Deletions of Xp22.2 including PIG-A locus lead to paroxysmal nocturnal hemoglobinuria von O'Keefe, C L, Sugimori, C, Afable, M, Clemente, M, Shain, K, Araten, D J, List, A, Epling-Burnette, P K, Maciejewski, J P

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Dynamics of hematopoiesis in paroxysmal nocturnal hemoglobinuria (PNH): no evidence for intrinsic growth advantage of PNH clones von ARATEN, D. J, BESSLER, M, MCKENZIE, S, CASTRO-MALASPINA, H, CHILDS, B. H, BOULAD, F, KARADIMITRIS, A, NOTARO, R, LUZZATTO, L

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Clonal Populations of Hematopoietic Cells with Paroxysmal Nocturnal Hemoglobinuria Genotype and Phenotype Are Present in Normal Individuals von Araten, David J., Nafa, Khedoudja, Pakdeesuwan, Kriangsak, Luzzatto, Lucio

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Paroxysmal nocturnal hemoglobinuria and concurrent JAK2(V617F) mutation von Sugimori, C, Padron, E, Caceres, G, Shain, K, Sokol, L, Zhang, L, Tiu, R, O'Keefe, C L, Afable, M, Clemente, M, Lee, J M, Maciejewski, J P, List, A F, Epling-Burnette, P K, Araten, D J

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Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria von Karadimitris, Anastasios, Manavalan, John S., Thaler, Howard T., Notaro, Rosario, Araten, David J., Nafa, Khedoudja, Roberts, Irene A.G., Weksler, Marc E., Luzzatto, Lucio

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Allogeneic bone marrow transplantation for paroxysmal nocturnal hemoglobinuria von Araten, D J, Luzzatto, L

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No evidence of hypermutability in red cells from patients with paroxysmal nocturnal hemoglobinuria using the XK gene von Araten, David J, Zamechek, Leah, Halverson, Gregory

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Paroxysmal nocturnal hemoglobinuria and concurrent JAK2V617F mutation von Sugimori, C, Padron, E, Caceres, G, Shain, K, Sokol, L, Zhang, L, Tiu, R, O'Keefe, C L, Afable, M, Clemente, M, Lee, J M, Maciejewski, J P, List, A F, Epling-Burnette, P K, Araten, D J

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Association of clonal T‐cell large granular lymphocyte disease and paroxysmal nocturnal haemoglobinuria (PNH): further evidence for a pathogenetic link between T cells, aplastic an... von Karadimitris, Anastasios, Li, Ke, Notaro, Rosario, Araten, David J., Nafa, Khedoudja, Thertulien, Raymond, Ladanyi, Marc, Stevens, Ann E., Rosenfeld, Calvin S., Roberts, Irene A. G., Luzzatto, Lucio

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Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria von Araten, David J., Swirsky, David, Karadimitris, Anastasios, Notaro, Rosario, Nafa, Khedoudja, Bessler, Monica, Thaler, Howard T., Castro‐Malaspina, Hugo, Childs, Barrett H., Boulad, Farid, Weiss, Mark, Anagnostopoulos, Nikolaos, Kutlar, Abdullah, Savage, David G., Maziarz, Richard T., Jhanwar, Suresh, Luzzatto, Lucio

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Thrombolytic therapy is effective in paroxysmal nocturnal hemoglobinuria: a series of nine patients and a review of the literature von ARATEN, David J, NOTARO, Rosario, CHAFFEE, Sara, GONSKY, Jason, THERTULIEN, Raymond, TARQUINI, Roberto, LUZZATTO, Lucio, THALER, Howard T, KERNAN, Nancy, BOULAD, Farid, CASTRO-MALASPINA, Hugo, SMALL, Trudy, SCARADAVOU, Andromachi, MAGNAN, Heather, PROCKOP, Susan

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A quantitative measurement of the human somatic mutation rate von ARATEN, David J, GOLDE, David W, ZHANG, Rong H, THALER, Howard T, GARGIULO, Lucia, NOTARO, Rosario, LUZZATTO, Lucio

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High incidence of thrombosis in African-American and Latin-American patients with Paroxysmal Nocturnal Haemoglobinuria von Araten, David J., Thaler, Howard T., Luzzatto, Lucio

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Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria von Karadimitris, Anastasios, Manavalan, John S., Thaler, Howard T., Notaro, Rosario, Araten, David J., Nafa, Khedoudja, Roberts, Irene A.G., Weksler, Marc E., Luzzatto, Lucio

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Severe telomere shortening in patients with paroxysmal nocturnal hemoglobinuria affects both GPI– and GPI+ hematopoiesis von Karadimitris, Anastasios, Araten, David J., Luzzatto, Lucio, Notaro, Rosario

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In vitro alloreactivity against host antigens in an adult HLA-mismatched bone marrow transplant recipient despite in vivo host tolerance von ARATEN, D. J, LAWTON, T, FERRARA, J, ANTIN, J. H, MILFORD, E, CARPENTER, C. B, MAZIARZ, R. T

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Measurement of the Human Mutation Rate

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Changing prognosis in paroxysmal nocturnal haemoglobinuria disease subcategories: an analysis of the International PNH Registry von Socié, G., Schrezenmeier, H., Muus, P., Lisukov, I., Röth, A., Kulasekararaj, A., Lee, J. W., Araten, D., Hill, A., Brodsky, R., Urbano-Ispizua, A., Szer, J., Wilson, A., Hillmen, P.

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Cephalosporin resistance, tolerance, and approaches to improve their activities von Araten, Alison H., Brooks, Rachel S., Choi, Sarah D. W., Esguerra, Laura L., Savchyn, Diana, Wu, Emily J., Leon, Gabrielle, Sniezek, Katherine J., Brynildsen, Mark P.

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Low Rate of Clinically Evident Extravascular Hemolysis in Patients with Paroxysmal Nocturnal Hemoglobinuria Treated with a Complement C5 Inhibitor: Results from a Large, Multicente... von Shammo, Jamile, Gajra, Ajeet, Patel, Yogesh, Tomazos, Ioannis, Kish, Jonathan, Hill, Anita, Sierra, J. Rafael, Araten, David

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