-
1
-
-
0344153222
-
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. Ann Intern Med. 1972;76:643-652
-
(1972)
Ann Intern Med
, vol.76
, pp. 643-652
-
-
Powars, D.1
Wilson, B.2
Imbus, C.3
Pegelow, C.4
Allen, J.5
-
2
-
-
0031965089
-
Cerebrovascular accidents in sickle cell disease: Rates and risk factors
-
Ohene-Frempong K, Weiner SJ, Sleeper LA, Miller ST, Embury S, Moohr JW, Wethers DL, Pegelow CH, Gill FM, and the Cooperative Study of Sickle Cell Disease. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. 1998;1:288-294
-
(1998)
Blood
, vol.1
, 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
Wethers, D.L.7
Pegelow, C.H.8
Gill, F.M.9
-
3
-
-
9344223367
-
The spectrum of central nervous system abnormalities in sickle cell disease as defined by magnetic resonance imaging: A report from the Cooperative Study of Sickle Cell Disease
-
Moser FG, Miller ST, Bello JA, et al. The spectrum of central nervous system abnormalities in sickle cell disease as defined by magnetic resonance imaging: a report from the Cooperative Study of Sickle Cell Disease. AJNR. 1996;17:965-972
-
(1996)
AJNR
, vol.17
, pp. 965-972
-
-
Moser, F.G.1
Miller, S.T.2
Bello, J.A.3
-
4
-
-
15844366370
-
Cognitive functioning and brain magnetic resonance imaging in children with sickle cell disease
-
Armstrong FD, Thompson RJ, Wang W, Zimmerman R, Pegelow CH, Miller S, Moser F, Bello J, Hurtig A, Vass K, for the Neuropsychology Committee of the Cooperative Study of Sickle Cell Disease. Cognitive functioning and brain magnetic resonance imaging in children with sickle cell disease. Pediatrics. 1996;97:864-870
-
(1996)
Pediatrics
, vol.97
, pp. 864-870
-
-
Armstrong, F.D.1
Thompson, R.J.2
Wang, W.3
Zimmerman, R.4
Pegelow, C.H.5
Miller, S.6
Moser, F.7
Bello, J.8
Hurtig, A.9
Vass, K.10
-
5
-
-
0020323557
-
The Cooperative Study of Sickle Cell Disease: Review of design and objectives
-
Gaston M, Rosse WF. The Cooperative Study of Sickle Cell Disease: review of design and objectives. Am J Pediatr Hematol Oncol. 1982;4: 197-201
-
(1982)
Am J Pediatr Hematol Oncol
, vol.4
, pp. 197-201
-
-
Gaston, M.1
Rosse, W.F.2
-
6
-
-
0023478475
-
Recruitment in the Cooperative Study of Sickle Cell Disease
-
Gaston M, Smith J, Gallagher D, et al. Recruitment in the Cooperative Study of Sickle Cell Disease. Control Clin Trials. 1987;8(suppl):131S-140S
-
(1987)
Control Clin Trials
, vol.8
, Issue.SUPPL.
-
-
Gaston, M.1
Smith, J.2
Gallagher, D.3
-
7
-
-
0021875567
-
Cooperative Study of Sickle Cell Disease: Demographics and socioeconomic characteristics of patients and families with sickle cell disease
-
Farber M, Koshy M, Kinney TR, and the Cooperative Study of Sickle Cell Disease. Cooperative Study of Sickle Cell Disease: demographics and socioeconomic characteristics of patients and families with sickle cell disease. J Chron Dis. 1985;38:495-505
-
(1985)
J Chron Dis
, vol.38
, pp. 495-505
-
-
Farber, M.1
Koshy, M.2
Kinney, T.R.3
-
8
-
-
36949068851
-
Estimation of small percentages of foetal haemoglobin
-
Betke K, Marti HR, Schlicht I. Estimation of small percentages of foetal haemoglobin. Nature. 1959;184:1877-1878
-
(1959)
Nature
, vol.184
, pp. 1877-1878
-
-
Betke, K.1
Marti, H.R.2
Schlicht, I.3
-
9
-
-
0018581641
-
α-Globin gene organization in blacks precludes the severe form of α-thalassemia
-
Dozy AM, Kan YW, Embury SH, et al. α-Globin gene organization in blacks precludes the severe form of α-thalassemia. Nature. 1979;280: 605-607
-
(1979)
Nature
, vol.280
, pp. 605-607
-
-
Dozy, A.M.1
Kan, Y.W.2
Embury, S.H.3
-
10
-
-
0019219843
-
Two different molecular organizations account for the single α-globin gene in the α-thalassemia-2 genotype
-
Embury SH Miller JA, Dozy Am, et al. Two different molecular organizations account for the single α-globin gene in the α-thalassemia-2 genotype. J Clin Invest. 1980;66:1319-1325
-
(1980)
J Clin Invest
, vol.66
, pp. 1319-1325
-
-
Embury, S.H.1
Miller, J.A.2
Dozy, A.3
-
11
-
-
0021946139
-
DNA polymorphism and molecular pathology of the human globin gene clusters
-
Antonarakis SE, Kazarian HH Jr, Orkin SH. DNA polymorphism and molecular pathology of the human globin gene clusters. Hum Genet. 1985;69:1-14
-
(1985)
Hum Genet
, vol.69
, pp. 1-14
-
-
Antonarakis, S.E.1
Kazarian H.H., Jr.2
Orkin, S.H.3
-
12
-
-
0021933164
-
Developmental pattern of splenic dysfunction in sickle cell disorders
-
Pearson HA, Gallagher D, Chilcote R, Sullivan E, Wilmas J, Espeland M, Ritchey AK, and the Cooperative Study of Sickle Cell Disease. Developmental pattern of splenic dysfunction in sickle cell disorders. Pediatrics. 1985;76:392-397
-
(1985)
Pediatrics
, vol.76
, pp. 392-397
-
-
Pearson, H.A.1
Gallagher, D.2
Chilcote, R.3
Sullivan, E.4
Wilmas, J.5
Espeland, M.6
Ritchey, A.K.7
-
14
-
-
0028291736
-
Mortality in sickle cell disease: Life expectancy and risk factors for early death
-
Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP. Mortality in sickle cell disease: life expectancy and risk factors for early death. N Engl J Med. 1994;30:1639-1644
-
(1994)
N Engl J Med
, vol.30
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
Milner, P.F.4
Castro, O.5
Steinberg, M.H.6
Klug, P.P.7
-
15
-
-
0024446352
-
Mortality in children and adolescents with sickle cell disease
-
Leiken SL, Gallagher D, Kinney TR. et al. Mortality in children and adolescents with sickle cell disease. Pediatrics. 1989;84:500-508
-
(1989)
Pediatrics
, vol.84
, pp. 500-508
-
-
Leiken, S.L.1
Gallagher, D.2
Kinney, T.R.3
-
16
-
-
0024500054
-
Neuropsychological test findings in subjects with leukoaraiosis
-
Rao SM, Mittenberg W, Bernardin L, Haughton V, Leo GJ. Neuropsychological test findings in subjects with leukoaraiosis. Arch Neurol 1989;46:40-44
-
(1989)
Arch Neurol
, vol.46
, pp. 40-44
-
-
Rao, S.M.1
Mittenberg, W.2
Bernardin, L.3
Haughton, V.4
Leo, G.J.5
-
17
-
-
0021343093
-
Is there a threshold of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?
-
Powars DR, Weiss JN, Chan LS, et al. Is there a threshold of fetal hemoglobin that ameliorates morbidity in sickle cell anemia? Blood. 1984;63:921-926
-
(1984)
Blood
, vol.63
, pp. 921-926
-
-
Powars, D.R.1
Weiss, J.N.2
Chan, L.S.3
-
18
-
-
0025109527
-
The variable expression of sickle cell disease is genetically determined
-
Powars DR, Chan LS, Schroeder WA. The variable expression of sickle cell disease is genetically determined. Semin Hematol. 1990;27:360-376
-
(1990)
Semin Hematol
, vol.27
, pp. 360-376
-
-
Powars, D.R.1
Chan, L.S.2
Schroeder, W.A.3
-
19
-
-
0344153218
-
Abnormalities of the central nervous system in very young children with sickle cell anemia: MRI, MRA, and neuropsychometric testing
-
September 15-20, Washington, DC
-
Wang W, Langston J, Steen G, et al. Abnormalities of the central nervous system in very young children with sickle cell anemia: MRI, MRA, and neuropsychometric testing. Presented at the 22th Annual Meeting of the National Sickle Cell Disease Program, September 15-20, 1997, Washington, DC
-
(1997)
22th Annual Meeting of the National Sickle Cell Disease Program
-
-
Wang, W.1
Langston, J.2
Steen, G.3
-
20
-
-
0015525420
-
Occlusion of large cerebral vessels in sickle cell anemia
-
Stockman JA, Nigro MA, Mishkin MM, et al. Occlusion of large cerebral vessels in sickle cell anemia. N Engl J Med. 1972;287:846-849
-
(1972)
N Engl J Med
, vol.287
, pp. 846-849
-
-
Stockman, J.A.1
Nigro, M.A.2
Mishkin, M.M.3
-
21
-
-
0026558470
-
The use of transcranial ultrasonography to predict stroke in sickle cell disease
-
Adams R, McKie V, Nichols F, et al. The use of transcranial ultrasonography to predict stroke in sickle cell disease. N Engl J Med. 1992;326: 605-610
-
(1992)
N Engl J Med
, vol.326
, pp. 605-610
-
-
Adams, R.1
McKie, V.2
Nichols, F.3
-
22
-
-
0032474692
-
Prevention of first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial doppler ultrasonography
-
Adams RJ, McKie V, Hsu L, et al. Prevention of 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.2
Hsu, L.3
-
23
-
-
0029005136
-
Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions
-
Pegelow CH, Adams RJ, McKie V, et al. Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions. J Pediatr. 1995;126:896-899
-
(1995)
J Pediatr
, vol.126
, pp. 896-899
-
-
Pegelow, C.H.1
Adams, R.J.2
McKie, V.3
-
24
-
-
9344231922
-
Bone marrow transplantation for sickle cell disease
-
Walters MC, Patience M, Leisenring W, Eckman JR, Scott JP, Mentzer WC, Davies SC, Ohene-Frempong K, Bernaudin F, Matthews DC, Storb R, Sullivan K. Bone marrow transplantation for sickle cell disease. N Engl I Med. 1996;335:369-376
-
(1996)
N Engl I Med
, vol.335
, pp. 369-376
-
-
Walters, M.C.1
Patience, M.2
Leisenring, W.3
Eckman, J.R.4
Scott, J.P.5
Mentzer, W.C.6
Davies, S.C.7
Ohene-Frempong, K.8
Bernaudin, F.9
Matthews, D.C.10
Storb, R.11
Sullivan, K.12
-
25
-
-
0026631318
-
Hydroxyurea: Effect on hemoglobin F production in patients with sickle cell anemia
-
Charache S, Dover GJ, Moore RD, et al. Hydroxyurea: effect on hemoglobin F production in patients with sickle cell anemia. Blood. 1992;79: 2556-2565
-
(1992)
Blood
, vol.79
, pp. 2556-2565
-
-
Charache, S.1
Dover, G.J.2
Moore, R.D.3
-
26
-
-
0029129942
-
Hydroxyurea. An alternative to transfusion therapy for stroke in sickle cell anemia
-
Ware RE, Steinberg MH, Kinney TR. Hydroxyurea. An alternative to transfusion therapy for stroke in sickle cell anemia. Am J Hematol. 1995;50:140-143
-
(1995)
Am J Hematol
, vol.50
, pp. 140-143
-
-
Ware, R.E.1
Steinberg, M.H.2
Kinney, T.R.3
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