Causes Memory Impairment: Neuroprotective Role of Creatine.Differentiation of antemortem pulmonary thromboembolism and postmortem clot with unenhanced MRI: a case report.Young adults with coeliac disease may be at increased risk of early atherosclerosis.Thrombophilia testing in children: a 7 year experience.Prevalence of Homocysteine-Related Hypertension in Patients With Chronic Kidney Disease.Familial perinatal liver disease and fetal thrombotic vasculopathy.Sildenafil-related cerebral venous sinus thrombosis and papilledema: a case report of a rare entity.Xanthine calculi in a patient with Lesch-Nyhan syndrome and factor V Leiden treated with allopurinol: case report.
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Cardiology patient pages. Homocysteine and MTHFR mutations: relation to thrombosis and coronary artery disease.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Cardiology patient pages. Homo ...... s and coronary artery disease.
@en
Cardiology patient pages. Homo ...... s and coronary artery disease.
@nl
type
label
Cardiology patient pages. Homo ...... s and coronary artery disease.
@en
Cardiology patient pages. Homo ...... s and coronary artery disease.
@nl
prefLabel
Cardiology patient pages. Homo ...... s and coronary artery disease.
@en
Cardiology patient pages. Homo ...... s and coronary artery disease.
@nl
P2093
P1433
P1476
Cardiology patient pages. Homo ...... s and coronary artery disease.
@en
P2093
Amy C Sturm
Caron P Misita
Elizabeth A Varga
Stephan Moll
P304
P356
10.1161/01.CIR.0000165142.37711.E7
P407
P577
2005-05-01T00:00:00Z