Childhood emotional abuse and neglect as predictors of psychological and physical symptoms in women presenting to a primary care practice von Spertus, Ilyse L, Yehuda, Rachel, Wong, Cheryl M, Halligan, Sarah, Seremetis, Stephanie V

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Pharmacokinetic analysis of plasma-derived and recombinant F IX concentrates in previously treated patients with moderate or severe hemophilia B von Ewenstein, Bruce M., Joist, J. Heinrich, Shapiro, Amy D., Hofstra, Thomas C., Leissinger, Cindy A., Seremetis, Stephanie V., Broder, Martin, Mueller-Velten, Guenther, Schwartz, Bruce A.

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Effects of recombinant factor VIIa on platelet function and clot structure in blood with deficient prothrombin conversion von Carr, Marcus E., Martin, Erika J., Kuhn, Jan G., Seremetis, Stephanie V.

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The Upward Spiral of Drug Costs: A Time Series Analysis of Drugs Used in the Treatment of Hemophilia von Rogoff, Edward G., Guirguis, Hany S., Lipton, Richard A., Seremetis, Stephanie V., DiMichele, Donna M., Agnew, George M., Karpatkin, Margaret, Barish, Robert J., Jones, Robert L., Bianco, Celso, Knothe, Barbara D., Lee, Myung-Soo

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Safety of Recombinant Activated Coagulation Factor VII in Non-Hemophilia Patients von Skolnick, Brett E., Rojkjaer, Lisa Payne, Seremetis, Stephanie V.

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Variations in Ex-Vivo Assessments of Hemostasis von Gabriel, Don A., Skolnick, Brett E., Rojkjaer, Lisa Payne, Seremetis, Stephanie V.

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An Open-Label, Randomized, Parallel, Multi-Center Trial Comparing the Safety and Efficacy of rFVIIa When Administered as I.V. Bolus or I.V. Continuous Infusion to Hemophilia Patien... von Pruthi, Rajiv K., Mathew, Prasad, Valentino, Leonard A., Seremetis, Stephanie V.

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Three-year randomised study of high-purity or intermediate-purity factor VIII concentrates in symptom-free HIV-seropositive haemophiliacs: effects on immune status von Seremetis, S.V, Aledort, L.M, Lau, T-S, Bergman, G.E, Bona, R, Rickles, F, Bray, G, Kessler, C, Brettler, D, Eyster, M.E, Lusher, J

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Impact of hemophilia treatment on the management of HIV disease von Seremetis, Stephanie V

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Modern treatment of haemophilia: choice of products for the treatment of haemophilia A and B von SEREMETIS, STEPHANIE V.

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High frequency of clonal immunoglobulin or T cell receptor gene rearrangements in acute myelogenous leukemia expressing terminal deoxyribonucleotidyltransferase von SEREMETIS, S. V, PELICCI, P.-G, TABILIO, A, UBRIACO, A, GRIGNANI, F, CUTTNER, J, WINCHESTER, R. J, KNOWLES, D. M. II, DALLA-FAVERA, R

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Congenital bleeding disorders : rational treatment options von SEREMETIS, S. V, ALEDORT, L. M

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HL-T, A New Cell Line Derived From HL-60 Promyelocytic Leukemia Cell Cultures Expressing Terminal Transferase and Secreting Suppressor Activity von Paietta, Elisabeth, Stockert, Richard J., Calvelli, Theresa, Papenhausen, Peter, Seremetis, Stephanie V., Fotino, Marilena, Wiernik, Peter H., Chang, Lucy, Bollum, Fred J.

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Risk factors for inhibitor formation in haemophilia: a prevalent case-control study von RAGNI, M. V., OJEIFO, O., FENG, J., YAN, J., HILL, K. A., SOMMER, S. S., TRUCCO, M. N., BRAMBILLA, D. J.

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TdT-Positive Acute Leukemia With Monocytoid Characteristics: Clinical, Cytochemical, Cytogenetic, and Immunologic Findings von Cuttner, Janet, Seremetis, Stephanie, Najfeld, Vesna, Dimitriu-Bona, Alexandra, Winchester, Robert A.

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Trisomy 22—A new abnormality found in acute leukemia characterized by eosinophilia and monocytoid blasts expressing immature differentiation antigens von Najfeld, Vesna, Seremetis, Stephanie, Troy, Kevin, Uehlinger, Joan, Schwartz, Paula, Cuttner, Janet

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