arginine and Hemorrhagic Disorders
arginine has been researched along with Hemorrhagic Disorders in 5 studies
Research
Studies (5)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (40.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors
Authors | Studies |
---|---|
Arai, N; Matsumoto, T; Nogami, K; Ogiwara, K; Sasai, K; Shima, M | 1 |
Akhavan, S; De Cristofaro, R; Landolfi, R; Lavoretano, S; Mannucci, PM; Peyvandi, F | 1 |
GLUECK, HI | 1 |
Brennan, SO; Carrell, RW; Lewis, JH; Owen, MC | 1 |
Casonato, A; Gaucher, C; Girolami, A; Mazurier, C; Pontara, E; Zerbinati, P; Zucchetto, A | 1 |
Other Studies
5 other study(ies) available for arginine and Hemorrhagic Disorders
Article | Year |
---|---|
A novel simultaneous clot-fibrinolysis waveform analysis for assessing fibrin formation and clot lysis in haemorrhagic disorders.
Topics: Arginine; Fibrin; Fibrin Clot Lysis Time; Fibrinolysis; Hemorrhagic Disorders; Humans; Kinetics; Pipecolic Acids; Sulfonamides; Thrombomodulin; Tranexamic Acid | 2019 |
Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype.
Topics: Arginine; Blood Coagulation Disorders; Cell Line; Consanguinity; Factor Va; Factor Xa; Female; Fibrinopeptide A; Hemorrhagic Disorders; Heparin Cofactor II; Histidine; Homozygote; Humans; Hydrolysis; Infant; Mutagenesis, Site-Directed; Mutation; Protein C; Prothrombin; Receptor, PAR-1; Receptors, Thrombin; Thrombin; Thrombomodulin; Thromboplastin; Transfection | 2002 |
The utilization of a synthetic substrate (TAMe) to measure the plasma prothrombin in coagulation disorders.
Topics: Arginine; Blood Coagulation Disorders; Hemorrhagic Disorders; Humans; Plasma; Prothrombin; Prothrombin Time; Sulfonamides; Tosylarginine Methyl Ester | 1957 |
Mutation of antitrypsin to antithrombin. alpha 1-antitrypsin Pittsburgh (358 Met leads to Arg), a fatal bleeding disorder.
Topics: Adolescent; alpha 1-Antitrypsin; Amino Acid Sequence; Antithrombin III; Arginine; Genetic Variation; Hemorrhagic Disorders; Humans; Male; Methionine; Mutation; Pancreatic Elastase; Plasma Exchange; Wounds and Injuries | 1983 |
Type 2N von Willebrand disease due to Arg91Gln substitution and a cytosine deletion in exon 18 of the von Willebrand factor gene.
Topics: Arginine; Cytosine; Exons; Female; Gene Deletion; Hemorrhagic Disorders; Heterozygote; Humans; Middle Aged; Pedigree; Point Mutation; von Willebrand Diseases; von Willebrand Factor | 1998 |