-
2
-
-
0037335688
-
Therapeutic challenges in childhood sickle cell disease part 1: current and future treatment options
-
Armolia P.J., Almeida A., Halsey C., et al. Therapeutic challenges in childhood sickle cell disease part 1: current and future treatment options. Br J Haematol 120 (2003) 725-736
-
(2003)
Br J Haematol
, vol.120
, pp. 725-736
-
-
Armolia, P.J.1
Almeida, A.2
Halsey, C.3
-
3
-
-
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 88 (1996) 1960-1964
-
(1996)
Blood
, vol.88
, pp. 1960-1964
-
-
Ferster, A.1
Vermylen, C.2
Cornu, G.3
-
4
-
-
0037338359
-
Therapeutic challenges in childhood sickle cell disease part 2: a problem oriented approach
-
Armolia P.J., Almeida A., Davies S.C., et al. Therapeutic challenges in childhood sickle cell disease part 2: a problem oriented approach. Br J Haematol 120 (2003) 737-743
-
(2003)
Br J Haematol
, vol.120
, pp. 737-743
-
-
Armolia, P.J.1
Almeida, A.2
Davies, S.C.3
-
5
-
-
0031934441
-
Hydroxyurea in children with sickle cell disease: impact on splenic function and compliance with therapy
-
Olivieri N.F., and Vichinsky E.P. Hydroxyurea in children with sickle cell disease: impact on splenic function and compliance with therapy. J Pediatr Hematol Oncol 20 (1998) 26-31
-
(1998)
J Pediatr Hematol Oncol
, vol.20
, pp. 26-31
-
-
Olivieri, N.F.1
Vichinsky, E.P.2
-
6
-
-
27144448031
-
Long-term hydroxyurea therapy for infants with sickle cell anemia: The HUSOFT extention study
-
Hankins J.S., Ware R.E., Rogers Z.R., et al. Long-term hydroxyurea therapy for infants with sickle cell anemia: The HUSOFT extention study. Blood 106 (2005) 2269-2275
-
(2005)
Blood
, vol.106
, pp. 2269-2275
-
-
Hankins, J.S.1
Ware, R.E.2
Rogers, Z.R.3
-
7
-
-
0037414166
-
Hydroxyurea and sickle cell disease: a chance for every patient
-
Weiner D.L., and Brugnara C. Hydroxyurea and sickle cell disease: a chance for every patient. JAMA 289 (2003) 1692-1694
-
(2003)
JAMA
, vol.289
, pp. 1692-1694
-
-
Weiner, D.L.1
Brugnara, C.2
-
8
-
-
0037414164
-
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment
-
Steinberg M.H., Barton F., Castro O., et al. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment. JAMA 289 (2003) 1645-1651
-
(2003)
JAMA
, vol.289
, pp. 1645-1651
-
-
Steinberg, M.H.1
Barton, F.2
Castro, O.3
-
9
-
-
0036846955
-
The effect of hydroxyurea on vasculopathy in a child with sickle cell disease
-
Helton K.J., Wang W.C., Wynn L.W., et al. The effect of hydroxyurea on vasculopathy in a child with sickle cell disease. Am J Neuroradiol 23 (2002) 1692-1696
-
(2002)
Am J Neuroradiol
, vol.23
, pp. 1692-1696
-
-
Helton, K.J.1
Wang, W.C.2
Wynn, L.W.3
-
10
-
-
0036829459
-
Hydroxyurea (HU) for prevention of recurrent stroke in sickle cell anemia (SCA)
-
Sumoza A., De Bisotti R., Sumoza D., et al. Hydroxyurea (HU) for prevention of recurrent stroke in sickle cell anemia (SCA). Am J Hematol 71 (2002) 161-165
-
(2002)
Am J Hematol
, vol.71
, pp. 161-165
-
-
Sumoza, A.1
De Bisotti, R.2
Sumoza, D.3
-
11
-
-
0033229703
-
Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sicle cell disease
-
Ware R.E., Zimmerman S.A., and Schultz W.H. Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sicle 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
-
12
-
-
32544435138
-
Long-term hydroxyurea treatment in children with sickle cell disease: Tolerance and clinical outcomes
-
De Montalembert M., Brousse V., Elie C., et al. Long-term hydroxyurea treatment in children with sickle cell disease: Tolerance and clinical outcomes. Haematologica 91 (2006) 125-128
-
(2006)
Haematologica
, vol.91
, pp. 125-128
-
-
De Montalembert, M.1
Brousse, V.2
Elie, C.3
-
13
-
-
20144386780
-
Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: The Belgian experience
-
Gulbis B., Haberman D., Dutour D., et al. Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: The Belgian experience. Blood 105 (2005) 2685-2690
-
(2005)
Blood
, vol.105
, pp. 2685-2690
-
-
Gulbis, B.1
Haberman, D.2
Dutour, D.3
-
14
-
-
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., 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
-
15
-
-
0035383785
-
Five years of experience with hydroxyurea in children and young adults with sickle cell disease
-
Ferster A., Tahiri P., Vermylen C., et al. Five years of experience with hydroxyurea in children and young adults with sickle cell disease. Blood 97 (2001) 3628-3632
-
(2001)
Blood
, vol.97
, pp. 3628-3632
-
-
Ferster, A.1
Tahiri, P.2
Vermylen, C.3
-
16
-
-
0035525770
-
Is hydroxyurea leukemogenic in children with sickle cell disease?
-
De Montalembert M., and Davies S.C. Is hydroxyurea leukemogenic in children with sickle cell disease?. Blood 98 (2001) 2878-2879
-
(2001)
Blood
, vol.98
, pp. 2878-2879
-
-
De Montalembert, M.1
Davies, S.C.2
-
17
-
-
0032736850
-
Preliminary report of a toxicity study of hydroxyurea in sickle cell disease
-
De Montalembert M., Begue P., Bernaudin F., et al. Preliminary report of a toxicity study of hydroxyurea in sickle cell disease. Arch Dis Child 81 (1999) 437-439
-
(1999)
Arch Dis Child
, vol.81
, pp. 437-439
-
-
De Montalembert, M.1
Begue, P.2
Bernaudin, F.3
-
19
-
-
1542373662
-
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease
-
Zimmerman S.A., Schultz W.H., Dvis J.S., et al. Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in 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
Dvis, J.S.3
-
20
-
-
0037409211
-
The role of hydroxyurea in the management of sickle cell disease
-
Davies S.C., and Gilmore A. The role of hydroxyurea in the management of sickle cell disease. Blood Rev 17 (2003) 99-109
-
(2003)
Blood Rev
, vol.17
, pp. 99-109
-
-
Davies, S.C.1
Gilmore, A.2
-
21
-
-
0029025475
-
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia
-
Charache S., Terrin M.L., Moore R.D., et al. Effect of hydroxyurea on the frequency of painful crises 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
-
22
-
-
0035659819
-
Hydroxyurea in very young children with sickle cell anemia is not a cure-all
-
Powers D.R. Hydroxyurea in very young children with sickle cell anemia is not a cure-all. J Pediatr 139 (2001) 763-764
-
(2001)
J Pediatr
, vol.139
, pp. 763-764
-
-
Powers, D.R.1
-
23
-
-
0035666461
-
A two-years pilot trial of hydroxyurea in very young children with sickle cell anemia
-
Wang W.C., Wynn L.W., Rogers Z.R., et al. A two-years pilot trial of hydroxyurea in very young children with sickle cell anemia. J Pediatr 139 (2001) 790-796
-
(2001)
J Pediatr
, vol.139
, pp. 790-796
-
-
Wang, W.C.1
Wynn, L.W.2
Rogers, Z.R.3
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