arginine and Hemorrhagic Disorders

arginine has been researched along with Hemorrhagic Disorders in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19902 (40.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arai, N; Matsumoto, T; Nogami, K; Ogiwara, K; Sasai, K; Shima, M1
Akhavan, S; De Cristofaro, R; Landolfi, R; Lavoretano, S; Mannucci, PM; Peyvandi, F1
GLUECK, HI1
Brennan, SO; Carrell, RW; Lewis, JH; Owen, MC1
Casonato, A; Gaucher, C; Girolami, A; Mazurier, C; Pontara, E; Zerbinati, P; Zucchetto, A1

Other Studies

5 other study(ies) available for arginine and Hemorrhagic Disorders

ArticleYear
A novel simultaneous clot-fibrinolysis waveform analysis for assessing fibrin formation and clot lysis in haemorrhagic disorders.
    British journal of haematology, 2019, Volume: 187, Issue:4

    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.
    Blood, 2002, Aug-15, Volume: 100, Issue:4

    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.
    The Journal of laboratory and clinical medicine, 1957, Volume: 49, Issue:1

    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.
    The New England journal of medicine, 1983, Sep-22, Volume: 309, Issue:12

    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.
    British journal of haematology, 1998, Volume: 103, Issue:1

    Topics: Arginine; Cytosine; Exons; Female; Gene Deletion; Hemorrhagic Disorders; Heterozygote; Humans; Middle Aged; Pedigree; Point Mutation; von Willebrand Diseases; von Willebrand Factor

1998
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