arginine and Hemophilia A

arginine has been researched along with Hemophilia A in 27 studies

Research

Studies (27)

Timeframe	Studies, this research(%)	All Research%
pre-1990	5 (18.52)	18.7374
1990's	14 (51.85)	18.2507
2000's	5 (18.52)	29.6817
2010's	2 (7.41)	24.3611
2020's	1 (3.70)	2.80

Authors

Authors	Studies
Chantarangkul, V; Clerici, M; Padovan, L; Peyvandi, F; Scalambrino, E; Tripodi, A	1
Fay, PJ; Nogami, K; Shima, M; Wakabayashi, H; Yada, K	1
Eckhardt, CL; Fijnvandraat, K; Geskus, RB; Kamphuisen, PW; Menke, LA; Peters, M; van der Lee, JH; van Ommen, CH	1
Griffiths, AB; Nath, SV; Revesz, T; Williams, VK	1
Buhot, C; Burny, W; Chaux, P; Demotte, N; Jacquemin, M; Lavend'homme, R; Maillere, B; Peerlinck, K; Saint-Remy, JM; van der Bruggen, P; Vantomme, V; Vermylen, J	1
Fay, PJ; Nogami, K; Wakabayashi, H; Zhou, Q	1
Bayry, J; Christophe, O; Dasgupta, S; Delignat, S; Friboulet, A; Hoebeke, J; Kaveri, SV; Kazatchkine, MD; Lacroix-Desmazes, S; Nagaraja, V; Reinbolt, J; Saenko, E; Wootla, B	1
Hamada, M; Matsui, H; Mizuno, T; Shida, Y; Sugimoto, M; Yoshioka, A	1
Mihara, H; Satsuma, J; Yoshihara, H	1
Kamisue, S; Kuramoto, A; Morichika, S; Nakai, H; Nishimura, T; Shima, M; Takata, N; Tanaka, I; Yoshioka, A	1
Arai, M; Fukutake, K; Gale, K; Inoue, M; Kagawa, K; Kamisue, S; Morichika, S; Nakai, H; Shima, M; Suzuki, H; Tanaka, I; Tuddenham, EG; Yoshioka, A	1
Healey, JF; Liu, M; Lollar, P; Murphy, ME; Saenko, EL; Scandella, D; Thompson, AR	1
Amano, K; Kaufman, RJ; Michnick, DA; Moussalli, M	1
Gu, J; Lavergne, JM; Meyer, D; Ruan, C	1
Eickhorst, AN; Kaufman, RJ; McKinley, SH; Pipe, SW; Saenko, EL	1
Antonarakis, SE; Enayat, MS; Higuchi, M; Hill, FG; Kazazian, HH; Theophilus, BD	1
Bardin, JM; Baudis, M; Deburgrave, N; Delpech, M; Kaplan, JC; Nafa, K; Sultan, Y	1
Acquila, M; Krepelová, A; Mori, P; Vorlová, Z	1
Reiner, AP; Stray, SM; Thompson, AR	1
Bottema, CD; Ketterling, RP; Koeberl, DD; Sommer, SS; Taylor, SA	1
Antonarakis, SE; Arai, M; Higuchi, M; Hoyer, LW; Janco, RL; Kazazian, HH; Phillips, JA	1
O'Brien, DP; Pattinson, JK; Tuddenham, EG	1
Bertina, RM; Cupers, R; Mannucci, PM; Poort, SR; Reinalda-Poot, HH; Reitsma, PH; van der Linden, IK	1
Antonarakis, SE; Fujimaki, M; Inaba, H; Kazazian, HH	1
Antonarakis, SE; Arai, M; Fujimaki, M; Higuchi, M; Hoyer, LW; Inaba, H; Kazazian, HH	1
Mannucci, PM; Pareti, FI; Ruggeri, ZM	1
Gardikas, C; Stavridis, J	1

Other Studies

27 other study(ies) available for arginine and Hemophilia A

Article	Year
Effect of emicizumab on global coagulation assays for plasma supplemented with apixaban or argatroban. Journal of thrombosis and thrombolysis, 2020, Volume: 49, Issue:3 Topics: Antibodies, Bispecific; Antibodies, Monoclonal, Humanized; Arginine; Hemophilia A; Humans; Partial Thromboplastin Time; Pipecolic Acids; Plasma; Pyrazoles; Pyridones; Sulfonamides	2020
The mild phenotype in severe hemophilia A with Arg1781His mutation is associated with enhanced binding affinity of factor VIII for factor X. Thrombosis and haemostasis, 2013, Volume: 109, Issue:6 Topics: Adult; Arginine; Factor VIII; Factor X; Factor Xa; Gene Expression Regulation; Genotype; Hemophilia A; Hemostasis; Histidine; Humans; Kinetics; Male; Mutagenesis; Mutation; Phenotype; Protein Binding; Recombinant Proteins; Thrombelastography; Thrombin	2013
Intensive peri-operative use of factor VIII and the Arg593-->Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A. Journal of thrombosis and haemostasis : JTH, 2009, Volume: 7, Issue:6 Topics: Adolescent; Adult; Arginine; Autoantibodies; Cysteine; Factor VIII; Hemophilia A; Humans; Longitudinal Studies; Middle Aged; Mutation; Perioperative Care; Retrospective Studies; Risk Factors; Severity of Illness Index; Young Adult	2009
Discrepancy in factor VIII 1-stage/2-stage activity in a child with Arg(531)--> His mutation. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2010, Volume: 21, Issue:5 Topics: Amino Acid Substitution; Arginine; Child; Factor VIII; Hemophilia A; Histidine; Humans; Male; Mutation, Missense	2010
CD4+ T-cell clones specific for wild-type factor VIII: a molecular mechanism responsible for a higher incidence of inhibitor formation in mild/moderate hemophilia A. Blood, 2003, Feb-15, Volume: 101, Issue:4 Topics: Antibodies; Antigen Presentation; Arginine; CD4-Positive T-Lymphocytes; Clone Cells; Epitope Mapping; Factor VIII; Hemophilia A; Histidine; Histocompatibility Antigens Class II; HLA-DR Antigens; HLA-DRB1 Chains; HLA-DRB4 Chains; Humans; Lymphocyte Activation; Middle Aged; Mutation; Peptide Fragments; Recombinant Proteins	2003
Thrombin-catalyzed activation of factor VIII with His substituted for Arg372 at the P1 site. Blood, 2005, Jun-01, Volume: 105, Issue:11 Topics: Amino Acid Substitution; Arginine; Catalysis; Factor VIII; Factor Xa; Hemophilia A; Histidine; Humans; Hydrolysis; Kinetics; Thrombin	2005
Catalytic IgG from patients with hemophilia A inactivate therapeutic factor VIII. Journal of immunology (Baltimore, Md. : 1950), 2006, Jul-15, Volume: 177, Issue:2 Topics: Adolescent; Adult; Aged; Antibodies, Catalytic; Arginine; Binding Sites, Antibody; Blood Coagulation; Child; Coumarins; Factor VIII; Hemophilia A; Humans; Hydrolysis; Immunoglobulin G; Middle Aged; Oligopeptides; Phenylalanine; Proline	2006
Visual evaluation of blood coagulation during mural thrombogenesis under high shear blood flow. Thrombosis research, 2008, Volume: 121, Issue:6 Topics: Adult; Anticoagulants; Arginine; Blood Coagulation; Blood Flow Velocity; Blood Platelets; Collagen; Dose-Response Relationship, Drug; Factor VIIa; Fibrin; Hemolysis; Hemophilia A; Hemorheology; Heparin; Humans; Male; Microscopy, Confocal; Microscopy, Electron, Scanning; Middle Aged; Perfusion; Pipecolic Acids; Sulfonamides; Surface Properties; Thrombosis	2008
[Mathematical simulation of the blood coagulation system]. Nihon seirigaku zasshi. Journal of the Physiological Society of Japan, 1984, Volume: 46, Issue:4 Topics: Adult; Anticoagulants; Antithrombin III; Antithrombin III Deficiency; Arginine; Blood Coagulation; Factor VII; Factor VIIa; Hemophilia A; Heparin; Humans; Male; Mathematics; Microcomputers; Models, Biological; Partial Thromboplastin Time; Pipecolic Acids; Prothrombin; Prothrombin Time; Sulfonamides	1984
Abnormal factor VIII Hiroshima: defect in crucial proteolytic cleavage by thrombin at Arg1689 detected by a novel ELISA. British journal of haematology, 1994, Volume: 86, Issue:1 Topics: Arginine; Base Sequence; DNA; Dose-Response Relationship, Drug; Enzyme-Linked Immunosorbent Assay; Factor VIII; Gene Amplification; Hemophilia A; Humans; Immunoblotting; Male; Molecular Sequence Data; Thrombin	1994
Factor VIII Ise (R2159C) in a patient with mild hemophilia A, an abnormal factor VIII with retention of function but modification of C2 epitopes. Thrombosis and haemostasis, 1997, Volume: 77, Issue:5 Topics: Adolescent; Amino Acid Sequence; Antibodies, Monoclonal; Arginine; Base Sequence; Cysteine; Deamino Arginine Vasopressin; DNA Primers; Enzyme-Linked Immunosorbent Assay; Epitopes; Exons; Factor VIII; Hemophilia A; Humans; Isoantibodies; Male; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; von Willebrand Factor	1997
Loss of tolerance to exogenous and endogenous factor VIII in a mild hemophilia A patient with an Arg593 to Cys mutation. Blood, 1997, Sep-01, Volume: 90, Issue:5 Topics: Adult; Arginine; Cysteine; Factor VIII; Hemophilia A; Humans; Immune Tolerance; Male; Point Mutation	1997
Mutation at either Arg336 or Arg562 in factor VIII is insufficient for complete resistance to activated protein C (APC)-mediated inactivation: implications for the APC resistance test. Thrombosis and haemostasis, 1998, Volume: 79, Issue:3 Topics: Animals; Arginine; Cricetinae; Drug Resistance; Factor VIII; Fibrinolytic Agents; Hemophilia A; Humans; Point Mutation; Protein C	1998
Detection by denaturing gradient gel electrophoresis of an Arg1689Cys mutation in a Chinese patient with mild hemophilia A. Chinese medical journal, 1997, Volume: 110, Issue:2 Topics: Adolescent; Arginine; Cysteine; Electrophoresis, Gel, Pulsed-Field; Factor VIII; Hemophilia A; Humans; Male; Point Mutation; Polymerase Chain Reaction; Sequence Analysis, DNA	1997
Mild hemophilia A caused by increased rate of factor VIII A2 subunit dissociation: evidence for nonproteolytic inactivation of factor VIIIa in vivo. Blood, 1999, Jan-01, Volume: 93, Issue:1 Topics: Amino Acid Substitution; Animals; Arginine; COS Cells; Factor VIIIa; Hemophilia A; Histidine; Humans; Hydrolysis; Mutagenesis, Site-Directed; Peptide Hydrolases; Phenotype; Protein Binding; Recombinant Proteins; Thrombin	1999
Independent occurrence of the novel Arg2163 to His mutation in the factor VIII gene in three unrelated families with haemophila A with different phenotypes. Mutations in brief no. 126. Online. Human mutation, 1998, Volume: 11, Issue:4 Topics: Amino Acid Substitution; Arginine; Factor VIII; Hemophilia A; Histidine; Humans; Mutation; Phenotype	1998
A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia A. Human mutation, 1992, Volume: 1, Issue:1 Topics: Arginine; Base Sequence; Blotting, Southern; Codon; DNA; Exons; Factor VIII; Female; Guanine; Hemophilia A; Humans; Leucine; Male; Middle Aged; Point Mutation; Polymerase Chain Reaction; Thymine	1992
GAA(Glu)272----AAA(Lys) and CGA(Arg)1941----CAA(Gln) in the factor VIII gene in two haemophilia A patients of Czech origin. British journal of haematology, 1992, Volume: 81, Issue:3 Topics: Amino Acid Sequence; Arginine; Base Sequence; Czechoslovakia; DNA; Factor VIII; Glutamates; Glutamic Acid; Hemophilia A; Humans; Lysine; Polymerase Chain Reaction; White People	1992
Three missense mutations in Arg codons of the factor VIII genes of mild to moderately severe hemophilia A patients. Thrombosis research, 1992, Apr-01, Volume: 66, Issue:1 Topics: Amino Acid Sequence; Arginine; Base Sequence; Codon; Factor VIII; Genetic Testing; Hemophilia A; Humans; Molecular Sequence Data; Mutation; Sequence Homology	1992
Mutations at arginine residues in two Asian hemophilia B patients. Nucleic acids research, 1990, Apr-11, Volume: 18, Issue:7 Topics: Arginine; Asia; Codon; Factor X; Hemophilia A; Humans; Mutation; Polymorphism, Restriction Fragment Length	1990
Characterization of a thrombin cleavage site mutation (Arg 1689 to Cys) in the factor VIII gene of two unrelated patients with cross-reacting material-positive hemophilia A. Blood, 1990, Jan-15, Volume: 75, Issue:2 Topics: Arginine; Base Sequence; Cross Reactions; Factor VIII; Hemophilia A; Humans; Immunosorbent Techniques; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Thrombin	1990
Purification and characterization of factor VIII 372-Cys: a hypofunctional cofactor from a patient with moderately severe hemophilia A. Blood, 1990, Apr-15, Volume: 75, Issue:8 Topics: Amino Acid Sequence; Arginine; Blotting, Western; Codon; Cysteine; DNA; Factor VIII; Hemophilia A; Humans; Molecular Sequence Data; Mutation; Nucleic Acid Hybridization; Plasma; Thrombin; von Willebrand Factor	1990
Mutations in hemophilia Bm occur at the Arg180-Val activation site or in the catalytic domain of factor IX. The Journal of biological chemistry, 1990, Jul-05, Volume: 265, Issue:19 Topics: Amino Acid Sequence; Antibodies, Monoclonal; Arginine; Binding Sites; Binding, Competitive; Chymotrypsin; DNA Restriction Enzymes; Factor IX; Factor VIIa; Factor X; Factor XIa; Hemophilia A; Humans; Molecular Sequence Data; Molecular Weight; Mutation; Protein Conformation; Prothrombin Time; Thromboplastin; Valine	1990
Mild hemophilia A resulting from Arg-to-Leu substitution in exon 26 of the factor VIII gene. Human genetics, 1989, Volume: 81, Issue:4 Topics: Arginine; Base Sequence; Codon; DNA Probes; Exons; Factor VIII; Female; Hemophilia A; Humans; Leucine; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; RNA, Messenger	1989
Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine). Proceedings of the National Academy of Sciences of the United States of America, 1989, Volume: 86, Issue:11 Topics: Arginine; Base Sequence; Factor VIII; Genes; Hemophilia A; Histidine; Humans; Immunoblotting; Molecular Sequence Data; Mutation; Thrombin	1989
Letter: Enhanced factor VIII activity in von Willebrand's disease. The New England journal of medicine, 1974, May-30, Volume: 290, Issue:22 Topics: Arginine; Blood Coagulation Tests; Blood Platelets; Factor VIII; Hemophilia A; Humans; Ristocetin; Vasopressins; von Willebrand Diseases	1974
Trypsin activity of haemophilic blood. Acta haematologica, 1970, Volume: 44, Issue:3 Topics: Amides; Ammonia; Arginine; Hemophilia A; Humans; Trypsin	1970