The β-Thalassemias von Olivieri, Nancy F

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Iron-chelating therapy and the treatment of thalassemia von OLIVIERI, N. F, BRITTENHAM, G. M

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Haemoglobin E β thalassaemia in Sri Lanka von Premawardhena, A, Fisher, CA, Olivieri, NF, de Silva, S, Arambepola, M, Perera, W, O'Donnell, A, Peto, TEA, Viprakasit, V, Merson, L, Muraca, G, Weatherall, DJ

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Long-Term Safety and Effectiveness of Iron-Chelation Therapy with Deferiprone for Thalassemia Major von Olivieri, Nancy F, Brittenham, Gary M, McLaren, Christine E, Templeton, Douglas M, Cameron, Ross G, McClelland, Robert A, Burt, Alastair D, Fleming, Kenneth A

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The Therapeutic Reactivation of Fetal Haemoglobin von Olivieri, Nancy F., Weatherall, D. J.

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Iron-Chelation Therapy with Oral Deferiprone in Patients with Thalassemia Major von Olivieri, Nancy F, Brittenham, Gary M, Matsui, Doreen, Berkovitch, Matitiahu, Blendis, Laurence M, Cameron, Ross G, McClelland, Robert A, Liu, Peter P, Templeton, Douglas M, Koren, Gideon

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A Short-Term Trial of Butyrate to Stimulate Fetal-Globin-Gene Expression in the β-Globin Disorders von Perrine, Susan P, Ginder, Gordon D, Faller, Douglas V, Dover, George H, Ikuta, Tohru, Witkowska, H. Ewa, Cai, Shi-ping, Vichinsky, Elliott P, Olivieri, Nancy F

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Treatment of thalassaemia major with phenylbutyrate and hydroxyurea von Olivieri, Nancy F, Rees, David C, Ginder, Gordon D, Thein, Swee Lay, Brittenham, Gary M, Waye, John S, Weatherall, DJ

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Genetic determinants of jaundice and gallstones in haemoglobin E β thalassaemia von Premawardhena, A, Fisher, CA, Fathiu, F, de Silva, S, Perera, W, Peto, TEA, Olivieri, NF, Weatherall, DJ

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Uptake of non-transferrin-bound iron by both reductive and nonreductive processes is modulated by intracellular iron von RANDELL, E. W, PARKES, J. G, OLIVIERI, N. F, TEMPLETON, D. M

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Regression of extramedullary haemopoiesis and augmentation of fetal haemoglobin concentration during hydroxyurea therapy in β thalassaemia von Saxon, Ben R., Rees, David, Olivieri, Nancy F.

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Trying to improve compliance with prophylactic penicillin therapy in children with sickle cell disease von Berkovitch, Matitiahu, Papadouris, Dimitrios, Shaw, Dianne, Onuaha, Nzenalu, Dias, Carla, Olivieri, Nancy F.

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Secondary iron overload von Kushner, J P, Porter, J P, Olivieri, N F

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Comparison of oral iron chelator L1 and desferrioxamine in iron-loaded patients von Olivieri, N.F., Freedman, M.H., Koren, G., Hermann, C., Bentur, Y., Chung, D., Klein, J., Olivieri, N.F., Koren, G., Freedman, M.H., St. Louis, P., Templeton, D.M., McClelland, R.A., Templeton, D.M.

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Experimental verocytotoxemia in rabbits von RICHARDSON, S. E, ROTMAN, T. A, VENITA JAY, SMITH, C. R, BECKER, L. E, PETRIC, M, OLIVEIRI, N. F, KARMALI, M. A

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Identification of Microdeletions Spanning the Diamond-Blackfan Anemia Locus on 19q13 and Evidence for Genetic Heterogeneity von Gustavsson, Peter, Garelli, Emanuela, Draptchinskaia, Natalia, Ball, Sarah, Willig, Thiébaut-Noël, Tentler, Dimitri, Dianzani, Irma, Punnett, Hope H., Shafer, Frank E., Cario, Holger, Ramenghi, Ugo, Glomstein, Anders, Pfeiffer, Rudolf A., Goringe, Andy, Olivieri, Nancy F., Smibert, Elizabeth, Tchernia, Gil, Elinder, Göran, Dahl, Niklas

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Deferiprone versus desferrioxamine in thalassaemia, and T2 validation and utility von Brittenham, GM, Nathan, DG, Olivieri, NF, Pippard, MJ, Weatherall, DJ

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Hydroxyurea in children with sickle cell disease : Impact on splenic function and compliance with therapy von OLIVIERI, N. F, VICHINSKY, E. P

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Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo von SHALEV, O, REPKA, T, GOLDFARB, A, GRINBERG, L, ABRAHAMOV, A, OLIVIERI, N. F, RACHMILEWITZ, E. A, HEBBEL, R. P

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Compliance assessed by the Medication Event Monitoring System von Olivieri, N F, Matsui, D, Hermann, C, Koren, G

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