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1
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0026576594
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Natural antibodies to factor VIII (antihemophilic factor) in healthy individuals
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Algiman M, Dietrich G, Nydegger UE, Boieldieu D, Sultan Y, Kazatchkine (1992) Natural antibodies to factor VIII (antihemophilic factor) in healthy individuals. Proc Natl Acad Sci USA 89:3795-3799
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Algiman, M.1
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Nydegger, U.E.3
Boieldieu, D.4
Sultan, Y.5
Kazatchkine6
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2
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0024400371
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A monoclonal antibody to von Willebrand factor (vWF) inhibits factor VIII binding. Localization of its antigenic determinant to a nonadecapeptide at the amino terminus of the mature vWF polypeptide
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Bahou WF, Ginsburg D, Sikkink R, Litwiller R, Pass DN (1991) A monoclonal antibody to von Willebrand factor (vWF) inhibits factor VIII binding. Localization of its antigenic determinant to a nonadecapeptide at the amino terminus of the mature vWF polypeptide. J Clin Invest 84:56-61
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4
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15844362843
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Antibodies to factor VIII in plasma of patients with hemophilia A and normal subjects
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Batlle J, Gómez E, Castiñeira P, Lourés E, Couselo M, Vila P, Sedano C, Tusell X, Magallón M, Quintana M, González-Boullosa R, López Fernández MF (1996) Antibodies to factor VIII in plasma of patients with hemophilia A and normal subjects. Ann Hematol 72:321-326
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An alloantibody to von Willebrand factor selectively inhibiting the binding of von Willebrand factor to collagen in a patient with severe von Willebrand disease
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abstract
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Budde U, Effenberg W, Oldenburg J, Schneppenheim R, van Genderen P, Drewke E, Brackmann HH (1995) An alloantibody to von Willebrand factor selectively inhibiting the binding of von Willebrand factor to collagen in a patient with severe von Willebrand disease. Thromb Haemost 73:1161 (abstract)
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6
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0023217139
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A major factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand factor
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Foster PA, Fulcher CA, Marti T, Titani K, Zimmerman TS (1987) A major factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand factor. J Biol Chem 262:8443-8446
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7
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A synthetic factor VIII peptide of eight amino acid residues (1677-1684) contains the binding region of an anti-factor VIII antibody which inhibits the binding of factor VIII to von Willebrand factor
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Foster PA, Fulcher CA, Hounghten RA, Zimmerman TS (1990) A synthetic factor VIII peptide of eight amino acid residues (1677-1684) contains the binding region of an anti-factor VIII antibody which inhibits the binding of factor VIII to von Willebrand factor. Thromb Haemost 63:403-406
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8
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Characterization of the human factor VIII procoagulant protein with a heterologous precipitating antibody
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Fulcher, C.A.1
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Localization of human factor VIII inhibitor epitopes to two polypeptide fragments
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10
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Apparent IgG anti-factor VIII antibodies in normal individuals are specific for ABO blood group substances
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abstract
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Gill JC, Stephany K, Newton-Nash D, Foster PA (1995) Apparent IgG anti-factor VIII antibodies in normal individuals are specific for ABO blood group substances. Blood 86:611a (abstract)
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Replacement therapy for surgery in type III von Willebrand patient with inhibitors to factor VIII procoagulant
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abstract
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Hanna, W.T.1
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0016665839
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A more uniform measurement of factor VIII inhibitors
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Kasper CK, Aledort LM, Counts RB, Edson JR, Fratantoni J, Green D, Hampton JW, Hilgartner M, Lazerson J, Levine PH, McMillan CW, Pool JG, Shapiro SS, Shulman NR, van Eys J (1975) A more uniform measurement of factor VIII inhibitors. Thromb Diath Haemorrh 34:869-872
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Production and characterization of recombinant factor VIII
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15
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0026562062
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Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII
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López Fernández MF, Blanco López MJ, Castiñeira MP, Batlle J (1992) Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII. Am J Hematol 40:20-27
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17
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A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction
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Mazurier C, Dieval J, Jorieux S, Delobel J, Goudemand M (1990) A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction. Blood 75:20-26
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18
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0025116340
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Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed as mild hemophilia A and hemophilia A carriers: Consequences for therapy and genetic counselling
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Mazurier C, Gaucher C, Jorieux S, Parquet-Gernez A, Goudemand M (1990) Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed as mild hemophilia A and hemophilia A carriers: consequences for therapy and genetic counselling. Br J Haematol 76:372-379
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19
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0024425034
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Nishino M, Girma JP, Rothschild C, Fressinaud E, Meyer D (1989) New variant of von Willebrand disease with defective binding to factor VIII. Blood 74:1591-1599
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A case of recessive type 2N von Willebrand's disease due to Arg 53 Trp substitution
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Two distinct forms of factor VIII coagulant protein in human plasma. Cleavage by thrombin and differences in coagulant activity and association with von Willebrand factor
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