-
1
-
-
0023525879
-
Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia
-
Appelbaum FR, Barrall J, Storb R, Ramberg R, Doney K, Sale GE, Thomas ED. Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia. Exp Hematol 1987;15:1134-9.
-
(1987)
Exp Hematol
, vol.15
, pp. 1134-1139
-
-
Appelbaum, F.R.1
Barrall, J.2
Storb, R.3
Ramberg, R.4
Doney, K.5
Sale, G.E.6
Thomas, E.D.7
-
2
-
-
44449158040
-
Cytogenetic features in myelodysplastic syndromes
-
Haase D. Cytogenetic features in myelodysplastic syndromes. Ann Hematol 2008;87:515-26.
-
(2008)
Ann Hematol
, vol.87
, pp. 515-526
-
-
Haase, D.1
-
3
-
-
0036566542
-
Distinct clinical outcomes for cytogenetic abnormalities evolving from aplastic anemia
-
Maciejewski JP, Risitano A, Sloand EM, Nunez O, Young NS. Distinct clinical outcomes for cytogenetic abnormalities evolving from aplastic anemia. Blood 2002;99:3129-35.
-
(2002)
Blood
, vol.99
, pp. 3129-3135
-
-
Maciejewski, J.P.1
Risitano, A.2
Sloand, E.M.3
Nunez, O.4
Young, N.S.5
-
4
-
-
34047220891
-
World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes
-
Bernasconi P, Klersy C, Boni M, et al. World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes. Br J Haematol 2007;137:193-205.
-
(2007)
Br J Haematol
, vol.137
, pp. 193-205
-
-
Bernasconi, P.1
Klersy, C.2
Boni, M.3
-
5
-
-
77955477205
-
The characteristics and clinical outcome of adult patients with aplastic anemia and abnormal cytogenetics at diagnosis
-
Kim SY, Lee JW, Lee SE, et al. The characteristics and clinical outcome of adult patients with aplastic anemia and abnormal cytogenetics at diagnosis. Genes Chromosom Cancer 2010;49:844-50.
-
(2010)
Genes Chromosom Cancer
, vol.49
, pp. 844-850
-
-
Kim, S.Y.1
Lee, J.W.2
Lee, S.E.3
-
6
-
-
84858830672
-
New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge
-
Schanz J, Tuchler H, Sole F, et al. New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge. J Clin Oncol 2012;30:820-9.
-
(2012)
J Clin Oncol
, vol.30
, pp. 820-829
-
-
Schanz, J.1
Tuchler, H.2
Sole, F.3
-
7
-
-
33744824138
-
Clinical relevance of cytogenetic abnormalities at diagnosis of acquired aplastic anaemia in adults
-
Gupta V, Brooker C, Tooze JA, Yi QL, Sage D, Turner D, Kangasabapathy P, Marsh JC. Clinical relevance of cytogenetic abnormalities at diagnosis of acquired aplastic anaemia in adults. Br J Haematol 2006;134:95-9.
-
(2006)
Br J Haematol
, vol.134
, pp. 95-99
-
-
Gupta, V.1
Brooker, C.2
Tooze, J.A.3
Yi, Q.L.4
Sage, D.5
Turner, D.6
Kangasabapathy, P.7
Marsh, J.C.8
-
8
-
-
0030326426
-
Cytogenetic abnormalities in patients with severe aplastic anemia
-
Mikhailova N, Sessarego M, Fugazza G, et al. Cytogenetic abnormalities in patients with severe aplastic anemia. Haematologica 1996;81:418-22.
-
(1996)
Haematologica
, vol.81
, pp. 418-422
-
-
Mikhailova, N.1
Sessarego, M.2
Fugazza, G.3
-
9
-
-
39649094569
-
New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: Evidence from a core dataset of 2124 patients
-
Haase D, Germing U, Schanz J, et al. New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: Evidence from a core dataset of 2124 patients. Blood 2007;110:4385-95.
-
(2007)
Blood
, vol.110
, pp. 4385-4395
-
-
Haase, D.1
Germing, U.2
Schanz, J.3
-
10
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P, Cox C, LeBeau MM, et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997;89:2079-88.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
-
11
-
-
23044473715
-
Preferential suppression of trisomy 8 compared with normal hematopoietic cell growth by autologous lymphocytes in patients with trisomy 8 myelodysplastic syndrome
-
Sloand EM, Mainwaring L, Fuhrer M, Ramkissoon S, Risitano AM, Keyvanafar K, Lu J, Basu A, Barrett AJ, Young NS. Preferential suppression of trisomy 8 compared with normal hematopoietic cell growth by autologous lymphocytes in patients with trisomy 8 myelodysplastic syndrome. Blood 2005;106:841-51.
-
(2005)
Blood
, vol.106
, pp. 841-851
-
-
Sloand, E.M.1
Mainwaring, L.2
Fuhrer, M.3
Ramkissoon, S.4
Risitano, A.M.5
Keyvanafar, K.6
Lu, J.7
Basu, A.8
Barrett, A.J.9
Young, N.S.10
-
12
-
-
0033592318
-
Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes
-
Dunn DE, Tanawattanacharoen P, Boccuni P, Nagakura S, Green SW, Kirby MR, Kumar MS, Rosenfeld S, Young NS. Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes. Ann Intern Med 1999;131:401-8.
-
(1999)
Ann Intern Med
, vol.131
, pp. 401-408
-
-
Dunn, D.E.1
Tanawattanacharoen, P.2
Boccuni, P.3
Nagakura, S.4
Green, S.W.5
Kirby, M.R.6
Kumar, M.S.7
Rosenfeld, S.8
Young, N.S.9
-
13
-
-
0036893544
-
Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome
-
Wang H, Chuhjo T, Yasue S, Omine M, Nakao S. Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome. Blood 2002;100:3897-902.
-
(2002)
Blood
, vol.100
, pp. 3897-3902
-
-
Wang, H.1
Chuhjo, T.2
Yasue, S.3
Omine, M.4
Nakao, S.5
-
14
-
-
58149235125
-
Detection of paroxysmal nocturnal hemoglobinuria clones in patients with myelodysplastic syndromes and related bone marrow diseases, with emphasis on diagnostic pitfalls and caveats
-
Wang SA, Pozdnyakova O, Jorgensen JL, Medeiros LJ, Stachurski D, Anderson M, Raza A, Woda BA. Detection of paroxysmal nocturnal hemoglobinuria clones in patients with myelodysplastic syndromes and related bone marrow diseases, with emphasis on diagnostic pitfalls and caveats. Haematologica 2009;94:29-37.
-
(2009)
Haematologica
, vol.94
, pp. 29-37
-
-
Wang, S.A.1
Pozdnyakova, O.2
Jorgensen, J.L.3
Medeiros, L.J.4
Stachurski, D.5
Anderson, M.6
Raza, A.7
Woda, B.A.8
-
15
-
-
0035726553
-
Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria
-
Araten DJ, Swirsky D, Karadimitris A, et al. Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria. Br J Haematol 2001;115:360-8.
-
(2001)
Br J Haematol
, vol.115
, pp. 360-368
-
-
Araten, D.J.1
Swirsky, D.2
Karadimitris, A.3
-
16
-
-
84870463231
-
Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO 'MDS-U' designation
-
Hosokawa K, Katagiri T, Sugimori N, Ishiyama K, Sasaki Y, Seiki Y, Sato-Otsubo A, Sanada M, Ogawa S, Nakao S. Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO 'MDS-U' designation. Haematologica 2012;97:1845-1849.
-
(2012)
Haematologica
, vol.97
, pp. 1845-1849
-
-
Hosokawa, K.1
Katagiri, T.2
Sugimori, N.3
Ishiyama, K.4
Sasaki, Y.5
Seiki, Y.6
Sato-Otsubo, A.7
Sanada, M.8
Ogawa, S.9
Nakao, S.10
-
17
-
-
0141484361
-
Cytogenetic abnormalities in paroxysmal nocturnal haemoglobinuria usually occur in haematopoietic cells that are glycosylphosphatidylinositol-anchored protein (GPI-AP) positive
-
Sloand EM, Fuhrer M, Keyvanfar K, Mainwaring L, Maciejewski J, Wang Y, Johnson S, Barrett AJ, Young NS. Cytogenetic abnormalities in paroxysmal nocturnal haemoglobinuria usually occur in haematopoietic cells that are glycosylphosphatidylinositol-anchored protein (GPI-AP) positive. Br J Haematol 2003;123:173-6.
-
(2003)
Br J Haematol
, vol.123
, pp. 173-176
-
-
Sloand, E.M.1
Fuhrer, M.2
Keyvanfar, K.3
Mainwaring, L.4
Maciejewski, J.5
Wang, Y.6
Johnson, S.7
Barrett, A.J.8
Young, N.S.9
-
18
-
-
0026696775
-
Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria
-
Parlier V, Tiainen M, Beris P, Miescher PA, Knuutila S, Jotterand Bellomo M. Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria. Br J Haematol 1992;81:296-304.
-
(1992)
Br J Haematol
, vol.81
, pp. 296-304
-
-
Parlier, V.1
Tiainen, M.2
Beris, P.3
Miescher, P.A.4
Knuutila, S.5
Jotterand Bellomo, M.6
-
19
-
-
0028234052
-
Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease
-
Longo L, Bessler M, Beris P, Swirsky D, Luzzatto L. Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease. Br J Haematol 1994;87:401-3.
-
(1994)
Br J Haematol
, vol.87
, pp. 401-403
-
-
Longo, L.1
Bessler, M.2
Beris, P.3
Swirsky, D.4
Luzzatto, L.5
-
20
-
-
39149083040
-
Hypocellularity in myelodysplastic syndrome is an independent factor which predicts a favorable outcome
-
Yue G, Hao S, Fadare O, Baker S, Pozdnyakova O, Galili N, Woda BA, Raza A, Wang SA. Hypocellularity in myelodysplastic syndrome is an independent factor which predicts a favorable outcome. Leuk Res 2008;32:553-8.
-
(2008)
Leuk Res
, vol.32
, pp. 553-558
-
-
Yue, G.1
Hao, S.2
Fadare, O.3
Baker, S.4
Pozdnyakova, O.5
Galili, N.6
Woda, B.A.7
Raza, A.8
Wang, S.A.9
-
21
-
-
0003676646
-
-
International Standing Committee on Human Cytogenetic Nomenclature, Basel; Unionville, CT: Karger
-
International Standing Committee on Human Cytogenetic Nomenclature, Shaffer LG, Slovak ML, Campbell LJ. ISCN 2009: An International System for Human Cytogenetic Nomenclature. Basel; Unionville, CT: Karger, 2009.
-
(2009)
ISCN 2009: An International System for Human Cytogenetic Nomenclature
-
-
Shaffer, L.G.1
Slovak, M.L.2
Campbell, L.J.3
-
22
-
-
33745968917
-
Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia
-
Cheson BD, Greenberg PL, Bennett JM, et al. Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia. Blood 2006;108:419-25.
-
(2006)
Blood
, vol.108
, pp. 419-425
-
-
Cheson, B.D.1
Greenberg, P.L.2
Bennett, J.M.3
-
23
-
-
0025205057
-
Immunosuppressive therapy for aplastic anemia: indications, agents, mechanisms, and results
-
Camitta BM, Doney K. Immunosuppressive therapy for aplastic anemia: indications, agents, mechanisms, and results. Am J Pediatr Hematol Oncol 1990;12:411-24.
-
(1990)
Am J Pediatr Hematol Oncol
, vol.12
, pp. 411-424
-
-
Camitta, B.M.1
Doney, K.2
-
24
-
-
32644434385
-
Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia
-
Sugimori C, Chuhjo T, Feng X, Yamazaki H, Takami A, Teramura M, Mizoguchi H, Omine M, Nakao S. Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia. Blood 2006;107:1308-14.
-
(2006)
Blood
, vol.107
, pp. 1308-1314
-
-
Sugimori, C.1
Chuhjo, T.2
Feng, X.3
Yamazaki, H.4
Takami, A.5
Teramura, M.6
Mizoguchi, H.7
Omine, M.8
Nakao, S.9
-
25
-
-
0033609114
-
Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals
-
Araten DJ, Nafa K, Pakdeesuwan K, Luzzatto L. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals. Proc Natl Acad Sci USA 1999;96:5209-14.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 5209-5214
-
-
Araten, D.J.1
Nafa, K.2
Pakdeesuwan, K.3
Luzzatto, L.4
-
26
-
-
70349218024
-
Origin and fate of blood cells deficient in glycosylphosphatidylinositol-anchored protein among patients with bone marrow failure
-
Sugimori C, Mochizuki K, Qi Z, Sugimori N, Ishiyama K, Kondo Y, Yamazaki H, Takami A, Okumura H, Nakao S. Origin and fate of blood cells deficient in glycosylphosphatidylinositol-anchored protein among patients with bone marrow failure. Br J Haematol 2009;147:102-12.
-
(2009)
Br J Haematol
, vol.147
, pp. 102-112
-
-
Sugimori, C.1
Mochizuki, K.2
Qi, Z.3
Sugimori, N.4
Ishiyama, K.5
Kondo, Y.6
Yamazaki, H.7
Takami, A.8
Okumura, H.9
Nakao, S.10
-
27
-
-
84870454857
-
Prognostic value of minor PNH clones in aplastic anaemia patients treated with ATG-based immunosuppression: results of a two-centre prospective study
-
Kulagin A, Golubovskaya I, Ganapiev A, et al. Prognostic value of minor PNH clones in aplastic anaemia patients treated with ATG-based immunosuppression: results of a two-centre prospective study. Bone Marrow Transplant 2011;46:S83-4.
-
(2011)
Bone Marrow Transplant
, vol.46
, pp. S83-S84
-
-
Kulagin, A.1
Golubovskaya, I.2
Ganapiev, A.3
-
28
-
-
28444483571
-
Diagnosis and management of paroxysmal nocturnal hemoglobinuria
-
Parker C, Omine M, Richards S, et al. Diagnosis and management of paroxysmal nocturnal hemoglobinuria. Blood 2005;106:3699-709.
-
(2005)
Blood
, vol.106
, pp. 3699-3709
-
-
Parker, C.1
Omine, M.2
Richards, S.3
-
29
-
-
84875215709
-
Investigation of the freely available easy-to-use software 'EZR' for medical statistics
-
Kanda Y. Investigation of the freely available easy-to-use software 'EZR' for medical statistics. Bone Marrow Transplant 2013;48:452-458.
-
(2013)
Bone Marrow Transplant
, vol.48
, pp. 452-458
-
-
Kanda, Y.1
-
30
-
-
84878018531
-
Increased plasma thrombopoietin levels in patients with myelodysplastic syndrome: a reliable marker for a benign subset of bone marrow failure
-
Seiki Y, Sasaki Y, Hosokawa K, Saito C, Sugimori N, Yamazaki H, Takami A, Nakao S. Increased plasma thrombopoietin levels in patients with myelodysplastic syndrome: a reliable marker for a benign subset of bone marrow failure. Haematologica 2013;98:901-907.
-
(2013)
Haematologica
, vol.98
, pp. 901-907
-
-
Seiki, Y.1
Sasaki, Y.2
Hosokawa, K.3
Saito, C.4
Sugimori, N.5
Yamazaki, H.6
Takami, A.7
Nakao, S.8
-
31
-
-
33947224233
-
CD34 cells from patients with trisomy 8 myelodysplastic syndrome (MDS) express early apoptotic markers but avoid programmed cell death by up-regulation of antiapoptotic proteins
-
Sloand EM, Pfannes L, Chen G, Shah S, Solomou EE, Barrett J, Young NS. CD34 cells from patients with trisomy 8 myelodysplastic syndrome (MDS) express early apoptotic markers but avoid programmed cell death by up-regulation of antiapoptotic proteins. Blood 2007;109:2399-405.
-
(2007)
Blood
, vol.109
, pp. 2399-2405
-
-
Sloand, E.M.1
Pfannes, L.2
Chen, G.3
Shah, S.4
Solomou, E.E.5
Barrett, J.6
Young, N.S.7
-
32
-
-
84055223059
-
Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia
-
Katagiri T, Sato-Otsubo A, Kashiwase K, et al. Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia. Blood 2011;118:6601-9.
-
(2011)
Blood
, vol.118
, pp. 6601-6609
-
-
Katagiri, T.1
Sato-Otsubo, A.2
Kashiwase, K.3
-
33
-
-
84866621729
-
Revised international prognostic scoring system for myelodysplastic syndromes
-
Greenberg PL, Tuechler H, Schanz J, et al. Revised international prognostic scoring system for myelodysplastic syndromes. Blood 2012;120:2454-65.
-
(2012)
Blood
, vol.120
, pp. 2454-2465
-
-
Greenberg, P.L.1
Tuechler, H.2
Schanz, J.3
-
34
-
-
84867447235
-
Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes
-
Saumell S, Florensa L, Luno E, et al. Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes. Br J Haematol 2012;159:311-21.
-
(2012)
Br J Haematol
, vol.159
, pp. 311-321
-
-
Saumell, S.1
Florensa, L.2
Luno, E.3
|