Sickle Cell Disease: New Opportunities and Challenges in Africa von Ohene-Frempong, K., Wonkam, A., Nnodu, Obiageli E., Ofori-Acquah, Solomon F., Makani, J.

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S129: IMPLEMENTATION OF HYDROXYUREA THERAPY FOR SICKLE CELL DISEASE ON A LARGE SCALE IN GHANA von Ohene‐Frempong, K, Segbefia, C, Spector, J, Amoah, E, Asubonteng, A, Hammond‐Addo, R, Odame, I, Odame, I

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P‐002: MULTISPECTRAL IMAGING FOR MICROCHIP ELECTROPHORESIS ENABLES POINT‐OF‐CARE NEWBORN HEMOGLOBIN VARIANT SCREENING von R., AN, Y., HUANG, A., ROCHELEAU, A., AVANAKI, P., THOTA, Q., ZHANG, Y., MAN, Z., SEKYONDA, C., SEGBEFIA, Y., DEI‐ADOMAKOH, E., MENSAH, K., OHENE‐FREMPONG, I., ODAME, A., OWUSU‐ANSAH, U., GURKAN

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5‐hydroxymethyl‐2‐furfural modifies intracellular sickle haemoglobin and inhibits sickling of red blood cells von Abdulmalik, Osheiza, Safo, Martin K., Chen, Qiukan, Yang, Jisheng, Brugnara, Carlo, Ohene‐Frempong, Kwaku, Abraham, Donald J., Asakura, Toshio

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Effect of myeloablative bone marrow transplantation on growth in children with sickle cell anaemia: results of the multicenter study of haematopoietic cell transplantation for sick... von Eggleston, B., Patience, M., Edwards, S., Adamkiewicz, T., Buchanan, G. R., Davies, S. C., Dickerhoff, R., Donfield, S., Feig, S. A., Giller, R. H., Haight, A., Horan, J., Hsu, L. L., Kamani, N., Lane, P., Levine, J. E., Margolis, D., Moore, T. B., Ohene‐Frempong, K., Redding‐Lallinger, R., Roberts, I. A. G., Rogers, Z. R., Sanders, J. E., Scott, J. P., Sleight, B., Thompson, A. A., Sullivan, K. M., Walters, M. C.

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Silent Cerebral Infarcts in Sickle Cell Anemia: A Risk Factor Analysis von Kinney, Thomas R, Sleeper, Lynn A, Wang, Winfred C, Zimmerman, Robert A, Pegelow, Charles H, Ohene-Frempong, Kwaku, Wethers, Doris L, Bello, Jacqueline A, Vichinsky, Elliott P, Moser, Franklin G, Gallagher, Dianne M, DeBaun, Michael R, Platt, Orah S, Miller, Scott T, Cooperative Study of Sickle Cell Disease

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Sickle Cell Disease: Reference Values and Interhemispheric Differences of Nonimaging Transcranial Doppler Blood Flow Parameters von ARKUSZEWSKI, M, KREJZA, J, CHEN, R, KWIATKOWSKI, J. L, ICHORD, R, ZIMMERMAN, R, OHENE-FREMPONG, K, DESIDERIO, L, MELHEM, E. R

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Sickle cell and the brain von Adams, R J, Ohene-Frempong, K, Wang, W

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The spectrum of brain MR abnormalities in sickle-cell disease: a report from the Cooperative Study of Sickle Cell Disease von Moser, FG, Miller, ST, Bello, JA, Pegelow, CH, Zimmerman, RA, Wang, WC, Ohene- Frempong, K, Schwartz, A, Vichinsky, EP, Gallagher, D, Kinney, TR

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Different hematological phenotypes caused by the interaction of triplicated α‐globin genes and heterozygous β‐thalassemia von Camaschella, C., Kattamis, A.C., Petroni, D., Roetto, A., Sivera, P., Sbaiz, L., Cohen, A., Ohene‐Frempong, K., Trifillis, P., Surrey, S., Fortina, P.

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Association of Pulsatility Index in the Middle Cerebral Artery with Intelligence Quotient in Children with Sickle Cell Disease von Krejza, J., Arkuszewski, M., Radcliffe, J., Flynn, T.B., Chen, R., Kwiatkowski, J.L., Ichord, R., Zimmerman, R., Bilello, M., Ohene-Frempong, K., Melhem, E.R.

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Sickle Cell Disease in Children: Accuracy of Imaging Transcranial Doppler Ultrasonography in Detection of Intracranial Arterial Stenosis von Arkuszewski, M., Krejza, J., Chen, R., Kwiatkowski, J.L., Ichord, R., Zimmerman, R., Ohene-Frempong, K., Melhem, E.R.

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Cerebrovascular Accidents in Sickle Cell Disease: Rates and Risk Factors von Ohene-Frempong, Kwaku, Weiner, Steven J., Sleeper, Lynn A., Miller, Scott T., Embury, Stephen, Moohr, John W., Wethers, Doris L., Pegelow, Charles H., Gill, Frances M.

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Indications for red cell transfusion in sickle cell disease von Ohene-Frempong, Kwaku

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Safety of Hydroxyurea in Children With Sickle Cell Anemia: Results of the HUG-KIDS Study, a Phase I/II Trial von Kinney, Thomas R., Helms, Ronald W., O'Branski, Erin E., Ohene-Frempong, Kwaku, Wang, Winfred, Daeschner, Charles, Vichinsky, Elliott, Redding-Lallinger, Rupa, Gee, Beatrice, Platt, Orah S., Ware, Russell E.

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Plasma zinc status, growth, and maturation in children with sickle cell disease von Leonard, Mary B., Zemel, Babette S., Kawchak, Deborah A., Ohene-Frempong, Kwaku, Virginia, Virginia A.

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Epidemiology of human parvovirus B19 in children with sickle cell disease von Smith-Whitley, Kim, Zhao, Huaqing, Hodinka, Richard L., Kwiatkowski, Janet, Cecil, Renèe, Cecil, Tamara, Cnaan, Avital, Ohene-Frempong, Kwaku

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Indications for red cell transfusion in sickle cell disease von Ohene-Frempong, Kwaku

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Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke von Scothorn, Douglas J., Price, Cynthia, Schwartz, Daniel, Terrill, Cindy, Buchanan, George R., Shurney, Wanda, Sarniak, Ingrid, Fallon, Robert, Chu, Jen-Yih, Pegelow, Charles H., Wang, Winfred, Casella, James F., Resar, Linda S., Berman, Brian, Adamkiewicz, Thomas, Hsu, Lewis L., Ohene-Frempong, Kwaku, Smith-Whitley, Kim, Mahoney, Donald, Scott, J.Paul, Woods, Gerald M., Watanabe, Masayo, DeBaun, Michael R.

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Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: A report from the Cooperative Study of Sickle Cell Disease von Miller, Scott T., Macklin, Eric A., Pegelow, Charles H., Kinney, Thomas R., Sleeper, Lynn A., Bello, Jacqueline A., DeWitt, L.Dana, Gallagher, Dianne M., Guarini, Ludovico, Moser, Franklin G., Ohene-Frempong, Kwaku, Sanchez, Nelson, Vichinsky, Elliott P., Wang, Winfred C., Wethers, Doris L., Younkin, Donald P., Zimmerman, Robert A., DeBaun, Michael R.

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