Compounds > arginine

arginine and von Willebrand Diseases

arginine has been researched along with von Willebrand Diseases in 14 studies

Research

Studies (14)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (7.14)	18.7374
1990's	11 (78.57)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (14.29)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Arion, C; Buga-Corbu, I	1
Budde, U; Castaman, G; Eikenboom, J; Federici, AB; Goodeve, A; Goudemand, J; Hampshire, D; Hickson, N; James, P; Peake, I; Rodeghiero, F; Schneppenheim, R; Winship, P	1
Batlle, J; Daly, M; Peake, I; Pérez-Casal, M	1
Harrison, P; Inbal, A; Kornbrot, N; Randi, AM; Sadler, JE	1
Alessi, MC; Boyer-Neumann, C; Lavergne, JM; Meyer, D; Piao, YC; Schandelong, A	1
Berntorp, E; Dahlbäck, B; Donnér, M; Holmberg, L; Kristoffersson, AC; Nilsson, IM; Scheibel, E; Thorsen, S	1
Arai, M; Fukutake, K; Hagiwara, T; Hanabusa, H; Inaba, H; Nagaizumi, K; Yoshida, S	1
Casonato, A; Gaucher, C; Girolami, A; Mazurier, C; Pontara, E; Zerbinati, P; Zucchetto, A	1
Aznar, JA; Casaña, P; Haya, S; Martínez, F	1
Bahnak, BR; De Paillette, L; Fressinaud, E; Lavergne, JM; Meyer, D; Pietu, G; Ribba, AS	1
Arnout, J; Briët, E; Eikenboom, JC; Peerlinck, K; Ploos Van Amstel, HK; Reitsma, PH; Sangtawesin, W; Vermylen, J	1
Andersson, AM; Dahlbäck, B; Donnér, M; Holmberg, L; Kristoffersson, AC; Nilsson, IM	1
Fahs, SA; Friedman, KD; Kroner, PA; Montgomery, RR; Scott, JP	1
Mannucci, PM; Pareti, FI; Ruggeri, ZM	1

Reviews

1 review(s) available for arginine and von Willebrand Diseases

Article	Year
Up to date concepts about Von Willebrand disease and the diagnose of this hemostatic disorder. Journal of medicine and life, 2014, Sep-15, Volume: 7, Issue:3 Topics: Arginine; Gene Components; Hemostasis; Humans; Models, Biological; Pipecolic Acids; Platelet Adhesiveness; Platelet Aggregation; Platelet Aggregation Inhibitors; Sulfonamides; von Willebrand Diseases; von Willebrand Factor	2014

Other Studies

13 other study(ies) available for arginine and von Willebrand Diseases

Article	Year
von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels. Journal of thrombosis and haemostasis : JTH, 2010, Volume: 8, Issue:9 Topics: ABO Blood-Group System; Alleles; Arginine; Case-Control Studies; Factor VIII; Founder Effect; Genetic Variation; Genotype; Glutamine; Heterozygote; Humans; Mutation; Phenotype; Recombinant Proteins; von Willebrand Diseases; von Willebrand Factor	2010
A case of recessive type 2N von Willebrand's disease due to Arg 53 Trp substitution. American journal of hematology, 1995, Volume: 48, Issue:2 Topics: Adolescent; Adult; Arginine; Factor VIII; Female; Humans; Male; Mutation; Polymerase Chain Reaction; Tryptophan; von Willebrand Diseases; von Willebrand Factor	1995
Effect of type IIB von Willebrand disease mutation Arg(545)Cys on platelet glycoprotein Ib binding--studies with recombinant von Willebrand factor. Thrombosis and haemostasis, 1993, Dec-20, Volume: 70, Issue:6 Topics: Arginine; Base Sequence; Blood Platelets; Cysteine; Humans; Molecular Sequence Data; Mutation; Platelet Membrane Glycoproteins; Recombinant Proteins; Ristocetin; von Willebrand Diseases; von Willebrand Factor	1993
Arg578Gln mutations in the von Willebrand factor gene in three unrelated cases of type IIB von Willebrand disease. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1993, Volume: 4, Issue:5 Topics: Adult; Aged; Arginine; Base Sequence; Child, Preschool; DNA, Complementary; Female; Glutamine; Humans; Male; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; von Willebrand Diseases; von Willebrand Factor	1993
Two new candidate mutations in type IIA von Willebrand's disease (Arg834-->Gly, Gly846-->Arg) and one polymorphism (Tyr821-->Cys) in the A2 region of the von Willebrand factor. European journal of haematology, 1993, Volume: 51, Issue:1 Topics: Adolescent; Adult; Alleles; Amino Acid Sequence; Arginine; Base Sequence; Child; Cysteine; DNA; Female; Genetic Markers; Glycine; Humans; Male; Molecular Sequence Data; Oligodeoxyribonucleotides; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Tyrosine; von Willebrand Diseases; von Willebrand Factor	1993
A novel mutation Gly 1672-->Arg in type 2A and a homozygous mutation in type 2B von Willebrand disease. Thrombosis and haemostasis, 1996, Volume: 76, Issue:2 Topics: Arginine; Asian People; Case-Control Studies; DNA; DNA Mutational Analysis; Exons; Glycine; Homozygote; Humans; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; von Willebrand Diseases	1996
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
Identification of a new candidate mutation, G1629R, in a family with type 2A von Willebrand disease. American journal of hematology, 1999, Volume: 60, Issue:4 Topics: Arginine; Base Sequence; Deoxyribonucleases, Type II Site-Specific; Female; Glycine; Humans; Male; Mutation; Pedigree; Spain; von Willebrand Diseases; von Willebrand Factor	1999
Defects in type IIA von Willebrand disease: a cysteine 509 to arginine substitution in the mature von Willebrand factor disrupts a disulphide loop involved in the interaction with platelet glycoprotein Ib-IX. British journal of haematology, 1992, Volume: 82, Issue:1 Topics: Arginine; Base Sequence; Cysteine; Electrophoresis, Polyacrylamide Gel; Humans; Molecular Sequence Data; Platelet Membrane Glycoproteins; Polymerase Chain Reaction; von Willebrand Diseases; von Willebrand Factor	1992
A patient with von Willebrand's disease characterized by a compound heterozygosity for a substitution of Arg854 by Gln in the putative factor-VIII-binding domain of von Willebrand factor (vWF) on one allele and very low levels of mRNA from the second vWF British journal of haematology, 1992, Volume: 80, Issue:3 Topics: Adult; Alleles; Arginine; Base Sequence; Factor VIII; Female; Glutamine; Heterozygote; Humans; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; RNA, Messenger; von Willebrand Diseases; von Willebrand Factor	1992
An Arg545----Cys545 substitution mutation of the von Willebrand factor in type IIB von Willebrand's disease. European journal of haematology, 1991, Volume: 47, Issue:5 Topics: Adult; Aged; Arginine; Base Sequence; Codon; Cysteine; DNA Probes; Family Health; Humans; Male; Molecular Sequence Data; Mutation; von Willebrand Diseases; von Willebrand Factor	1991
Abnormal binding of factor VIII is linked with the substitution of glutamine for arginine 91 in von Willebrand factor in a variant form of von Willebrand disease. The Journal of biological chemistry, 1991, Oct-15, Volume: 266, Issue:29 Topics: Arginine; Autoradiography; Base Sequence; Cell Line; Electrophoresis, Polyacrylamide Gel; Factor VIII; Gene Expression; Glutamine; Humans; Molecular Sequence Data; Mutation; Polymorphism, Genetic; RNA, Messenger; von Willebrand Diseases; von Willebrand Factor	1991
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