-
1
-
-
0016687781
-
Natural history of sickle cell disease - The first ten years
-
Powars D. Natural history of sickle cell disease - the first ten years. Semin Hematol 1975;12:267-85.
-
(1975)
Semin Hematol
, vol.12
, pp. 267-285
-
-
Powars, D.1
-
2
-
-
0028291736
-
Mortality in sickle cell disease. Life expectancy and risk factors for early death
-
Platt O, Brambilla D, Rosse W, et al. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med 1994;330:1639-44.
-
(1994)
N Engl J Med
, vol.330
, pp. 1639-1644
-
-
Platt, O.1
Brambilla, D.2
Rosse, W.3
-
3
-
-
0031959197
-
New considerations in the treatment of sickle cell disease
-
Reed W, Vichinsky E. New considerations in the treatment of sickle cell disease. Annu Rev Med 1998;49:461-74.
-
(1998)
Annu Rev Med
, vol.49
, pp. 461-474
-
-
Reed, W.1
Vichinsky, E.2
-
4
-
-
0030703240
-
Circulating activated endothelial cells in sickle cell anemia
-
Solovey A, Lin Y, Browne P, et al. Circulating activated endothelial cells in sickle cell anemia. N Engl J Med 1997;337:1584-90.
-
(1997)
N Engl J Med
, vol.337
, pp. 1584-1590
-
-
Solovey, A.1
Lin, Y.2
Browne, P.3
-
5
-
-
0030895689
-
Decrease of very late activation antigen-4 and CD36 on reticulocytes in patients treated with hydroxyurea
-
Styles L, Lubin B, Vichinsky E, et al. Decrease of very late activation antigen-4 and CD36 on reticulocytes in patients treated with hydroxyurea. Blood 1997;89:2554-9.
-
(1997)
Blood
, vol.89
, pp. 2554-2559
-
-
Styles, L.1
Lubin, B.2
Vichinsky, E.3
-
6
-
-
0032080802
-
Tissue factor expression by endothetial cells in sickle cell anemia
-
Solovey A, Gui L, Hebbel R. Tissue factor expression by endothetial cells in sickle cell anemia. J Clin Invest 1998;101:1899-904.
-
(1998)
J Clin Invest
, vol.101
, pp. 1899-1904
-
-
Solovey, A.1
Gui, L.2
Hebbel, R.3
-
7
-
-
0029025475
-
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the multicenter study of hydroxyurea in sickle cell anemia
-
Charache S, Termin M, Moore R. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med 1995;322:1317-22.
-
(1995)
N Engl J Med
, vol.322
, pp. 1317-1322
-
-
Charache, S.1
Termin, M.2
Moore, R.3
-
8
-
-
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 1996;88:1960-4.
-
(1996)
Blood
, vol.88
, pp. 1960-1964
-
-
Ferster, A.1
Vermylen, C.2
Cornu, G.3
-
9
-
-
9344231922
-
Bone marrow transplantation for sickle cell disease
-
Walters M, Patience M, Leisenring W, et al. Bone marrow transplantation for sickle cell disease. N Engl J Med 1996;335:369-76.
-
(1996)
N Engl J Med
, vol.335
, pp. 369-376
-
-
Walters, M.1
Patience, M.2
Leisenring, W.3
-
10
-
-
0030815760
-
Umbilical cord blood stem cells: Application for the treatment of patients with hemoglobinopathies
-
Kelly P, Kurtzberg J, Vichinsky E, Lubin B. Umbilical cord blood stem cells: application for the treatment of patients with hemoglobinopathies. J Pediatr 1997;130:695-703.
-
(1997)
J Pediatr
, vol.130
, pp. 695-703
-
-
Kelly, P.1
Kurtzberg, J.2
Vichinsky, E.3
Lubin, B.4
-
11
-
-
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
-
12
-
-
0032474690
-
Sickle cell disease - New treatments, new questions
-
Cohen A. Sickle cell disease - new treatments, new questions (editorial). N Engl J Med 1998;339:42-4.
-
(1998)
N Engl J Med
, vol.339
, pp. 42-44
-
-
Cohen, A.1
-
13
-
-
0031007362
-
Chronic transfusion programmes in sickle cell disease: Problem or panacea?
-
Serjeant G. Chronic transfusion programmes in sickle cell disease: problem or panacea? Br J Haematol 1997;97:253-5.
-
(1997)
Br J Haematol
, vol.97
, Issue.25
, pp. 3-5
-
-
Serjeant, G.1
-
14
-
-
0028143269
-
Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples
-
Isola J, DeVries S, Chu L, et al. Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples. Am J Pathol 1994;145:1301-8.
-
(1994)
Am J Pathol
, vol.145
, pp. 1301-1308
-
-
Isola, J.1
DeVries, S.2
Chu, L.3
-
15
-
-
0019595547
-
Combined sickle cell disease and autoimmune hemolytic anemia
-
Chaplin H Jr, Zarkowsky HS. Combined sickle cell disease and autoimmune hemolytic anemia. Arch Intern Med 1981;141:1091-3.
-
(1981)
Arch Intern Med
, vol.141
, pp. 1091-1093
-
-
Chaplin H., Jr.1
Zarkowsky, H.S.2
-
16
-
-
0001827318
-
Severe autoimmune hemolytic anemia induced by transfusion in two alloimmunized patients with sickle cell disease
-
Sosler SD, Perkins JT, Saporito C, et al. Severe autoimmune hemolytic anemia induced by transfusion in two alloimmunized patients with sickle cell disease (abstract). Transfusion 1989;29(Suppl):49S.
-
(1989)
Transfusion
, vol.29
, Issue.SUPPL.
-
-
Sosler, S.D.1
Perkins, J.T.2
Saporito, C.3
-
17
-
-
0032950197
-
Erythrocyte autoantibodies in pediatric patients with sickle cell disease receiving transfusion therapy: Frequency, characteristics, and significance
-
Castellino SM, Combs MR, Zimmerman MA, et al. Erythrocyte autoantibodies in pediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics, and significance. Br J Haematol 1999;104:189-94.
-
(1999)
Br J Haematol
, vol.104
, pp. 189-194
-
-
Castellino, S.M.1
Combs, M.R.2
Zimmerman, M.A.3
-
18
-
-
0030950506
-
The sickle cell hemolytic transfusion reaction syndrome
-
Petz LD, Calhoun L, Shulman IA, et al. 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
-
19
-
-
0018941865
-
Delayed hemolytic transfusion reaction presenting as sickle-cell crisis
-
Diamond WJ, Brown FL Jr, Bitterman P, et al. Delayed hemolytic transfusion reaction presenting as sickle-cell crisis. Ann Intern Med 1980;93:231-4.
-
(1980)
Ann Intern Med
, vol.93
, pp. 231-234
-
-
Diamond, W.J.1
Brown F.L., Jr.2
Bitterman, P.3
-
20
-
-
0030948542
-
Delayed hemolytic reactions in sickle cell disease: Simultaneous destruction of recipient's red cells
-
King K, Shirey R, Lankiewicz M, et al. Delayed hemolytic reactions in sickle cell disease: simultaneous destruction of recipient's red cells. Transfusion 1997;37:376-81.
-
(1997)
Transfusion
, vol.37
, pp. 376-381
-
-
King, K.1
Shirey, R.2
Lankiewicz, M.3
-
21
-
-
0023093035
-
Variability of the erythropoietic response in autoimmune hemolytic anemia: Analysis of 109 cases
-
Liesveld JL, Rowe JM, Lichtman MA. Variability of the erythropoietic response in autoimmune hemolytic anemia: analysis of 109 cases. Blood 1987;69:820-6.
-
(1987)
Blood
, vol.69
, pp. 820-826
-
-
Liesveld, J.L.1
Rowe, J.M.2
Lichtman, M.A.3
-
22
-
-
0020074626
-
Autoimmune hemolytic anemia with reticulocytopenia and erythroid marrow
-
Conley CL, Lippman SM, Ness PM, et al. Autoimmune hemolytic anemia with reticulocytopenia and erythroid marrow. N Engl J Med 1982;306:281-6.
-
(1982)
N Engl J Med
, vol.306
, pp. 281-286
-
-
Conley, C.L.1
Lippman, S.M.2
Ness, P.M.3
-
24
-
-
0026795418
-
Evidence that the antigens of the Yt blood group system are located on human erythrocyte acetylcholinesterase
-
Spring F, Gardner B, Anstee D. Evidence that the antigens of the Yt blood group system are located on human erythrocyte acetylcholinesterase. Blood 1992;80:2136-41.
-
(1992)
Blood
, vol.80
, pp. 2136-2141
-
-
Spring, F.1
Gardner, B.2
Anstee, D.3
-
27
-
-
0027517150
-
Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for the Yt blood group polymorphism
-
Bartels C, Zelinski T, Lockridge O. Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for the Yt blood group polymorphism. Am J Hum Genet 1993;52:928-36.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 928-936
-
-
Bartels, C.1
Zelinski, T.2
Lockridge, O.3
-
29
-
-
0028040030
-
Defective regulation of complement by the sickle erythrocyte: Evidence for a defect in control of membrane attack complex formation
-
Test ST, Woolworth VS. Defective regulation of complement by the sickle erythrocyte: evidence for a defect in control of membrane attack complex formation. Blood 1994;83:842-52.
-
(1994)
Blood
, vol.83
, pp. 842-852
-
-
Test, S.T.1
Woolworth, V.S.2
-
30
-
-
0030893806
-
Severe reactions associated with transfusion in patients with sickle cell disease
-
Garratty G. Severe reactions associated with transfusion in patients with sickle cell disease. Transfusion 1997;37:357-61.
-
(1997)
Transfusion
, vol.37
, pp. 357-361
-
-
Garratty, G.1
-
31
-
-
0021930572
-
Acute splenic sequestration in homozygous sickle cell disease: Natural history and management
-
Emond A, Collins R, Darvill D. Acute splenic sequestration in homozygous sickle cell disease: natural history and management. J Pediatr 1985;107:201-6.
-
(1985)
J Pediatr
, vol.107
, pp. 201-206
-
-
Emond, A.1
Collins, R.2
Darvill, D.3
-
32
-
-
0017760208
-
Benign course of extreme hyperbilirubinemia in sickle cell anemia: Analysis of six cases
-
Buchanan G, Glader B. Benign course of extreme hyperbilirubinemia in sickle cell anemia: analysis of six cases. J Pediatr 1977;91:21-4.
-
(1977)
J Pediatr
, vol.91
, pp. 21-24
-
-
Buchanan, G.1
Glader, B.2
-
33
-
-
0031035337
-
Acute chest syndrome in sickle cell disease: Clinical presentation and course
-
Vichinsky EP, Styles LA, Colangelo LH, et al. Acute chest syndrome in sickle cell disease: clinical presentation and course. Blood 1997;89:1787-92.
-
(1997)
Blood
, vol.89
, pp. 1787-1792
-
-
Vichinsky, E.P.1
Styles, L.A.2
Colangelo, L.H.3
-
34
-
-
0031048148
-
Parvovirus B19 in human disease
-
Brown K, Young N. Parvovirus B19 in human disease. Annu Rev Med 1997;48:59-67.
-
(1997)
Annu Rev Med
, vol.48
, pp. 59-67
-
-
Brown, K.1
Young, N.2
-
35
-
-
0027050207
-
Clostridial sepsis with massive intravascular hemolysis: Rapid diagnosis and successful treatment
-
Batge B, Filejski W, Kurowski V, et al. Clostridial sepsis with massive intravascular hemolysis: rapid diagnosis and successful treatment. Intensive Care Med 1992;18:488-90.
-
(1992)
Intensive Care Med
, vol.18
, pp. 488-490
-
-
Batge, B.1
Filejski, W.2
Kurowski, V.3
-
36
-
-
0028898660
-
Functional asplenia in hemoglobin SC disease
-
Lane P, O'Connell J, Lear J, et al. Functional asplenia in hemoglobin SC disease. Blood 1995;85:2238-44.
-
(1995)
Blood
, vol.85
, pp. 2238-2244
-
-
Lane, P.1
O'Connell, J.2
Lear, J.3
-
37
-
-
0029034749
-
Fatal hemolysis induced by ceftriaxone in a child with sickle cell disease
-
Bernini J, Mustafa M, Sutor L, Buchanan G. Fatal hemolysis induced by ceftriaxone in a child with sickle cell disease. J Pediatr 1995;126:813-5.
-
(1995)
J Pediatr
, vol.126
, pp. 813-815
-
-
Bernini, J.1
Mustafa, M.2
Sutor, L.3
Buchanan, G.4
-
38
-
-
0025924845
-
A fatal case of ceftriaxone-induced hemolytic anemia associated with intravascular immune hemolysis
-
Garratty G, Postaway N, Schwellenbach J, McMahill P. A fatal case of ceftriaxone-induced hemolytic anemia associated with intravascular immune hemolysis. Transfusion 1991;31:176-9.
-
(1991)
Transfusion
, vol.31
, pp. 176-179
-
-
Garratty, G.1
Postaway, N.2
Schwellenbach, J.3
McMahill, P.4
-
39
-
-
0031965089
-
Cerebrovascular accidents in sickle cell disease: Rates and risk factors
-
Ohene-Frempong K, Weiner S, Sleeper L, 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.2
Sleeper, L.3
|