-
1
-
-
79955909191
-
Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG)
-
Wang WC, Ware RE, Miller ST, et al. Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG). Lancet 2011;377:1663-72.
-
(2011)
Lancet
, vol.377
, pp. 1663-1672
-
-
Wang, W.C.1
Ware, R.E.2
Miller, S.T.3
-
3
-
-
77957751077
-
Pregnancy in sickle cell disease: maternal and fetal outcomes in a population receiving prophylactic partial exchange transfusions
-
Ngo C, Kayem G, Habibi A, Benachi A, Goffinet F, Galacteros F, Haddad B. Pregnancy in sickle cell disease: maternal and fetal outcomes in a population receiving prophylactic partial exchange transfusions. Eur J Obstet Gynecol Reprod Biol 2010;152:138-42.
-
(2010)
Eur J Obstet Gynecol Reprod Biol
, vol.152
, pp. 138-142
-
-
Ngo, C.1
Kayem, G.2
Habibi, A.3
Benachi, A.4
Goffinet, F.5
Galacteros, F.6
Haddad, B.7
-
4
-
-
79957528030
-
Sickle-cell disease and compromised cognition
-
Wang WC. Sickle-cell disease and compromised cognition. Pediatr Blood Cancer 2011;56:705-6.
-
(2011)
Pediatr Blood Cancer
, vol.56
, pp. 705-706
-
-
Wang, W.C.1
-
5
-
-
80052601209
-
Mortality and causes of death in children with sickle cell disease in the Netherlands, before the introduction of neonatal screening
-
van der Plas EM, van den Tweel XW, Geskus RB, Heijboer H, Biemond BJ, Peters M, Fijnvandraat K. Mortality and causes of death in children with sickle cell disease in the Netherlands, before the introduction of neonatal screening. Br J Haematol 2011;155:106-10.
-
(2011)
Br J Haematol
, vol.155
, pp. 106-110
-
-
van der Plas, E.M.1
van den Tweel, X.W.2
Geskus, R.B.3
Heijboer, H.4
Biemond, B.J.5
Peters, M.6
Fijnvandraat, K.7
-
6
-
-
65649136953
-
Usefulness and limitations of Bayesian network model as a mortality risk assessment tool in sickle cell anemia
-
Anoop PB, Bevan DH, Chakrabarti S. Usefulness and limitations of Bayesian network model as a mortality risk assessment tool in sickle cell anemia. Am J Hematol 2009;84:312-3.
-
(2009)
Am J Hematol
, vol.84
, pp. 312-313
-
-
Anoop, P.B.1
Bevan, D.H.2
Chakrabarti, S.3
-
7
-
-
77954423200
-
Prevalence and clinical correlates of microalbuminuria in children with sickle cell disease
-
Becton LJ, Kalpatthi RV, Rackoff E, Disco D, Orak JK, Jackson SM, Shatat IF. Prevalence and clinical correlates of microalbuminuria in children with sickle cell disease. Pediatr Nephrol 2010;25:1505-11.
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 1505-1511
-
-
Becton, L.J.1
Kalpatthi, R.V.2
Rackoff, E.3
Disco, D.4
Orak, J.K.5
Jackson, S.M.6
Shatat, I.F.7
-
8
-
-
0028291736
-
Mortality in sickle cell disease. Life expectancy and risk factors for early death
-
Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med 1994;330:1639-44.
-
(1994)
N Engl J Med
, vol.330
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
Milner, P.F.4
Castro, O.5
Steinberg, M.H.6
Klug, P.P.7
-
9
-
-
27344441977
-
Health related quality of life in sickle cell patients: the PiSCES project
-
McClish DK, Penberthy LT, Bovbjerg VE, Roberts JD, Aisiku IP, Levenson JL, Roseff SD, Smith WR. Health related quality of life in sickle cell patients: the PiSCES project. Health Qual Life Outcomes 2005;3:50.
-
(2005)
Health Qual Life Outcomes
, vol.3
, pp. 50
-
-
McClish, D.K.1
Penberthy, L.T.2
Bovbjerg, V.E.3
Roberts, J.D.4
Aisiku, I.P.5
Levenson, J.L.6
Roseff, S.D.7
Smith, W.R.8
-
10
-
-
77951712618
-
Improved survival of children and adolescents with sickle cell disease
-
Quinn CT, Rogers ZR, McCavit TL, Buchanan GR. Improved survival of children and adolescents with sickle cell disease. Blood 2010;115:3447-52.
-
(2010)
Blood
, vol.115
, pp. 3447-3452
-
-
Quinn, C.T.1
Rogers, Z.R.2
McCavit, T.L.3
Buchanan, G.R.4
-
11
-
-
9344231922
-
Bone marrow transplantation for sickle cell disease
-
Walters MC, Patience M, Leisenring W, et al. Bone marrow transplantation for sickle cell disease. N Engl J Med 1996;335:369-76.
-
(1996)
N Engl J Med
, vol.335
, pp. 369-376
-
-
Walters, M.C.1
Patience, M.2
Leisenring, W.3
-
12
-
-
85028101011
-
Allogeneic cellular gene therapy in hemoglobinopathies-evaluation of hematopoietic SCT in sickle cell anemia
-
Lucarelli G, Gaziev J, Isgro A, et al. Allogeneic cellular gene therapy in hemoglobinopathies-evaluation of hematopoietic SCT in sickle cell anemia. Bone Marrow Transplant 2011;47:227-30.
-
(2011)
Bone Marrow Transplant
, vol.47
, pp. 227-230
-
-
Lucarelli, G.1
Gaziev, J.2
Isgro, A.3
-
13
-
-
77952427892
-
Outcome of hematopoietic cell transplantation in children with sickle cell disease, a single center's experience
-
Majumdar S, Robertson Z, Robinson A, Starnes S, Iyer R, Megason G. Outcome of hematopoietic cell transplantation in children with sickle cell disease, a single center's experience. Bone Marrow Transplant 2010;45:895-900.
-
(2010)
Bone Marrow Transplant
, vol.45
, pp. 895-900
-
-
Majumdar, S.1
Robertson, Z.2
Robinson, A.3
Starnes, S.4
Iyer, R.5
Megason, G.6
-
14
-
-
34247858963
-
Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research
-
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;137:479-85.
-
(2007)
Br J Haematol
, vol.137
, pp. 479-485
-
-
Panepinto, J.A.1
Walters, M.C.2
Carreras, J.3
-
15
-
-
84871021631
-
TC-related myeloablative stem cell transplantation (SCT) to cure sickle cell anemia (SCA): update of French results
-
abstract
-
Bernaudin F, Robin M, Ferry C. TC-related myeloablative stem cell transplantation (SCT) to cure sickle cell anemia (SCA): update of French results. Blood 2010;116:abstract 3518.
-
(2010)
Blood
, vol.116
, pp. 3518
-
-
Bernaudin, F.1
Robin, M.2
Ferry, C.3
-
16
-
-
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;22:1-6.
-
(1998)
Bone Marrow Transplant
, vol.22
, pp. 1-6
-
-
Vermylen, C.1
Cornu, G.2
Ferster, A.3
-
17
-
-
34948830175
-
Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease
-
Bernaudin F, Socie G, Kuentz M, et al. Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease. Blood 2007;110:2749-56.
-
(2007)
Blood
, vol.110
, pp. 2749-2756
-
-
Bernaudin, F.1
Socie, G.2
Kuentz, M.3
-
18
-
-
11144354570
-
Hydroxyurea treatment for sickle cell disease: impact on haematopoietic stem cell transplantation's outcome
-
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;33:799-803.
-
(2004)
Bone Marrow Transplant
, vol.33
, pp. 799-803
-
-
Brachet, C.1
Azzi, N.2
Demulder, A.3
-
19
-
-
0037443543
-
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease
-
Locatelli F, Rocha V, Reed W, et al. Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease. Blood 2003;101:2137-43.
-
(2003)
Blood
, vol.101
, pp. 2137-2143
-
-
Locatelli, F.1
Rocha, V.2
Reed, W.3
-
20
-
-
34347371274
-
Children with sickle cell disease: growth and gonadal function after hematopoietic stem cell transplantation
-
Brachet C, Heinrichs C, Tenoutasse S, Devalck C, Azzi N, Ferster A. Children with sickle cell disease: growth and gonadal function after hematopoietic stem cell transplantation. J Pediatr Hematol Oncol 2007;29:445-50.
-
(2007)
J Pediatr Hematol Oncol
, vol.29
, pp. 445-450
-
-
Brachet, C.1
Heinrichs, C.2
Tenoutasse, S.3
Devalck, C.4
Azzi, N.5
Ferster, A.6
-
21
-
-
77949390689
-
Stem-cell transplantation for sickle cell disease
-
author reply 6.
-
Walters MC, Sullivan KM. Stem-cell transplantation for sickle cell disease. N Engl J Med 2010;362:955-6; author reply 6.
-
(2010)
N Engl J Med
, vol.362
, pp. 955-956
-
-
Walters, M.C.1
Sullivan, K.M.2
-
22
-
-
84869813639
-
HLA-haploidentical bone marrow transplantation with post-transplant cyclophosphamide expands the donor pool for patients with sickle cell disease
-
Bolanos-Meade J, Fuchs EJ, Luznik L, Lanzkron SM, Gamper CJ, Jones RJ, Brodsky RA. HLA-haploidentical bone marrow transplantation with post-transplant cyclophosphamide expands the donor pool for patients with sickle cell disease. Blood 2012;120:4285-91.
-
(2012)
Blood
, vol.120
, pp. 4285-4291
-
-
Bolanos-Meade, J.1
Fuchs, E.J.2
Luznik, L.3
Lanzkron, S.M.4
Gamper, C.J.5
Jones, R.J.6
Brodsky, R.A.7
-
23
-
-
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
-
Horan JT, Liesveld JL, Fenton P, Blumberg N, Walters MC. 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. Bone Marrow Transplant 2005;35:171-7.
-
(2005)
Bone Marrow Transplant
, vol.35
, pp. 171-177
-
-
Horan, J.T.1
Liesveld, J.L.2
Fenton, P.3
Blumberg, N.4
Walters, M.C.5
-
24
-
-
36148986518
-
Fludarabine-based nonmyeloablative stem cell transplantation for sickle cell disease with and without renal failure: clinical outcome and pharmacokinetics
-
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;13:1422-6.
-
(2007)
Biol Blood Marrow Transplant
, vol.13
, pp. 1422-1426
-
-
Horwitz, M.E.1
Spasojevic, I.2
Morris, A.3
-
25
-
-
71849118976
-
Allogeneic hematopoietic stem-cell transplantation for sickle cell disease
-
Hsieh MM, Kang EM, Fitzhugh CD, Link MB, Bolan CD, Kurlander R, Childs RW, Rodgers GP, Powell JD, Tisdale JF. Allogeneic hematopoietic stem-cell transplantation for sickle cell disease. N Engl J Med 2009;361:2309-17.
-
(2009)
N Engl J Med
, vol.361
, pp. 2309-2317
-
-
Hsieh, M.M.1
Kang, E.M.2
Fitzhugh, C.D.3
Link, M.B.4
Bolan, C.D.5
Kurlander, R.6
Childs, R.W.7
Rodgers, G.P.8
Powell, J.D.9
Tisdale, J.F.10
-
26
-
-
53749086728
-
Stable long-term donor engraftment following reduced-intensity hematopoietic cell transplantation for sickle cell disease
-
Krishnamurti L, Kharbanda S, Biernacki MA, Zhang W, Baker KS, Wagner JE, Wu CJ. Stable long-term donor engraftment following reduced-intensity hematopoietic cell transplantation for sickle cell disease. Biol Blood Marrow Transplant 2008;14:1270-8.
-
(2008)
Biol Blood Marrow Transplant
, vol.14
, pp. 1270-1278
-
-
Krishnamurti, L.1
Kharbanda, S.2
Biernacki, M.A.3
Zhang, W.4
Baker, K.S.5
Wagner, J.E.6
Wu, C.J.7
-
27
-
-
0034779987
-
Allogeneic stem cell transplantation for sickle cell disease. A study of patients' decisions
-
van Besien K, Koshy M, Anderson-Shaw L, Talishy N, Dorn L, Devine S, Yassine M, Kodish E. Allogeneic stem cell transplantation for sickle cell disease. A study of patients' decisions. Bone Marrow Transplant 2001;28:545-9.
-
(2001)
Bone Marrow Transplant
, vol.28
, pp. 545-549
-
-
van Besien, K.1
Koshy, M.2
Anderson-Shaw, L.3
Talishy, N.4
Dorn, L.5
Devine, S.6
Yassine, M.7
Kodish, E.8
-
28
-
-
77950948797
-
Monitoring of adenovirus load in stool by real-time PCR permits early detection of impending invasive infection in patients after allogeneic stem cell transplantation
-
Lion T, Kosulin K, Landlinger C, et al. Monitoring of adenovirus load in stool by real-time PCR permits early detection of impending invasive infection in patients after allogeneic stem cell transplantation. Leukemia 2010;24:706-14.
-
(2010)
Leukemia
, vol.24
, pp. 706-714
-
-
Lion, T.1
Kosulin, K.2
Landlinger, C.3
-
29
-
-
84859796684
-
Molecular diagnosis and management of viral infections in hematopoietic stem cell transplant recipients
-
Breuer S, Rauch M, Matthes-Martin S, Lion T. Molecular diagnosis and management of viral infections in hematopoietic stem cell transplant recipients. Mol Diagn Ther 2012;16:63-77.
-
(2012)
Mol Diagn Ther
, vol.16
, pp. 63-77
-
-
Breuer, S.1
Rauch, M.2
Matthes-Martin, S.3
Lion, T.4
-
30
-
-
84864876080
-
The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantation
-
Lion T, Watzinger F, Preuner S, et al. The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantation. Leukemia 2012;26:1821-8.
-
(2012)
Leukemia
, vol.26
, pp. 1821-1828
-
-
Lion, T.1
Watzinger, F.2
Preuner, S.3
-
31
-
-
78651363574
-
Safety and efficacy of targeted busulfan therapy in children undergoing myeloablative matched sibling donor BMT for sickle cell disease
-
McPherson ME, Hutcherson D, Olson E, Haight AE, Horan J, Chiang KY. Safety and efficacy of targeted busulfan therapy in children undergoing myeloablative matched sibling donor BMT for sickle cell disease. Bone Marrow Transplant 2011;46:27-33.
-
(2011)
Bone Marrow Transplant
, vol.46
, pp. 27-33
-
-
McPherson, M.E.1
Hutcherson, D.2
Olson, E.3
Haight, A.E.4
Horan, J.5
Chiang, K.Y.6
-
32
-
-
43449108586
-
Sickle cell disease-related organ damage occurs irrespective of pain rate: implications for clinical practice
-
van Beers EJ, van Tuijn CF, Mac Gillavry MR, van der Giessen A, Schnog JJ, Biemond BJ. Sickle cell disease-related organ damage occurs irrespective of pain rate: implications for clinical practice. Haematologica 2008;93:757-60.
-
(2008)
Haematologica
, vol.93
, pp. 757-760
-
-
van Beers, E.J.1
van Tuijn, C.F.2
Mac Gillavry, M.R.3
van der Giessen, A.4
Schnog, J.J.5
Biemond, B.J.6
-
33
-
-
38949117897
-
Risk-adjusted outcome measurement in pediatric allogeneic stem cell transplantation
-
Matthes-Martin S, Potschger U, Bergmann K, Frommlet F, Brannath W, Bauer P, Klingebiel T. Risk-adjusted outcome measurement in pediatric allogeneic stem cell transplantation. Biol Blood Marrow Transplant 2008;14:335-43.
-
(2008)
Biol Blood Marrow Transplant
, vol.14
, pp. 335-343
-
-
Matthes-Martin, S.1
Potschger, U.2
Bergmann, K.3
Frommlet, F.4
Brannath, W.5
Bauer, P.6
Klingebiel, T.7
-
34
-
-
34247226169
-
A survey on patient perception of reduced-intensity transplantation in adults with sickle cell disease
-
Chakrabarti S, Bareford D. A survey on patient perception of reduced-intensity transplantation in adults with sickle cell disease. Bone Marrow Transplant 2007;39:447-51.
-
(2007)
Bone Marrow Transplant
, vol.39
, pp. 447-451
-
-
Chakrabarti, S.1
Bareford, D.2
-
35
-
-
84866945470
-
Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen
-
Boztug H, Karitnig-Weiss C, Ausserer B, et al. Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen. Pediatr Hematol Oncol 2012;29:585-94.
-
(2012)
Pediatr Hematol Oncol
, vol.29
, pp. 585-594
-
-
Boztug, H.1
Karitnig-Weiss, C.2
Ausserer, B.3
-
36
-
-
9144225345
-
Treatment of CD40 ligand deficiency by hematopoietic stem cell transplantation: a survey of the European experience, 1993-2002
-
Gennery AR, Khawaja K, Veys P, et al. Treatment of CD40 ligand deficiency by hematopoietic stem cell transplantation: a survey of the European experience, 1993-2002. Blood 2004;103:1152-7.
-
(2004)
Blood
, vol.103
, pp. 1152-1157
-
-
Gennery, A.R.1
Khawaja, K.2
Veys, P.3
-
37
-
-
79952536230
-
Long-term remission in pediatric Wegener granulomatosis following allo-SCT after reduced-intensity conditioning
-
Lawitschka A, Peters C, Seidel MG, Havranek A, Heitger A, Fazekas T, Gueclue ED, Gadner H, Matthes-Martin S. Long-term remission in pediatric Wegener granulomatosis following allo-SCT after reduced-intensity conditioning. Bone Marrow Transplant 2011;46:462-3.
-
(2011)
Bone Marrow Transplant
, vol.46
, pp. 462-463
-
-
Lawitschka, A.1
Peters, C.2
Seidel, M.G.3
Havranek, A.4
Heitger, A.5
Fazekas, T.6
Gueclue, E.D.7
Gadner, H.8
Matthes-Martin, S.9
-
38
-
-
0142182271
-
Lineage-specific chimaerism after stem cell transplantation in children following reduced intensity conditioning: potential predictive value of NK cell chimaerism for late graft rejection
-
Matthes-Martin S, Lion T, Haas OA, et al. Lineage-specific chimaerism after stem cell transplantation in children following reduced intensity conditioning: potential predictive value of NK cell chimaerism for late graft rejection. Leukemia 2003;17:1934-42.
-
(2003)
Leukemia
, vol.17
, pp. 1934-1942
-
-
Matthes-Martin, S.1
Lion, T.2
Haas, O.A.3
-
39
-
-
67049164916
-
Selective engraftment of donor CD4 + 25high FOXP3-positive T cells in IPEX syndrome after nonmyeloablative hematopoietic stem cell transplantation
-
Seidel MG, Fritsch G, Lion T, Jurgens B, Heitger A, Bacchetta R, Lawitschka A, Peters C, Gadner H, Matthes-Martin S. Selective engraftment of donor CD4 + 25high FOXP3-positive T cells in IPEX syndrome after nonmyeloablative hematopoietic stem cell transplantation. Blood 2009;113:5689-91.
-
(2009)
Blood
, vol.113
, pp. 5689-5691
-
-
Seidel, M.G.1
Fritsch, G.2
Lion, T.3
Jurgens, B.4
Heitger, A.5
Bacchetta, R.6
Lawitschka, A.7
Peters, C.8
Gadner, H.9
Matthes-Martin, S.10
-
40
-
-
23744481272
-
Improved outcome of treatment-resistant high-risk Langerhans cell histiocytosis after allogeneic stem cell transplantation with reduced-intensity conditioning
-
Steiner M, Matthes-Martin S, Attarbaschi A, et al. Improved outcome of treatment-resistant high-risk Langerhans cell histiocytosis after allogeneic stem cell transplantation with reduced-intensity conditioning. Bone Marrow Transplant 2005;36:215-25.
-
(2005)
Bone Marrow Transplant
, vol.36
, pp. 215-225
-
-
Steiner, M.1
Matthes-Martin, S.2
Attarbaschi, A.3
-
41
-
-
12144289379
-
Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia
-
Iannone R, Casella JF, Fuchs EJ, Chen AR, Jones RJ, Woolfrey A, Amylon M, Sullivan KM, Storb RF, Walters MC. Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia. Biol Blood Marrow Transplant 2003;9:519-28.
-
(2003)
Biol Blood Marrow Transplant
, vol.9
, 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
-
42
-
-
0033836980
-
Fludarabine-based conditioning for allogeneic transplantation in adults with sickle cell disease
-
van Besien K, Bartholomew A, Stock W, Peace D, Devine S, Sher D, Sosman J, Chen YH, Koshy M, Hoffman R. Fludarabine-based conditioning for allogeneic transplantation in adults with sickle cell disease. Bone Marrow Transplant 2000;26:445-9.
-
(2000)
Bone Marrow Transplant
, vol.26
, 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
-
43
-
-
0038743168
-
Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies
-
Krishnamurti L, Abel S, Maiers M, Flesch S. Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies. Bone Marrow Transplant 2003;31:547-50.
-
(2003)
Bone Marrow Transplant
, vol.31
, pp. 547-550
-
-
Krishnamurti, L.1
Abel, S.2
Maiers, M.3
Flesch, S.4
-
44
-
-
78650991791
-
Quantitatively different red cell/nucleated cell chimerism in patients with long-term, persistent 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 cell/nucleated cell chimerism in patients with long-term, persistent hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease. Haematologica 2011;96:128-33.
-
(2011)
Haematologica
, vol.96
, pp. 128-133
-
-
Andreani, M.1
Testi, M.2
Gaziev, J.3
-
45
-
-
34848927819
-
Mixed haematopoietic chimerism for sickle cell disease prevents intravascular haemolysis
-
Wu CJ, Gladwin M, Tisdale J, et al. Mixed haematopoietic chimerism for sickle cell disease prevents intravascular haemolysis. Br J Haematol 2007;139:504-7.
-
(2007)
Br J Haematol
, vol.139
, pp. 504-507
-
-
Wu, C.J.1
Gladwin, M.2
Tisdale, J.3
-
46
-
-
27744469194
-
Evidence for ineffective erythropoiesis in severe sickle cell disease
-
Wu CJ, Krishnamurti L, Kutok JL, Biernacki M, Rogers S, Zhang W, Antin JH, Ritz J. Evidence for ineffective erythropoiesis in severe sickle cell disease. Blood 2005;106:3639-45.
-
(2005)
Blood
, vol.106
, pp. 3639-3645
-
-
Wu, C.J.1
Krishnamurti, L.2
Kutok, J.L.3
Biernacki, M.4
Rogers, S.5
Zhang, W.6
Antin, J.H.7
Ritz, J.8
-
47
-
-
84862268473
-
Allogeneic hematopoietic stem cell transplantation in children with sickle cell disease
-
Locatelli F, Pagliara D. Allogeneic hematopoietic stem cell transplantation in children with sickle cell disease. Pediatr Blood Cancer 2012;59:372-6.
-
(2012)
Pediatr Blood Cancer
, vol.59
, pp. 372-376
-
-
Locatelli, F.1
Pagliara, D.2
|