-
1
-
-
67749121655
-
Sickle cell disease population estimation: Application of available contemporary data to traditional methods
-
Washington, DC
-
Hassell K. Sickle cell disease population estimation: application of available contemporary data to traditional methods. In: 35th Anniversary Convention of the National Sickle Cell Disease Program; 2007; Washington, DC.
-
(2007)
35th Anniversary Convention of the National Sickle Cell Disease Program
-
-
Hassell, K.1
-
2
-
-
0018679483
-
Adhesion of normal and sickle erythrocytes to endothelial monolayer cultures
-
Hoover R, Rubin R, Wise G, Warren R. Adhesion of normal and sickle erythrocytes to endothelial monolayer cultures. Blood 1979; 54:872-876.
-
(1979)
Blood
, vol.54
, pp. 872-876
-
-
Hoover, R.1
Rubin, R.2
Wise, G.3
Warren, R.4
-
3
-
-
0018885938
-
Erythrocyte adherence to endothelium in sickle cell anemia: A possible determinant of disease severity
-
Hebbel RP, Boogaerts MA, Eaton JW, et al. Erythrocyte adherence to endothelium in sickle cell anemia: a possible determinant of disease severity. N Engl J Med 1980; 302:992-995.
-
(1980)
N Engl J Med
, vol.302
, pp. 992-995
-
-
Hebbel, R.P.1
Boogaerts, M.A.2
Eaton, J.W.3
-
4
-
-
10244278094
-
Sickle cell vasoocclusion: Heterotypic, multicellular aggregations driven by leukocyte adhesion
-
Frenette PS. Sickle cell vasoocclusion: heterotypic, multicellular aggregations driven by leukocyte adhesion. Microcirculation 2004; 11:167-177.
-
(2004)
Microcirculation
, vol.11
, pp. 167-177
-
-
Frenette, P.S.1
-
5
-
-
0034307274
-
Activated monocytes in sickle cell disease: Potential role in the activation of vascular endothelium and vasoocclusion
-
Belcher JD, Marker PH, Weber JP, et al. Activated monocytes in sickle cell disease: potential role in the activation of vascular endothelium and vasoocclusion. Blood 2000; 96:2451-2459.
-
(2000)
Blood
, vol.96
, pp. 2451-2459
-
-
Belcher, J.D.1
Marker, P.H.2
Weber, J.P.3
-
6
-
-
0025350965
-
Enhancement of sickle erythrocyte adherence to endothelium by autologous platelets
-
Antonucci R, Walker R, Herion J, Orringer E. Enhancement of sickle erythrocyte adherence to endothelium by autologous platelets. Am J Hematol 1990; 34:44-48.
-
(1990)
Am J Hematol
, vol.34
, pp. 44-48
-
-
Antonucci, R.1
Walker, R.2
Herion, J.3
Orringer, E.4
-
7
-
-
0031147997
-
Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia
-
Wun T, Paglieroni T, Tablin F, et al. Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia. J Lab Clin Med 1997; 129:507-516.
-
(1997)
J Lab Clin Med
, vol.129
, pp. 507-516
-
-
Wun, T.1
Paglieroni, T.2
Tablin, F.3
-
8
-
-
3242792093
-
The endothelial biology of sickle cell disease: Inflammation and a chronic vasculopathy
-
Hebbel RP, Osarogiagbon R, Kaul D. The endothelial biology of sickle cell disease: inflammation and a chronic vasculopathy. Microcirculation 2004; 11:129-151.
-
(2004)
Microcirculation
, vol.11
, pp. 129-151
-
-
Hebbel, R.P.1
Osarogiagbon, R.2
Kaul, D.3
-
10
-
-
0016794848
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Role of hybrid tetramer formation in gelation of haemoglobin S
-
Bookchin RM, Nagel RL, Balazs T. Role of hybrid tetramer formation in gelation of haemoglobin S. Nature 1975; 256:667-668.
-
(1975)
Nature
, vol.256
, pp. 667-668
-
-
Bookchin, R.M.1
Nagel, R.L.2
Balazs, T.3
-
11
-
-
65949124657
-
Mechanisms of vasculopathy in sickle cell disease and thalassemia
-
Morris CR. Mechanisms of vasculopathy in sickle cell disease and thalassemia. Hematology Am Soc Hematol Educ Program 2008; 2008: 177-185.
-
(2008)
Hematology Am Soc Hematol Educ Program 2008
, pp. 177-185
-
-
Morris, C.R.1
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12
-
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33846279380
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Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes
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Kato GJ, Gladwin MT, Steinberg MH. Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Rev 2007; 21:37-47.
-
(2007)
Blood Rev
, vol.21
, pp. 37-47
-
-
Kato, G.J.1
Gladwin, M.T.2
Steinberg, M.H.3
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13
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33644775612
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Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease
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Kato GJ, McGowan V, Machado RF, et al. Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease. Blood 2006; 107:2279-2285.
-
(2006)
Blood
, vol.107
, pp. 2279-2285
-
-
Kato, G.J.1
McGowan, V.2
Machado, R.F.3
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14
-
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0025969263
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Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells
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Ballas SK. Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells. Am J Hematol 1991; 36:122-130.
-
(1991)
Am J Hematol
, vol.36
, pp. 122-130
-
-
Ballas, S.K.1
-
15
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4143132048
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Are there clinical phenotypes of homozygous sickle cell disease?
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Alexander N, Higgs D, Dover G, Serjeant GR. Are there clinical phenotypes of homozygous sickle cell disease? Br J Haematol 2004; 126:606-611.
-
(2004)
Br J Haematol
, vol.126
, pp. 606-611
-
-
Alexander, N.1
Higgs, D.2
Dover, G.3
Serjeant, G.R.4
-
16
-
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62449189504
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Risk factors for hospital readmission within 30 days: A new quality measure for children with sickle cell disease
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This study finds that lack of outpatient follow-up within 30 days after hospital discharge is a risk for readmission
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Frei-Jones MJ, Field JJ, DeBaun MR. Risk factors for hospital readmission within 30 days: a new quality measure for children with sickle cell disease. Pediatr Blood Cancer 2009; 52:481-485. This study finds that lack of outpatient follow-up within 30 days after hospital discharge is a risk for readmission.
-
(2009)
Pediatr Blood Cancer
, vol.52
, pp. 481-485
-
-
Frei-Jones, M.J.1
Field, J.J.2
DeBaun, M.R.3
-
17
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38749109710
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Daily assessment of pain in adults with sickle cell disease
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This study establishes that adults with sickle cell disease frequently manage acute pain events at home without physician contact
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Smith WR, Penberthy LT, Bovbjerg VE, et al. Daily assessment of pain in adults with sickle cell disease. Ann Intern Med 2008; 148:94-101. This study establishes that adults with sickle cell disease frequently manage acute pain events at home without physician contact
-
(2008)
Ann Intern Med
, vol.148
, pp. 94-101
-
-
Smith, W.R.1
Penberthy, L.T.2
Bovbjerg, V.E.3
-
18
-
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33747478249
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Painful episodes in children with sickle cell disease and asthma are temporally associated with respiratory symptoms
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Glassberg J, Spivey JF, Strunk R, et al. Painful episodes in children with sickle cell disease and asthma are temporally associated with respiratory symptoms. J Pediatr Hematol Oncol 2006; 28:481-485.
-
(2006)
J Pediatr Hematol Oncol
, vol.28
, pp. 481-485
-
-
Glassberg, J.1
Spivey, J.F.2
Strunk, R.3
-
19
-
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54049147444
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Association between wind speed and the occurrence of sickle cell acute painful episodes: Results of a case-crossover study
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Nolan VG, Zhang Y, Lash T, et al. Association between wind speed and the occurrence of sickle cell acute painful episodes: results of a case-crossover study. Br J Haematol 2008; 143:433-438.
-
(2008)
Br J Haematol
, vol.143
, pp. 433-438
-
-
Nolan, V.G.1
Zhang, Y.2
Lash, T.3
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20
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33644788545
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Windy weather and low humidity are associated with an increased number of hospital admissions for acute pain and sickle cell disease in an urban environment with a maritime temperate climate
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Jones S, Duncan ER, Thomas N, et al. Windy weather and low humidity are associated with an increased number of hospital admissions for acute pain and sickle cell disease in an urban environment with a maritime temperate climate. Br J Haematol 2005; 131:530-533.
-
(2005)
Br J Haematol
, vol.131
, pp. 530-533
-
-
Jones, S.1
Duncan, E.R.2
Thomas, N.3
-
21
-
-
18044397307
-
Hospital readmission for adult acute sickle cell painful episodes: Frequency, etiology, and prognostic significance
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Ballas SK, Lusardi M. Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significance. Am J Hematol 2005; 79:17-25.
-
(2005)
Am J Hematol
, vol.79
, pp. 17-25
-
-
Ballas, S.K.1
Lusardi, M.2
-
22
-
-
11144279969
-
Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease
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Panepinto JA, Brousseau DC, Hillery CA, Scott JP. Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease. Pediatr Blood Cancer 2005; 44:182-186.
-
(2005)
Pediatr Blood Cancer
, vol.44
, pp. 182-186
-
-
Panepinto, J.A.1
Brousseau, D.C.2
Hillery, C.A.3
Scott, J.P.4
-
23
-
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62449175675
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A question of quality in sickle cell disease
-
Quinn CT. A question of quality in sickle cell disease. Pediatr Blood Cancer 2009; 52:435-436.
-
(2009)
Pediatr Blood Cancer
, vol.52
, pp. 435-436
-
-
Quinn, C.T.1
-
24
-
-
0037265771
-
Examining the validity, reliability, and preference of three pediatric pain measurement tools in African-American children
-
Luffy R, Grove SK. Examining the validity, reliability, and preference of three pediatric pain measurement tools in African-American children. Pediatr Nurs 2003; 29:54-59.
-
(2003)
Pediatr Nurs
, vol.29
, pp. 54-59
-
-
Luffy, R.1
Grove, S.K.2
-
25
-
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0347763461
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Patient-controlled analgesia for sickle cell pain crisis in a pediatric emergency department
-
Melzer-Lange MD, Walsh-Kelly CM, Lea G, et al. Patient-controlled analgesia for sickle cell pain crisis in a pediatric emergency department. Pediatr Emerg Care 2004; 20:2-4.
-
(2004)
Pediatr Emerg Care
, vol.20
, pp. 2-4
-
-
Melzer-Lange, M.D.1
Walsh-Kelly, C.M.2
Lea, G.3
-
26
-
-
0025768807
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Intermittent injection vs patientcontrolled analgesia for sickle cell crisis pain. Comparison in patients in the emergency department
-
Gonzalez ER, Bahal N, Hansen LA, et al. Intermittent injection vs patientcontrolled analgesia for sickle cell crisis pain. Comparison in patients in the emergency department. Arch Intern Med 1991; 151:1373-1378.
-
(1991)
Arch Intern Med
, vol.151
, pp. 1373-1378
-
-
Gonzalez, E.R.1
Bahal, N.2
Hansen, L.A.3
-
27
-
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35549003236
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Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial
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This study demonstrates that patient-controlled analgesia reduces the consumption of morphine during an acute pain event and is equally effective at controlling pain compared to a continuous infusion
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van Beers EJ, van Tuijn CF, Nieuwkerk PT, et al. Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial. Am J Hematol 2007; 82:955-960. This study demonstrates that patient-controlled analgesia reduces the consumption of morphine during an acute pain event and is equally effective at controlling pain compared to a continuous infusion.
-
(2007)
Am J Hematol
, vol.82
, pp. 955-960
-
-
van Beers, E.J.1
van Tuijn, C.F.2
Nieuwkerk, P.T.3
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