-
1
-
-
0032474692
-
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography
-
Adams RJ, McKie VC, Hsu L, et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N Engl J Med 1998;339:5–11.
-
(1998)
N Engl J Med
, vol.339
, pp. 5-11
-
-
Adams, R.J.1
McKie, V.C.2
Hsu, L.3
-
2
-
-
0029005136
-
Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions
-
Pegelow CH, Adams RJ, McKie V, et al. Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions. J Pediatr 1995;126:896–9.
-
(1995)
J Pediatr
, vol.126
, pp. 896-899
-
-
Pegelow, C.H.1
Adams, R.J.2
McKie, V.3
-
3
-
-
29544444495
-
Discontinuing prophylactic transfusions used to prevent stroke in sickle cell disease
-
Adams RJ, Brambilla D; Optimizing Primary Stroke Prevention in Sickle Cell Anemia (STOP 2) Trial Investigators. Discontinuing prophylactic transfusions used to prevent stroke in sickle cell disease. N Engl J Med 2005;353:2769–78.
-
(2005)
N Engl J Med
, vol.353
, pp. 2769-2778
-
-
Adams, R.J.1
Brambilla, D.2
-
4
-
-
84902783655
-
Cardiac iron overload in sickle-cell disease
-
Meloni A, Puliyel M, Pepe A, et al. Cardiac iron overload in sickle-cell disease. Am J Hematol 2014;89:678–83.
-
(2014)
Am J Hematol
, vol.89
, pp. 678-683
-
-
Meloni, A.1
Puliyel, M.2
Pepe, A.3
-
5
-
-
66149149084
-
Hepatic iron overload in children with sickle cell anemia on chronic transfusion therapy
-
Brown K, Subramony C, May W, et al. Hepatic iron overload in children with sickle cell anemia on chronic transfusion therapy. J Pediatr Hematol Oncol 2009;31:309–12.
-
(2009)
J Pediatr Hematol Oncol
, vol.31
, pp. 309-312
-
-
Brown, K.1
Subramony, C.2
May, W.3
-
6
-
-
84857997579
-
Persistence and compliance of deferoxamine versus deferasirox in Medicaid patients with sickle-cell disease
-
Jordan LB, Vekeman F, Sengupta A, et al. Persistence and compliance of deferoxamine versus deferasirox in Medicaid patients with sickle-cell disease. J Clin Pharm Ther 2012;37:173–81.
-
(2012)
J Clin Pharm Ther
, vol.37
, pp. 173-181
-
-
Jordan, L.B.1
Vekeman, F.2
Sengupta, A.3
-
7
-
-
84870916333
-
Long-term persistency and costs associated with the use of iron chelation therapies in the treatment of sickle cell disease within Medicaid programs
-
Armstrong EP, Skrepnek GH, Sasane M, et al. Long-term persistency and costs associated with the use of iron chelation therapies in the treatment of sickle cell disease within Medicaid programs. J Med Econ 2013;16:10–8.
-
(2013)
J Med Econ
, vol.16
, pp. 10-18
-
-
Armstrong, E.P.1
Skrepnek, G.H.2
Sasane, M.3
-
8
-
-
0027958085
-
Erythrocytapheresis therapy to reduce iron overload in chronically transfused patients with sickle cell disease
-
Kim HC, Dugan NP, Silber JH, et al. Erythrocytapheresis therapy to reduce iron overload in chronically transfused patients with sickle cell disease. Blood 1994;83:1136–42.
-
(1994)
Blood
, vol.83
, pp. 1136-1142
-
-
Kim, H.C.1
Dugan, N.P.2
Silber, J.H.3
-
9
-
-
0032735280
-
Erythrocytapheresis for chronically transfused children with sickle cell disease: an effective method for maintaining a low hemoglobin S level and reducing iron overload
-
Singer ST, Quirolo K, Nishi K, et al. Erythrocytapheresis for chronically transfused children with sickle cell disease: an effective method for maintaining a low hemoglobin S level and reducing iron overload. J Clin Apher 1999;14:122–5.
-
(1999)
J Clin Apher
, vol.14
, pp. 122-125
-
-
Singer, S.T.1
Quirolo, K.2
Nishi, K.3
-
10
-
-
0031824987
-
Erythrocytapheresis limits iron accumulation in chronically transfused sickle cell patients
-
Hilliard LM, Williams BF, Lounsbury AE, et al. Erythrocytapheresis limits iron accumulation in chronically transfused sickle cell patients. Am J Hematol 1998;59:28–35.
-
(1998)
Am J Hematol
, vol.59
, pp. 28-35
-
-
Hilliard, L.M.1
Williams, B.F.2
Lounsbury, A.E.3
-
11
-
-
0030040223
-
Erythrocytapheresis can reduce iron overload and prevent the need for chelation therapy in chronically transfused pediatric patients
-
Adams DM, Schultz WH, Ware RE, et al. Erythrocytapheresis can reduce iron overload and prevent the need for chelation therapy in chronically transfused pediatric patients. J Pediatr Hematol Oncol 1996;18:46–50.
-
(1996)
J Pediatr Hematol Oncol
, vol.18
, pp. 46-50
-
-
Adams, D.M.1
Schultz, W.H.2
Ware, R.E.3
-
12
-
-
80051546628
-
Advantages of isovolemic hemodilution-red cell exchange therapy to prevent recurrent stroke in sickle cell anemia patients
-
Sarode R, Matevosyan K, Rogers ZR, et al. Advantages of isovolemic hemodilution-red cell exchange therapy to prevent recurrent stroke in sickle cell anemia patients. J Clin Apher 2011;26:200–7.
-
(2011)
J Clin Apher
, vol.26
, pp. 200-207
-
-
Sarode, R.1
Matevosyan, K.2
Rogers, Z.R.3
-
13
-
-
84881421476
-
Partial manual exchange reduces iron accumulation during chronic red cell transfusions for sickle cell disease
-
Savage WJ, Reddoch S, Wolfe J, et al. Partial manual exchange reduces iron accumulation during chronic red cell transfusions for sickle cell disease. J Pediatr Hematol Oncol 2013;35:434–6.
-
(2013)
J Pediatr Hematol Oncol
, vol.35
, pp. 434-436
-
-
Savage, W.J.1
Reddoch, S.2
Wolfe, J.3
-
14
-
-
84896950902
-
Consequences and management of iron overload in sickle cell disease
-
Porter J, Garbowski M. Consequences and management of iron overload in sickle cell disease. Hematology Am Soc Hematol Educ Program 2013;2013:447–56.
-
(2013)
Hematology Am Soc Hematol Educ Program
, vol.2013
, pp. 447-456
-
-
Porter, J.1
Garbowski, M.2
-
15
-
-
79958816234
-
Red cell exchange does not appear to increase the rate of allo- and auto-immunization in chronically transfused children with sickle cell disease
-
Venkateswaran L, Teruya J, Bustillos C, et al. Red cell exchange does not appear to increase the rate of allo- and auto-immunization in chronically transfused children with sickle cell disease. Pediatr Blood Cancer 2011;57:294–6.
-
(2011)
Pediatr Blood Cancer
, vol.57
, pp. 294-296
-
-
Venkateswaran, L.1
Teruya, J.2
Bustillos, C.3
-
16
-
-
84870988240
-
Lower alloimmunization rates in pediatric sickle cell patients on chronic erythrocytapheresis compared to chronic simple transfusions
-
Wahl SK, Garcia A, Hagar W, et al. Lower alloimmunization rates in pediatric sickle cell patients on chronic erythrocytapheresis compared to chronic simple transfusions. Transfusion 2012;52:2671–6.
-
(2012)
Transfusion
, vol.52
, pp. 2671-2676
-
-
Wahl, S.K.1
Garcia, A.2
Hagar, W.3
-
17
-
-
84923020660
-
Immunohematologic tolerance of chronic transfusion exchanges with erythrocytapheresis in sickle cell disease
-
Michot JM, Driss F, Guitton C, et al. Immunohematologic tolerance of chronic transfusion exchanges with erythrocytapheresis in sickle cell disease. Transfusion 2015;55:357–63.
-
(2015)
Transfusion
, vol.55
, pp. 357-363
-
-
Michot, J.M.1
Driss, F.2
Guitton, C.3
-
18
-
-
84925350470
-
Evidence gaps in the management of sickle cell disease: a summary of needed research
-
Savage WJ, Buchanan GR, Yawn BP, et al. Evidence gaps in the management of sickle cell disease: a summary of needed research. Am J Hematol 2015;90:273–5.
-
(2015)
Am J Hematol
, vol.90
, pp. 273-275
-
-
Savage, W.J.1
Buchanan, G.R.2
Yawn, B.P.3
-
19
-
-
84862512649
-
Transfusion protocol for patients with sickle hemoglobinopathies at Children's National Medical Center
-
Fasano RM, Paul W, Siegal E, et al. Transfusion protocol for patients with sickle hemoglobinopathies at Children's National Medical Center. Immunohematology 2012;28:13–6.
-
(2012)
Immunohematology
, vol.28
, pp. 13-16
-
-
Fasano, R.M.1
Paul, W.2
Siegal, E.3
-
20
-
-
11244355277
-
Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance
-
St Pierre TG, Clark PR, Chua-anusorn W, et al. Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance. Blood 2005;105:855–61.
-
(2005)
Blood
, vol.105
, pp. 855-861
-
-
St Pierre, T.G.1
Clark, P.R.2
Chua-anusorn, W.3
-
21
-
-
84900835793
-
Multicenter validation of spin-density projection-assisted R2-MRI for the noninvasive measurement of liver iron concentration
-
St Pierre TG, El-Beshlawy A, Elalfy M, et al. Multicenter validation of spin-density projection-assisted R2-MRI for the noninvasive measurement of liver iron concentration. Magn Reson Med 2014;71:2215–23.
-
(2014)
Magn Reson Med
, vol.71
, pp. 2215-2223
-
-
St Pierre, T.G.1
El-Beshlawy, A.2
Elalfy, M.3
-
22
-
-
84904758882
-
Use of magnetic resonance imaging to monitor iron overload
-
Wood JC. Use of magnetic resonance imaging to monitor iron overload. Hematol Oncol Clin North Am 2014;28:747–64, vii.
-
(2014)
Hematol Oncol Clin North Am
, vol.28
, pp. 747-764
-
-
Wood, J.C.1
-
23
-
-
69249192580
-
Transfusion management of sickle cell patients during bone marrow transplantation with matched sibling donor
-
McPherson ME, Anderson AR, Haight AE, et al. Transfusion management of sickle cell patients during bone marrow transplantation with matched sibling donor. Transfusion 2009;49:1977–86.
-
(2009)
Transfusion
, vol.49
, pp. 1977-1986
-
-
McPherson, M.E.1
Anderson, A.R.2
Haight, A.E.3
-
24
-
-
0031001278
-
Iron-chelating therapy and the treatment of thalassemia
-
Olivieri NF, Brittenham GM. Iron-chelating therapy and the treatment of thalassemia. Blood 1997;89:739–61.
-
(1997)
Blood
, vol.89
, pp. 739-761
-
-
Olivieri, N.F.1
Brittenham, G.M.2
-
25
-
-
84925441832
-
Deferasirox for iron chelation in multitransfused children with sickle cell disease; long-term experience in the East London clinical haemoglobinopathy network
-
Tsouana E, Kaya B, Gadong N, et al. Deferasirox for iron chelation in multitransfused children with sickle cell disease; long-term experience in the East London clinical haemoglobinopathy network. Eur J Haematol 2015;94:336–42.
-
(2015)
Eur J Haematol
, vol.94
, pp. 336-342
-
-
Tsouana, E.1
Kaya, B.2
Gadong, N.3
-
26
-
-
84886874276
-
High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors
-
Chou ST, Jackson T, Vege S, et al. High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors. Blood 2013;122:1062–71.
-
(2013)
Blood
, vol.122
, pp. 1062-1071
-
-
Chou, S.T.1
Jackson, T.2
Vege, S.3
-
27
-
-
84860348352
-
Stroke With Transfusions Changing to Hydroxyurea (SWiTCH)
-
Ware RE, Helms RW; SWiTCH Investigators. Stroke With Transfusions Changing to Hydroxyurea (SWiTCH). Blood 2012;119:3925–32.
-
(2012)
Blood
, vol.119
, pp. 3925-3932
-
-
Ware, R.E.1
Helms, R.W.2
-
28
-
-
84923172219
-
A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patients
-
Kuo KH, Ward R, Kaya B, et al. A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patients. Br J Haematol 2015;170:425–8.
-
(2015)
Br J Haematol
, vol.170
, pp. 425-428
-
-
Kuo, K.H.1
Ward, R.2
Kaya, B.3
-
29
-
-
84877626207
-
Long-term red blood cell exchange in children with sickle cell disease: manual or automatic?
-
Duclos C, Merlin E, Paillard C, et al. Long-term red blood cell exchange in children with sickle cell disease: manual or automatic? Transfus Apher Sci 2013;48:219–22.
-
(2013)
Transfus Apher Sci
, vol.48
, pp. 219-222
-
-
Duclos, C.1
Merlin, E.2
Paillard, C.3
-
30
-
-
55249115625
-
Stochastic modeling of human RBC alloimmunization: evidence for a distinct population of immunologic responders
-
Higgins JM, Sloan SR. Stochastic modeling of human RBC alloimmunization: evidence for a distinct population of immunologic responders. Blood 2008;112:2546–53.
-
(2008)
Blood
, vol.112
, pp. 2546-2553
-
-
Higgins, J.M.1
Sloan, S.R.2
|