arginine has been researched along with Deficiency, Protein S in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (60.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Maldonado, A | 1 |
| Chan, LC; Chan, NP; Chan, TL; Fan, YH; Lam, CW; Lam, WW; Leung, TW; Liu, HS; Siu, DY; Wong, KS; Yip, SF | 1 |
| Dahlbäck, B; Zöller, B | 1 |
| Hamaguchi, M; Kagami, K; Katsumi, A; Kojima, T; Okamoto, Y; Saito, H; Sugiura, I; Takamatsu, J; Yamazaki, T | 1 |
| Alving, BM; Carrington, LR; Gillespie, DL; Griffin, JH | 1 |
5 other study(ies) available for arginine and Deficiency, Protein S
| Article | Year |
|---|---|
Argatroban and catheter-directed thrombolysis with alteplase for limb- and graft-threatening thromboses in a patient with a history of HIT.
Topics: Aged; Antibodies, Anticardiolipin; Anticoagulants; Arginine; Catheterization; Contraindications; Drug Therapy, Combination; Femoral Vein; Heparin; Humans; Iliac Vein; Infusions, Intravenous; Ischemia; Kidney; Kidney Transplantation; Male; Pipecolic Acids; Popliteal Vein; Postoperative Complications; Protein S Deficiency; Purpura, Thrombocytopenic, Idiopathic; Renal Veins; Sulfonamides; Thrombolytic Therapy; Thrombophilia; Tissue Plasminogen Activator; Vena Cava Filters; Venous Thrombosis; Warfarin | 2009 |
Genetic predisposition of white matter infarction with protein S deficiency and R355C mutation.
Topics: Adolescent; Adult; Aged; Arginine; Brain; Cerebral Infarction; Child; Cysteine; Female; Genetic Predisposition to Disease; Haplotypes; Hong Kong; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Molecular Sequence Annotation; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Protein S; Protein S Deficiency; Risk Factors; Young Adult | 2010 |
Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis.
Topics: Alleles; Arginine; Base Sequence; DNA; DNA Primers; Factor V; Female; Genetic Linkage; Humans; Male; Molecular Sequence Data; Partial Thromboplastin Time; Pedigree; Point Mutation; Polymerase Chain Reaction; Protein C; Protein S Deficiency; Radioimmunoassay; Thrombophlebitis | 1994 |
Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474.
Topics: Androgen-Binding Protein; Animals; Arginine; Base Sequence; Binding Sites; Cattle; Cell Line, Transformed; Chlorocebus aethiops; CHO Cells; Consanguinity; Cricetinae; Cysteine; DNA, Complementary; Female; Genetic Predisposition to Disease; Genetic Vectors; Humans; Laminin; Male; Middle Aged; Molecular Sequence Data; Point Mutation; Protein S; Protein S Deficiency; Rabbits; Rats; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Thrombosis | 1996 |
Resistance to activated protein C: a common inherited cause of venous thrombosis.
Topics: Adolescent; Adult; Anticoagulants; Antithrombin III; Arginine; Contraceptives, Oral; DNA; Drug Resistance; Factor V; Female; Glutamine; Humans; Male; Middle Aged; Mutation; Obesity; Pregnancy; Protein C; Protein C Deficiency; Protein S Deficiency; Recurrence; Risk Factors; Thromboembolism; Thrombophlebitis | 1996 |