-
1
-
-
0029025475
-
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia
-
see comments
-
Charache S, Terrin ML, Moore RD, et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia [see comments]. N Engl J Med. 1995;332(20):1317-1322.
-
(1995)
N Engl J Med
, vol.332
, Issue.20
, pp. 1317-1322
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
-
2
-
-
0029845949
-
Hydroxyurea for treatment of severe sickle cell anemia: A pediatric clinical trial
-
Ferster A, Vermylen C, Cornu G, et al. Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial. Blood. 1996;88(6):1960-1964. (Pubitemid 26307897)
-
(1996)
Blood
, vol.88
, Issue.6
, pp. 1960-1964
-
-
Ferster, A.1
Vermylen, C.2
Cornu, G.3
Buyse, M.4
Corazza, F.5
Devalck, C.6
Fondu, P.7
Toppet, M.8
Sariban, E.9
-
3
-
-
0025217816
-
Hematologic responses of patients with sickle cell disease to treatment with hydroxyurea
-
Rodgers GP, Dover GJ, Noguchi CT, Schechter AN, Nienhuis AW. Hematologic responses of patients with sickle cell disease to treatment with hydroxyurea. N Engl J Med. 1990;322(15):1037-1045. (Pubitemid 20146662)
-
(1990)
New England Journal of Medicine
, vol.322
, Issue.15
, pp. 1037-1045
-
-
Rodgers, G.P.1
Dover, G.J.2
Noguchi, C.T.3
Schechter, A.N.4
Nienhuis, A.W.5
-
4
-
-
0034307369
-
Financial analysis of chronic transfusion for stroke prevention in sickle cell disease
-
Wayne AS, Schoenike SE, Pegelow CH. Financial analysis of chronic transfusion for stroke prevention in sickle cell disease. Blood. 2000;96(7):2369-2372.
-
(2000)
Blood
, vol.96
, Issue.7
, pp. 2369-2372
-
-
Wayne, A.S.1
Schoenike, S.E.2
Pegelow, C.H.3
-
5
-
-
79251628870
-
Impact of early transcranial Doppler screening and intensive therapy on cerebral vasculopathy outcome in a newborn sickle cell anemia cohort
-
Bernaudin F, Verlhac S, Arnaud C, et al. Impact of early transcranial Doppler screening and intensive therapy on cerebral vasculopathy outcome in a newborn sickle cell anemia cohort. Blood. 2011;117(4):1130-1140.
-
(2011)
Blood
, vol.117
, Issue.4
, pp. 1130-1140
-
-
Bernaudin, F.1
Verlhac, S.2
Arnaud, C.3
-
6
-
-
79952158820
-
Effect of transfusion therapy on transcranial Doppler ultrasonography velocities in children with sickle cell disease
-
Kwiatkowski JL, Yim E, Miller S, Adams RJ. Effect of transfusion therapy on transcranial Doppler ultrasonography velocities in children with sickle cell disease. Pediatr Blood Cancer. 2011;56(5):777-782.
-
(2011)
Pediatr Blood Cancer
, vol.56
, Issue.5
, pp. 777-782
-
-
Kwiatkowski, J.L.1
Yim, E.2
Miller, S.3
Adams, R.J.4
-
7
-
-
78751697297
-
Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
-
Jan 20
-
Hulbert ML, McKinstry RC, Lacey JL, et al. Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease. Blood. Jan 20;117(3):772-779.
-
Blood
, vol.117
, Issue.3
, pp. 772-779
-
-
Hulbert, M.L.1
McKinstry, R.C.2
Lacey, J.L.3
-
8
-
-
77958552396
-
Antibody development in pediatric sickle cell patients undergoing erythrocytapheresis
-
Godfrey GJ, Lockwood W, Kong M, Bertolone S, Raj A. Antibody development in pediatric sickle cell patients undergoing erythrocytapheresis. Pediatr Blood Cancer. 2010;55(6):1134-1137.
-
(2010)
Pediatr Blood Cancer
, vol.55
, Issue.6
, pp. 1134-1137
-
-
Godfrey, G.J.1
Lockwood, W.2
Kong, M.3
Bertolone, S.4
Raj, A.5
-
9
-
-
80051563022
-
Extended red blood cell antigen matching for transfusions in sickle cell disease: A review of a 14-year experience from a single center
-
published online ahead of print February 18, 2011 doi: 10.1111/j.1537-2995.2010.03045.x
-
Lasalle-Williams M, Nuss R, Le T, et al. Extended red blood cell antigen matching for transfusions in sickle cell disease: a review of a 14-year experience from a single center [published online ahead of print February 18, 2011]. Transfusion. doi: 10.1111/j.1537-2995.2010.03045.x.
-
Transfusion
-
-
Lasalle-Williams, M.1
Nuss, R.2
Le, T.3
-
10
-
-
77649128081
-
HLA alloimmunization is associated with RBC antibodies in multiply transfused patients with sickle cell disease
-
McPherson ME, Anderson AR, Castillejo MI, et al. HLA alloimmunization is associated with RBC antibodies in multiply transfused patients with sickle cell disease. Pediatr Blood Cancer. 2010;54(4):552-558.
-
(2010)
Pediatr Blood Cancer
, vol.54
, Issue.4
, pp. 552-558
-
-
McPherson, M.E.1
Anderson, A.R.2
Castillejo, M.I.3
-
11
-
-
34948830175
-
Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease
-
DOI 10.1182/blood-2007-03-079665
-
Bernaudin F, Socie G, Kuentz M, et al. Long-term results of related, myeloablative stem cell transplantation to cure sickle cell disease. Blood. 2007;110(7):2749-2756. (Pubitemid 47523201)
-
(2007)
Blood
, vol.110
, Issue.7
, pp. 2749-2756
-
-
Bernaudin, F.1
Socie, G.2
Kuentz, M.3
Chevret, S.4
Duval, M.5
Bertrand, Y.6
Vannier, J.-P.7
Yakouben, K.8
Thuret, I.9
Bordigoni, P.10
Fischer, A.11
Lutz, P.12
Stephan, J.-L.13
Dhedin, N.14
Plouvier, E.15
Margueritte, G.16
Bories, D.17
Verlhac, S.18
Esperou, H.19
Coic, L.20
Vernant, J.-P.21
Gluckman, E.22
more..
-
12
-
-
9344231922
-
Bone marrow transplantation for sickle cell disease
-
DOI 10.1056/NEJM199608083350601
-
Walters MC, Patience M, Leisenring W, et al. Bone marrow transplantation for sickle cell disease. N Engl J Med. 1996 335(6):369-376. (Pubitemid 26257244)
-
(1996)
New England Journal of Medicine
, vol.335
, Issue.6
, pp. 369-376
-
-
Walters, M.C.1
Patience, M.2
Leisenring, W.3
Eckman, J.R.4
Scott, J.P.5
Mentzer, W.C.6
Davies, S.C.7
Ohene-Frempong, K.8
Bernaudin, F.9
Matthews, D.C.10
Storb, R.11
Sullivan, K.M.12
-
13
-
-
74049151134
-
Cardiopulmonary complications leading to premature deaths in adult patients with sickle cell disease
-
Fitzhugh CD, Lauder N, Jonassaint JC, et al. Cardiopulmonary complications leading to premature deaths in adult patients with sickle cell disease. Am J Hematol. 2010;85(1):36-40.
-
(2010)
Am J Hematol
, vol.85
, Issue.1
, pp. 36-40
-
-
Fitzhugh, C.D.1
Lauder, N.2
Jonassaint, J.C.3
-
14
-
-
27944496081
-
Outcome of sickle cell anemia: A 4-decade observational study of 1056 patients
-
DOI 10.1097/01.md.0000189089.45003.52
-
Powars DR, Chan LS, Hiti A, Ramicone E, Johnson C. Outcome of sickle cell anemia: a 4-decade observational study of 1056 patients. Medicine (Baltimore). 2005;84(6):363-376. (Pubitemid 41668935)
-
(2005)
Medicine
, vol.84
, Issue.6
, pp. 363-376
-
-
Powars, D.R.1
Chan, L.S.2
Hiti, A.3
Ramicone, E.4
Johnson, C.5
-
15
-
-
10744233940
-
Pulmonary hypertension as a risk factor for death in patients with sickle cell disease
-
Gladwin Mt, Sachdev V, Jison ML, et al. Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med. 2004;350(9):886-895.
-
(2004)
N Engl J Med
, vol.350
, Issue.9
, pp. 886-895
-
-
Gladwin, Mt.1
Sachdev, V.2
Jison, M.L.3
-
16
-
-
0025939624
-
Chronic renal failure in sickle cell disease: Risk factors, clinical course, and mortality
-
Powars DR, Elliott-Mills DD, Chan L, et al. Chronic renal failure in sickle cell disease: risk factors, clinical course, and mortality. Ann Intern Med. 1991;115(8):614-620.
-
(1991)
Ann Intern Med
, vol.115
, Issue.8
, pp. 614-620
-
-
Powars, D.R.1
Elliott-Mills, D.D.2
Chan, L.3
-
17
-
-
0023279105
-
Prognosis of the nephrotic syndrome in sickle glomerulopathy. A retrospective study
-
Bakir AA, Hathiwala SC, Ainis H, et al. Prognosis of the nephrotic syndrome in sickle glomerulopathy. A retrospective study. Am J Nephrol. 1987;7(2):110-115. (Pubitemid 17094643)
-
(1987)
American Journal of Nephrology
, vol.7
, Issue.2
, pp. 110-115
-
-
Bakir, A.A.1
Hathiwala, S.C.2
Ainis, H.3
-
18
-
-
33750600143
-
Circumstances of death in adult sickle cell disease patients
-
DOI 10.1002/ajh.20685
-
Darbari DS, Kple-Faget P, Kwagyan J, Rana S, Gordeuk VR, Castro O. Circumstances of death in adult sickle cell disease patients. Am J Hematol. 2006;81(11):858-863. (Pubitemid 44682188)
-
(2006)
American Journal of Hematology
, vol.81
, Issue.11
, pp. 858-863
-
-
Darbari, D.S.1
Kple-Faget, P.2
Kwagyan, J.3
Rana, S.4
Gordeuk, V.R.5
Castro, O.6
-
19
-
-
22244448421
-
Sickle cell hepatopathy: Clinical presentation, treatment, and outcome in pediatric and adult patients
-
DOI 10.1002/pbc.20317
-
Ahn H, Li CS, Wang W. Sickle cell hepatopathy: clinical presentation, treatment, and outcome in pediatric and adult patients. Pediatr Blood Cancer. 2005;45(2):184-190. (Pubitemid 40993585)
-
(2005)
Pediatric Blood and Cancer
, vol.45
, Issue.2
, pp. 184-190
-
-
Ahn, H.1
Li, C.-S.2
Wang, W.3
-
20
-
-
0021593369
-
Bone-marrow transplantation in a patient with sickle-cell anemia
-
Johnson FL, Look AT, Gockerman J, Ruggiero MR, Dalla-Pozza L, Billings FT 3rd. Bone-marrow transplantation in a patient with sickle-cell anemia. N Engl J Med. 1984;311(12):780-783. (Pubitemid 14026230)
-
(1984)
New England Journal of Medicine
, vol.311
, Issue.12
, pp. 780-783
-
-
Johnson, F.L.1
Look, A.T.2
Gockerman, J.3
-
21
-
-
0027185471
-
Bone marrow transplantation in sickle cell disease: The Belgian experience
-
Vermylen C, Cornu G, Ferster A, Ninane J, Sariban E. Bone marrow transplantation in sickle cell disease: the Belgian experience. Bone Marrow Transplant. 1993;12(suppl 1):116-117. (Pubitemid 23231081)
-
(1993)
Bone Marrow Transplantation
, vol.12
, Issue.SUPPL. 1
, pp. 116-117
-
-
Vermylen, C.1
Cornu, G.2
Ferster, A.3
Ninane, J.4
Sariban, E.5
-
22
-
-
0027268493
-
Bone marrow transplantation (BMT) in 14 children with severe sickle cell disease (SCD): The French experience
-
Bernaudin F, Souillet G, Vannier JP, et al. Bone marrow transplantation (BMT) in 14 children with severe sickle cell disease (SCD): the French experience. GEGMO. Bone Marrow Transplant. 1993;12(suppl 1):118-121. (Pubitemid 23231082)
-
(1993)
Bone Marrow Transplantation
, vol.12
, Issue.SUPPL. 1
, pp. 118-121
-
-
Bernaudin, F.1
Souillet, G.2
Vannier, J.P.3
Plouvier, E.4
Lemerle, S.5
Michel, G.6
Bordigoni, P.7
Lutz, P.8
Kuentz, M.9
-
23
-
-
0028966027
-
Neurologic complications after allogeneic marrow transplantation for sickle cell anemia
-
see comments
-
Walters MC, Sullivan KM, Bernaudin F, et al. Neurologic complications after allogeneic marrow transplantation for sickle cell anemia [see comments]. Blood. 1995;85(4):879-884.
-
(1995)
Blood
, vol.85
, Issue.4
, pp. 879-884
-
-
Walters, M.C.1
Sullivan, K.M.2
Bernaudin, F.3
-
24
-
-
0031870487
-
Haematopoietic stem cell transplantation for sickle cell anaemia: The first 50 patients transplanted in Belgium
-
Vermylen C, Cornu G, Ferster A, et al. Haematopoietic stem cell transplantation for sickle cell anaemia: the first 50 patients transplanted in Belgium. Bone Marrow Transplant. 1998;22(1):1-6. (Pubitemid 28330528)
-
(1998)
Bone Marrow Transplantation
, vol.22
, Issue.1
, pp. 1-6
-
-
Vermylen, C.1
Cornu, G.2
Ferster, A.3
Brichard, B.4
Ninane, J.5
Ferrant, A.6
Zenebergh, A.7
Macs, P.8
Dhooge, C.9
Benoit, Y.10
Beguin, Y.11
Dresse, M.F.12
Sariban, E.13
-
25
-
-
0035544031
-
Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia
-
Walters MC, Patience M, Leisenring W, et al. Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia. Biol Blood Marrow Transplant. 2001;7(12):665-673. (Pubitemid 34055819)
-
(2001)
Biology of Blood and Marrow Transplantation
, vol.7
, Issue.12
, pp. 665-673
-
-
Walters, M.C.1
Patience, M.2
Leisenring, W.3
Rogers, Z.R.4
Aquino, V.M.5
Buchanan, G.R.6
Roberts, I.A.G.7
Yeager, A.M.8
Hsu, L.9
Adamkiewicz, T.10
Kurtzberg, J.11
Vichinsky, E.12
Storer, B.13
Storb, R.14
Sullivan, K.M.15
-
26
-
-
11144354570
-
Hydroxyurea treatment for sickle cell disease: Impact on haematopoietic stem cell transplantation's outcome
-
DOI 10.1038/sj.bmt.1704443
-
Brachet C, Azzi N, Demulder A, et al. Hydroxyurea treatment for sickle cell disease: impact on haematopoietic stem cell transplantation's outcome. Bone Marrow Transplant. 2004;33(8):799-803. (Pubitemid 38519240)
-
(2004)
Bone Marrow Transplantation
, vol.33
, Issue.8
, pp. 799-803
-
-
Brachet, C.1
Azzi, N.2
Demulder, A.3
Devalck, C.4
Gourdin, A.5
Gulbis, B.6
Klein, A.7
Le, P.Q.8
Loop, M.9
Sariban, E.10
Ferster, A.11
-
27
-
-
34247858963
-
Matched-related donor transplantation for sickle cell disease: Report from the Center for International Blood and Transplant Research
-
DOI 10.1111/j.1365-2141.2007.06592.x
-
Panepinto JA, Walters MC, Carreras J, et al. Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research. Br J Haematol. 2007;137(5):479-485. (Pubitemid 46698289)
-
(2007)
British Journal of Haematology
, vol.137
, Issue.5
, pp. 479-485
-
-
Panepinto, J.A.1
Walters, M.C.2
Carreras, J.3
Marsh, J.4
Bredeson, C.N.5
Gale, R.P.6
Hale, G.A.7
Horan, J.8
Hows, J.M.9
Klein, J.P.10
Pasquini, R.11
Roberts, I.12
Sullivan, K.13
Eapen, M.14
Ferster, A.15
-
28
-
-
34848927819
-
Mixed haematopoietic chimerism for sickle cell disease prevents intravascular haemolysis [1]
-
DOI 10.1111/j.1365-2141.2007.06803.x
-
Wu CJ, Gladwin M, Tisdale J, et al. Mixed haematopoietic chimerism for sickle cell disease prevents intravascular haemolysis. Br J Haematol. 2007;139(3):504-507. (Pubitemid 47512177)
-
(2007)
British Journal of Haematology
, vol.139
, Issue.3
, pp. 504-507
-
-
Wu, C.J.1
Gladwin, M.2
Tisdale, J.3
Hsieh, M.4
Law, T.5
Biernacki, M.6
Rogers, S.7
Wang, X.8
Walters, M.9
Zahrieh, D.10
Antin, J.H.11
Ritz, J.12
Krishnamurti, L.13
-
29
-
-
3042753988
-
Reduced intensity haemopoietic stem-cell transplantation for treatment of non-malignant diseases in children
-
DOI 10.1016/S0140-6736(04)16628-2, PII S0140673604166282
-
Jacobsohn DA, Duerst R, Tse W, Kletzel M. Reduced intensity haemopoietic stem-cell transplantation for treatment of non-malignant diseases in children. Lancet. 2004;364(9429):156-162. (Pubitemid 38891687)
-
(2004)
Lancet
, vol.364
, Issue.9429
, pp. 156-162
-
-
Jacobsohn, D.A.1
Duerst, R.2
Tse, W.3
Kletzel, M.4
-
30
-
-
35648951105
-
Has stem cell transplantation come of age in the treatment of sickle cell disease?
-
DOI 10.1038/sj.bmt.1705779, PII 1705779
-
Shenoy S. Has stem cell transplantation come of age in the treatment of sickle cell disease? Bone Marrow Transplant. 2007;40(9):813-821. (Pubitemid 350020314)
-
(2007)
Bone Marrow Transplantation
, vol.40
, Issue.9
, pp. 813-821
-
-
Shenoy, S.1
-
31
-
-
70350764819
-
Defining the intensity of conditioning regimens: Working definitions
-
Bacigalupo A, Ballen K, Rizzo D, et al. Defining the intensity of conditioning regimens: working definitions. Biol Blood Marrow Transplant. 2009;15(12):1628-1633.
-
(2009)
Biol Blood Marrow Transplant
, vol.15
, Issue.12
, pp. 1628-1633
-
-
Bacigalupo, A.1
Ballen, K.2
Rizzo, D.3
-
32
-
-
0034648702
-
Regression of metastatic renal-cell carcinoma after non-myeloablative allogeneic peripheral-blood stemcell transplantation
-
Childs R, Chernoff A, Contentin N, et al. Regression of metastatic renal-cell carcinoma after non-myeloablative allogeneic peripheral-blood stemcell transplantation. N Engl J Med. 2000;343(11):750-758.
-
(2000)
N Engl J Med
, vol.343
, Issue.11
, pp. 750-758
-
-
Childs, R.1
Chernoff, A.2
Contentin, N.3
-
33
-
-
33645454939
-
Overcoming graft rejection in heavily transfused and allo-immunised patients with bone marrow failure syndromes using fludarabine-based haematopoietic cell transplantation
-
Srinivasan R, Takahashi Y, McCoy JP, et al. Overcoming graft rejection in heavily transfused and allo-immunised patients with bone marrow failure syndromes using fludarabine-based haematopoietic cell transplantation. Br J Haematol. 2006;133(3):305-314.
-
(2006)
Br J Haematol
, vol.133
, Issue.3
, pp. 305-314
-
-
Srinivasan, R.1
Takahashi, Y.2
McCoy, J.P.3
-
34
-
-
12144289379
-
Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia
-
DOI 10.1016/S1083-8791(03)00192-7, PII S1083879103001927
-
Iannone R, Casella JF, Fuchs EJ, et al. Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and betathalassemia. Biol Blood Marrow Transplant. 2003;9(8):519-528. (Pubitemid 38351796)
-
(2003)
Biology of Blood and Marrow Transplantation
, vol.9
, Issue.8
, pp. 519-528
-
-
Iannone, R.1
Casella, J.F.2
Fuchs, E.J.3
Chen, A.R.4
Jones, R.J.5
Woolfrey, A.6
Amylon, M.7
Sullivan, K.M.8
Storb, R.F.9
Walters, M.C.10
-
35
-
-
0033104824
-
Inhibition of cell cycle progression by rapamycin induces T cell clonal anergy even in the presence of costimulation
-
Powell JD, Lerner CG, Schwartz RH. Inhibition of cell cycle progression by rapamycin induces T cell clonal anergy even in the presence of costimulation. J Immunol. 1999;162(5):2775-2784. (Pubitemid 29309302)
-
(1999)
Journal of Immunology
, vol.162
, Issue.5
, pp. 2775-2784
-
-
Powell, J.D.1
Lerner, C.G.2
Schwartz, R.H.3
-
36
-
-
29344456390
-
Low-dose radiation plus rapamycin promotes long-term bone marrow chimerism
-
DOI 10.1097/01.tp.0000185299.72295.90
-
Powell JD, Fitzhugh C, Kang EM, Hsieh M, Schwartz RH, Tisdale JF. Low-dose radiation plus rapamycin promotes long-term bone marrow chimerism. Transplantation. 2005;80(11):1541-1545. (Pubitemid 43005862)
-
(2005)
Transplantation
, vol.80
, Issue.11
, pp. 1541-1545
-
-
Powell, J.D.1
Fitzhugh, C.2
Kang, E.M.3
Hsieh, M.4
Schwartz, R.H.5
Tisdale, J.F.6
-
37
-
-
0032495656
-
Granulocytosis causing sickle-cell crisis
-
Abboud M, Laver J, Blau CA. Granulocytosis causing sickle-cell crisis [letter]. Lancet. 1998;351(9107):959. (Pubitemid 28138477)
-
(1998)
Lancet
, vol.351
, Issue.9107
, pp. 959
-
-
Abboud, M.1
Laver, J.2
Blau, C.A.3
-
38
-
-
0035874493
-
Fatal sickle cell crisis after granulocyte colony-stimulating factor administration
-
Adler BK, Salzman DE, Carabasi MH, Vaughan WP, Reddy VV, Prchal JT. Fatal sickle cell crisis after granulocyte colony-stimulating factor administration. Blood. 2001;97(10):3313-3314.
-
(2001)
Blood
, vol.97
, Issue.10
, pp. 3313-3314
-
-
Adler, B.K.1
Salzman, D.E.2
Carabasi, M.H.3
Vaughan, W.P.4
Reddy, V.V.5
Prchal, J.T.6
-
39
-
-
0035878007
-
Granulocyte colony-stimulating factorinduced sickle cell crisis and multiorgan dysfunction in a patient with compound heterozygous sickle cell/beta+ thalassemia
-
Grigg AP. Granulocyte colony-stimulating factorinduced sickle cell crisis and multiorgan dysfunction in a patient with compound heterozygous sickle cell/beta+ thalassemia. Blood. 2001;97(12):3998-3999.
-
(2001)
Blood
, vol.97
, Issue.12
, pp. 3998-3999
-
-
Grigg, A.P.1
-
40
-
-
68049130981
-
Granulocyte colony-stimulating factor (G-CSF) administration in individuals with sickle cell disease: Time for a moratorium?
-
Fitzhugh CD, Hsieh MM, Bolan CD, Saenz C, Tisdale JF. Granulocyte colony-stimulating factor (G-CSF) administration in individuals with sickle cell disease: time for a moratorium? Cytotherapy. 2009;11(4):464-471.
-
(2009)
Cytotherapy
, vol.11
, Issue.4
, pp. 464-471
-
-
Fitzhugh, C.D.1
Hsieh, M.M.2
Bolan, C.D.3
Saenz, C.4
Tisdale, J.F.5
-
41
-
-
0017056967
-
Freezing and deglycerolizing sickle trait red blood cells
-
Meryman HT, Hornblower M. Freezing and deglycerolizing sickle-trait red blood cells. Transfusion. 1976;16(6):627-632. (Pubitemid 8027823)
-
(1976)
Transfusion
, vol.16
, Issue.6
, pp. 627-632
-
-
Meryman, H.T.1
Hornblower, M.2
-
42
-
-
0027931352
-
White cell reduction in blood from donors with sickle cell trait
-
letter
-
Bodensteiner D. White cell reduction in blood from donors with sickle cell trait [letter]. Transfusion. 1994;34(1):84.
-
(1994)
Transfusion
, vol.34
, Issue.1
, pp. 84
-
-
Bodensteiner, D.1
-
43
-
-
0021246762
-
Transfusion of frozen erythrocytes from a donor with sickle trait
-
Kelleher JF Jr, Luban NL. Transfusion of frozen erythrocytes from a donor with sickle trait. Transfusion. 1984;24(2):167-168. (Pubitemid 14135428)
-
(1984)
Transfusion
, vol.24
, Issue.2
, pp. 167-168
-
-
Kelleher Jr., J.F.1
Luban, N.L.C.2
-
44
-
-
0036464660
-
Mobilization, collection, and processing of peripheral blood stem cells in individuals with sickle cell trait
-
DOI 10.1182/blood.V99.3.850
-
Kang EM, Areman EM, David-Ocampo V, et al. Mobilization, collection, and processing of peripheral blood stem cells in individuals with sickle cell trait. Blood. 2002;99(3):850-855. (Pubitemid 34525545)
-
(2002)
Blood
, vol.99
, Issue.3
, pp. 850-855
-
-
Kang, E.M.1
Areman, E.M.2
David-Ocampo, V.3
Fitzhugh, C.4
Link, M.E.5
Read, E.J.6
Leitman, S.F.7
Rodgers, G.P.8
Tisdale, J.F.9
-
45
-
-
13244269889
-
Hematopoietic stem cell transplantation for multiply transfused patients with sickle cell disease and thalassemia after low-dose total body irradiation, fludarabine, and rabbit anti-thymocyte globulin
-
DOI 10.1038/sj.bmt.1704745
-
Horan JT, Liesveld JL, Fenton P, Blumberg N, Walters MC. Hematopoietic stem cell transplantation for multiply transfused patients with sicklecell disease and thalassemia after low-dose total body irradiation, fludarabine, and rabbit anti-thymocyte globulin. Bone Marrow Transplant. 2005;35(2):171-177. (Pubitemid 40185933)
-
(2005)
Bone Marrow Transplantation
, vol.35
, Issue.2
, pp. 171-177
-
-
Horan, J.T.1
Liesveld, J.L.2
Fenton, P.3
Blumberg, N.4
Walters, M.C.5
-
46
-
-
0034307366
-
In vivo CAMPATH-1H prevents graft-versus-host disease following nonmyeloablative stem cell transplantation
-
Kottaridis PD, Milligan DW, Chopra R, et al. In vivo CAMPATH-1H prevents graft-versus-host disease following nonmyeloablative stem cell transplantation. Blood. 2000;96(7):2419-2425.
-
(2000)
Blood
, vol.96
, Issue.7
, pp. 2419-2425
-
-
Kottaridis, P.D.1
Milligan, D.W.2
Chopra, R.3
-
47
-
-
0036464657
-
Limiting transplantation-related mortality following unrelated donor stem cell transplantation by using a nonmyeloablative conditioning regimen
-
DOI 10.1182/blood.V99.3.1071
-
Chakraverty R, Peggs K, Chopra R, et al. Limiting transplantation-related mortality following unrelated donor stem cell transplantation by using a nonmyeloablative conditioning regimen. Blood. 2002;99(3):1071-1078. (Pubitemid 34525573)
-
(2002)
Blood
, vol.99
, Issue.3
, pp. 1071-1078
-
-
Chakraverty, R.1
Peggs, K.2
Chopra, R.3
Milligan, D.W.4
Kottaridis, P.D.5
Verfuerth, S.6
Geary, J.7
Thuraisundaram, D.8
Branson, K.9
Chakrabarti, S.10
Mahendra, P.11
Craddock, C.12
Parker, A.13
Hunter, A.14
Hale, G.15
Waldmann, H.16
Williams, C.D.17
Yong, K.18
Linch, D.C.19
Goldstone, A.H.20
Mackinnon, S.21
more..
-
48
-
-
71849118976
-
Allogeneic hematopoietic stem-cell transplantation for sickle cell disease
-
Hsieh MM, Kang EM, Fitzhugh CD, et al. Allogeneic hematopoietic stem-cell transplantation for sickle cell disease. N Engl J Med. 2009;361(24): 2309-2317.
-
(2009)
N Engl J Med
, vol.361
, Issue.24
, pp. 2309-2317
-
-
Hsieh, M.M.1
Kang, E.M.2
Fitzhugh, C.D.3
-
49
-
-
38949124765
-
Late effects of myeloablative bone marrow transplantation (BMT) in sickle cell disease (SCD)
-
author reply 1744
-
Fitzhugh CD, Perl S, Hsieh MM. Late effects of myeloablative bone marrow transplantation (BMT) in sickle cell disease (SCD). Blood. 2008;111(3):1742- 1743; author reply 1744.
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1742-1743
-
-
Fitzhugh, C.D.1
Perl, S.2
Hsieh, M.M.3
-
50
-
-
53749086728
-
Stable long-term donor engraftment following reduced-intensity hematopoietic cell transplantation for sickle cell disease
-
Krishnamurti L, Kharbanda S, Biernacki MA, et al. Stable long-term donor engraftment following reduced-intensity hematopoietic cell transplantation for sickle cell disease. Biol Blood Marrow Transplant. 2008;14(11):1270-1278.
-
(2008)
Biol Blood Marrow Transplant
, vol.14
, Issue.11
, pp. 1270-1278
-
-
Krishnamurti, L.1
Kharbanda, S.2
Biernacki, M.A.3
-
51
-
-
36148986518
-
Fludarabine-Based Nonmyeloablative Stem Cell Transplantation for Sickle Cell Disease with and without Renal Failure: Clinical Outcome and Pharmacokinetics
-
DOI 10.1016/j.bbmt.2007.08.050, PII S1083879107004569
-
Horwitz ME, Spasojevic I, Morris A, et al. Fludarabine- based nonmyeloablative stem cell transplantation for sickle cell disease with and without renal failure: clinical outcome and pharmacokinetics. Biol Blood Marrow Transplant. 2007;13(12):1422-1426. (Pubitemid 350107733)
-
(2007)
Biology of Blood and Marrow Transplantation
, vol.13
, Issue.12
, pp. 1422-1426
-
-
Horwitz, M.E.1
Spasojevic, I.2
Morris, A.3
Telen, M.4
Essell, J.5
Gasparetto, C.6
Sullivan, K.7
Long, G.8
Chute, J.9
Chao, N.10
Rizzieri, D.11
-
52
-
-
59449098985
-
Gene therapy for immunodeficiency due to adenosine deaminase deficiency
-
Aiuti A, Cattaneo F, Galimberti S, et al. Gene therapy for immunodeficiency due to adenosine deaminase deficiency. N Engl J Med. 2009;360(5):447-458.
-
(2009)
N Engl J Med
, vol.360
, Issue.5
, pp. 447-458
-
-
Aiuti, A.1
Cattaneo, F.2
Galimberti, S.3
-
53
-
-
77954833516
-
Efficacy of gene therapy for X-linked severe combined immunodeficiency
-
Hacein-Bey-Abina S, Hauer J, Lim A, et al. Efficacy of gene therapy for X-linked severe combined immunodeficiency. N Engl J Med. 2010;363(4):355-364.
-
(2010)
N Engl J Med
, vol.363
, Issue.4
, pp. 355-364
-
-
Hacein-Bey-Abina, S.1
Hauer, J.2
Lim, A.3
-
54
-
-
76249131912
-
Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease
-
Stein S, Ott MG, Schultze-Strasser S, et al. Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease. Nat Med. 2010;16(2):198-204.
-
(2010)
Nat Med
, vol.16
, Issue.2
, pp. 198-204
-
-
Stein, S.1
Ott, M.G.2
Schultze-Strasser, S.3
-
55
-
-
0035874519
-
Functional requirements for phenotypic correction of murine beta-thalassemia: Implications for human gene therapy
-
Persons DA, Allay ER, Sabatino DE, Kelly P, Bodine DM, Nienhuis AW. Functional requirements for phenotypic correction of murine beta-thalassemia: implications for human gene therapy. Blood. 2001;97(10):3275-3282.
-
(2001)
Blood
, vol.97
, Issue.10
, pp. 3275-3282
-
-
Persons, D.A.1
Allay, E.R.2
Sabatino, D.E.3
Kelly, P.4
Bodine, D.M.5
Nienhuis, A.W.6
-
56
-
-
78650991791
-
Quantitatively different red cells/nucleated cell chimerism in patients with long-term persistant hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease
-
Andreani M, Testi M, Gaziev J, et al. Quantitatively different red cells/nucleated cell chimerism in patients with long-term persistant hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease. Haematologica. 2011;96(1):128-133.
-
(2011)
Haematologica
, vol.96
, Issue.1
, pp. 128-133
-
-
Andreani, M.1
Testi, M.2
Gaziev, J.3
-
57
-
-
14644418544
-
A novel reduced-intensity stem cell transplant regimen for nonmalignant disorders
-
DOI 10.1038/sj.bmt.1704795
-
Shenoy S, Grossman WJ, DiPersio J, et al. A novel reduced-intensity stem cell transplant regimen for nonmalignant disorders. Bone Marrow Transplant. 2005;35(4):345-352. (Pubitemid 40309479)
-
(2005)
Bone Marrow Transplantation
, vol.35
, Issue.4
, pp. 345-352
-
-
Shenoy, S.1
Grossman, W.J.2
DiPersio, J.3
Yu, L.C.4
Wilson, D.5
Barnes, Y.J.6
Mohanakumar, T.7
Rao, A.8
Hayashi, R.J.9
-
58
-
-
0033836980
-
Fludarabine-based conditioning for allogeneic transplantation in adults with sickle cell disease
-
van Besien K, Bartholomew A, Stock W, et al. Fludarabine-based conditioning for allogeneic transplantation in adults with sickle cell disease. Bone Marrow Transplant. 2000;26(4):445-449. (Pubitemid 30649562)
-
(2000)
Bone Marrow Transplantation
, vol.26
, Issue.4
, pp. 445-449
-
-
Van Besien, K.1
Bartholomew, A.2
Stock, W.3
Peace, D.4
Devine, S.5
Sher, D.6
Sosman, J.7
Chen, Y.-H.8
Koshy, M.9
Hoffman, R.10
-
59
-
-
47749098306
-
Relationship between mixed chimerism and rejection after bone marrow transplantation in thalassaemia
-
DOI 10.2450/2008.0051-07
-
Andreani M, Testi M, Battarra M, et al. Relationship between mixed chimerism and rejection after bone marrow transplantation in thalassaemia. Blood Transfus. 2008;6(3):143-149. (Pubitemid 352031647)
-
(2008)
Blood Transfusion
, vol.6
, Issue.3
, pp. 143-149
-
-
Andreani, M.1
Testi, M.2
Battarra, M.3
Indigeno, P.4
Guagnano, A.5
Polchi, P.6
Federici, G.7
Lucarelli, G.8
-
60
-
-
0033996420
-
Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation
-
Andreani M, Nesci S, Lucarelli G, et al. Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation. Bone Marrow Transplant. 2000;25(4):401-404. (Pubitemid 30114034)
-
(2000)
Bone Marrow Transplantation
, vol.25
, Issue.4
, pp. 401-404
-
-
Andreani, M.1
Nesci, S.2
Lucarelli, G.3
Tonucci, P.4
Rapa, S.5
Angelucci, E.6
Persini, B.7
Agostinelli, F.8
Donati, M.9
Manna, M.10
-
61
-
-
0026784785
-
Mixed chimerism in thalassemic patients after bone marrow transplantation
-
Nesci S, Manna M, Andreani M, Fattorini P, Graziosi G, Lucarelli G. Mixed chimerism in thalassemic patients after bone marrow transplantation. Bone Marrow Transplant. 1992;10(2):143-146.
-
(1992)
Bone Marrow Transplant
, vol.10
, Issue.2
, pp. 143-146
-
-
Nesci, S.1
Manna, M.2
Andreani, M.3
Fattorini, P.4
Graziosi, G.5
Lucarelli, G.6
-
62
-
-
0026040687
-
Bone marrow transplantation for sickle cell disease.Astudy of parents' decisions
-
Kodish E, Lantos J, Stocking C, Singer PA, Siegler M, Johnson FL. Bone marrow transplantation for sickle cell disease.Astudy of parents' decisions. N Engl J Med. 1991;325(19):1349-1353.
-
(1991)
N Engl J Med
, vol.325
, Issue.19
, pp. 1349-1353
-
-
Kodish, E.1
Lantos, J.2
Stocking, C.3
Singer, P.A.4
Siegler, M.5
Johnson, F.L.6
-
63
-
-
0030133622
-
Barriers to bone marrow transplantation for sickle cell anemia
-
Walters MC, Patience M, Leisenring W, et al. Barriers to bone marrow transplantation for sickle cell anemia. Biol Blood Marrow Transplant. 1996;2(2):100-104. (Pubitemid 126488201)
-
(1996)
Biology of Blood and Marrow Transplantation
, vol.2
, Issue.2
, pp. 100-104
-
-
Walters, M.C.1
Patience, M.2
Leisenring, W.3
Eckman, J.R.4
Buchanan, G.R.5
Rogers, Z.R.6
Olivieri, N.F.7
Vichinsky, E.8
Davies, S.C.9
Mentzer, W.C.10
Powars, D.11
Scott, J.P.12
Bernadin, F.13
Ohene-Frempong, K.14
Darbyshire, P.J.15
Wayne, A.16
Roberts, I.A.G.17
Dinndorf, P.18
Brandalise, S.19
Sanders, J.E.20
Matthews, D.C.21
Appelbaum, F.R.22
Storb, R.23
Sullivan, K.M.24
more..
-
64
-
-
0030051313
-
Persistence of fetal hemoglobin production after successful transplantation of cord blood stem cells in a patient with sickle cell anemia
-
DOI 10.1016/S0022-3476(96)70398-0
-
Brichard B, Vermylen C, Ninane J, Cornu G. Persistence of fetal hemoglobin production after successful transplantation of cord blood stem cells in a patient with sickle cell anemia [see comments]. J Pediatr. 1996;128(2):241-243. (Pubitemid 26065950)
-
(1996)
Journal of Pediatrics
, vol.128
, Issue.2
, pp. 241-243
-
-
Brichard, B.1
Vermylen, C.2
Ninane, J.3
Cornu, G.4
-
65
-
-
17544400218
-
Cord blood transplantation (CBT) in hemoglobinopathies
-
Miniero R, Rocha V, Saracco P, et al. Cord blood transplantation (CBT) in hemoglobinopathies. Eurocord. Bone Marrow Transplant. 1998;22(suppl 1):S78-S79. (Pubitemid 28375290)
-
(1998)
Bone Marrow Transplantation
, vol.22
, Issue.SUPPL. 1
-
-
Miniero, R.1
Rochau, V.2
Saracco, P.3
Locatelli, F.4
Brichard, B.5
Nagler, A.6
Roberts, I.7
Yaniv, I.8
Beksac, M.9
Bernaudin, F.10
Gluckman, E.11
-
66
-
-
0034268110
-
Successful cord blood transplantation for sickle cell anemia from a sibling who is human leukocyte Antigen-Identical: Implications for comprehensive care
-
DOI 10.1097/00043426-200009000-00010
-
Gore L, Lane PA, Quinones RR, Giller RH. Successful cord blood transplantation for sickle cell anemia from a sibling who is human leukocyte antigen-identical: implications for comprehensive care. J Pediatr Hematol Oncol. 2000;22(5):437-440. (Pubitemid 33599752)
-
(2001)
Journal of Pediatric Hematology/Oncology
, vol.22
, Issue.5
, pp. 437-440
-
-
Gore, L.1
Lane, P.A.2
Quinones, R.R.3
Giller, R.H.4
-
67
-
-
0037443543
-
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease
-
DOI 10.1182/blood-2002-07-2090
-
Locatelli F, Rocha V, Reed W, et al. Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease. Blood. 2003;101(6):2137-2143. (Pubitemid 36302049)
-
(2003)
Blood
, vol.101
, Issue.6
, pp. 2137-2143
-
-
Locatelli, F.1
Rocha, V.2
Reed, W.3
Bernaudin, F.4
Ertem, M.5
Grafakos, S.6
Brichard, B.7
Li, X.8
Nagler, A.9
Giorgiani, G.10
Haut, P.R.11
Brochstein, J.A.12
Nugent, D.J.13
Blatt, J.14
Woodard, P.15
Kurtzberg, J.16
Rubin, C.M.17
Miniero, R.18
Lutz, P.19
Raja, T.20
Roberts, I.21
Will, A.M.22
Yaniv, I.23
Vermylen, C.24
Tannoia, N.25
Garnier, F.26
Ionescu, I.27
Walters, M.C.28
Lubin, B.H.29
Gluckman, E.30
more..
-
68
-
-
29744465280
-
Sibling donor cord blood transplantation for thalassemia major: Experience of the sibling donor cord blood program
-
DOI 10.1196/annals.1345.025
-
Walters MC, Quirolo L, Trachtenberg ET, et al. Sibling donor cord blood transplantation for thalassemia major: Experience of the Sibling Donor Cord Blood Program. Ann NY Acad Sci. 2005;1054:206-213. (Pubitemid 43031026)
-
(2005)
Annals of the New York Academy of Sciences
, vol.1054
, pp. 206-213
-
-
Walters, M.C.1
Quirolo, L.2
Trachtenberg, E.T.3
Edwards, S.4
Hale, L.5
Lee, J.6
Morton-Wiley, J.7
Quirolo, K.8
Robertson, S.9
Saba, J.10
Lubin, B.11
-
69
-
-
34547428427
-
Unrelated cord blood transplantation in children with sickle cell disease: Review of four-center experience
-
DOI 10.1111/j.1399-3046.2007.00725.x
-
Adamkiewicz TV, Szabolcs P, Haight A, et al. Unrelated cord blood transplantation in children with sickle cell disease: review of four-center experience. Pediatr Transplant. Sep. 2007;11(6):641-644. (Pubitemid 47174392)
-
(2007)
Pediatric Transplantation
, vol.11
, Issue.6
, pp. 641-644
-
-
Adamkiewicz, T.V.1
Szabolcs, P.2
Haight, A.3
Baker, K.S.4
Staba, S.5
Kedar, A.6
Chiang, K.Y.7
Krishnamurti, L.8
Boyer, M.W.9
Kurtzberg, J.10
Wagner, J.E.11
Wingard, J.R.12
Yeager, A.M.13
-
70
-
-
33845712655
-
Transplantation of a child with sickle cell anemia with an unrelated cord blood unit after reduced intensity conditioning
-
DOI 10.1097/MPH.0b013e31802d3e53, PII 0004342620061200000015
-
Mazur M, Kurtzberg J, Halperin E, Ciocci G, Szabolcs P. Transplantation of a child with sickle cell anemia with an unrelated cord blood unit after reduced intensity conditioning. J Pediatr Hematol Oncol. 2006;28(12):840-844. (Pubitemid 44967683)
-
(2006)
Journal of Pediatric Hematology/Oncology
, vol.28
, Issue.12
, pp. 840-844
-
-
Mazur, M.1
Kurtzberg, J.2
Halperin, E.3
Ciocci, G.4
Szabolcs, P.5
-
71
-
-
77955014034
-
Successful unrelated donor cord blood transplantation for adult sickle cell disease and Hodgkin lymphoma
-
Sauter C, Rausen AR, Barker JN. Successful unrelated donor cord blood transplantation for adult sickle cell disease and Hodgkin lymphoma. Bone Marrow Transplant. 2010;45(7):1252.
-
(2010)
Bone Marrow Transplant
, vol.45
, Issue.7
, pp. 1252
-
-
Sauter, C.1
Rausen, A.R.2
Barker, J.N.3
-
72
-
-
0038743168
-
Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies
-
DOI 10.1038/sj.bmt.1703887
-
Krishnamurti L, Abel S, Maiers M, Flesch S. Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies. Bone Marrow Transplant. 2003;31(7):547-550. (Pubitemid 36546831)
-
(2003)
Bone Marrow Transplantation
, vol.31
, Issue.7
, pp. 547-550
-
-
Krishnamurti, L.1
Abel, S.2
Maiers, M.3
Flesch, S.4
-
73
-
-
33644847688
-
Identification of unrelated cord blood units for hematopoietic stem cell transplantation in children with sickle cell disease
-
PII 0004342620060100000006
-
Adamkiewicz TV, Boyer MW, Bray R, Haight A, Yeager AM. Identification of unrelated cord blood units for hematopoietic stem cell transplantation in children with sickle cell disease. J Pediatr Hematol Oncol. 2006;28(1):29-32. (Pubitemid 43361615)
-
(2006)
Journal of Pediatric Hematology/Oncology
, vol.28
, Issue.1
, pp. 29-32
-
-
Adamkiewicz, T.V.1
Boyer, M.W.2
Bray, R.3
Haight, A.4
Yeager, A.M.5
-
74
-
-
80051564402
-
Results of alternative donor search in adult patients with severe sickle cell disease (SCD) eligible for hematopoietic stem cell transplantation (HSCT)
-
Paper presented at
-
Hsieh M, Wilder J, Fitzhugh C, Link B, Tisdale JF. Results of alternative donor search in adult patients with severe sickle cell disease (SCD) eligible for hematopoietic stem cell transplantation (HSCT). Paper presented at Annual Meeting of the American Society of Hematology Annual Meetingm Atlanta, GA, December 2007.
-
Annual Meeting of the American Society of Hematology Annual Meetingm Atlanta, GA, December 2007
-
-
Hsieh, M.1
Wilder, J.2
Fitzhugh, C.3
Link, B.4
Tisdale, J.F.5
-
75
-
-
47249083472
-
Paucity of HLA-Identical Unrelated Donors for African-Americans with Hematologic Malignancies: The Need for New Donor Options
-
DOI 10.1016/j.bbmt.2008.06.005, PII S1083879108002486
-
Dew A, Collins D, Artz A, et al. Paucity of HLAidentical unrelated donors for African-Americans with hematologic malignancies: the need for new donor options. Biol Blood Marrow Transplant. 2008;14(8):938-941. (Pubitemid 351985032)
-
(2008)
Biology of Blood and Marrow Transplantation
, vol.14
, Issue.8
, pp. 938-941
-
-
Dew, A.1
Collins, D.2
Artz, A.3
Rich, E.4
Stock, W.5
Swanson, K.6
Van Besien, K.7
-
76
-
-
0042738792
-
Allogeneic hematopoietic stem cell transplantation from family members other than HLA-identical siblings over the last decade (1991-2000)
-
DOI 10.1182/blood-2003-02-0430
-
Kanda Y, Chiba S, Hirai H, et al. Allogeneic hematopoietic stem cell transplantation from family members other than HLA-identical siblings over the last decade (1991-2000). Blood. 2003;102(4):1541-1547. (Pubitemid 36988069)
-
(2003)
Blood
, vol.102
, Issue.4
, pp. 1541-1547
-
-
Kanda, Y.1
Chiba, S.2
Hirai, H.3
Sakamaki, H.4
Iseki, T.5
Kodera, Y.6
Karasuno, T.7
Okamoto, S.8
Hirabayashi, N.9
Iwato, K.10
Maruta, A.11
Fujimori, Y.12
Furukawa, T.13
Mineishi, S.14
Matsuo, K.15
Hamajima, N.16
Imamura, M.17
-
77
-
-
0024537269
-
Effect of HLA compatibility on engraftment of bone marrow transplants in patients with leukemia or lymphoma
-
Anasetti C, Amos D, Beatty PG, et al. Effect of HLA compatibility on engraftment of bone marrow transplants in patients with leukemia or lymphoma. N Engl J Med. 1989;320(4):197-204. (Pubitemid 19034144)
-
(1989)
New England Journal of Medicine
, vol.320
, Issue.4
, pp. 197-204
-
-
Anasetti, C.1
Amos, D.2
Beatty, P.G.3
Appelbaum, F.R.4
Bensinger, W.5
Buckner, C.D.6
Clift, R.7
Doney, K.8
Martin, P.J.9
Mickelson, E.10
Nisperos, B.11
O'Quigley, J.12
Ramberg, R.13
Sanders, J.E.14
Stewart, P.15
Storb, R.16
Sullivan, K.M.17
Witherspoon, R.P.18
Thomas, E.D.19
Hansen, J.A.20
more..
-
78
-
-
0025011798
-
Effect of HLA incompatibility on graft-versus-host disease, relapse, and survival after marrow transplantation for patients with leukemia or lymphoma
-
DOI 10.1016/0198-8859(90)90071-V
-
Anasetti C, Beatty PG, Storb R, et al. Effect of HLA incompatibility on graft-versus-host disease, relapse, and survival after marrow transplantation for patients with leukemia or lymphoma. Hum Immunol. 1990;29(2):79-91. (Pubitemid 20357658)
-
(1990)
Human Immunology
, vol.29
, Issue.2
, pp. 79-91
-
-
Anasetti, C.1
Beatty, P.G.2
Storb, R.3
Martin, P.J.4
Mori, M.5
Sanders, J.E.6
Thomas, E.D.7
Hansen, J.A.8
-
79
-
-
67651149659
-
Haploidentical hematopoietic stem cell transplantation in child hematologic malignancies with G-CSF-mobilized marrow grafts without T-cell depletion: A single-center report of 45 cases
-
Wang HX, Yan HM, Duan LN, et al. Haploidentical hematopoietic stem cell transplantation in child hematologic malignancies with G-CSF-mobilized marrow grafts without T-cell depletion: a single-center report of 45 cases. Pediatr Hematol Oncol. 2009;26(3):119-128.
-
(2009)
Pediatr Hematol Oncol
, vol.26
, Issue.3
, pp. 119-128
-
-
Wang, H.X.1
Yan, H.M.2
Duan, L.N.3
-
80
-
-
66549125203
-
Haploidentical stem cell transplantation after a reduced- intensity conditioning regimen for the treatment of advanced hematologic malignancies: Posttransplantation CD8-depleted donor lymphocyte infusions contribute to improve T-cell recovery
-
Dodero A, Carniti C, Raganato A, et al. Haploidentical stem cell transplantation after a reduced- intensity conditioning regimen for the treatment of advanced hematologic malignancies: posttransplantation CD8-depleted donor lymphocyte infusions contribute to improve T-cell recovery. Blood. 2009;113(19):4771-4779.
-
(2009)
Blood
, vol.113
, Issue.19
, pp. 4771-4779
-
-
Dodero, A.1
Carniti, C.2
Raganato, A.3
-
81
-
-
64749113174
-
Haploidentical hematopoietic stem cell transplantation without in vitro T cell depletion for treatment of hematologic malignancies in children
-
Huang X, Liu D, Liu K, et al. Haploidentical hematopoietic stem cell transplantation without in vitro T cell depletion for treatment of hematologic malignancies in children. Biol Blood Marrow Transplant. 2009;15(1 suppl):91-94.
-
(2009)
Biol Blood Marrow Transplant
, vol.15
, Issue.1 SUPPL.
, pp. 91-94
-
-
Huang, X.1
Liu, D.2
Liu, K.3
-
82
-
-
33746936705
-
Haploidentical hematopoietic stem cell transplantation without in vitro T-cell depletion for the treatment of hematological malignancies
-
Huang XJ, Liu DH, Liu KY, et al. Haploidentical hematopoietic stem cell transplantation without in vitro T-cell depletion for the treatment of hematological malignancies. Bone Marrow Transplant. 2006;38(4):291-297.
-
(2006)
Bone Marrow Transplant
, vol.38
, Issue.4
, pp. 291-297
-
-
Huang, X.J.1
Liu, D.H.2
Liu, K.Y.3
-
83
-
-
43449091559
-
HLA-Haploidentical Bone Marrow Transplantation for Hematologic Malignancies Using Nonmyeloablative Conditioning and High-Dose, Posttransplantation Cyclophosphamide
-
DOI 10.1016/j.bbmt.2008.03.005, PII S1083879108001146
-
Luznik L, O'Donnell PV, Symons HJ, et al. HLA-haploidentical bone marrow transplantation for hematologic malignancies using nonmyeloablative conditioning and high-dose, posttransplantation cyclophosphamide. Biol Blood Marrow Transplant. 2008;14(6):641-650. (Pubitemid 351664058)
-
(2008)
Biology of Blood and Marrow Transplantation
, vol.14
, Issue.6
, pp. 641-650
-
-
Luznik, L.1
O'Donnell, P.V.2
Symons, H.J.3
Chen, A.R.4
Leffell, M.S.5
Zahurak, M.6
Gooley, T.A.7
Piantadosi, S.8
Kaup, M.9
Ambinder, R.F.10
Huff, C.A.11
Matsui, W.12
Bolanos-Meade, J.13
Borrello, I.14
Powell, J.D.15
Harrington, E.16
Warnock, S.17
Flowers, M.18
Brodsky, R.A.19
Sandmaier, B.M.20
Storb, R.F.21
Jones, R.J.22
Fuchs, E.J.23
more..
-
84
-
-
2442420923
-
Successful Treatment of Refractory Autoimmune Hemolytic Anemia with Monthly Rituximab Following Nonmyeloablative Stem Cell Transplantation for Sickle Cell Disease
-
DOI 10.1097/00043426-200405000-00011
-
Raj A, Bertolone S, Cheerva A. Successful treatment of refractory autoimmune hemolytic anemia with monthly rituximab following nonmyeloablative stem cell transplantation for sickle cell disease. J Pediatr Hematol Oncol. 2004;26(5):312-314. (Pubitemid 38621373)
-
(2004)
Journal of Pediatric Hematology/Oncology
, vol.26
, Issue.5
, pp. 312-314
-
-
Raj, A.1
Bertolone, S.2
Cheerva, A.3
-
85
-
-
55549090680
-
Reduced intensity HLAhaploidentical BMT with post transplantation cyclophosphamide in nonmalignant hematologic diseases
-
Brodsky RA, Luznik L, Bolanos-Meade J, Leffell MS, Jones RJ, Fuchs EJ. Reduced intensity HLAhaploidentical BMT with post transplantation cyclophosphamide in nonmalignant hematologic diseases. Bone Marrow Transplant. 2008;42(8):523-527.
-
(2008)
Bone Marrow Transplant
, vol.42
, Issue.8
, pp. 523-527
-
-
Brodsky, R.A.1
Luznik, L.2
Bolanos-Meade, J.3
Leffell, M.S.4
Jones, R.J.5
Fuchs, E.J.6
-
86
-
-
0034724857
-
Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease
-
DOI 10.1126/science.288.5466.669
-
Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, et al. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease [see comments]. Science. 2000;288(5466):669-672. (Pubitemid 30241569)
-
(2000)
Science
, vol.288
, Issue.5466
, pp. 669-672
-
-
Cavazzana-Calvo, M.1
Hacein-Bey, S.2
De Saint, B.G.3
Gross, F.4
Yvon, E.5
Nusbaum, P.6
Selz, F.7
Hue, C.8
Certain, S.9
Casanova, J.-L.10
Bousso, P.11
Le, D.F.12
Fischer, A.13
-
87
-
-
18444376150
-
Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement [1]
-
DOI 10.1038/nm0502-423
-
Aiuti A, Vai S, Mortellaro A, et al. Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement. Nat Med. 2002;8(5):423-425. (Pubitemid 34546725)
-
(2002)
Nature Medicine
, vol.8
, Issue.5
, pp. 423-425
-
-
Aiuti, A.1
Vai, S.2
Mortellaro, A.3
Casorati, G.4
Ficara, F.5
Andolfi, G.6
Ferrari, G.7
Tabucchi, A.8
Carlucci, F.9
Ochs, H.D.10
Notarangelo, L.D.11
Roncarolo, M.G.12
Bordignon, C.13
-
88
-
-
0037189401
-
Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning
-
DOI 10.1126/science.1070104
-
Aiuti A, Slavin S, Aker M, et al. Correction of ADASCID by stem cell gene therapy combined with nonmyeloablative conditioning. Science. 2002;296(5577):2410-2413. (Pubitemid 34734219)
-
(2002)
Science
, vol.296
, Issue.5577
, pp. 2410-2413
-
-
Aiuti, A.1
Slavin, S.2
Aker, M.3
Ficara, F.4
Deola, S.5
Mortellaro, A.6
Morecki, S.7
Andolfi, G.8
Tabucchi, A.9
Carlucci, F.10
Marinello, E.11
Cattaneo, F.12
Vai, S.13
Servida, P.14
Miniero, R.15
Roncarolo, M.G.16
Bordignon, C.17
-
89
-
-
33645734405
-
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1
-
Ott MG, Schmidt M, Schwarzwaelder K, et al. Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1. Nat Med. 2006;12(4):401-409.
-
(2006)
Nat Med
, vol.12
, Issue.4
, pp. 401-409
-
-
Ott, M.G.1
Schmidt, M.2
Schwarzwaelder, K.3
-
90
-
-
34547686397
-
Multilineage hematopoietic reconstitution without clonal selection in ADA-SCID patients treated with stem cell gene therapy
-
DOI 10.1172/JCI31666
-
Aiuti A, Cassani B, Andolfi G, et al. Multilineage hematopoietic reconstitution without clonal selection in ADA-SCID patients treated with stem cell gene therapy. J Clin Invest. 2007;117(8):2233-2240. (Pubitemid 47219568)
-
(2007)
Journal of Clinical Investigation
, vol.117
, Issue.8
, pp. 2233-2240
-
-
Aiuti, A.1
Cassani, B.2
Andolfi, G.3
Mirolo, M.4
Biasco, L.5
Recchia, A.6
Urbinati, F.7
Valacca, C.8
Scaramuzza, S.9
Aker, M.10
Slavin, S.11
Cazzola, M.12
Sartori, D.13
Ambrosi, A.14
Di, S.C.15
Roncarolo, M.G.16
Mavilio, F.17
Bordignon, C.18
-
91
-
-
0343628721
-
Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin
-
DOI 10.1038/35017565
-
May C, Rivella S, Callegari J, et al. Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin. Nature. 2000;406(6791):82-86. (Pubitemid 30460215)
-
(2000)
Nature
, vol.406
, Issue.6791
, pp. 82-86
-
-
Chad, M.1
Rivella, S.2
Callegari, J.3
Heller, G.4
Gaensler, K.M.L.5
Luzzatto, L.6
Sadelain, M.7
-
92
-
-
0037772187
-
Successful treatment of murine beta-thalassemia using in vivo selection of genetically modified, drug-resistant hematopoietic stem cells
-
DOI 10.1182/blood-2003-03-0677
-
Persons DA, Allay ER, Sawai N, et al. Successful treatment of murine beta-thalassemia using in vivo selection of genetically modified, drug-resistant hematopoietic stem cells. Blood. 2003;102(2):506-513. (Pubitemid 36841967)
-
(2003)
Blood
, vol.102
, Issue.2
, pp. 506-513
-
-
Persons, D.A.1
Allay, E.R.2
Sawai, N.3
Hargrove, P.W.4
Brent, T.P.5
Hanawa, H.6
Nienhuis, A.W.7
Sorrentino, B.P.8
-
93
-
-
0037443467
-
The degree of phenotypic correction of murine beta-thalassemia intermedia following lentiviral-mediated transfer of a human gamma-globin gene is influenced by chromosomal position effects and vector copy number
-
DOI 10.1182/blood-2002-07-2211
-
Persons DA, Hargrove PW, Allay ER, Hanawa H, Nienhuis AW. The degree of phenotypic correction of murine beta -thalassemia intermedia following lentiviral-mediated transfer of a human gamma-globin gene is influenced by chromosomal position effects and vector copy number. Blood. 2003;101(6):2175- 2183. (Pubitemid 36302055)
-
(2003)
Blood
, vol.101
, Issue.6
, pp. 2175-2183
-
-
Persons, D.A.1
Hargrove, P.W.2
Allay, E.R.3
Hanawa, H.4
Nienhuis, A.W.5
-
94
-
-
0035861452
-
Correction of sickle cell disease in transgenic mouse models by gene therapy
-
DOI 10.1126/science.1065806
-
Pawliuk R, Westerman KA, Fabry ME, et al. Correction of sickle cell disease in transgenic mouse models by gene therapy. Science. 2001;294(5550):2368-2371. (Pubitemid 33140563)
-
(2001)
Science
, vol.294
, Issue.5550
, pp. 2368-2371
-
-
Pawliuk, R.1
Westerman, K.A.2
Fabry, M.E.3
Payen, E.4
Tighe, R.5
Bouhassira, E.E.6
Acharya, S.A.7
Ellis, J.8
London, I.M.9
Eaves, C.J.10
Humphries, R.K.11
Beuzard, Y.12
Nagel, R.L.13
Leboulch, P.14
-
95
-
-
0037195091
-
Permanent and panerythroid correction of murine beta thalassemia by multiple lentiviral integration in hematopoietic stem cells
-
DOI 10.1073/pnas.212507099
-
Imren S, Payen E, Westerman KA, et al. Permanent and panerythroid correction of murine beta thalassemia by multiple lentiviral integration in hematopoietic stem cells. Proc Natl Acad Sci U S A. 2002;99(22):14380-14385. (Pubitemid 35257680)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.22
, pp. 14380-14385
-
-
Imren, S.1
Payen, E.2
Westerman, K.A.3
Pawliuk, R.4
Fabry, M.E.5
Eaves, C.J.6
Cavilla, B.7
Wadsworth, L.D.8
Beuzard, Y.9
Bouhassira, E.E.10
Russell, R.11
London, I.M.12
Nagel, R.L.13
Leboulch, P.14
Humphries, R.K.15
-
96
-
-
79958017228
-
3′UTR-truncated Hmga2 cDNA causes MPN-like hematopoiesis by conferring a clonal growth advantage at the level of HSC in mice
-
Ikeda K, Mason PJ, Bessler M. 3′UTR-truncated Hmga2 cDNA causes MPN-like hematopoiesis by conferring a clonal growth advantage at the level of HSC in mice. Blood. 2011;117(22):5860-5869.
-
(2011)
Blood
, vol.117
, Issue.22
, pp. 5860-5869
-
-
Ikeda, K.1
Mason, P.J.2
Bessler, M.3
|