-
1
-
-
0029843953
-
Thalassemia - A global public health problem
-
Weatherall DJ, Clegg JB. Thalassemia - a global public health problem. Nat Med 1996; 2: 847-9.
-
(1996)
Nat Med
, vol.2
, pp. 847-849
-
-
Weatherall, D.J.1
Clegg, J.B.2
-
2
-
-
0037716416
-
Les β-thalassémies en France métropolitaine
-
Badens C, North ML, Lena-Russo D. Les β-thalassémies en France métropolitaine. Presse Med 2003; 32: 1016-21.
-
(2003)
Presse Med
, vol.32
, pp. 1016-1021
-
-
Badens, C.1
North, M.L.2
Lena-Russo, D.3
-
4
-
-
0025970809
-
Transfusion requirements and effects in thalassemia major
-
Rebulla P, Modell B. Transfusion requirements and effects in thalassemia major. Lancet 1991; 337: 277-80.
-
(1991)
Lancet
, vol.337
, pp. 277-280
-
-
Rebulla, P.1
Modell, B.2
-
5
-
-
7044260046
-
Erythrocytapheresis to reduce iron loading in thalassemia
-
Friedman DF, Jawad AF, Martin MB, Horiuchi K, Mitchell CF, Cohen AR. Erythrocytapheresis to reduce iron loading in thalassemia. Blood 2003; 102: 121a.
-
(2003)
Blood
, vol.102
-
-
Friedman, D.F.1
Jawad, A.F.2
Martin, M.B.3
Horiuchi, K.4
Mitchell, C.F.5
Cohen, A.R.6
-
6
-
-
0031850655
-
Hydroxyurea therapy in thalassemia
-
Loukopoulos D, Voskaridou E, Stamoulakatou A, Papassotiriou Y, Kalotychou V, Loutradi A, et al. Hydroxyurea therapy in thalassemia. Ann N Y Acad Sci 1998; 850: 120-8.
-
(1998)
Ann N Y Acad Sci
, vol.850
, pp. 120-128
-
-
Loukopoulos, D.1
Voskaridou, E.2
Stamoulakatou, A.3
Papassotiriou, Y.4
Kalotychou, V.5
Loutradi, A.6
-
7
-
-
0042237715
-
Hydroxyurea can eliminate transfusion requirements in children with severe β-thalassemia
-
Bradai M, Abad MT, Pissard S, Lamraoui F, Skopinski L, de Montalembert M. Hydroxyurea can eliminate transfusion requirements in children with severe β-thalassemia. Blood 2003; 102: 1529-30.
-
(2003)
Blood
, vol.102
, pp. 1529-1530
-
-
Bradai, M.1
Abad, M.T.2
Pissard, S.3
Lamraoui, F.4
Skopinski, L.5
De Montalembert, M.6
-
8
-
-
0027363440
-
Epidemiological and clinical study of sickle cell disease in France, French Guiana and Algeria
-
de Montalembert M, Guilloud-Bataille M, Feingold J, Girot R. Epidemiological and clinical study of sickle cell disease in France, French Guiana and Algeria. Eur J Haematol 1993; 51: 136-40.
-
(1993)
Eur J Haematol
, vol.51
, pp. 136-140
-
-
De Montalembert, M.1
Guilloud-Bataille, M.2
Feingold, J.3
Girot, R.4
-
9
-
-
0034642592
-
Prediction of adverse outcomes in children with sickle cell disease
-
Miller ST, Sleeper LA, Pegelow CH, Enos LE, Wang WC, Weiner SJ, et al. Prediction of adverse outcomes in children with sickle cell disease. N Engl J Med 2000; 342: 83-9.
-
(2000)
N Engl J Med
, vol.342
, pp. 83-89
-
-
Miller, S.T.1
Sleeper, L.A.2
Pegelow, C.H.3
Enos, L.E.4
Wang, W.C.5
Weiner, S.J.6
-
10
-
-
0035944843
-
Haematological response to parvovirus B19 infection in homozygous sickle-cell disease
-
Serjeant BE, Hambleton IR, Kerr S, Kilty CG, Serjeant GR. Haematological response to parvovirus B19 infection in homozygous sickle-cell disease. Lancet 2001; 358: 1779-80.
-
(2001)
Lancet
, vol.358
, pp. 1779-1780
-
-
Serjeant, B.E.1
Hambleton, I.R.2
Kerr, S.3
Kilty, C.G.4
Serjeant, G.R.5
-
11
-
-
0742316143
-
The epidemiology of human parvovirus B19 in children with sickle cell disease
-
Smith-Whitley K, Zhao H, Hodinka RL, Kwiatkowski J, Cecil R, Cecil T, et al. The epidemiology of human parvovirus B19 in children with sickle cell disease. Blood 2004; 103: 422-7.
-
(2004)
Blood
, vol.103
, pp. 422-427
-
-
Smith-Whitley, K.1
Zhao, H.2
Hodinka, R.L.3
Kwiatkowski, J.4
Cecil, R.5
Cecil, T.6
-
12
-
-
0025526556
-
Management of acute splenic sequestration in sickle cell disease
-
Grover R, Wethers DL. Management of acute splenic sequestration in sickle cell disease. Asso Acad Minor Phys 1990; 1: 67-70.
-
(1990)
Asso Acad Minor Phys
, vol.1
, pp. 67-70
-
-
Grover, R.1
Wethers, D.L.2
-
13
-
-
0025362309
-
Long-terme management of splenic sequestration in children with sickle cell disease
-
Kinney TR, Ware RE, Schultz WH, Filston HC. Long-terme management of splenic sequestration in children with sickle cell disease. J Pediatr 1990; 117: 194-9.
-
(1990)
J Pediatr
, vol.117
, pp. 194-199
-
-
Kinney, T.R.1
Ware, R.E.2
Schultz, W.H.3
Filston, H.C.4
-
14
-
-
0027510623
-
Transfusion management of sickle cell disease
-
Wayne AS, Kevy SV, Nathan DG. Transfusion management of sickle cell disease. Blood 1993; 81: 1109-23.
-
(1993)
Blood
, vol.81
, pp. 1109-1123
-
-
Wayne, A.S.1
Kevy, S.V.2
Nathan, D.G.3
-
15
-
-
0027737943
-
Association of sickle cell disease, priapism, exchange transfusion and neurological events: ASPEN syndrome
-
Siegel JF, Rich MA, Brock WA. Association of sickle cell disease, priapism, exchange transfusion and neurological events: ASPEN syndrome. J Urol 1993; 150: 1480-2.
-
(1993)
J Urol
, vol.150
, pp. 1480-1482
-
-
Siegel, J.F.1
Rich, M.A.2
Brock, W.A.3
-
16
-
-
0028345470
-
Acute multiorgan failure syndrome: A potentially catastrophic complication of severe sickle cell pain episodes
-
Hassell KL, Eckman JR, Lane PA. Acute multiorgan failure syndrome: a potentially catastrophic complication of severe sickle cell pain episodes. Am J Med 1994; 96: 155-62.
-
(1994)
Am J Med
, vol.96
, pp. 155-162
-
-
Hassell, K.L.1
Eckman, J.R.2
Lane, P.A.3
-
17
-
-
0035133221
-
Indications for red cells transfusion in sickle cell disease
-
Ohene-Frempong K. Indications for red cells transfusion in sickle cell disease. Semin Hematol 2001; 38(Suppl 1): 5-13.
-
(2001)
Semin Hematol
, vol.38
, Issue.SUPPL. 1
, pp. 5-13
-
-
Ohene-Frempong, K.1
-
18
-
-
0029027701
-
A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease
-
Vichinsky EP, Haberkern CM, Neumayr L, Earles AN, Black D, Koshy M, et al. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. N Engl J Med 1995; 333: 206-13.
-
(1995)
N Engl J Med
, vol.333
, pp. 206-213
-
-
Vichinsky, E.P.1
Haberkern, C.M.2
Neumayr, L.3
Earles, A.N.4
Black, D.5
Koshy, M.6
-
19
-
-
4243247414
-
Controversies in transfusion in sickle cell disease
-
Rosse WF, Telen M, Ware RE, eds . AABB Press
-
Rosse WF, Telen M, Ware RE. Controversies in transfusion in sickle cell disease. In: Rosse WF, Telen M, Ware RE, eds. Transfusion support for patients with sickle cell disease. AABB Press, 1998: 63-71.
-
(1998)
Transfusion Support for Patients with Sickle Cell Disease
, pp. 63-71
-
-
Rosse, W.F.1
Telen, M.2
Ware, R.E.3
-
20
-
-
0031106184
-
The endothelial biology of sickle cell disease
-
Hebbel RP, Vercellotti GM. The endothelial biology of sickle cell disease. J Lab Clin Med 1997; 129: 288-93.
-
(1997)
J Lab Clin Med
, vol.129
, pp. 288-293
-
-
Hebbel, R.P.1
Vercellotti, G.M.2
-
21
-
-
0035869387
-
Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilatation
-
Belhassen L, Pelle G, Sediame S, Bachir D, Carville C, Bucherer C, et al. Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilatation. Blood 2001; 97: 1584-9.
-
(2001)
Blood
, vol.97
, pp. 1584-1589
-
-
Belhassen, L.1
Pelle, G.2
Sediame, S.3
Bachir, D.4
Carville, C.5
Bucherer, C.6
-
22
-
-
0023002273
-
Sickle cell anemia and central nervous system infarction: A neuropathological study
-
Rothman SM, Fulling KH, Nelson JS. Sickle cell anemia and central nervous system infarction: a neuropathological study. Ann Neurol 1986; 20: 684-94.
-
(1986)
Ann Neurol
, vol.20
, pp. 684-694
-
-
Rothman, S.M.1
Fulling, K.H.2
Nelson, J.S.3
-
23
-
-
0032474692
-
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial doppler untrasonography
-
Adams RJ, McKie VC, Hsu L, Files B, Vichinsky E, Pegelow C, et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial doppler untrasonography. 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
Files, B.4
Vichinsky, E.5
Pegelow, C.6
-
24
-
-
0031965089
-
Cerebrovascular accidents in sickle cell disease: Rates and risk factors
-
Ohene-Frempong K, Weiner SJ, Sleeper L, Miller ST, Embury S, Moohr JW, et al. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood 1998; 91: 288-94.
-
(1998)
Blood
, vol.91
, pp. 288-294
-
-
Ohene-Frempong, K.1
Weiner, S.J.2
Sleeper, L.3
Miller, S.T.4
Embury, S.5
Moohr, J.W.6
-
25
-
-
0026034335
-
High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease
-
Wang WC, Kovnar EH, Tonkin IL, Mulhern RK, Langston JW, Day SW, 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 1991; 118: 377-82.
-
(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
-
26
-
-
0033229703
-
Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease
-
Ware RE, Zimmerman SZ, Schultz WH. Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease. Blood 1999; 94: 3022-6.
-
(1999)
Blood
, vol.94
, pp. 3022-3026
-
-
Ware, R.E.1
Zimmerman, S.Z.2
Schultz, W.H.3
-
27
-
-
0035659821
-
Impact of chronic transfusion on pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia
-
Miller ST, Wright E, Abboud M, Berman B, Files B, Scher CD, et al. Impact of chronic transfusion on pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia. J Pediatr 2001; 139: 785-9.
-
(2001)
J Pediatr
, vol.139
, pp. 785-789
-
-
Miller, S.T.1
Wright, E.2
Abboud, M.3
Berman, B.4
Files, B.5
Scher, C.D.6
-
28
-
-
0023716354
-
Prophylactic red-cell transfusion in pregnant patients with sickle cell disease
-
Koshy M, Burd L, Wallace D, Moawad A, Baron J. Prophylactic red-cell transfusion in pregnant patients with sickle cell disease. N Engl J Med 1988; 319: 1447-52.
-
(1988)
N Engl J Med
, vol.319
, pp. 1447-1452
-
-
Koshy, M.1
Burd, L.2
Wallace, D.3
Moawad, A.4
Baron, J.5
-
29
-
-
0032975423
-
Drépanocytose et grossesse. Complications et prise en charge
-
Berkane N, Nizard J, Dreux B, Uzan S, Girot R. Drépanocytose et grossesse. Complications et prise en charge. Path Biol 1999; 47: 46-54.
-
(1999)
Path Biol
, vol.47
, pp. 46-54
-
-
Berkane, N.1
Nizard, J.2
Dreux, B.3
Uzan, S.4
Girot, R.5
-
30
-
-
0034631379
-
Survival in β-thalassemia major in the UK: Data from the UK Thalassemia register
-
Modell B, Khan M, Darlison M. Survival in β-thalassemia major in the UK: data from the UK Thalassemia register. Lancet 2000; 355: 2051-2.
-
(2000)
Lancet
, vol.355
, pp. 2051-2052
-
-
Modell, B.1
Khan, M.2
Darlison, M.3
-
31
-
-
0028086414
-
Survival in medically treated patients with homozygous β-thalassemia
-
Olivieiri NF, Nathan DG, MacMillan JH, Wayne AS, Liu PP, McGee A, et al. Survival in medically treated patients with homozygous β-thalassemia. N Engl J Med 1994; 331: 574-8.
-
(1994)
N Engl J Med
, vol.331
, pp. 574-578
-
-
Olivieiri, N.F.1
Nathan, D.G.2
MacMillan, J.H.3
Wayne, A.S.4
Liu, P.P.5
McGee, A.6
-
32
-
-
0035137382
-
Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease
-
Ballas SK. Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease. Semin Hematol 2001; 38(Suppl 1): 30-6.
-
(2001)
Semin Hematol
, vol.38
, Issue.SUPPL. 1
, pp. 30-36
-
-
Ballas, S.K.1
-
33
-
-
0034094839
-
Safety profile of the oral iron chelator deferiprone: A multicenter study
-
Cohen AR, Galanello R, Piga A, Dipalma A, Vullo C, Tricta F. Safety profile of the oral iron chelator deferiprone: a multicenter study. Br J Haematol 2000; 108: 305-12.
-
(2000)
Br J Haematol
, vol.108
, pp. 305-312
-
-
Cohen, A.R.1
Galanello, R.2
Piga, A.3
Dipalma, A.4
Vullo, C.5
Tricta, F.6
-
34
-
-
0031784438
-
Combined therapy with deferiprone and desferrioxamine
-
Wonke B, Wright C, Hoffbrand AV. Combined therapy with deferiprone and desferrioxamine. Br J Haematol 1998; 103: 361-4.
-
(1998)
Br J Haematol
, vol.103
, pp. 361-364
-
-
Wonke, B.1
Wright, C.2
Hoffbrand, A.V.3
-
35
-
-
0037761474
-
Safety and efficay of combining deferiprone and deferoxamine in iron chelation therapy in patients with thalassemia
-
abstract
-
Kattamis A, Kassou C, Ladis V, Berdoussi H, Papasotiriou I, Kattamis C. Safety and efficay of combining deferiprone and deferoxamine in iron chelation therapy in patients with thalassemia. Blood 2002; 100: 443; [abstract].
-
(2002)
Blood
, vol.100
, pp. 443
-
-
Kattamis, A.1
Kassou, C.2
Ladis, V.3
Berdoussi, H.4
Papasotiriou, I.5
Kattamis, C.6
-
36
-
-
0012773702
-
Phase II study of oral chelator ICL 670 in thalassemia patients with transfusional iron overload: Safety, pharmacokinetics (PK) and pharmacodynamics (PD) after 6 months of therapy
-
abstract
-
Piga A, Galanello R, Cappellini MD, Forni GL, Opitz H, Ford JM, et al. Phase II study of oral chelator ICL 670 in thalassemia patients with transfusional iron overload: safety, pharmacokinetics (PK) and pharmacodynamics (PD) after 6 months of therapy. Blood 2002; 100: 5; [abstract].
-
(2002)
Blood
, vol.100
, pp. 5
-
-
Piga, A.1
Galanello, R.2
Cappellini, M.D.3
Forni, G.L.4
Opitz, H.5
Ford, J.M.6
-
37
-
-
0031824987
-
Erythrocytapheresis limits iron accumulation in chronically transfused sickle cell patients
-
Hilliard LM, Williams BF, Lounsbury AE, Howard TH. 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
Howard, T.H.4
-
38
-
-
0025372673
-
Alloimmunization in sickle cell anemia and transfusion of racially unmatched blood
-
Vichinsky EP, Earles A, Johnson RA, Hoag MS, Williams A, Lubin B. Alloimmunization in sickle cell anemia and transfusion of racially unmatched blood. N Engl J Med 1990; 322: 1617-21.
-
(1990)
N Engl J Med
, vol.322
, pp. 1617-1621
-
-
Vichinsky, E.P.1
Earles, A.2
Johnson, R.A.3
Hoag, M.S.4
Williams, A.5
Lubin, B.6
-
39
-
-
0036892762
-
Rare RHCE phenotypes in black individuals of Afro-caribbean origin: Identification and transfusion safety
-
Noizat-Pirenne F, Lee K, Pennec PY, Simon P, Kazup P, Bachir D, et al. Rare RHCE phenotypes in black individuals of Afro-caribbean origin: identification and transfusion safety. Blood 2002; 100: 4223-31.
-
(2002)
Blood
, vol.100
, pp. 4223-4231
-
-
Noizat-Pirenne, F.1
Lee, K.2
Pennec, P.Y.3
Simon, P.4
Kazup, P.5
Bachir, D.6
-
40
-
-
0030950506
-
The sickle cell hemolytic transfusion reaction syndrome
-
Petz LD, Calhoun L, Shulman IA, Johnson C, Herron RM. The sickle cell hemolytic transfusion reaction syndrome. Transfusion 1997; 37: 382-92.
-
(1997)
Transfusion
, vol.37
, pp. 382-392
-
-
Petz, L.D.1
Calhoun, L.2
Shulman, I.A.3
Johnson, C.4
Herron, R.M.5
-
41
-
-
17344391561
-
Delayed hemolytic transfusion/hyperhemolysis syndrome in children with sickle cell disease
-
Talano JA, Hillery CA, Gottschall JL, Bayelrian DM, Scott JP. Delayed hemolytic transfusion/hyperhemolysis syndrome in children with sickle cell disease. Pediatrics 2003; 11: 661-5.
-
(2003)
Pediatrics
, vol.11
, pp. 661-665
-
-
Talano, J.A.1
Hillery, C.A.2
Gottschall, J.L.3
Bayelrian, D.M.4
Scott, J.P.5
-
42
-
-
0033559323
-
Structural and functional consequences of antigenic modulation of red blood cells with methoxypoly (Ethylene Glycol)
-
Murad KL, Mahany KL, Brugnara C, Kuypers FA, Eaton JW, Scott MD. Structural and functional consequences of antigenic modulation of red blood cells with methoxypoly (Ethylene Glycol). Blood 1999; 93: 2121-7.
-
(1999)
Blood
, vol.93
, pp. 2121-2127
-
-
Murad, K.L.1
Mahany, K.L.2
Brugnara, C.3
Kuypers, F.A.4
Eaton, J.W.5
Scott, M.D.6
-
43
-
-
0026660391
-
Prevalence of markers for human immunodeficiency virus type 1 and 2, human T-lymphotrophic virus type I, cytomegalovirus, and hepatitis B and C virus in multiply transfused thalassemia patients
-
de Montalembert M, Costagliola DG, Lefrère JJ, Cornu G, Lombardo T, Cosentino S, et al. Prevalence of markers for human immunodeficiency virus type 1 and 2, human T-lymphotrophic virus type I, cytomegalovirus, and hepatitis B and C virus in multiply transfused thalassemia patients. Transfusion 1992; 32: 509-12.
-
(1992)
Transfusion
, vol.32
, pp. 509-512
-
-
Montalembert, M.1
Costagliola, D.G.2
Lefrère, J.J.3
Cornu, G.4
Lombardo, T.5
Cosentino, S.6
-
44
-
-
0035132761
-
Current issues with blood transfusions in sickle cell disease
-
Vichinsky EP. Current issues with blood transfusions in sickle cell disease. Semin Hematol 2001; 38(Suppl 1): 14-22.
-
(2001)
Semin Hematol
, vol.38
, Issue.SUPPL. 1
, pp. 14-22
-
-
Vichinsky, E.P.1
-
45
-
-
2342427166
-
Risque résiduel de transmission du VIH, du VHC et du VHB par transfusion sanguine entre 1992 et 2002 en France et impact du dépistage génomique viral
-
Pillonel J, Laperche S. Risque résiduel de transmission du VIH, du VHC et du VHB par transfusion sanguine entre 1992 et 2002 en France et impact du dépistage génomique viral. Trans Clin Biol 2004; 11: 81-6.
-
(2004)
Trans Clin Biol
, vol.11
, pp. 81-86
-
-
Pillonel, J.1
Laperche, S.2
-
46
-
-
0036191089
-
Successful long-term erythrocytapheresis therapy in a patient with symptomatic sickle-cell disease using an arterio-venous fistula
-
Hartwig D, Schlager F, Bucsky P, Kirchner H, Schlenke P. Successful long-term erythrocytapheresis therapy in a patient with symptomatic sickle-cell disease using an arterio-venous fistula. Transf Med 2002; 12: 75-7.
-
(2002)
Transf Med
, vol.12
, pp. 75-77
-
-
Hartwig, D.1
Schlager, F.2
Bucsky, P.3
Kirchner, H.4
Schlenke, P.5
|