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Thrombosis Research|April 12, 2001
In hemophilia A and autoantibody inhibitor patients: the factor VIII A2 domain and light chain are most immunogenicD H Scandella, H Nakai, M Felch, et al.
The Journal of Biological Chemistry|June 16, 1995
Residues 484-508 contain a major determinant of the inhibitory epitope in the A2 domain of human factor VIIIJ F Healey, I M Lubin, H Nakai, et al.
The New England Journal of Medicine|April 28, 1977
A co-operative study for the detection of the carrier state of classic hemophiliaH G Klein, L M Aledort, B N Bouma, et al.
American Journal of Hematology|November 1, 1995
Acquired von Willebrand's disease: a rare manifestation of postpartum thyroiditisC A Aylesworth, R C Smallridge, M E Rick, et al.
Thrombosis Research|May 1, 1982
The identification and functional significance of factor VIII components on normal plateletsM A Flaum, J A Donlon, H R Gralnick, et al.
The British Journal of Ophthalmology|October 1, 1986
Retinal cotton-wool spots: an early finding in diabetic retinopathy?M S Roy, M E Rick, K E Higgins, et al.
Blood|March 1, 1987
Thrombocytopenia associated with pregnancy in a patient with type IIB von Willebrand's diseaseM E Rick, S B Williams, R A Sacher, et al.
The Journal of Clinical Investigation|June 1, 1994
Inhibition of human factor VIIIa by anti-A2 subunit antibodiesP Lollar, E T Parker, J E Curtis, et al.
Blood|January 15, 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 AM Arai, M Higuchi, S E Antonarakis, et al.
Blood|September 1, 1981
Normal pregnancy in a patient with a prior postpartum factor VIII inhibitor: with observations on pathogenesis and prognosisB S Coller, M B Hultin, L W Hoyer, et al.
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