메뉴 건너뛰기




Volumn 1, Issue 26, 2017, Pages 2563-2567

The case for HLA-identical sibling hematopoietic stem cell transplantation in children with symptomatic sickle cell anemia

Author keywords

[No Author keywords available]

Indexed keywords


EID: 85048804221     PISSN: 24739529     EISSN: 24739537     Source Type: Journal    
DOI: 10.1182/bloodadvances.2017007708     Document Type: Article
Times cited : (19)

References (58)
  • 1
    • 84987899339 scopus 로고    scopus 로고
    • Renal failure in sickle cell disease: Prevalence, predictors of disease, mortality and effect on length of hospital stay
    • Yeruva SL, Paul Y, Oneal P, NouraieM. Renal failure in sickle cell disease: prevalence, predictors of disease, mortality and effect on length of hospital stay. Hemoglobin. 2016;40(5):295-299.
    • (2016) Hemoglobin. , vol.40 , Issue.5 , pp. 295-299
    • Yeruva, S.L.1    Paul, Y.2    Oneal, P.3    Nouraie, M.4
  • 2
    • 0034105690 scopus 로고    scopus 로고
    • Renal abnormalities in sickle cell disease
    • Ataga KI, Orringer EP. Renal abnormalities in sickle cell disease. Am J Hematol. 2000;63(4):205-211.
    • (2000) Am J Hematol. , vol.63 , Issue.4 , pp. 205-211
    • Ataga, K.I.1    Orringer, E.P.2
  • 4
    • 0025797297 scopus 로고
    • Stroke in sickle cell disease: Demographic, clinical, and therapeutic considerations
    • Ohene-Frempong K. Stroke in sickle cell disease: demographic, clinical, and therapeutic considerations. Semin Hematol. 1991;28(3):213-219.
    • (1991) Semin Hematol. , vol.28 , Issue.3 , pp. 213-219
    • Ohene-Frempong, K.1
  • 5
    • 0034828316 scopus 로고    scopus 로고
    • Neuropsychologic performance in schoolaged children with sickle cell disease: A report from the Cooperative Study of Sickle Cell Disease
    • Wang W, Enos L, Gallagher D, et al; Cooperative Study of Sickle Cell Disease. Neuropsychologic performance in schoolaged children with sickle cell disease: a report from the Cooperative Study of Sickle Cell Disease. J Pediatr. 2001;139(3):391-397.
    • (2001) J Pediatr. , vol.139 , Issue.3 , pp. 391-397
    • Wang, W.1    Enos, L.2    Gallagher, D.3
  • 6
    • 45749124385 scopus 로고    scopus 로고
    • Detection and assessment of stroke in patients with sickle cell disease: Neuropsychological functioning and magnetic resonance imaging
    • Gold JI, Johnson CB, Treadwell MJ, Hans N, Vichinsky E. Detection and assessment of stroke in patients with sickle cell disease: neuropsychological functioning and magnetic resonance imaging. Pediatr Hematol Oncol. 2008;25(5):409-421.
    • (2008) Pediatr Hematol Oncol. , vol.25 , Issue.5 , pp. 409-421
    • Gold, J.I.1    Johnson, C.B.2    Treadwell, M.J.3    Hans, N.4    Vichinsky, E.5
  • 7
    • 74049151134 scopus 로고    scopus 로고
    • 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
  • 8
    • 70349492889 scopus 로고    scopus 로고
    • The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization
    • Carroll CP, Haywood C Jr, Fagan P, Lanzkron S. The course and correlates of high hospital utilization in sickle cell disease: evidence from a large, urban Medicaid managed care organization. Am J Hematol. 2009;84(10):666-670.
    • (2009) Am J Hematol. , vol.84 , Issue.10 , pp. 666-670
    • Carroll, C.P.1    Haywood, C.2    Fagan, P.3    Lanzkron, S.4
  • 9
    • 33845254119 scopus 로고    scopus 로고
    • Hospitalization rates and costs of care of patients with sickle-cell anemia in the state of Maryland in the era of hydroxyurea
    • Lanzkron S, Haywood C Jr, Segal JB, Dover GJ. Hospitalization rates and costs of care of patients with sickle-cell anemia in the state of Maryland in the era of hydroxyurea. Am J Hematol. 2006;81(12):927-932.
    • (2006) Am J Hematol. , vol.81 , Issue.12 , pp. 927-932
    • Lanzkron, S.1    Haywood, C.2    Segal, J.B.3    Dover, G.J.4
  • 10
    • 77950478131 scopus 로고    scopus 로고
    • Acute care utilization and rehospitalizations for sickle cell disease
    • Brousseau DC, Owens PL, Mosso AL, Panepinto JA, Steiner CA. Acute care utilization and rehospitalizations for sickle cell disease. JAMA. 2010;303(13):1288-1294.
    • (2010) JAMA , vol.303 , Issue.13 , pp. 1288-1294
    • Brousseau, D.C.1    Owens, P.L.2    Mosso, A.L.3    Panepinto, J.A.4    Steiner, C.A.5
  • 12
    • 66849138584 scopus 로고    scopus 로고
    • The cost of health care for children and adults with sickle cell disease
    • Kauf TL, Coates TD, Huazhi L, Mody-Patel N, Hartzema AG. The cost of health care for children and adults with sickle cell disease. Am J Hematol. 2009;84(6):323-327.
    • (2009) Am J Hematol. , vol.84 , Issue.6 , pp. 323-327
    • Kauf, T.L.1    Coates, T.D.2    Huazhi, L.3    Mody-Patel, N.4    Hartzema, A.G.5
  • 13
    • 84869803950 scopus 로고    scopus 로고
    • Impact of hydroxyurea on clinical events in the BABY HUG trial
    • quiz 4448
    • Thornburg CD, Files BA, Luo Z, et al; BABY HUG Investigators. Impact of hydroxyurea on clinical events in the BABY HUG trial. Blood. 2012;120(22):4304-4310, quiz 4448.
    • (2012) Blood. , vol.120 , Issue.22 , pp. 4304-4310
    • Thornburg, C.D.1    Files, B.A.2    Luo, Z.3
  • 14
    • 79955909191 scopus 로고    scopus 로고
    • Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG)
    • Wang WC, Ware RE, Miller ST, et al; BABY HUG investigators. Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG). Lancet. 2011;377(9778):1663-1672.
    • (2011) Lancet. , vol.377 , Issue.9778 , pp. 1663-1672
    • Wang, W.C.1    Ware, R.E.2    Miller, S.T.3
  • 15
    • 0030358260 scopus 로고    scopus 로고
    • Clinical and hematologic effects of hydroxyurea in children with sickle cell anemia
    • Jayabose S, Tugal O, Sandoval C, et al. Clinical and hematologic effects of hydroxyurea in children with sickle cell anemia. J Pediatr. 1996;129(4):559-565
    • (1996) J Pediatr. , vol.129 , Issue.4 , pp. 559-565
    • Jayabose, S.1    Tugal, O.2    Sandoval, C.3
  • 16
    • 0029845949 scopus 로고    scopus 로고
    • 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.
    • (1996) Blood. , vol.88 , Issue.6 , pp. 1960-1964
    • Ferster, A.1    Vermylen, C.2    Cornu, G.3
  • 17
    • 84913590685 scopus 로고    scopus 로고
    • Medication adherence among pediatric patients with sickle cell disease: A systematic review
    • Walsh KE, Cutrona SL, Kavanagh PL, et al. Medication adherence among pediatric patients with sickle cell disease: a systematic review. Pediatrics. 2014;134(6):1175-1183.
    • (2014) Pediatrics. , vol.134 , Issue.6 , pp. 1175-1183
    • Walsh, K.E.1    Cutrona, S.L.2    Kavanagh, P.L.3
  • 18
    • 10744233940 scopus 로고    scopus 로고
    • 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, M.T.1    Sachdev, V.2    Jison, M.L.3
  • 19
    • 84957570980 scopus 로고    scopus 로고
    • Hydroxyurea-increased fetal hemoglobin is associated with less organ damage and longer survival in adults with sickle cell anemia
    • Fitzhugh CD, Hsieh MM, Allen D, et al. Hydroxyurea-increased fetal hemoglobin is associated with less organ damage and longer survival in adults with sickle cell anemia. PLoS One. 2015;10(11):e0141706.
    • (2015) PLoS One. , vol.10 , Issue.11
    • Fitzhugh, C.D.1    Hsieh, M.M.2    Allen, D.3
  • 20
    • 77951712618 scopus 로고    scopus 로고
    • 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(17):3447-3452.
    • (2010) Blood. , vol.115 , Issue.17 , pp. 3447-3452
    • Quinn, C.T.1    Rogers, Z.R.2    McCavit, T.L.3    Buchanan, G.R.4
  • 21
    • 77949482609 scopus 로고    scopus 로고
    • Population estimates of sickle cell disease in the U.S
    • Hassell KL. Population estimates of sickle cell disease in the U.S. Am J Prev Med. 2010;38(4 Suppl):S512-S521.
    • (2010) Am J Prev Med. , vol.38 , Issue.4 , pp. S512-S521
    • Hassell, K.L.1
  • 22
    • 85016981659 scopus 로고    scopus 로고
    • Risk factors for mortality in adult patients with sickle cell disease: A metaanalysis of studies in North America and Europe
    • Maitra P, Caughey M, Robinson L, et al. Risk factors for mortality in adult patients with sickle cell disease: a metaanalysis of studies in North America and Europe. Haematologica. 2017;102(4):626-636.
    • (2017) Haematologica. , vol.102 , Issue.4 , pp. 626-636
    • Maitra, P.1    Caughey, M.2    Robinson, L.3
  • 23
    • 84921418905 scopus 로고    scopus 로고
    • Health-related quality of life in children with sickle cell anemia: Impact of blood transfusion therapy
    • Beverung LM, Strouse JJ, Hulbert ML, et al; SIT trial investigators. Health-related quality of life in children with sickle cell anemia: impact of blood transfusion therapy. Am J Hematol. 2015;90(2):139-143.
    • (2015) Am J Hematol. , vol.90 , Issue.2 , pp. 139-143
    • Beverung, L.M.1    Strouse, J.J.2    Hulbert, M.L.3
  • 24
    • 84924256397 scopus 로고    scopus 로고
    • Clinically meaningful interpretation of pediatric health-related quality of life in sickle cell disease
    • Beverung LM, Varni JW, Panepinto JA. Clinically meaningful interpretation of pediatric health-related quality of life in sickle cell disease. J Pediatr Hematol Oncol. 2015;37(2): 128-133.
    • (2015) J Pediatr Hematol Oncol. , vol.37 , Issue.2 , pp. 128-133
    • Beverung, L.M.1    Varni, J.W.2    Panepinto, J.A.3
  • 25
    • 49649112089 scopus 로고    scopus 로고
    • Daily functioning and quality of life in children with sickle cell disease pain: Relationship with family and neighborhood socioeconomic distress
    • Palermo TM, Riley CA, Mitchell BA. Daily functioning and quality of life in children with sickle cell disease pain: relationship with family and neighborhood socioeconomic distress. J Pain. 2008;9(9):833-840.
    • (2008) J Pain. , vol.9 , Issue.9 , pp. 833-840
    • Palermo, T.M.1    Riley, C.A.2    Mitchell, B.A.3
  • 26
    • 23844458936 scopus 로고    scopus 로고
    • Quality of life in children with sickle cell hemoglobinopathy
    • Patel AB, Pathan HG. Quality of life in children with sickle cell hemoglobinopathy. Indian J Pediatr. 2005;72(7):567-571.
    • (2005) Indian J Pediatr. , vol.72 , Issue.7 , pp. 567-571
    • Patel, A.B.1    Pathan, H.G.2
  • 27
    • 0029810145 scopus 로고    scopus 로고
    • Pain, quality of life, and coping in sickle cell disease
    • Fuggle P, Shand PA, Gill LJ, Davies SC. Pain, quality of life, and coping in sickle cell disease. Arch Dis Child. 1996;75(3): 199-203.
    • (1996) Arch Dis Child. , vol.75 , Issue.3 , pp. 199-203
    • Fuggle, P.1    Shand, P.A.2    Gill, L.J.3    Davies, S.C.4
  • 28
    • 84958239480 scopus 로고    scopus 로고
    • Indications and results of HLA-identical sibling hematopoietic cell transplantation for sickle cell disease
    • Walters MC, De Castro LM, Sullivan KM, et al. Indications and results of HLA-identical sibling hematopoietic cell transplantation for sickle cell disease. Biol Blood Marrow Transplant. 2016;22(2):207-211.
    • (2016) Biol Blood Marrow Transplant. , vol.22 , Issue.2 , pp. 207-211
    • Walters, M.C.1    De Castro, L.M.2    Sullivan, K.M.3
  • 29
    • 85015934863 scopus 로고    scopus 로고
    • Sickle cell disease: An international survey of results of HLA-identical sibling hematopoietic stem cell transplantation
    • Gluckman E, Cappelli B, Bernaudin F, et al; Eurocord, the Pediatric Working Party of the European Society for Blood and Marrow Transplantation, and the Center for International Blood and Marrow Transplant Research. Sickle cell disease: an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation. Blood. 2017;129(11):1548-1556.
    • (2017) Blood. , vol.129 , Issue.11 , pp. 1548-1556
    • Gluckman, E.1    Cappelli, B.2    Bernaudin, F.3
  • 30
    • 84898444338 scopus 로고    scopus 로고
    • Haematopoietic stem cell transplantation for severe sickle cell disease in childhood: A single centre experience of 50 patients
    • Dedeken L, Lê PQ, Azzi N, et al. Haematopoietic stem cell transplantation for severe sickle cell disease in childhood: a single centre experience of 50 patients. Br J Haematol. 2014;165(3):402-408.
    • (2014) Br J Haematol. , vol.165 , Issue.3 , pp. 402-408
    • Dedeken, L.1    Lê, P.Q.2    Azzi, N.3
  • 31
    • 84929239251 scopus 로고    scopus 로고
    • Treosulfan-based conditioning regimen for allogeneic haematopoietic stem cell transplantation in children with sickle cell disease
    • Strocchio L, Zecca M, Comoli P, et al. Treosulfan-based conditioning regimen for allogeneic haematopoietic stem cell transplantation in children with sickle cell disease. Br J Haematol. 2015;169(5):726-736.
    • (2015) Br J Haematol. , vol.169 , Issue.5 , pp. 726-736
    • Strocchio, L.1    Zecca, M.2    Comoli, P.3
  • 32
    • 84924278004 scopus 로고    scopus 로고
    • Health-related quality of life after allogeneic hematopoietic stem cell transplantation for sickle cell disease
    • Bhatia M, Kolva E, Cimini L, et al. Health-related quality of life after allogeneic hematopoietic stem cell transplantation for sickle cell disease. Biol Blood Marrow Transplant. 2015;21(4): 666-672.
    • (2015) Biol Blood Marrow Transplant. , vol.21 , Issue.4 , pp. 666-672
    • Bhatia, M.1    Kolva, E.2    Cimini, L.3
  • 33
    • 84905682255 scopus 로고    scopus 로고
    • Health-related quality of life in pediatric patients after allogeneic SCT: Development of the PedsQL Stem Cell Transplant module and results of a pilot study
    • Lawitschka A, Güclü ED, Varni JW, et al. Health-related quality of life in pediatric patients after allogeneic SCT: development of the PedsQL Stem Cell Transplant module and results of a pilot study. Bone Marrow Transplant. 2014;49(8):1093-1097.
    • (2014) Bone Marrow Transplant. , vol.49 , Issue.8 , pp. 1093-1097
    • Lawitschka, A.1    Güclü, E.D.2    Varni, J.W.3
  • 34
    • 84879108970 scopus 로고    scopus 로고
    • Pediatric allo-SCT for malignant and non-malignant diseases: Impact on healthrelated quality of life outcomes
    • Oberg JA, Bender JG, Morris E, et al. Pediatric allo-SCT for malignant and non-malignant diseases: impact on healthrelated quality of life outcomes. Bone Marrow Transplant. 2013;48(6):787-793.
    • (2013) Bone Marrow Transplant. , vol.48 , Issue.6 , pp. 787-793
    • Oberg, J.A.1    Bender, J.G.2    Morris, E.3
  • 35
    • 79956038028 scopus 로고    scopus 로고
    • Prospective assessment of health-related quality of life in pediatric patients with betathalassemia following hematopoietic stem cell transplantation
    • Caocci G, Efficace F, Ciotti F, et al. Prospective assessment of health-related quality of life in pediatric patients with betathalassemia following hematopoietic stem cell transplantation. Biol Blood Marrow Transplant. 2011;17(6):861-866.
    • (2011) Biol Blood Marrow Transplant. , vol.17 , Issue.6 , pp. 861-866
    • Caocci, G.1    Efficace, F.2    Ciotti, F.3
  • 36
    • 84886897873 scopus 로고    scopus 로고
    • Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLAidentical sibling
    • Locatelli F, Kabbara N, Ruggeri A, et al; Eurocord and European Blood and Marrow Transplantation (EBMT) group. Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLAidentical sibling. Blood. 2013;122(6):1072-1078.
    • (2013) Blood. , vol.122 , Issue.6 , pp. 1072-1078
    • Locatelli, F.1    Kabbara, N.2    Ruggeri, A.3
  • 38
    • 0030051313 scopus 로고    scopus 로고
    • Persistence of fetal hemoglobin production after successful transplantation of cord blood stem cells in a patient with sickle cell anemia
    • 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. J Pediatr. 1996;128(2):241-243.
    • (1996) J Pediatr. , vol.128 , Issue.2 , pp. 241-243
    • Brichard, B.1    Vermylen, C.2    Ninane, J.3    Cornu, G.4
  • 39
    • 0034268110 scopus 로고    scopus 로고
    • Successful cord blood transplantation for sickle cell anemia from a sibling who is human leukocyte antigen-identical: Implications for comprehensive care
    • 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.
    • (2000) J Pediatr Hematol Oncol. , vol.22 , Issue.5 , pp. 437-440
    • Gore, L.1    Lane, P.A.2    Quinones, R.R.3    Giller, R.H.4
  • 40
    • 53749086728 scopus 로고    scopus 로고
    • 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
  • 41
    • 84875254453 scopus 로고    scopus 로고
    • Stem cell transplantation after reduced-intensity conditioning for sickle cell disease
    • Matthes-Martin S, Lawitschka A, Fritsch G, et al. Stem cell transplantation after reduced-intensity conditioning for sickle cell disease. Eur J Haematol. 2013;90(4):308-312.
    • (2013) Eur J Haematol. , vol.90 , Issue.4 , pp. 308-312
    • Matthes-Martin, S.1    Lawitschka, A.2    Fritsch, G.3
  • 42
    • 84903882984 scopus 로고    scopus 로고
    • Reduced toxicity, myeloablative conditioning with BU, fludarabine, alemtuzumab and SCT from sibling donors in children with sickle cell disease
    • Bhatia M, Jin Z, Baker C, et al. Reduced toxicity, myeloablative conditioning with BU, fludarabine, alemtuzumab and SCT from sibling donors in children with sickle cell disease. Bone Marrow Transplant. 2014;49(7):913-920.
    • (2014) Bone Marrow Transplant. , vol.49 , Issue.7 , pp. 913-920
    • Bhatia, M.1    Jin, Z.2    Baker, C.3
  • 43
    • 84954230957 scopus 로고    scopus 로고
    • Successful matched sibling donor marrow transplantation following reduced intensity conditioning in children with hemoglobinopathies
    • King AA, Kamani N, Bunin N, et al. Successful matched sibling donor marrow transplantation following reduced intensity conditioning in children with hemoglobinopathies. Am J Hematol. 2015;90(12):1093-1098.
    • (2015) Am J Hematol. , vol.90 , Issue.12 , pp. 1093-1098
    • King, A.A.1    Kamani, N.2    Bunin, N.3
  • 44
    • 0035544031 scopus 로고    scopus 로고
    • Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia
    • Walters MC, Patience M, Leisenring W, et al; Multicenter Investigation of Bone Marrow Transplantation for Sickle Cell Disease. Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia. Biol Blood Marrow Transplant. 2001;7(12):665-673.
    • (2001) Biol Blood Marrow Transplant. , vol.7 , Issue.12 , pp. 665-673
    • Walters, M.C.1    Patience, M.2    Leisenring, W.3
  • 45
    • 57349083313 scopus 로고    scopus 로고
    • Donor/recipient mixed chimerism does not predict graft failure in children with betathalassemia given an allogeneic cord blood transplant from an HLA-identical sibling
    • Lisini D, Zecca M, Giorgiani G, et al. Donor/recipient mixed chimerism does not predict graft failure in children with betathalassemia given an allogeneic cord blood transplant from an HLA-identical sibling. Haematologica. 2008;93(12): 1859-1867.
    • (2008) Haematologica. , vol.93 , Issue.12 , pp. 1859-1867
    • Lisini, D.1    Zecca, M.2    Giorgiani, G.3
  • 46
    • 84903625438 scopus 로고    scopus 로고
    • Nonmyeloablative HLA-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype
    • Hsieh MM, Fitzhugh CD, Weitzel RP, et al. Nonmyeloablative HLA-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype. JAMA. 2014;312(1):48-56.
    • (2014) JAMA , vol.312 , Issue.1 , pp. 48-56
    • Hsieh, M.M.1    Fitzhugh, C.D.2    Weitzel, R.P.3
  • 47
    • 85073817370 scopus 로고    scopus 로고
    • Non-myeloablative alemtuzumab/low dose total body irradiation conditioning for children undergoing HLA-matched sibling donor haematopoietic cell transplantation for sickle cell diseaes
    • 28 March, Marseille, France.
    • Guilcher G, Monagel D, Leaker M, et al. Non-myeloablative alemtuzumab/low dose total body irradiation conditioning for children undergoing HLA-matched sibling donor haematopoietic cell transplantation for sickle cell diseaes. Presented at the 43rd Annual Meeting of the European Society for Blood and Marrow Transplantation. 28 March 2017. Marseille, France.
    • (2017) The 43rd Annual Meeting of the European Society for Blood and Marrow Transplantation
    • Guilcher, G.1    Monagel, D.2    Leaker, M.3
  • 48
    • 84908601771 scopus 로고    scopus 로고
    • Transfusions for silent cerebral infarcts in sickle cell anemia
    • DeBaun MR, Casella JF. Transfusions for silent cerebral infarcts in sickle cell anemia. N Engl J Med. 2014;371(19): 1841-1842.
    • (2014) N Engl J Med. , vol.371 , Issue.19 , pp. 1841-1842
    • Debaun, M.R.1    Casella, J.F.2
  • 49
    • 75149170038 scopus 로고    scopus 로고
    • Pulmonary, gonadal, and central nervous system status after bone marrow transplantation for sickle cell disease
    • Walters MC, Hardy K, Edwards S, et al; Multicenter Study of Bone Marrow Transplantation for Sickle Cell Disease. Pulmonary, gonadal, and central nervous system status after bone marrow transplantation for sickle cell disease. Biol Blood Marrow Transplant. 2010;16(2):263-272.
    • (2010) Biol Blood Marrow Transplant. , vol.16 , Issue.2 , pp. 263-272
    • Walters, M.C.1    Hardy, K.2    Edwards, S.3
  • 50
    • 85008674713 scopus 로고    scopus 로고
    • Reversal of pre-capillary pulmonary hypertension in a patient with sickle cell anemia who underwent haploidentical peripheral blood stem cell transplantation
    • Pittman C, Hsieh MM, Coles W, Tisdale JF, Weir NA, Fitzhugh CD. Reversal of pre-capillary pulmonary hypertension in a patient with sickle cell anemia who underwent haploidentical peripheral blood stem cell transplantation. Bone Marrow Transplant. 2017;52(4):641-642.
    • (2017) Bone Marrow Transplant. , vol.52 , Issue.4 , pp. 641-642
    • Pittman, C.1    Hsieh, M.M.2    Coles, W.3    Tisdale, J.F.4    Weir, N.A.5    Fitzhugh, C.D.6
  • 51
    • 34948830175 scopus 로고    scopus 로고
    • Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease
    • Bernaudin F, Socie G, Kuentz M, et al; SFGM-TC. Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease. Blood. 2007;110(7):2749-2756.
    • (2007) Blood. , vol.110 , Issue.7 , pp. 2749-2756
    • Bernaudin, F.1    Socie, G.2    Kuentz, M.3
  • 52
    • 84963628522 scopus 로고    scopus 로고
    • Long-term treatment follow-up of children with sickle cell disease monitored with abnormal transcranial Doppler velocities
    • Bernaudin F, Verlhac S, Arnaud C, et al. Long-term treatment follow-up of children with sickle cell disease monitored with abnormal transcranial Doppler velocities. Blood. 2016;127(14):1814-1822.
    • (2016) Blood. , vol.127 , Issue.14 , pp. 1814-1822
    • Bernaudin, F.1    Verlhac, S.2    Arnaud, C.3
  • 53
    • 77958616980 scopus 로고    scopus 로고
    • Toward a coherent account of pediatric decision making
    • Iltis AS. Toward a coherent account of pediatric decision making. J Med Philos. 2010;35(5):526-552.
    • (2010) J Med Philos. , vol.35 , Issue.5 , pp. 526-552
    • Iltis, A.S.1
  • 54
    • 84909981898 scopus 로고    scopus 로고
    • Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia
    • Lucarelli G, Isgrò A, Sodani P, et al. Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia. Bone Marrow Transplant. 2014;49(11):1376-1381.
    • (2014) Bone Marrow Transplant. , vol.49 , Issue.11 , pp. 1376-1381
    • Lucarelli, G.1    Isgrò, A.2    Sodani, P.3
  • 55
    • 78651363574 scopus 로고    scopus 로고
    • 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(1): 27-33.
    • (2011) Bone Marrow Transplant. , vol.46 , Issue.1 , pp. 27-33
    • McPherson, M.E.1    Hutcherson, D.2    Olson, E.3    Haight, A.E.4    Horan, J.5    Chiang, K.Y.6
  • 56
    • 77952427892 scopus 로고    scopus 로고
    • 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(5):895-900.
    • (2010) Bone Marrow Transplant. , vol.45 , Issue.5 , pp. 895-900
    • Majumdar, S.1    Robertson, Z.2    Robinson, A.3    Starnes, S.4    Iyer, R.5    Megason, G.6
  • 57
    • 34247858963 scopus 로고    scopus 로고
    • 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; Non-Malignant Marrow Disorders Working Committee, Center for International Blood and Marrow Transplant Research. 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.
    • (2007) Br J Haematol. , vol.137 , Issue.5 , pp. 479-485
    • Panepinto, J.A.1    Walters, M.C.2    Carreras, J.3
  • 58
    • 0031870487 scopus 로고    scopus 로고
    • 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.
    • (1998) Bone Marrow Transplant. , vol.22 , Issue.1 , pp. 1-6
    • Vermylen, C.1    Cornu, G.2    Ferster, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.