-
1
-
-
0001661081
-
The involvement of the nervous system in sickle cell anemia
-
Hughes J.G., Diggs L.W., Gillespie C.E. The involvement of the nervous system in sickle cell anemia. J Pediatr. 17:1940;166-184
-
(1940)
J Pediatr
, vol.17
, pp. 166-184
-
-
Hughes, J.G.1
Diggs, L.W.2
Gillespie, C.E.3
-
3
-
-
0004655593
-
Studies in sickle cell anemia, XXI: Clinico-pathological aspects of neurological manifestations
-
Baird R.L., Weiss D.L., Ferguson A.D., French J.H., Scott R.B. Studies in sickle cell anemia, XXI: clinico-pathological aspects of neurological manifestations. Pediatrics. 34:1964;92-100
-
(1964)
Pediatrics
, vol.34
, pp. 92-100
-
-
Baird, R.L.1
Weiss, D.L.2
Ferguson, A.D.3
French, J.H.4
Scott, R.B.5
-
4
-
-
0023730856
-
Cerebral infarction in sickle cell anemia: Mechanism based on CT and MRI
-
Adams R.J., Nichols F.T., McKie V., McKie K., Milner P., Gammal T.E. Cerebral infarction in sickle cell anemia: mechanism based on CT and MRI. Neurology. 38:1988;1012-1017
-
(1988)
Neurology
, vol.38
, pp. 1012-1017
-
-
Adams, R.J.1
Nichols, F.T.2
McKie, V.3
McKie, K.4
Milner, P.5
Gammal, T.E.6
-
5
-
-
0017822187
-
The natural history of stroke in sickle cell disease
-
Powars D., Wilson B., Imbus C., Pegelow C., Allen J. The natural history of stroke in sickle cell disease. Am J Med. 65:1978;461-471
-
(1978)
Am J Med
, vol.65
, pp. 461-471
-
-
Powars, D.1
Wilson, B.2
Imbus, C.3
Pegelow, C.4
Allen, J.5
-
7
-
-
0025109527
-
The variable expression of sickle cell disease is genetically determined
-
Powars D., Chan L.S., Schroeder W.A. The variable expression of sickle cell disease is genetically determined. Semin Hematol. 27:1990;360-376
-
(1990)
Semin Hematol
, vol.27
, pp. 360-376
-
-
Powars, D.1
Chan, L.S.2
Schroeder, W.A.3
-
8
-
-
0025797297
-
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. 28:1991;213-219
-
(1991)
Semin Hematol
, vol.28
, pp. 213-219
-
-
Ohene-Frempong, K.1
-
9
-
-
0026541648
-
Stroke in a cohort of patients with homozygous sickle cell disease
-
Balkaran B., Char G., Morris J.S., Thomas T.W., Serjeant B.E., Serjeant G.R. Stroke in a cohort of patients with homozygous sickle cell disease. J Pediatr. 120:1992;360-366
-
(1992)
J Pediatr
, vol.120
, pp. 360-366
-
-
Balkaran, B.1
Char, G.2
Morris, J.S.3
Thomas, T.W.4
Serjeant, B.E.5
Serjeant, G.R.6
-
10
-
-
0031965089
-
Cerebrovascular accidents in sickle cell disease: Rates and risk factors
-
Ohene-Frempong K., Weiner S.J., Sleeper L.A., Miller S.T., Embury S., Moohr J.W., et al. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. 91:1998;288-294
-
(1998)
Blood
, vol.91
, pp. 288-294
-
-
Ohene-Frempong, K.1
Weiner, S.J.2
Sleeper, L.A.3
Miller, S.T.4
Embury, S.5
Moohr, J.W.6
-
11
-
-
0033844765
-
Serving the family from birth to the medical home: Newborn screening: A blueprint for the future
-
AAP Newborn Screening Taskforce. Serving the family from birth to the medical home: newborn screening: a blueprint for the future. Pediatrics. 106:(suppl):2000;383-427
-
(2000)
Pediatrics
, vol.106
, Issue.SUPPL.
, pp. 383-427
-
-
Newborn Screening Taskforce, A.1
-
12
-
-
0019231082
-
Cerebral vascular accidents in sickle cell anemia
-
Powars D., Imbus C. Cerebral vascular accidents in sickle cell anemia. Texas Reports Biol Med. 40:1980;293-304
-
(1980)
Texas Reports Biol Med
, vol.40
, pp. 293-304
-
-
Powars, D.1
Imbus, C.2
-
13
-
-
0021335218
-
Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease
-
Russell M.O., Goldberg H.I., Hodson A., Kim H.C., Halus J., Reivich M., et al. Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease. Blood. 63:1984;162-169
-
(1984)
Blood
, vol.63
, pp. 162-169
-
-
Russell, M.O.1
Goldberg, H.I.2
Hodson, A.3
Kim, H.C.4
Halus, J.5
Reivich, M.6
-
14
-
-
0017196848
-
A prophylactic transfusion program for children with sickle cell anemia complicated by CNS infarction
-
Lusher J.M., Haghighat H., Khalifa A.S. A prophylactic transfusion program for children with sickle cell anemia complicated by CNS infarction. Am J Hematol. 1:1976;265-273
-
(1976)
Am J Hematol
, vol.1
, pp. 265-273
-
-
Lusher, J.M.1
Haghighat, H.2
Khalifa, A.S.3
-
15
-
-
84886616693
-
Transfusion therapy for cerebrovascular abnormalities in sickle cell disease
-
Russell M.O., Goldberg H.I., Reis L., Friedman S., Slater R., Reivich M., et al. Transfusion therapy for cerebrovascular abnormalities in sickle cell disease. J Pediatr. 88:1976;382-387
-
(1976)
J Pediatr
, vol.88
, pp. 382-387
-
-
Russell, M.O.1
Goldberg, H.I.2
Reis, L.3
Friedman, S.4
Slater, R.5
Reivich, M.6
-
16
-
-
0029005136
-
Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions
-
Pegelow C.H., Adams R.J., McKie V., Abboud M., Berman B., Miller S.T., et al. Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions. J Pediatr. 126:1995;896-899
-
(1995)
J Pediatr
, vol.126
, pp. 896-899
-
-
Pegelow, C.H.1
Adams, R.J.2
McKie, V.3
Abboud, M.4
Berman, B.5
Miller, S.T.6
-
17
-
-
0036220398
-
Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke
-
Scothorn D.J., Price C., Schwartz D., Terrill C., Buchanan G.R., Shurney W., et al. Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke. J Pediatr. 140:2002;348-354
-
(2002)
J Pediatr
, vol.140
, pp. 348-354
-
-
Scothorn, D.J.1
Price, C.2
Schwartz, D.3
Terrill, C.4
Buchanan, G.R.5
Shurney, W.6
-
18
-
-
0029942003
-
The risk of transfusion-transmitted viral infections: The Retrovirus Epidemiology Donor Study
-
Schreiber G.B., Busch M.P., Kleinman S.H., Korelitz J.J. The risk of transfusion-transmitted viral infections: the Retrovirus Epidemiology Donor Study. N Engl J Med. 334:1996;1685-1690
-
(1996)
N Engl J Med
, vol.334
, pp. 1685-1690
-
-
Schreiber, G.B.1
Busch, M.P.2
Kleinman, S.H.3
Korelitz, J.J.4
-
19
-
-
0025155742
-
Transfusion and alloimmunization in sickle cell disease
-
Rosse W.F., Gallagher D., Kinney T.R., Castro O., Dosik H., Moohr J., et al. Transfusion and alloimmunization in sickle cell disease. Blood. 76:1990;1431-1437
-
(1990)
Blood
, vol.76
, pp. 1431-1437
-
-
Rosse, W.F.1
Gallagher, D.2
Kinney, T.R.3
Castro, O.4
Dosik, H.5
Moohr, J.6
-
20
-
-
0034858110
-
Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: A multicenter transfusion trial
-
Vichinsky E.P., Luban N.L., Wright E., Olivieri N., Driscoll C., Pegelow C.H., et al. Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial. Transfusion. 41:2001;1086-1092
-
(2001)
Transfusion
, vol.41
, pp. 1086-1092
-
-
Vichinsky, E.P.1
Luban, N.L.2
Wright, E.3
Olivieri, N.4
Driscoll, C.5
Pegelow, C.H.6
-
21
-
-
0032950197
-
Erythrocyte autoantibodies in pediatric patients receiving transfusion therapy: Frequency, characteristics, and significance
-
Castellino S.M., Combs M.R., Zimmerman S.A., Issitt P.D., Ware R.E. Erythrocyte autoantibodies in pediatric patients receiving transfusion therapy: frequency, characteristics, and significance. Br J Haematol. 104:1999;189-194
-
(1999)
Br J Haematol
, vol.104
, pp. 189-194
-
-
Castellino, S.M.1
Combs, M.R.2
Zimmerman, S.A.3
Issitt, P.D.4
Ware, R.E.5
-
22
-
-
0035137382
-
Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease
-
Ballas S.K. Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease. Semin Hematol. 38:(suppl):2001;30-36
-
(2001)
Semin Hematol
, vol.38
, Issue.SUPPL.
, pp. 30-36
-
-
Ballas, S.K.1
-
23
-
-
0036255547
-
Longitudinal changes in ferritin during chronic transfusion: A report from the stroke prevention trial in sickle cell anemia (STOP)
-
Files B., Brambilla D., Kutlar A., Miller S., Vichinsky E., Wang W., et al. Longitudinal changes in ferritin during chronic transfusion: a report from the stroke prevention trial in sickle cell anemia (STOP). J Pediatr Hematol/Oncol. 24:2002;284-290
-
(2002)
J Pediatr Hematol/Oncol
, vol.24
, pp. 284-290
-
-
Files, B.1
Brambilla, D.2
Kutlar, A.3
Miller, S.4
Vichinsky, E.5
Wang, W.6
-
24
-
-
0029129942
-
Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia
-
Ware R.E., Steinberg M.H., Kinney T.R. Hydroxyurea: an alternative to transfusion therapy for stroke in sickle cell anemia. Am J Hematol. 50:1995;140-143
-
(1995)
Am J Hematol
, vol.50
, pp. 140-143
-
-
Ware, R.E.1
Steinberg, M.H.2
Kinney, T.R.3
-
25
-
-
0033229703
-
Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease
-
Ware R.E., Zimmerman S.A., Schultz W.H. Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease. Blood. 94:1999;3022-3026
-
(1999)
Blood
, vol.94
, pp. 3022-3026
-
-
Ware, R.E.1
Zimmerman, S.A.2
Schultz, W.H.3
-
26
-
-
0026631318
-
Hydroxyurea: Effects on hemoglobin F production in patients with sickle cell disease
-
Charache S., Dover G.J., Moore R.D., Eckert S., Ballas S.K., Koshy M., et al. Hydroxyurea: effects on hemoglobin F production in patients with sickle cell disease. Blood. 79:1992;2555-2565
-
(1992)
Blood
, vol.79
, pp. 2555-2565
-
-
Charache, S.1
Dover, G.J.2
Moore, R.D.3
Eckert, S.4
Ballas, S.K.5
Koshy, M.6
-
27
-
-
13044277572
-
Safety of hydroxyurea in children with sickle cell anemia: Results of the HUG-KIDS study, a Phase I/II trial
-
Kinney T.R., Helms R.W., O'Branski E.E., Ohene-Frempong K., Wang W., Daeschner C., et al. Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a Phase I/II trial. Blood. 94:1999;1550-1554
-
(1999)
Blood
, vol.94
, pp. 1550-1554
-
-
Kinney, T.R.1
Helms, R.W.2
O'Branski, E.E.3
Ohene-Frempong, K.4
Wang, W.5
Daeschner, C.6
-
28
-
-
0030040223
-
Erythrocytapheresis can reduce iron overload and prevent the need for chelation therapy in chronically transfused pediatric patients
-
Adams D.M., Schultz W.H., Ware R.E., Kinney T.R. Erythrocytapheresis can reduce iron overload and prevent the need for chelation therapy in chronically transfused pediatric patients. J Pediatr Hematol/Oncol. 18:1996;46-50
-
(1996)
J Pediatr Hematol/Oncol
, vol.18
, pp. 46-50
-
-
Adams, D.M.1
Schultz, W.H.2
Ware, R.E.3
Kinney, T.R.4
-
29
-
-
0018888412
-
Efficacy of transfusion therapy for one to two years in patients with sickle cell disease and cerebrovascular accidents
-
Wilimas J., Goff J.R., Anderson H.R. Jr., Langston J.W., Thompson E. Efficacy of transfusion therapy for one to two years in patients with sickle cell disease and cerebrovascular accidents. J Pediatr. 96:1980;205-208
-
(1980)
J Pediatr
, vol.96
, pp. 205-208
-
-
Wilimas, J.1
Goff, J.R.2
Anderson Jr., H.R.3
Langston, J.W.4
Thompson, E.5
-
30
-
-
0026034335
-
High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease
-
Wang W.C., Kovnar E.H., Tonkin I.L., Mulhern R.K., Langston J.W., Day S.W., et al. High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease. J Pediatr. 118:1991;377-382
-
(1991)
J Pediatr
, vol.118
, pp. 377-382
-
-
Wang, W.C.1
Kovnar, E.H.2
Tonkin, I.L.3
Mulhern, R.K.4
Langston, J.W.5
Day, S.W.6
-
31
-
-
79960971743
-
Variable approaches to therapeutic options for children with sickle cell disease (SCD): A practice survey of the American Society of Pediatric Hematology/Oncology (ASPH/O)
-
Lane P.A., Buchanan G.R., Ware R.E. Variable approaches to therapeutic options for children with sickle cell disease (SCD): a practice survey of the American Society of Pediatric Hematology/Oncology (ASPH/O). Blood. 98:2001;784a
-
(2001)
Blood
, vol.98
-
-
Lane, P.A.1
Buchanan, G.R.2
Ware, R.E.3
-
32
-
-
0035138526
-
Progression of iron overload in sickle cell disease
-
Olivieri N.F. Progression of iron overload in sickle cell disease. Semin Hematol. 38:(suppl):2001;57-62
-
(2001)
Semin Hematol
, vol.38
, Issue.SUPPL.
, pp. 57-62
-
-
Olivieri, N.F.1
-
33
-
-
0035135479
-
Improving adherence with deferoxamine regimens for patients receiving chronic transfusion therapy
-
Treadwell M.J., Weissman L. Improving adherence with deferoxamine regimens for patients receiving chronic transfusion therapy. Semin Hematol. 38:(suppl):2001;77-84
-
(2001)
Semin Hematol
, vol.38
, Issue.SUPPL.
, pp. 77-84
-
-
Treadwell, M.J.1
Weissman, L.2
-
34
-
-
0029025475
-
Effect of hydroxyurea on frequency of painful crisis in sickle cell anemia
-
Charache S., Terrin M.L., Moore R.D., Dover G.J., Barton F.B., Eckert S.V., et al. Effect of hydroxyurea on frequency of painful crisis in sickle cell anemia. N Engl J Med. 332:1995;1317-1322
-
(1995)
N Engl J Med
, vol.332
, pp. 1317-1322
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
Dover, G.J.4
Barton, F.B.5
Eckert, S.V.6
-
35
-
-
0030853711
-
Pathogenesis and treatment of sickle cell disease
-
Bunn H.F. Pathogenesis and treatment of sickle cell disease. N Engl J Med. 337:1997;762-769
-
(1997)
N Engl J Med
, vol.337
, pp. 762-769
-
-
Bunn, H.F.1
-
36
-
-
0028053133
-
A cautionary note regarding hydroxyurea in sickle cell disease
-
Vichinsky E.P., Lubin B.H. A cautionary note regarding hydroxyurea in sickle cell disease. Blood. 83:1994;1124-1128
-
(1994)
Blood
, vol.83
, pp. 1124-1128
-
-
Vichinsky, E.P.1
Lubin, B.H.2
-
37
-
-
0029982591
-
Hydroxyurea therapy in children severely affected with sickle cell disease
-
Scott J.P., Hillery C.A., Brown E.R., Misiewicz V., Labotka R.J. Hydroxyurea therapy in children severely affected with sickle cell disease. J Pediatr. 128:1996;820-828
-
(1996)
J Pediatr
, vol.128
, pp. 820-828
-
-
Scott, J.P.1
Hillery, C.A.2
Brown, E.R.3
Misiewicz, V.4
Labotka, R.J.5
-
38
-
-
0030696806
-
Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease: The French Study Group on Sickle Cell Disease
-
de Montalembert M., Belloy M., Bernaudin F., Gouraud F., Capdeville R., Mardini R., et al. Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease: the French Study Group on Sickle Cell Disease. J Pediatr Hematol/Oncol. 19:1997;313-318
-
(1997)
J Pediatr Hematol/Oncol
, vol.19
, pp. 313-318
-
-
De Montalembert, M.1
Belloy, M.2
Bernaudin, F.3
Gouraud, F.4
Capdeville, R.5
Mardini, R.6
-
39
-
-
1542373662
-
Sustained long-term hematological efficacy of hydroxyurea therapy for children with sickle cell disease
-
Zimmerman S.A., Schultz W.H., Davis J.S., Pickens C.V., Mortier N.A., Howard T.A., et al. Sustained long-term hematological efficacy of hydroxyurea therapy for children with sickle cell disease. Blood. 103:2004;2039-2045
-
(2004)
Blood
, vol.103
, pp. 2039-2045
-
-
Zimmerman, S.A.1
Schultz, W.H.2
Davis, J.S.3
Pickens, C.V.4
Mortier, N.A.5
Howard, T.A.6
-
40
-
-
0030848104
-
Phlebotomy to reduce iron overload in patients cured of thalassemia by bone marrow transplantation
-
Angelucci E., Muretto P., Lucarelli G., Ripalti M., Baronciani D., Erer B., et al. Phlebotomy to reduce iron overload in patients cured of thalassemia by bone marrow transplantation. Blood. 90:1997;994-998
-
(1997)
Blood
, vol.90
, pp. 994-998
-
-
Angelucci, E.1
Muretto, P.2
Lucarelli, G.3
Ripalti, M.4
Baronciani, D.5
Erer, B.6
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