-
1
-
-
0032416228
-
Sickle cell disease: Clinical management
-
Ballas SK. Sickle cell disease: clinical management. Baillieres Clin Haematol. 1998;11(1):185-214.
-
(1998)
Baillieres Clin Haematol
, vol.11
, Issue.1
, pp. 185-214
-
-
Ballas, S.K.1
-
3
-
-
60749094795
-
Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion
-
Conran N, Franco-Penteado CF, Costa FF. Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion. Hemoglobin. 2009;33(1):1-16.
-
(2009)
Hemoglobin
, vol.33
, Issue.1
, pp. 1-16
-
-
Conran, N.1
Franco-Penteado, C.F.2
Costa, F.F.3
-
4
-
-
0028340716
-
The painful crisis of homozygous sickle cell disease: Clinical features
-
Serjeant GR, Ceulaer CD, Lethbridge R, Morris J, Singhal A, Thomas PW. The painful crisis of homozygous sickle cell disease: clinical features. Br J Haematol. 1994; 87(3):586-591.
-
(1994)
Br J Haematol
, vol.87
, Issue.3
, pp. 586-591
-
-
Serjeant, G.R.1
Ceulaer, C.D.2
Lethbridge, R.3
Morris, J.4
Singhal, A.5
Thomas, P.W.6
-
5
-
-
0025973855
-
Is the painful crisis of sickle-cell disease due to sickling?
-
Bailey S, Higgs DR, Morris J, Serjeant GR. Is the painful crisis of sickle-cell disease due to sickling? Lancet. 1991;337(8743):735.
-
(1991)
Lancet
, vol.337
, Issue.8743
, pp. 735
-
-
Bailey, S.1
Higgs, D.R.2
Morris, J.3
Serjeant, G.R.4
-
6
-
-
0025770390
-
Pain in sickle cell disease. Rates and risk factors
-
Platt OS, Thorington BD, Brambilla DJ, Milner PF, Rosse WF, Vichinsky E, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med. 1991;325(1):11-16.
-
(1991)
N Engl J Med
, vol.325
, Issue.1
, pp. 11-16
-
-
Platt, O.S.1
Thorington, B.D.2
Brambilla, D.J.3
Milner, P.F.4
Rosse, W.F.5
Vichinsky, E.6
-
7
-
-
0030464953
-
Hydroxyurea and sickle cell anemia. Clinical utility of a myelosuppressive switching agent. The Multicenter Study of Hydroxyurea in Sickle Cell Anemia
-
(Baltimore)
-
Charache S, Barton FB, Moore RD, Terrin ML, Steinberg MH, Dover GJ, et al. Hydroxyurea and sickle cell anemia. Clinical utility of a myelosuppressive switching agent. The Multicenter Study of Hydroxyurea in Sickle Cell Anemia. Medicine (Baltimore). 1996;75(6):300-326.
-
(1996)
Medicine
, vol.75
, Issue.6
, pp. 300-326
-
-
Charache, S.1
Barton, F.B.2
Moore, R.D.3
Terrin, M.L.4
Steinberg, M.H.5
Dover, G.J.6
-
8
-
-
18044397307
-
Hospital readmission for adult acute sickle cell painful episodes: Frequency, etiology, and prognostic significance
-
Ballas SK, Lusardi M. Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significance. Am J Hematol. 2005;79(1):17-25.
-
(2005)
Am J Hematol
, vol.79
, Issue.1
, pp. 17-25
-
-
Ballas, S.K.1
Lusardi, M.2
-
10
-
-
0026463664
-
Subclinical ischaemic episodes during the steady state of sickle cell anaemia
-
Akinola NO, Stevens SM, Franklin IM, Nash GB, Stuart J. Subclinical ischaemic episodes during the steady state of sickle cell anaemia. J Clin Pathol. 1992;45(10): 902-906.
-
(1992)
J Clin Pathol
, vol.45
, Issue.10
, pp. 902-906
-
-
Akinola, N.O.1
Stevens, S.M.2
Franklin, I.M.3
Nash, G.B.4
Stuart, J.5
-
11
-
-
0028347684
-
Monitoring the acute phase response to vaso-occlusive crisis in sickle cell disease
-
Stuart J, Stone PC, Akinola NO, Gallimore JR, Pepys MB. Monitoring the acute phase response to vaso-occlusive crisis in sickle cell disease. J Clin Pathol. 1994;47(2):166-169.
-
(1994)
J Clin Pathol
, vol.47
, Issue.2
, pp. 166-169
-
-
Stuart, J.1
Stone, P.C.2
Akinola, N.O.3
Gallimore, J.R.4
Pepys, M.B.5
-
12
-
-
0026687777
-
Rheological changes in the prodromal and established phases of sickle cell vaso-occlusive crisis
-
Akinola NO, Stevens SM, Franklin IM, Nash GB, Stuart J. Rheological changes in the prodromal and established phases of sickle cell vaso-occlusive crisis. Br J Haematol. 1992;81(4):598-602.
-
(1992)
Br J Haematol
, vol.81
, Issue.4
, pp. 598-602
-
-
Akinola, N.O.1
Stevens, S.M.2
Franklin, I.M.3
Nash, G.B.4
Stuart, J.5
-
13
-
-
0027483349
-
Is there an acute-phase response in steady-state sickle cell disease?
-
Singhal A, Doherty JF, Raynes JG, McAdam KP, Thomas PW, Serjeant BE, et al. Is there an acute-phase response in steady-state sickle cell disease? Lancet. 1993;341(8846): 651-653.
-
(1993)
Lancet
, vol.341
, Issue.8846
, pp. 651-653
-
-
Singhal, A.1
Doherty, J.F.2
Raynes, J.G.3
McAdam, K.P.4
Thomas, P.W.5
Serjeant, B.E.6
-
14
-
-
0026660955
-
Modified (mixed) erythrocyte sedimentation rate in sickle cell anemia
-
Sabio H, McKie VC. Modified (mixed) erythrocyte sedimentation rate in sickle cell anemia. Clinical hemorheology 1992;587: 587-592.
-
(1992)
Clinical Hemorheology
, vol.587
, pp. 587-592
-
-
Sabio, H.1
McKie, V.C.2
-
15
-
-
84920245672
-
Acute-phase response and sickle crisis
-
Stuart J. Acute-phase response and sickle crisis. Lancet. 1993;341(8846):664.
-
(1993)
Lancet
, vol.341
, Issue.8846
, pp. 664
-
-
Stuart, J.1
-
17
-
-
60849135703
-
Proteomic identification of altered apolipoprotein patterns in pulmonary hypertension and vasculopathy of sickle cell disease
-
Yuditskaya S, Tumblin A, Hoehn GT, Wang G, Drake SK, Xu X, et al. Proteomic identification of altered apolipoprotein patterns in pulmonary hypertension and vasculopathy of sickle cell disease. Blood. 2009;113(5):1122-1128.
-
(2009)
Blood
, vol.113
, Issue.5
, pp. 1122-1128
-
-
Yuditskaya, S.1
Tumblin, A.2
Hoehn, G.T.3
Wang, G.4
Drake, S.K.5
Xu, X.6
-
18
-
-
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. The American journal of medicine. 1994;96(2):155-162.
-
(1994)
The American Journal of Medicine
, vol.96
, Issue.2
, pp. 155-162
-
-
Hassell, K.L.1
Eckman, J.R.2
Lane, P.A.3
-
19
-
-
33644764856
-
Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia
-
Ballas SK, Marcolina MJ. Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia. Transfusion. 2006;46(1):105-110.
-
(2006)
Transfusion
, vol.46
, Issue.1
, pp. 105-110
-
-
Ballas, S.K.1
Marcolina, M.J.2
-
20
-
-
0014558319
-
Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease
-
Neely CL, Wajima T, Kraus AP, Diggs LW, Barreras L. Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease. Am J Clin Pathol. 1969;52(2):167-169.
-
(1969)
Am J Clin Pathol
, vol.52
, Issue.2
, pp. 167-169
-
-
Neely, C.L.1
Wajima, T.2
Kraus, A.P.3
Diggs, L.W.4
Barreras, L.5
-
21
-
-
0024390927
-
Creatine kinase activity in sickle cell disease
-
Hunt BJ, Korsah P, Eaton S, Brozovic M. Creatine kinase activity in sickle cell disease. J Clin Pathol. 1989;42(7):712-715.
-
(1989)
J Clin Pathol
, vol.42
, Issue.7
, pp. 712-715
-
-
Hunt, B.J.1
Korsah, P.2
Eaton, S.3
Brozovic, M.4
-
22
-
-
38749109710
-
Daily assessment of pain in adults with sickle cell disease
-
Smith WR, Penberthy LT, Bovbjerg VE, McClish DK, Roberts JD, Dahman B, et al. Daily assessment of pain in adults with sickle cell disease. Ann Intern Med. 2008;148(2):94-101.
-
(2008)
Ann Intern Med
, vol.148
, Issue.2
, pp. 94-101
-
-
Smith, W.R.1
Penberthy, L.T.2
Bovbjerg, V.E.3
McClish, D.K.4
Roberts, J.D.5
Dahman, B.6
-
23
-
-
0026463664
-
Subclinical ischaemicepisodes during the steady state of sickle cell anaemia
-
Akinola NO, Stevens SM, Franklin IM, Nash GB, Stuart J. Subclinical ischaemicepisodes during the steady state of sickle cell anaemia. J Clin Pathol. 1992;45(10): 902-906.
-
(1992)
J Clin Pathol
, vol.45
, Issue.10
, pp. 902-906
-
-
Akinola, N.O.1
Stevens, S.M.2
Franklin, I.M.3
Nash, G.B.4
Stuart, J.5
-
24
-
-
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, Terrin ML, Moore RD, Dover GJ, Barton FB, Eckert SV, et al. 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; 332(20):1317-1322.
-
(1995)
N Engl J Med
, vol.332
, Issue.20
, pp. 1317-1322
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
Dover, G.J.4
Barton, F.B.5
Eckert, S.V.6
-
25
-
-
0042604626
-
Serum paraoxonase: Effect of the apolipoprotein composition of HDL and the acute phase response
-
Cabana VG, Reardon CA, Feng N, Neath S, Lukens J, Getz GS. Serum paraoxonase: effect of the apolipoprotein composition of HDL and the acute phase response. J Lipid Res. 2003;44(4):780-792.
-
(2003)
J Lipid Res
, vol.44
, Issue.4
, pp. 780-792
-
-
Cabana, V.G.1
Reardon, C.A.2
Feng, N.3
Neath, S.4
Lukens, J.5
Getz, G.S.6
-
26
-
-
0020971452
-
Acute phase proteins with special reference to C-reactive protein and related proteins (pentaxins) and serum amyloid A protein
-
Pepys MB, Baltz ML. Acute phase proteins with special reference to C-reactive protein and related proteins (pentaxins) and serum amyloid A protein. Adv Immunol. 1983;34:141-212.
-
(1983)
Adv Immunol
, vol.34
, pp. 141-212
-
-
Pepys, M.B.1
Baltz, M.L.2
-
27
-
-
0034100717
-
Role of serum amyloid A during metabolism of acute-phase HDL by macrophages
-
Artl A, Marsche G, Lestavel S, Sattler W, Malle E. Role of serum amyloid A during metabolism of acute-phase HDL by macrophages. Arterioscler Thromb Vasc Biol. 2000;20(3):763-772.
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, Issue.3
, pp. 763-772
-
-
Artl, A.1
Marsche, G.2
Lestavel, S.3
Sattler, W.4
Malle, E.5
-
28
-
-
0028810664
-
Paradoxical increase of painful crises in sickle cell patients with alpha-thalassemia
-
Billett HH, Nagel RL, Fabry ME. Paradoxical increase of painful crises in sickle cell patients with alpha-thalassemia. Blood. 1995;86(11):4382.
-
(1995)
Blood
, vol.86
, Issue.11
, pp. 4382
-
-
Billett, H.H.1
Nagel, R.L.2
Fabry, M.E.3
-
29
-
-
0029017748
-
Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease
-
Gill FM, Sleeper LA, Weiner SJ, Brown AK, Bellevue R, Grover R, et al. Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease. Blood. 1995;86(2): 776-783.
-
(1995)
Blood
, vol.86
, Issue.2
, pp. 776-783
-
-
Gill, F.M.1
Sleeper, L.A.2
Weiner, S.J.3
Brown, A.K.4
Bellevue, R.5
Grover, R.6
-
30
-
-
0033062562
-
SAA-only HDL formed during the acute phase response in apoA-I+/+ andapoA-I-/- mice
-
Cabana VG, Reardon CA, Wei B, Lukens JR, Getz GS. SAA-only HDL formed during the acute phase response in apoA-I+/+ andapoA-I-/- mice. J Lipid Res. 1999;40(6): 1090-1103.
-
(1999)
J Lipid Res
, vol.40
, Issue.6
, pp. 1090-1103
-
-
Cabana, V.G.1
Reardon, C.A.2
Wei, B.3
Lukens, J.R.4
Getz, G.S.5
-
31
-
-
0032933232
-
Expression of serum amyloid A protein in the absence of the acute phase response does not reduce HDL cholesterol or apoA-I levels in human apoA-I transgenic mice
-
Hosoai H, Webb NR, Glick JM, Tietge UJ, Purdom MS, de Beer FC, et al. Expression of serum amyloid A protein in the absence of the acute phase response does not reduce HDL cholesterol or apoA-I levels in human apoA-I transgenic mice. J Lipid Res. 1999;40(4):648-653.
-
(1999)
J Lipid Res
, vol.40
, Issue.4
, pp. 648-653
-
-
Hosoai, H.1
Webb, N.R.2
Glick, J.M.3
Tietge, U.J.4
Purdom, M.S.5
de Beer, F.C.6
-
32
-
-
0022595156
-
Decreased apolipoprotein A-I and B content in plasma of individuals with sickle cell anemia
-
Pt 1
-
Sasaki J, Waterman MR, Cottam GL. Decreased apolipoprotein A-I and B content in plasma of individuals with sickle cell anemia. Clin Chem. 1986;32(1 Pt 1):226-227.
-
(1986)
Clin Chem
, vol.32
, Issue.1
, pp. 226-227
-
-
Sasaki, J.1
Waterman, M.R.2
Cottam, G.L.3
-
33
-
-
0023694748
-
Painful crises in sickle cell diseasepatients' perspectives
-
Murray N, May A. Painful crises in sickle cell diseasepatients' perspectives. Bmj. 1988;297(6646):452-454.
-
(1988)
Bmj
, vol.297
, Issue.6646
, pp. 452-454
-
-
Murray, N.1
May, A.2
-
34
-
-
0022966771
-
Transcriptional regulation of serum amyloid A gene expression
-
Lowell CA, Stearman RS, Morrow JF. Transcriptional regulation of serum amyloid A gene expression. J Biol Chem. 1986;261(18):8453-8461.
-
(1986)
J Biol Chem
, vol.261
, Issue.18
, pp. 8453-8461
-
-
Lowell, C.A.1
Stearman, R.S.2
Morrow, J.F.3
-
35
-
-
0033911818
-
Comparative analysis of lipid composition of normal and acute-phase high density lipoproteins
-
Pruzanski W, Stefanski E, de Beer FC, de Beer MC, Ravandi A, Kuksis A. Comparative analysis of lipid composition of normal and acute-phase high density lipoproteins. J Lipid Res. 2000;41(7):1035-1047.
-
(2000)
J Lipid Res
, vol.41
, Issue.7
, pp. 1035-1047
-
-
Pruzanski, W.1
Stefanski, E.2
de Beer, F.C.3
de Beer, M.C.4
Ravandi, A.5
Kuksis, A.6
-
36
-
-
33845910404
-
Severity of pulmonary hypertension during vasoocclusive pain crisis and exercise in patients with sickle cell disease
-
Machado RF, Mack AK, Martyr S, Barnett C, Macarthur P, Sachdev V, et al. Severity of pulmonary hypertension during vasoocclusive pain crisis and exercise in patients with sickle cell disease. Br J Haematol. 2007;136(2):319-325.
-
(2007)
Br J Haematol
, vol.136
, Issue.2
, pp. 319-325
-
-
Machado, R.F.1
Mack, A.K.2
Martyr, S.3
Barnett, C.4
Macarthur, P.5
Sachdev, V.6
-
37
-
-
0037986617
-
L-4F, an apolipoprotein A-1 mimetic, dramatically improves vasodilation in hypercholesterolemia and sickle cell disease
-
Ou J, Ou Z, Jones DW, Holzhauer S, Hatoum OA, Ackerman AW, et al. L-4F, an apolipoprotein A-1 mimetic, dramatically improves vasodilation in hypercholesterolemia and sickle cell disease. Circulation. 2003;107(18):2337-2341.
-
(2003)
Circulation
, vol.107
, Issue.18
, pp. 2337-2341
-
-
Ou, J.1
Ou, Z.2
Jones, D.W.3
Holzhauer, S.4
Hatoum, O.A.5
Ackerman, A.W.6
|