-
1
-
-
45349108763
-
Sickle cell disease: new insights into pathophysiology and treatment
-
Inati A., Koussa S., Taher A., et al. Sickle cell disease: new insights into pathophysiology and treatment. Pediatr Ann 37 (2008) 311-325
-
(2008)
Pediatr Ann
, vol.37
, pp. 311-325
-
-
Inati, A.1
Koussa, S.2
Taher, A.3
-
2
-
-
0028234283
-
The acute chest syndrome in sickle cell disease: incidence and risk factors. The Cooperative Study of Sickle Cell Disease
-
Castro O., Brambilla D.J., Thorington B., et al. The acute chest syndrome in sickle cell disease: incidence and risk factors. The Cooperative Study of Sickle Cell Disease. Blood 84 (1994) 643-649
-
(1994)
Blood
, vol.84
, pp. 643-649
-
-
Castro, O.1
Brambilla, D.J.2
Thorington, B.3
-
3
-
-
0029017748
-
Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease
-
Gill F.M., Sleeper L.A., Weiner S.J., et al. Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease. Blood 86 (1995) 776-783
-
(1995)
Blood
, vol.86
, pp. 776-783
-
-
Gill, F.M.1
Sleeper, L.A.2
Weiner, S.J.3
-
4
-
-
0031965089
-
Cerebrovascular accidents in sickle cell disease: rates and risk factors
-
Ohene-Frempong K., Weiner S.J., Sleeper L.A., 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
-
5
-
-
0022628893
-
Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial
-
Gaston M.H., Verter J.I., Woods G., et al. Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. N Engl J Med 314 (1986) 1593-1599
-
(1986)
N Engl J Med
, vol.314
, pp. 1593-1599
-
-
Gaston, M.H.1
Verter, J.I.2
Woods, G.3
-
6
-
-
0023906590
-
Newborn screening for sickle cell disease: effect on mortality
-
Vichinsky E., Hurst D., Earles A., et al. Newborn screening for sickle cell disease: effect on mortality. Pediatrics 81 (1988) 749-755
-
(1988)
Pediatrics
, vol.81
, pp. 749-755
-
-
Vichinsky, E.1
Hurst, D.2
Earles, A.3
-
7
-
-
0025832814
-
Comprehensive care in sickle cell disease: its impact on morbidity and mortality
-
Vichinsky E.P. Comprehensive care in sickle cell disease: its impact on morbidity and mortality. Semin Hematol 28 (1991) 220-226
-
(1991)
Semin Hematol
, vol.28
, pp. 220-226
-
-
Vichinsky, E.P.1
-
8
-
-
0032474692
-
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography
-
Adams R.J., McKie V.C., 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 339 (1998) 5-11
-
(1998)
N Engl J Med
, vol.339
, pp. 5-11
-
-
Adams, R.J.1
McKie, V.C.2
Hsu, L.3
-
9
-
-
0029027701
-
A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. The Preoperative Transfusion in Sickle Cell Disease Study Group
-
Vichinsky E.P., Haberkern C.M., Neumayr L., et al. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. The Preoperative Transfusion in Sickle Cell Disease Study Group. N Engl J Med 333 (1995) 206-213
-
(1995)
N Engl J Med
, vol.333
, pp. 206-213
-
-
Vichinsky, E.P.1
Haberkern, C.M.2
Neumayr, L.3
-
10
-
-
0035133221
-
Indications for red cell transfusion in sickle cell disease
-
Ohene-Frempong K. Indications for red cell transfusion in sickle cell disease. Semin Hematol 38 1 Suppl 1 (2001) 5-13
-
(2001)
Semin Hematol
, vol.38
, Issue.1 SUPPL. 1
, pp. 5-13
-
-
Ohene-Frempong, K.1
-
11
-
-
0029005136
-
Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions
-
Pegelow C.H., Adams R.J., McKie V., 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
-
12
-
-
29544444495
-
Optimizing Primary Stroke Prevention in Sickle Cell Anemia (STOP 2) Trial Investigators. Discontinuing prophylactic transfusions used to prevent stroke in sickle cell disease
-
Adams R.J., and 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 353 (2005) 2769-2778
-
(2005)
N Engl J Med
, vol.353
, pp. 2769-2778
-
-
Adams, R.J.1
Brambilla, D.2
-
13
-
-
0026646262
-
Serum non-transferrin bound iron in beta-thalassaemia major patients treated with desferrioxamine and L1
-
Al-Refaie F.N., Wickens D.G., Wonke B., et al. Serum non-transferrin bound iron in beta-thalassaemia major patients treated with desferrioxamine and L1. Br J Haematol 82 (1992) 431-436
-
(1992)
Br J Haematol
, vol.82
, pp. 431-436
-
-
Al-Refaie, F.N.1
Wickens, D.G.2
Wonke, B.3
-
14
-
-
33750600143
-
Circumstances of death in adult sickle cell disease patients
-
Darbari D.S., Kple-Faget P., Kwagyan J., et al. Circumstances of death in adult sickle cell disease patients. Am J Haematol 81 (2006) 858-863
-
(2006)
Am J Haematol
, vol.81
, pp. 858-863
-
-
Darbari, D.S.1
Kple-Faget, P.2
Kwagyan, J.3
-
15
-
-
73349100912
-
Mortality in sickle cell patient transitioning from pediatric to adult program: 10 years grady comprehensive sickle cell center experience
-
abstract 1426.
-
Aduloju S.O., Palmer S., and Eckman J.R. Mortality in sickle cell patient transitioning from pediatric to adult program: 10 years grady comprehensive sickle cell center experience. Blood 112 (2008) abstract 1426.
-
(2008)
Blood
, vol.112
-
-
Aduloju, S.O.1
Palmer, S.2
Eckman, J.R.3
-
16
-
-
50849084793
-
Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions
-
Fung E.B., Harmatz P.R., Milet M., et al. Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions. Transfusion 48 (2008) 1971-1980
-
(2008)
Transfusion
, vol.48
, pp. 1971-1980
-
-
Fung, E.B.1
Harmatz, P.R.2
Milet, M.3
-
17
-
-
73149097830
-
Tailoring iron chelation by iron intake and serum ferritin: prospective EPIC study of deferasirox in 1744 patients with transfusion-dependent anemias
-
[Epub ahead of print].
-
Cappellini M.D., Porter J., El-Beshlawy A., et al. Tailoring iron chelation by iron intake and serum ferritin: prospective EPIC study of deferasirox in 1744 patients with transfusion-dependent anemias. Haematologica (2009) [Epub ahead of print].
-
(2009)
Haematologica
-
-
Cappellini, M.D.1
Porter, J.2
El-Beshlawy, A.3
-
18
-
-
0033677772
-
The importance of non-transferrin bound iron in disorders of iron metabolism
-
Breuer W., Hershko C., and Cabantchik Z.I. The importance of non-transferrin bound iron in disorders of iron metabolism. Transfus Sci 23 (2000) 185-192
-
(2000)
Transfus Sci
, vol.23
, pp. 185-192
-
-
Breuer, W.1
Hershko, C.2
Cabantchik, Z.I.3
-
19
-
-
73349129282
-
Magnetic resonance imaging R2 mapping accurately estimates iron overload in sickle cell disease patients
-
abstract 1285.
-
Inati A., Taha M., Musallam K.M., et al. Magnetic resonance imaging R2 mapping accurately estimates iron overload in sickle cell disease patients. EHA (2009) abstract 1285.
-
(2009)
EHA
-
-
Inati, A.1
Taha, M.2
Musallam, K.M.3
-
20
-
-
85117738609
-
Iron overload indices rise linearly with transfusion rate in patients with sickle cell disease
-
in press
-
Inati A, Musallam KM, Wood JC, et al. Iron overload indices rise linearly with transfusion rate in patients with sickle cell disease. Blood; in press.
-
Blood
-
-
Inati, A.1
Musallam, K.M.2
Wood, J.C.3
-
21
-
-
70449499193
-
Absence of cardiac siderosis by MRI T2* despite transfusion burden, hepatic and serum iron overload in Lebanese patients with sickle cell disease
-
Inati A., Musallam K.M., Wood J.C., et al. Absence of cardiac siderosis by MRI T2* despite transfusion burden, hepatic and serum iron overload in Lebanese patients with sickle cell disease. Eur J Haematol 83 (2009) 565-571
-
(2009)
Eur J Haematol
, vol.83
, pp. 565-571
-
-
Inati, A.1
Musallam, K.M.2
Wood, J.C.3
-
22
-
-
73349127369
-
Magnetic resonance imaging T2* in the evaluation of cardiac iron overload in patients with sickle cell disease
-
abstract 1286.
-
Inati A., Musallam K.M., Taha M., et al. Magnetic resonance imaging T2* in the evaluation of cardiac iron overload in patients with sickle cell disease. EHA (2009) abstract 1286.
-
(2009)
EHA
-
-
Inati, A.1
Musallam, K.M.2
Taha, M.3
-
24
-
-
0013409935
-
-
and Division of Blood Diseases and Resources NIH, Bethesda, MD National Institutes of Health National Heart, Lung, and Blood Institute,
-
National Institutes of Health, National Heart, Lung, and Blood Institute, and and Division of Blood Diseases and Resources. The management of sickle cell disease (NIH Publication No 02-2117) (2002), NIH, Bethesda, MD
-
(2002)
The management of sickle cell disease (NIH Publication No 02-2117)
-
-
-
25
-
-
33846012866
-
A randomised comparison of deferasirox versus deferoxamine for the treatment of transfusional iron overload in sickle cell disease
-
Vichinsky E., Onyekwere O., Porter J., et al. A randomised comparison of deferasirox versus deferoxamine for the treatment of transfusional iron overload in sickle cell disease. Br J Haematol 136 (2007) 501-508
-
(2007)
Br J Haematol
, vol.136
, pp. 501-508
-
-
Vichinsky, E.1
Onyekwere, O.2
Porter, J.3
-
26
-
-
46049087344
-
Patient-reported outcomes of deferasirox (Exjade, ICL670) versus deferoxamine in sickle cell disease patients with transfusional hemosiderosis. Substudy of a randomized open-label phase II trial
-
Vichinsky E., Pakbaz Z., Onyekwere O., et al. Patient-reported outcomes of deferasirox (Exjade, ICL670) versus deferoxamine in sickle cell disease patients with transfusional hemosiderosis. Substudy of a randomized open-label phase II trial. Acta Haematol 119 (2008) 133-141
-
(2008)
Acta Haematol
, vol.119
, pp. 133-141
-
-
Vichinsky, E.1
Pakbaz, Z.2
Onyekwere, O.3
-
27
-
-
73349094282
-
-
Vichinsky E. Coates T, Thompson AA, et al. Deferasirox (Exjade®), the once-daily oral iron chelator, demonstrates safety and efficacy in patient with sickle cell disease CD: 3.5-year follow-up. ASH 2008: abstract 1420.
-
Vichinsky E. Coates T, Thompson AA, et al. Deferasirox (Exjade®), the once-daily oral iron chelator, demonstrates safety and efficacy in patient with sickle cell disease (CD: 3.5-year follow-up. ASH 2008: abstract 1420.
-
-
-
-
28
-
-
63649136756
-
Oral iron chelation and the treatment of iron overload in a pediatric hematology center
-
Raphael J.L., Bernhardt M.B., Mahoney D.H., et al. Oral iron chelation and the treatment of iron overload in a pediatric hematology center. Pediatr Blood Cancer 52 (2009) 616-620
-
(2009)
Pediatr Blood Cancer
, vol.52
, pp. 616-620
-
-
Raphael, J.L.1
Bernhardt, M.B.2
Mahoney, D.H.3
|