Hydroxyurea: Effects on Hemoglobin F Production in Patients With Sickle Cell Anemia von Charache, Samuel, Dover, George J., Moore, Richard D., Eckert, S., Ballas, Samir K., Koshy, Mabel, Milner, Paul F.A., Orringer, Eugene P., Phillips, George, Platt, Orah S., Thomas, George H.

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Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency von HASSOUN, H, VASSILIADIS, J. N, MURRAY, J, NJOLSTAD, P. R, ROGUS, J. J, BALLAS, S. K, SCHAFFER, F, JAROLIM, P, BRABEC, V, PALEK, J

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Erythropoietic activity in patients with sickle cell anaemia before and after treatment with hydroxyurea von Ballas, Samir, Marcolina, Mary, Dover, George, Barton, Franca

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Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency von JAROLIM, P, MURRAY, J. L, PALEK, J, RUBIN, H. L, TAYLOR, W. M, PRCHAL, J. T, BALLAS, S. K, SNYDER, L. M, CHROBAK, L, MELROSE, W. D, BRABEC, V

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Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24 von Grootenboer, Sabine, Schischmanoff, Pierre-Olivier, Laurendeau, Ingrid, Cynober, Thérèsa, Tchernia, Gil, Dommergues, Jean-Paul, Dhermy, Didier, Bost, Mireille, Varet, Bruno, Snyder, Michael, Ballas, Samir K., Ducot, Béatrice, Babron, Marie-Claude, Stewart, Gordon W., Gasparini, Paolo, Iolascon, Achille, Delaunay, Jean

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Drugs for preventing red blood cell dehydration in people with sickle cell disease von Singh, P C, Ballas, S K

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The risks and benefits of long‐term use of hydroxyurea in sickle cell anemia: A 17.5 year follow‐up von Steinberg, Martin H., McCarthy, William F., Castro, Oswaldo, Ballas, Samir K., Armstrong, F. Danny, Smith, Wally, Ataga, Kenneth, Swerdlow, Paul, Kutlar, Abdullah, DeCastro, Laura, Waclawiw, Myron A.

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Reticulocyte hemoglobin: An integrated parameter for evaluation of erythropoietic activity von BRUGNARA, C, ZELMANOVIC, D, SORETTE, M, BALLAS, S. K, PLATT, O

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Increased Preoperative Collection of Autologous Blood with Recombinant Human Erythropoietin Therapy von Goodnough, Lawrence Tim, Rudnick, Seth, Price, Thomas H, Ballas, Samir K, Collins, Myra L, Crowley, James P, Kosmin, Martin, Kruskall, Margot S, Lenes, Bruce A, Menitove, Jay E, Silberstein, Leslie E, Smith, Kenneth J, Wallas, Charles H, Abels, Robert, Von Tress, Mark

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Cost‐effectiveness of hydroxyurea in sickle cell anemia von Moore, Richard D., Charache, Samuel, Terrin, Michael L., Barton, Franca B., Ballas, Samir K.

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Sequential nitric oxide measurements during the emergency department treatment of acute vasoocclusive sickle cell crisis von Lopez, Bernard L., Davis‐Moon, Linda, Ballas, Samir K., Ma, Xin‐liang

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Revised transthyretin ile 122 allele frequency in African-Americans von JACOBSON, D. R, PASTORE, R, POOL, S, MALENDOWICZ, S, KANE, I, SHIVJI, A, EMBURY, S. H, BALLAS, S. K, BUXBAUM, J. N

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Rheologic Predictors of the Severity of the Painful Sickle Cell Crisis von Ballas, Samir K., Lamer, James, Smith, Eugene D., Surrey, Saul, Schwartz, Elias, Rappaport, Eric F.

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Molecular abnormality of erythrocyte pyruvate kinase deficiency in the Amish von KANNO, H, BALLAS, S. K, MIWA, S, FUJII, H, BOWMAN, H. S

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Band 3 Peptides Block the Adherence of Sickle Cells to Endothelial Cells In Vitro von Thevenin, Bernard J.-M., Crandall, Ian, Ballas, Samir K., Sherman, Irwin W., Shohet, Stephen B.

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Molecular Mimicry Between the Rabies Virus Glycoprotein and Human Immunodeficiency Virus-1 GP120: Cross-Reacting Antibodies Induced by Rabies Vaccination von Bracci, Luisa, Ballas, Samir K., Spreafico, Adriano, Neri, Paolo

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Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells von Ballas, Samir K.

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Nitrosylation of Sickle Cell Hemoglobin by Hydroxyurea von Xu, Yueping, Mull, Courtney D, Bonifant, Challice L, Yasaki, Genichiro, Palmer, Eric C, Shields, Howard, Ballas, Samir K, Kim-Shapiro, Daniel B, King, S. Bruce

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Pain measurement in hospitalized adults with sickle cell painful episodes von BALLAS, S. K, DELENGOWSKI, A

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Thrombosis, megaloblastic anaemia, and sickle cell disease: a unified hypothesis von Ballas, S K, Saidi, P

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