methionine has been researched along with Thrombophilia in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (30.00) | 18.2507 |
2000's | 7 (70.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
O'Donnell, J; Perry, DJ | 1 |
Battaglioli, T; Cattaneo, M; Mannucci, PM; Martinelli, I; Pedotti, P | 1 |
Favier, A; Galan, P; Guilland, JC; Hercberg, S; Potier de Courcy, G | 1 |
Abbate, R; Betti, I; Cappelli, S; Evangelisti, L; Fedi, S; Giusti, B; Marcucci, R; Menchini, U; Prisco, D; Sodi, A | 1 |
Alatri, A; Franchi, F; Moia, M | 1 |
Cattaneo, M; Lecchi, A; Lombardi, R; Zighetti, ML | 1 |
Cattaneo, M | 1 |
Robinson, K; van Guldener, C | 1 |
Boers, GH; Naughten, ER; Wilcken, B; Wilcken, DE; Yap, S | 1 |
Cattaneo, M; Chantarangkul, V; Mannucci, PM; Tripodi, A; Zighetti, ML | 1 |
5 review(s) available for methionine and Thrombophilia
Article | Year |
---|---|
Pharmacotherapy of hyperhomocysteinaemia in patients with thrombophilia.
Topics: Folic Acid; Homocysteine; Humans; Hyperhomocysteinemia; Methionine; Pyridoxine; Renal Insufficiency; Thrombophilia; Vitamin B 12; Vitamins | 2002 |
[Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease?. 1. Basic data].
Topics: Animals; Arteriosclerosis; Biomarkers; Cystathionine beta-Synthase; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Models, Biological; Nitric Oxide; Oxidative Stress; Oxidoreductases Acting on CH-NH Group Donors; Rats; Risk Factors; S-Adenosylmethionine; Signal Transduction; Thrombophilia; Vascular Diseases; Vasodilation; Vitamin B 6 Deficiency | 2003 |
Hyperhomocysteinemia, atherosclerosis and thrombosis.
Topics: Adult; Aged; Animals; Arteriosclerosis; Avitaminosis; Case-Control Studies; Clinical Trials as Topic; Cohort Studies; Cross-Sectional Studies; Cystathionine beta-Synthase; Female; Folic Acid; Gene Frequency; Homocysteine; Homocystinuria; Hormone Replacement Therapy; Humans; Hyperhomocysteinemia; Male; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Muscle, Smooth, Vascular; Oxidoreductases Acting on CH-NH Group Donors; Prevalence; Primates; Prospective Studies; Pyridoxine; Risk Factors; Smoking; Tamoxifen; Thrombophilia; Thrombosis; Vitamin B 12 | 1999 |
Homocysteine and renal disease.
Topics: Adult; Arteriosclerosis; Cardiovascular Diseases; Case-Control Studies; Child; Endothelium, Vascular; Female; Folic Acid; Folic Acid Deficiency; Follow-Up Studies; Homocysteine; Humans; Hyperhomocysteinemia; Kidney Diseases; Kidney Failure, Chronic; Kidney Transplantation; Life Tables; Male; Methionine; Peritoneal Dialysis; Prospective Studies; Pyridoxine; Renal Dialysis; Survival Analysis; Thrombophilia; Vitamin B 12; Vitamin B 12 Deficiency; Vitamin B 6 Deficiency | 2000 |
Vascular complications of severe hyperhomocysteinemia in patients with homocystinuria due to cystathionine beta-synthase deficiency: effects of homocysteine-lowering therapy.
Topics: Adolescent; Adult; Aged; Australia; Child; Child, Preschool; Cohort Studies; Cystine; Drug Resistance; Female; Folic Acid; Follow-Up Studies; Genetic Predisposition to Disease; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Infant; Ireland; Male; Methionine; Middle Aged; Netherlands; Pyridoxine; Risk; Risk Factors; Thrombophilia; Vascular Diseases; Vitamin B 12 | 2000 |
5 other study(ies) available for methionine and Thrombophilia
Article | Year |
---|---|
Hyperhomocysteinemia in cerebral vein thrombosis.
Topics: Adolescent; Adult; Case-Control Studies; Child; Female; Folic Acid; Homocystine; Humans; Hyperhomocysteinemia; Intracranial Thrombosis; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Oxidoreductases Acting on CH-NH Group Donors; Risk Factors; Thrombophilia; Venous Thrombosis; Vitamin B 12 | 2003 |
Genetic determinants of fasting and post-methionine hyperhomocysteinemia in patients with retinal vein occlusion.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Cystathionine beta-Synthase; Fasting; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Hyperhomocysteinemia; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Mutagenesis, Insertional; Mutation, Missense; Point Mutation; Polymorphism, Genetic; Retinal Vein Occlusion; Risk Factors; Thrombophilia | 2003 |
Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.
Topics: 3' Untranslated Regions; Adult; Aged; Brain Ischemia; Female; Genetic Predisposition to Disease; Homocysteine; Homozygote; Humans; Male; Methionine; Middle Aged; Prothrombin; Risk Factors; Thrombophilia; Thrombophlebitis | 1998 |
Is the oral methionine loading test insensitive to the remethylation pathway of homocysteine?
Topics: Artifacts; Folic Acid Deficiency; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Reproducibility of Results; Risk Factors; Thrombophilia | 1999 |
Determination of total homocysteine in plasma: comparison of the Abbott IMx immunoassay with high performance liquid chromatography.
Topics: Adult; Chromatography, High Pressure Liquid; False Negative Reactions; Fasting; Female; Homocysteine; Humans; Hyperhomocysteinemia; Immunoassay; Male; Methionine; Middle Aged; Photochemistry; Reagent Kits, Diagnostic; Reproducibility of Results; Sensitivity and Specificity; Thrombophilia; Thrombosis | 2002 |