Compounds > homocysteine

homocysteine and Antithrombin III Deficiency

homocysteine has been researched along with Antithrombin III Deficiency in 9 studies

Research

Studies (9)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	7 (77.78)	18.2507
2000's	1 (11.11)	29.6817
2010's	1 (11.11)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Freiberg, RA; Glueck, CJ; Jetty, V; Wang, P	1
Varga, E	1
de Vries, JI; Dekker, GA; Doelitzsch, PM; Huijgens, PC; Jakobs, C; van Geijn, HP; von Blomberg, BM	1
Clark, WM; Coull, BM	1
Florell, SR; Rodgers, GM	1
Bernardi, F; Coccheri, S; Ferraresi, P; Grauso, F; Grossi, G; Legnani, C; Marchetti, G; Palareti, G; Piazzi, S; Sassi, S	1
Kaplan, R; Rao, AK; Sheth, S	1
Ballerini, G; Gemmati, D; Mari, R; Moratelli, S; Scapoli, GL; Serino, ML	1
Arroliga, AC; Marelich, GP; Matthay, RA; Murin, S	1

Reviews

5 review(s) available for homocysteine and Antithrombin III Deficiency

Article	Year
Inherited thrombophilia: key points for genetic counseling. Journal of genetic counseling, 2007, Volume: 16, Issue:3 Topics: Abortion, Habitual; Antithrombin III Deficiency; Factor V; Female; Genetic Counseling; Genetic Predisposition to Disease; Genetic Testing; Homocysteine; Humans; Male; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Genetic; Pregnancy; Prothrombin; Referral and Consultation; Risk Assessment; Thromboembolism; Thrombophilia	2007
Abnormalities of hemostasis in ischemic stroke. The Medical clinics of North America, 1993, Volume: 77, Issue:1 Topics: Antithrombin III Deficiency; Cerebrovascular Disorders; Hemoglobin SC Disease; Hemostasis; Homocysteine; Humans; Myeloproliferative Disorders; Protein C Deficiency; Protein S Deficiency	1993
Inherited thrombotic disorders: an update. American journal of hematology, 1997, Volume: 54, Issue:1 Topics: Antithrombin III Deficiency; Blood Coagulation; Factor V; Female; Homocysteine; Humans; Male; Point Mutation; Protein C; Protein S; Thrombosis	1997
Inherited hypercoagulable states. Vascular medicine (London, England), 1997, Volume: 2, Issue:4 Topics: Antithrombin III Deficiency; Blood Coagulation Disorders; Female; Fibrinogen; Fibrinolysis; Genetic Variation; Homocysteine; Humans; Male; Mutation; Pregnancy; Protein C; Prothrombin; Risk Factors; Thromboembolism	1997
Hereditary thrombophilia and venous thromboembolism. American journal of respiratory and critical care medicine, 1998, Volume: 158, Issue:5 Pt 1 Topics: Antithrombin III Deficiency; Factor V; Genetic Predisposition to Disease; Homocysteine; Humans; Mutation; Prevalence; Protein C; Protein C Deficiency; Protein S Deficiency; Prothrombin; Thrombophilia; Venous Thrombosis	1998

Other Studies

4 other study(ies) available for homocysteine and Antithrombin III Deficiency

Article	Year
Venous Thromboembolism After Knee Arthroscopy in Undiagnosed Familial Thrombophilia. Orthopedics, 2016, Nov-01, Volume: 39, Issue:6 Topics: Antibodies, Anticardiolipin; Antithrombin III Deficiency; Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee; Arthroscopy; Blood Coagulation Factor Inhibitors; Blood Coagulation Factors; Factor V; Factor VIII; Factor XI; Female; Homocysteine; Humans; Knee Joint; Male; Methylenetetrahydrofolate Reductase (NADPH2); Mutation; Plasminogen Activator Inhibitor 1; Prothrombin; Thrombophilia; Venous Thromboembolism	2016
Underlying disorders associated with severe early-onset preeclampsia. American journal of obstetrics and gynecology, 1995, Volume: 173, Issue:4 Topics: Antibodies, Anticardiolipin; Antithrombin III Deficiency; Female; Homocysteine; Humans; Hypertension; Pre-Eclampsia; Pregnancy; Protein C; Protein S Deficiency; Thrombosis	1995
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects. Arteriosclerosis, thrombosis, and vascular biology, 1997, Volume: 17, Issue:11 Topics: Adult; Aged; Antithrombin III; Antithrombin III Deficiency; Disease Susceptibility; Enzyme Activation; Factor V; Gene Frequency; Genotype; Homocysteine; Homocystine; Humans; Italy; Male; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Protein C; Protein S Deficiency; Risk Factors; Thrombophilia	1997
Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1998, Volume: 9, Issue:2 Topics: Adult; Aged; Antithrombin III; Antithrombin III Deficiency; Factor V; Female; Homocysteine; Humans; Male; Mutation; Pedigree; Phenotype; Risk Factors; Thrombosis	1998