12th Congress of the European Hematology ... - Haematologica

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1490 Cytometry, 0494, 0791, 1262, 1367 Cytoskeleton, 0917 Cytotoxic T cell, 0192, 0282 Cytotoxic T lymphocyte, 0419, 0511 Cytotoxicity, 0204, 0296, 0616, 1120 D-dimer, 0827, 1171 Daunoxome, 1100 DC, 1347 decitabine, 0233, 0632 Deep venous thrombosis, 0347, 0350, 0355, 0992, 1370 deferiprone, 0798, 1146, 1158, 1203 Defibrotide, 0258, 1207 Demethylation, 1296 Dendritic cell, 0185, 0276, 0435, 0592, 0934, 0989, 1020, 1456, 1471 Dendritic cell vaccine, 0187 dexamethasone, 0737, 1054, 1128, 1352 DHPLC, 0438, 0569, 1129 Diagnosis, 0073, 0135, 0137, 0221, 0248, 0385, 0402, 0444, 0522, 0576, 0601, 0616, 0712, 0891, 0969, 0994, 1001, 1034, 1112, 1172, 1369, 1485, 1516 Diamond-Blackfan anemia, 0080 Differentiation, 0038, 0327, 0331, 0442, 0856, 0970, 0979, 1462 Diffuse large B cell lymphoma, 0407, 0408, 0704, 0708, 1082, 1175, 1177, 1246, 1261, 1436 Disseminated intravascular coagulation, 1378 DLBCL, 0702, 1007, 1474 DLI, 0194, 1353 DMT1, 0782 DNA damage, 0436, 0489 DNA methylation, 0162, 0233 DNA repair, 0167, 0696 DNA vaccine, 0192 Donor, 0368, 0457, 1000, 1014, 1385, 1424 Donor lymphocyte infusion, 0456, 0498, 1194 Dose intensity, 0550, 1489 Down Syndrome, 0042, 0492 Doxorubicin, 1034, 1302, 1535 Drug interaction, 0732, 1034, 1109 Drug resistance, 0034, 0098, 0162, 0481, 0523, 0789, 0927 Drug sensitivity, 0524, 0621, 1128 Dysplasia, 1366 EBV, 0213, 0282, 0293, 0740, 0921, 1082, 1249 Elderly, 0049, 0050, 0055, 0325, 0401, 0402, 0407, 0483, 0490, 0497, 0659, 0867, 0923, 0925, 1023, 1132, 1317, 1468 Endothelial, 0594, 1331 Endothelial cell, 0326, 0336, 0499, 0823, 0842, 0843, 0882, 1338 Endothelial dysfunction, 0594, 1141, 1159, 1234, 1318 Endothelial progenitor, 0389, 0629, 0840 Endothelial progenitor cell, 0242, 0334, 0846 Engraftment, 0370, 0457, 0505 Enzyme replacement therapy, 0596, 0681, 0734, 0735 Epidemiology, 0077, 0608, 0662, 0679, 0751, 0841, 1298, 1310 Epigenetic, 0019, 0228, 0250, 0631, 0667, 0923, 0930, 1077 EPO, 0222, 0241, 0427, 0894 Epoetin alfa, 1500 Erythrocyte, 0783, 0789 Erythrocytosis, 0241, 0894, 0931, 1482 Erythroid, 0785 Erythroid cells, 0231, 1377 Erythroid differentiation, 0161, 1272 Erythroid lineage, 0430 Erythroid progenitor, 0147, 0623, 1520 Erythropoieisis, 0768, 0799, 0913, 1045 Erythropoietin, 0078, 0079, 0249, 0770, 0776, 0931, 1171, 1183, 1206, 1315, 1493 Erythropoietin receptor, 0017 Essential Thrombocytemia, 0236, 0246, 0249, 0637, 0639, 0643, 0650, 0651, 0895, 0896, 0897, 0946, 0963, 1026, 1030, 1041, 1053, 1078, 1129, 1235, 1284, 1409, 1418, 1483, 1550 ETV6, 0134, 0382, 0877 EVI1, 0171, 0900, 1375, 1441 Ex vivo expansion, 0854, 0857, 1051, 1293, 1446 Expansion, 0855 Expression, 0155, 1273, 1541 Expression profiling, 1054, 1495 Extracorporeal photopheresis, 0588 Extranodal lymphoma, 0291, 0301, 0703, 0863, 1089, 1216, 1246, 1453, 1473 Factor IXa, 1270 Factor V, 0971, 1215 Factor V Leiden, 0354, 0817, 0830, 0937, 0952, 0992, 1169, 1224 Factor VIII Inhibitor, 0082, 1219 Factor XIII, 0340, 1370, 1433 Familial, 0627, 0647, 1229 Fanconi anemia, 0062, 0432, 0436 farnesyltransferase inhibitor, 0630, 1131 Fas, 0316, 1257 Fatigue, 0768, 0772 Fc receptor, 0581 FcGRIIIa polymorphism, 0306 FDG-PET, 0183, 0392, 1009, 1179, 1261, 1510 Febrile neutropenia, 0061, 0614 Ferritin, 0792, 0804, 0812, 1153, 1251, 1451, 1519 Fertility, 0204, 0540 Fetal, 0824, 0826, 1242 Fever, 1295 FGF, 1138 Fibrin, 0340 Fibrinogen, 0340 Fibrinolysis, 0338, 0340, 1114, 1323 Filgrastim, 1049 FIP1L1-PDGFRA, 0235 FISH, 0103, 0107, 0125, 0129, 0131, 0133, 0135, 0136, 0137, 0141, 0541, 0590, 0666, 0691, 0693, 0694, 0886, 0909, 0968, 1008, 1105, 1238, 1314, 1534 Flow cytometry, 0018, 0052, 0058, 0274, 0326, 0486, 0712, 0755, 0844, 0845, 0852, 0903, 0917, 0964, 0969, 0977, 1011, 1060, 1156, 1198, 1238, 1267, 12 th Congress of the European Hematology Association 1287, 1309, 1398, 1440, 1454, 1522, 1525 Flt3-ITD, 0035, 0056, 0174, 0397, 0469 FLT3, 0041, 0060, 0487, 0868, 0870, 1213 flt3 ligand, 0437 Fludarabine, 0049, 0062, 0113, 0120, 0364, 0451, 0465, 0496, 0523, 0524, 0709, 1073, 1342, 1438, 1511, 1530 Fludarabine phosphate, 0304 Fluorescence in situ hybridization, 0958, 1282, 1383 Follicular lymphoma, 0172, 0281, 0284, 0303, 0306, 0307, 0406, 0706, 0728, 0729, 0744, 0746, 0942, 1179, 1301, 1449, 1510 Follow-up, 0753, 1112, 1538 Free light chain, 0257, 1113, 1181, 1312 Fresh frozen plasma, 0832, 1219 Fungal infection, 0201, 0202, 0207, 0214, 0606, 0611, 0614, 0622, 0991, 1058, 1243, 1463 Fusion, 0024, 0382, 0502 G-CSF, 0205, 0531, 0615, 1048, 1358, 1373, 1531, 1540 G-CSF mobilization, 0431, 0505, 1455, 1457 G6PD, 1492 Gamma globin, 0200 Ganciclovir, 1292 Gastric MALT lymphoma, 1256 GATA-1, 1495 GATA-2, 1495 Gaucher disease, 0596, 0681, 0734, 0735, 0743, 1115 Geldanamycin, 0104 Gemcitabine, 1176, 1177, 1239, 1477 Gemtuzumab ozogamicin, 0048, 0049, 1023, 1068, 1537 Gender, 1506 Gene array, 0094, 0444, 0688 Gene expression, 0043, 0069, 0075, 0153, 0174, 0218, 0371, 0522, 0528, 0694, 0700, 0909, 1004, 1272, 1303, 1358 Gene expression profile, 0013, 0116, 0169, 0251, 0326, 0675, 0692, 0699, 0891, 0892, 0928, 0973, 1051 Gene polymorphism, 0613, 1074, 1111 Gene regulation, 0152, 0251, 0785 Gene therapy, 0043, 0189, 0191, 0196, 0416, 0436 Gene transfer, 0189, 0416 Genetic, 0165, 0228, 0870, 0871, 1105 Genetic instability, 0095, 0697 Genetic modifiers, 1232 Genetic polymorphism, 0529, 0536, 0821, 0822, 1221 Genomics, 0097, 0869, 1173 Genotype, 1080, 1205, 1427, 1526 Glanzmann, 1404 Gleevec (Glivec, Imatinib), 1233 Globin gene, 1145 Glycoprotein, 1367 Graft-versus-host disease (GVHD), 0158, 0188, 0190, 0194, 0195, 0197, 0462, 0499, 0579, 0580, 0581, 0585, 0586, 0592, 0836, 0851, 0933, 0951, 0956, 1097, 1200, 1381, 1407, 1509 Graft-versus-leukemia, 0195, 0419, 0579 Graft-versus-tumor effect, 0403, 0498, 0508 haematologica/the hematology journal | 2007; 92(s1) | c
12 th Congress of the European Hematology Association Granulocyte, 0776 Granulocyte transfusion, 0061 Granulopoiesis, 0439, 0440 Growth factor, 0147, 0602, 1281, 1466 Growth inhibition, 0935, 1360 GST, 0529, 1040 HAART, 1348 Hairy cell leukemia, 0117 Haploidentical, 0186 Haploidentical stem cell transplantation, 0194, 0450, 0457, 0951, 1381 Haplotype, 0779, 0830 Haplotype analysis, 0879 HDAC inhibitor, 0153 Health care, 0596, 0764, 0771, 1345 Healthy individuals, 0826 Heat shock protein, 0033, 0732, 1357 Helicobacter pylori, 0753, 1155, 1393, 1394 Hemangioblast, 0389 Hematocrit, 1482 Hematological malignancy, 0061, 0171, 0193, 0208, 0212, 0217, 0227, 0587, 0725, 1102, 1199, 1230, 1241, 1251, 1375 Hematopoiesis, 0335, 1250, 1450 Hematopoietic cell, 0200, 1250 Hematopoietic cell transplantation, 0019, 0186, 0370, 0451, 0464, 0587, 0950, 0999, 1199, 1274 Hematopoietic microenvironment, 0075, 0986, 1004 Hematopoietic stem and progenitor cells, 0331, 0852, 0986, 1004 Hematopoietic stem cell, 0075, 0240, 0432 Hematotoxicity, 1140 Heme, 0779, 0780 Hemochromatosis, 0165, 0778, 0781, 0792, 0812, 1158, 1203, 1329, 1402, 1526 Hemoglobin, 0377, 1388, 1493 Hemoglobin variants, 1168, 1388 Hemoglobinopathy, 0796, 0806, 0813, 1152, 1168, 1185, 1321, 1388, 1389 Hemolysis, 0065, 0378, 0379, 0380, 1356, 1378 Hemolytic anemia, 0203, 0783, 0784, 0785, 0786, 0794, 1160, 1185, 1321, 1325, 1335 Hemophilia, 0083, 0203, 0603, 0769, 0771, 0843, 0960, 1219, 1408, 1427 Hemophilia A, 0085, 0090, 1258, 1404 Hemophilia B, 0085 Hemorrhage, 0057, 0089, 1002, 1270, 1414 Hemostasis, 0057, 1018, 1173, 1202, 1252, 1361 Heparin, 0756 Heparin induced thrombocytopenia (HIT), 0757 Hepatitis B virus, 0978 Hepatitis C virus, 0139, 0716, 0723, 0726, 0730, 0978, 1329, 1427, 1436, 1478, 1517, 1526 Hepatocyte, 0502 Hepcidin, 0782, 1045, 1392 Hereditary spherocytosis, 0774, 0783, 0786, 0917, 1325 Herpesvirus, 0207, 0619, 0621, 1345, 1371 High-grade non-Hodgkins-lymphoma, 0410, 0723 d | haematologica/the hematology journal | 2007; 92(s1) High dose therapy, 0047, 0308, 0408, 0668, 0721, 0925, 1259 High risk, 1248 Histone deacetylase inhibitor, 0582 HIT, 0756 HIV, 0203, 0506, 0978, 1348, 1422 HIV related lymphoma, 0726 HLA, 0069, 0110, 0272, 1076 HLA mismatched, 0447 Hodgkin’s disease, 0204, 1066, 1072, 1209, 1232, 1304 Hodgkin’s lymphoma, 0177, 0178, 0179, 0180, 0182, 0391, 0392, 0393, 0394, 0395, 0921, 0950, 1022, 1218, 1227, 1239, 1430, 1461, 1468 Homeobox gene, 1139 Homocysteine, 0343, 0992 Hormone replacement therapy, 1141, 1328 HOX, 0752 HOXa9, 0045 HSCT, 0210, 0458, 0939, 0940, 0941 HTLV-1, 0145, 0310, 0733 Human immunodeficiency virus, 0731 Hydroxyurea, 0797, 0800, 0810, 0842, 1053, 1079, 1147, 1503 Hyperdiploid, 0467, 1092 Hypereosinophilic syndrome, 0640, 1086 Hypomethylation, 0428 Hypoxia-sensing, 0241 Ibritumomab tiuxetan, 0719, 0744 Id-KLH, 0418 Idiopathic myelofibrosis, 0414, 0644, 1009, 1217 Idiopathic thombocytopenic purpura (ITP), 0086, 0121, 0751, 0753, 0754, 1150, 1161, 1317, 1393 Idiotype, 0947 IFN-gamma, 1262 Ig and TCR gene rearrangement, 0008 IGH, 0908 IgH rearrangment, 0125, 0288, 0518, 1008, 1101, 1344, 1383 IgH translocation, 0107 Ikaros, 0006, 0150 IL-1, 1465 IL-10, 0437 IL-15, 0196 IL-6, 0106, 0954, 1012, 1465 IL-7, 0196 Imatinib, 0140, 0357, 0441, 0528, 0533, 0537, 0540, 0542, 0547, 0548, 0549, 0550, 0559, 0561, 0562, 0567, 0640, 0654, 0657, 0659, 0660, 0663, 0666, 0668, 0669, 0745, 0906, 0907, 1013, 1032, 1052, 1086, 1135, 1163, 1201, 1253, 1289, 1343, 1353, 1363, 1365, 1441, 1480, 1489, 1491, 1494, 1496, 1504, 1505, 1512 Imatinib resistance, 0026, 0321, 0330, 0356, 0358, 0359, 0526, 0534, 0535, 0554, 0557, 0563, 0655, 0656, 0862, 0904, 0905, 1231, 1491 Imids, 0234, 0363 Immune deficiency, 0416, 0725 Immune reconstitution, 0193, 0464, 1450 Immune response, 0285 Immune therapy, 0190, 0191, 0197, 0232, 0418, 0581 Immune thrombocytopenia (ITP), 0376, 0750, 1088, 1151, 1324, 1399 Immunodeficiency, 0289, 1249 Immunoglobulin gene, 1084, 1410 Immunohistochemistry, 0219, 0238, 0280, 0294, 0683, 0969, 1069, 1087, 1478 Immunomodulation, 0185, 0847 Immunomodulatory thalidomide analog, 0402 Immunophenotype, 0016, 0018, 0292, 0693, 0953, 0975, 0976, 1092, 1287 Immunosuppression, 0081, 0082, 0201, 0273, 0311, 0496, 0682, 0994, 1277 Immunosuppressive therapy, 0072 Immunotherapy, 0301, 0409, 0417, 0593, 0934, 0948 Incidence, 0067, 0209, 0751, 0994, 1088, 1217, 1452, 1552 Indolent non-Hodgkin’s lymphoma, 0709 Induction chemotherapy, 0053, 0256 Infant, 0014, 0088, 1245, 1366, 1437 Infection, 0188, 0208, 0216, 0291, 0608, 0611, 0613, 0614, 0617, 0618, 0620, 0621, 0682, 1036, 1050, 1085, 1165, 1247, 1264, 1292, 1443 Inflammation, 0064, 0285, 1173, 1329 Inherited thrombophilia, 0817, 1044 Inhibitor, 0090, 0269, 0439, 0520, 0603, 0954, 1028, 1215, 1219, 1258, 1404, 1408, 1523 Innate Immunity, 1255 Insertional mutagenesis, 0420 Interferon-alpha, 0387 Interferon, 0723, 1162, 1505 Interferon alpha, 0088, 0117, 0441, 0531, 0561, 0650, 0656 Interferon gamma, 0948 International prognostic index, 1474 Invasive aspergillosis, 0202, 0606, 0994 Iron, 0078, 0803, 1075, 1183 Iron chelation, 0598, 0636, 0782, 0798, 0805, 0808, 1027, 1075, 1146, 1147, 1328 Iron deficiency, 0079, 1000, 1521 Iron deficiency anemia, 1319, 1516, 1519 Iron overload, 0778, 0781, 0792, 0794, 0808, 0812, 1027, 1075, 1146, 1147, 1174, 1329, 1389, 1402, 1451, 1526 Irradiation, 0836 ITP, 0749, 1142, 1316, 1320, 1330 IVIg, 0833 JMML, 0235, 0957 JNK, 0034 Kaposi’s sarcoma, 1313 Ki-67, 0175, 0690, 1306, 1474 Killer immunoglobulin receptors (KIR), 0186, 0951, 1024 Kinase, 0324, 1542, 1550 Kinase domain mutant, 0655, 0904, 1129, 1435 Kinase inhibitor, 0041, 0313, 0324, 0554, 0738, 0904, 1435 Kinetics, 0433, KIR, 0595, 0940
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haematologica the hematology journa
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Information for readers, authors an
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EHA Executive Board E. Hellström-L
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Poster session I POSTER SESSION POS
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12 th Congress of the European Hema
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dasatinib. Methods. We studied Ikar
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Expression of the oncogene H-Ras an
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is the gene for the erythropoietin
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safety of a slow-release liposomal
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0029 OUTCOME OF THE TREATMENT OF AD
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drug-induced apoptotic response of
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41% in the PI3K- group (p=0.001). I
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Acute myeloid leukemia - Clinical I
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to 60 years (n=116, or 72%) receive
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0056 PROGNOSTIC SIGNIFICANCE OF FLT
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Anemia and Bone marrow failure 0061
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tified with the current protocol. S
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new cases of lead poisoning due to
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icance, from baseline to week 6 (p
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0086 THROMBELASTOGRAPHIC CHART RELI
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trials. The aim of this retrospecti
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tant function in this disease, nega
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ed to a favorable outcome. Bialleli
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stronger levels of p21 in the cell
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hematological centers in one countr
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ure 1). Conclusions. Results for re
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patients. After a median follow-up
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Cytogenetics and Molecular diagnost
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0135 ROUTINE DETECTION OF CYTOGENET
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(MMolR, defined as a BCR-ABL x 100
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0146 ARSENIC TRIOXIDE INDUCES ACCUM
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tinguish between genotypic B-cell l
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Genomics and proteomics 0158 PLASMA
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0164 EVALUATION OF MULTIPLEX LIGATI
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each patient’s replicate conditio
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0174 RELATION BETWEEN LOW PML-RARα
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0179 ESHAP VS GIN AS SALVAGE AND MO
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Immunology and gene therapy 0184 EA
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Cell viability was not affected by
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month is not relevant to chronic Gv
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Infection and supportive care I 020
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0206 POTENTIAL ROLE OF CMV IN THE O
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3H-thymidine uptake in cell culture
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0217 TUBERCULOSIS AMONG A COHORT OF
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0222 COMPARISON OF IWG 2006 AND IWG
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tem (IPSS) to h-MDS was also invest
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PCH97-19) were studied. Conventiona
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of erythroid colonies was reduced i
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0245 POTENT AND SELECTIVE INHIBITIO
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0250 INACTIVATION OF SUPPRESSOR OF
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Bortezomib 1.3 mg/m 2 days 1,4,8,11
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Response was defined according to E
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G-CSF can be used in neutropenic pa
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ence and functional activity of CD8
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itating tumor development, or engag
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phoma and SNT-13, -15 were establis
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usage (2/20 ie 10%) were observed.
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0294 MYCOSIS FUNGOIDES. IMMUNOHYSTO
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(range, 1-6) and 11 treatment cycle
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0306 RISK-ADAPTED IMMUNOCHEMOTHERAP
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functional activity was confirmed b
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No major toxicity, neither hematolo
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enewal potential of X-RAR-positive
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(50-99) respectively. Serial analys
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cell-interaction, adhesion and acti
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0340 ALTERED FIBRIN CLOT STRUCTURE
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Conclusions. This study demonstrate
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0354 FACTOR V LEIDEN HOMOZYGOUS GEN
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Results. From July 2005 through Mar
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0364 CLINICAL EFFICACY OF OXALIPLAT
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one marrow and peripheral blood ste
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ecently suggested (Boissel et al.,
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0378 SAFETY AND EFFICACY OF THE TER
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Cytogenetics and molecular diagnost
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0385 CYTOPLASMIC MUTATED NUCLEOPHOS
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0390 ELTROMBOPAG RAISES PLATELET CO
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factor for the achievement of CR wa
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The cases of RAS showed two peaks o
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is 85%. Seven out of the 25 relapse
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0409 FRACTIONATED RADIOIMMUNOTHERAP
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0414 COMPARATIVE ANALYSIS OF THE CO
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successfully managed with GM-CSF di
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49% for PCR positive patients (95%
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+8 (1 PR+1 HI) and 14/24 pts with c
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(e.g. bcr-abl leading to CML). CSC
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0438 TERC MUTATIONS ANALYSIS IN PAT
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observed in all mice. Analysis of l
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ex-vivo expansion of HUCB-derived H
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ic kidney disease in univariate or
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One hundred eleven CN AML patients,
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to asses intestinal epithelial dama
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genesis of acute myeloid leukaemia
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polymorphism at nucleotide 4889 of
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expression along with a decreased C
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0487 MUTATIONAL STATUS OF NUCLEOPHO
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previously reported, a single cours
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0497 SINGLE AGENT CLORETAZINE (VNP4
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ly received melphalan-based chemoth
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were similar among the 3 groups. Ho
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Methods. Several read-out systems w
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0518 SERUM AND CELLULAR EXPRESSION
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0523 DNA REPAIR INHIBITION IN RESTO
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held true when BMI-1 expression was
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Ph + cells in the bone marrow). We
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derivative chromosome (4p16, 7p14,
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0545 STABILIZED BONE MARROW IS NOT
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obtained in low (Sokal) risk patien
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median dose intensity being 800 (21
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from pivotal clinical trials. Metho
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Cytogenetics and Molecular diagnost
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to set up and optimize a D-HPLC-bas
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0576 WESTERN BLOT IDENTIFICATION OF
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Basic disease was AML (n=5), ALL (n
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0588 EXTRACORPOREAL PHOTOPHORESIS F
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acquire a cytolytic capacity agains
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informed vignettes describing healt
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using CHOP-21 in the UK, pegfilgras
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0609 SOFT TISSUE COMPLICATIONS IN P
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inding lectin (MBL) gene by polymer
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all infection rate (p=0.12) as well
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Myelodysplastic syndromes II 0623 M
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formation (in total 28 samples). Ti
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sion. In addition, confocal analysi
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Myeloproliferative disorders - Clin
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open-label, multi-centre study enro
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iopsies after 6 and 12 months treat
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Myeloproliferative disorders Chroni
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ash, muscolar cramps, diarrhoea, he
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induced significant apoptosis (mean
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Myeloma and other monoclonal gammop
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the therapy of choice for POEMS is
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er patient does not indicate such t
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Myeloma and other monoclonal gammop
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secutive patients with MM, referred
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whether gene expression values may
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0705 THE SHIFT OF TREATMENT FOR NAS
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0710 CLINICO-PATHOLOGICAL FEATURES,
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patients presented a stage IV disea
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plete remission or recurrent diseas
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known at NHL diagnosis, were includ
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0731 THE IMPACT OF HIV ON NON-HODGK
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patients had died of their underlyi
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scripts and proteins most affected
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modulated after 24 h (37 up- and 59
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0753 A SUSTAINED REMISSION OF IDIOP
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and treatment, has rarely been syst
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uncontrolled massive bleeding affec
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Results. A total of 396 patients we
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C30 questionnaire, and the correspo
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wave length of light of reflected r
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0783 PREVALENCE OF MEMBRANE PROTEIN
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erozygous mother has a more severe
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0794 CARDIAC MANIFESTATIONS IN A BR
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0799 INEFFECTIVE ERYTHROPOIESIS IN
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p=0.014 and p=0.003, respectively).
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0809 CURRENT APPROACH TO CHELATION
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Thrombosis II 0814 UNSUSPECTED PULM
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the 97.5th percentile (5.2 U/mL) ge
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symptoms of DVT, 3 (7.89%) previous
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Transfusion medicine and vascular b
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tions (most bacterial, 2 malaria, 6
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0844 INCREASED LEUKOCYTE-PLATELET I
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0851 CORD BLOOD DERIVED MESENCHYMAL
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SIMULTANEOUS SESSION II Chronic mye
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0862 COMPARISON OF DASATINIB TO HIG
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0867 COMPREHENSIVE GERIATRIC ASSESS
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0872 MN1 INDUCES LEUKEMIA IN MICE A
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0877 PAX5/TEL TRANSDUCED PRE-BI CEL
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0882 CISPLATIN INDUCES THROMBIN GEN
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have an early manifestation of typi
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0892 INTEGRATION OF GENOME WIDE SNP
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0897 THE PHENOTYPE OF JAK2V617F MUT
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gest diverse sequences of NPM mutan
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2004 to January, 2006. At enrollmen
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with a p value of ≥ 0.10. Sets of
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BRIC 126 and 4N1K) in cells lacking
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sclerosis[NS] and 12 Mixed cellular
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0927 MK-0457, A NOVEL MULTIKINASE I
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Publication Only 0933 CLINICAL FEAT
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HSCT from the available Asian as we
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that the incidence of JAK2 mutation
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without type 2 diabetes. Methods. T
Page 365 and 366:
pts (38.8%) that were isolated (abs
Page 367 and 368:
y using the Miltenyi CD34 isolation
Page 369 and 370:
0969 COMPARISON OF CD25 IMMUNOHISTO
Page 371 and 372:
cytes was 24 days (range 8-32 days)
Page 373 and 374:
a cytogenetic hallmark for M4/M5 su
Page 375 and 376:
normal human BM B progenitor cells
Page 377 and 378:
0994 INCIDENCE OF INVASIVE ASPERGIL
Page 379 and 380:
3 of disease relapse.TRM at day+100
Page 381 and 382:
survival of five years. This dismal
Page 383 and 384:
1011 FLOW CYTOMETRIC DNA INDEX AND
Page 385 and 386:
1018 THE EFFECT OF THE SUGARBAKER P
Page 387 and 388:
1024 KIR/HLA CLASS I MISMATCHING AN
Page 389 and 390:
ment details and thrombotic histori
Page 391 and 392:
1036 INCIDENCE AND SPECTRUM OF INFE
Page 393 and 394:
tinely by our stem cell lab prior t
Page 395 and 396:
tion to a translocation t(5;14)(q35
Page 397 and 398:
ment of CML and induces a high rate
Page 399 and 400:
due to reactivation and/or progress
Page 401 and 402:
1063 ABNORMAL METHYLATION STATUS OF
Page 403 and 404:
1069 CLINICAL RELEVANCE OF REGULATO
Page 405 and 406:
1076 SERUM LEVELS OF SOLUBLE HLA CL
Page 407 and 408:
patient is still undergoing intensi
Page 409 and 410:
nificant MVD differences were detec
Page 411 and 412:
dictor of OS (p=0.004). High dose t
Page 413 and 414:
1099 ALTERATIONS IN THE NATURAL KIL
Page 415 and 416:
1105 CYTOGENETIC ABNORMALITIES IN 3
Page 417 and 418:
1110 CONSTITUTIVE ACTIVATION OF STA
Page 419 and 420:
efficacy results with a well-tolera
Page 421 and 422:
unmutated VH genes, and high and lo
Page 423 and 424:
Aims. Aim of this study was to pred
Page 425 and 426:
tested across a wide range of human
Page 427 and 428:
were incidentally diagnosed (52%).
Page 429 and 430:
ß2GP1 may be considered as determi
Page 431 and 432:
characterized in 198 β thalassaemi
Page 433 and 434:
1155 PLATELET AGGREGATION IN CHILDR
Page 435 and 436:
to-pelvic or perineal trauma. No me
Page 437 and 438:
in age. High prevalence of LBM amon
Page 439 and 440:
ecause some of the patients were or
Page 441 and 442:
of the drug is crucial to allow lon
Page 443 and 444:
egarding cost analysis of ASCT in G
Page 445 and 446:
ID Allo-BMT, 1 family one mismatche
Page 447 and 448:
admitted to ICU were discharged des
Page 449 and 450:
events -Postoperative states: 9,19%
Page 451 and 452:
efficacy and decreased atherosclero
Page 453 and 454:
1217 INCIDENCE OF EARLY STAGE IDIOP
Page 455 and 456:
1691GA and 1 homozygous 1691AA. The
Page 457 and 458:
1230 ASSOCIATION OF HEPARANASE GENE
Page 459 and 460:
posed, was: DF = (CD43%+FMC7%+CD79b
Page 461 and 462:
treatment of acute promyelocityc le
Page 463 and 464:
loaded group and 35 (70%) were non-
Page 465 and 466:
mild. Fas and soluble Fas ligand le
Page 467 and 468:
1265 POSACONAZOLE THERAPY IN REFRAC
Page 469 and 470:
ly express the cytoplasmic (inactiv
Page 471 and 472:
findings confirmed the significant
Page 473 and 474:
a less favorable prognosis. Interes
Page 475 and 476:
disease (HD), 4 patients (9%) with
Page 477 and 478:
1295 HEMOPHAGOCYTIC LYMPHOHYSTIOCYT
Page 479 and 480:
phamide 750 mg/m 2 on day 1, vincri
Page 481 and 482:
nomenon is unclear. It has been sug
Page 483 and 484:
oped mild thrombocytopenia (platele
Page 485 and 486:
gle dose of 54mg/m 2 rituximab furt
Page 487 and 488:
patients (pts), 36 male, with acute
Page 489 and 490:
esulting alterations of the endothe
Page 491 and 492:
(range 1-7) and 28,6% of patients h
Page 493 and 494:
three decades. In vivo, Ara-C is tr
Page 495 and 496:
statistical analysis. Results. Seve
Page 497 and 498:
Results. Though there was no recogn
Page 499 and 500:
2% and 19% of patients with or with
Page 501 and 502:
were older than 65 y) which can be
Page 503 and 504:
1376 RESVERATROL INDUCED P53 MEDIAT
Page 505 and 506:
median time of 21 days to reach >0.
Page 507 and 508:
ly. Conclusions. 1. Combined intens
Page 509 and 510:
to the presence of IVS1-6 mutation
Page 511 and 512:
fy predictive factors for these abn
Page 513 and 514:
acute leukemia. However, we cannot
Page 515 and 516:
agents. They involve primarily the
Page 517 and 518:
voriconazole for 2 months followed
Page 519 and 520:
typed using a commercially availabl
Page 521 and 522:
low up of ABL KD mutations’ level
Page 523 and 524:
with development of BC/AP. 2. EVI-1
Page 525 and 526:
1447 THE IMPACT OF DISPARITY IN SHO
Page 527 and 528:
three had visual field defects, two
Page 529 and 530:
acquired mutation most prone to cau
Page 531 and 532:
1466 ROS GENERATION AND APOPTOSIS I
Page 533 and 534:
1473 DIARRHEIC SYNDROME, A CLINICAL
Page 535 and 536:
gene fusion is an independent progn
Page 537 and 538:
1484 EPIDEMIOLOGY AND RESPONSE TO T
Page 539 and 540:
1492 FREQUENCY OF MEDITERRANEAN GLU
Page 541 and 542:
immune globulin was administered at
Page 543 and 544:
maintained on Imatinib 400 mg. Afte
Page 545 and 546:
Hodgkin’s disease is well known,
Page 547 and 548: gram provided a unique chance to de
Page 549 and 550: even when ADP-induced plt activatio
Page 551 and 552: medullary involvement of multiple m
Page 553 and 554: 1540 ADMINISTRATION OF G-CSF AND CH
Page 555 and 556: 1548 QUALITY ANALYSIS OF THE MULTID
Page 557 and 558: Index of authors A Aapro, M., 0377,
Page 559 and 560: Bahr, J., 0148 Bai, M., 1551 Baia,
Page 561 and 562: Bottini, P.V., 1181 Botto, B., 0408
Page 563 and 564: Chaidos, A., 0456, 0498, 0599, 0686
Page 565 and 566: De Keersmaecker, K., 0442, 0875 De
Page 567 and 568: El-Sharkawy, N., 0016 Elwahidi, G.,
Page 569 and 570: Garcia-Frade, J., 0346, 0680, 1105
Page 571 and 572: H Haas, N., 0742 Haas, O.A., 0001,
Page 573 and 574: Jaksic, B., 0127, 0446 Jaksic, O.,
Page 575 and 576: Körmöczi, G., 0848 Kornblau, S.,
Page 577 and 578: Lin, L.-I., 0030, 0484 Lin, T., 012
Page 579 and 580: Massé, A., 0249 Massó, P., 1287,
Page 581 and 582: Musto, P., 0254, 0401, 0422, 0569,
Page 583 and 584: Papadavid, E., 1442 Papageorgiou, E
Page 585 and 586: Probatova, N., 0704 Prochazka, V.,
Page 587 and 588: Rykavicin, O., 0504 Ryningen, A., 0
Page 589 and 590: Sirard, C., 0127, 0128 Sirigou, A.,
Page 591 and 592: Thiebaut, A., 0454 Thieblemont, C.,
Page 593 and 594: Vincenzi, C., 1060 Viniou, N.-A., 0
Page 595 and 596: Zouabi, H., 0503, 0999 Zoumbos, N.C
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