-
1
-
-
9244250307
-
Sickle cell disease; a general overview
-
Schnog J.B., Duits A.J., Muskiet F.A., ten Cate H., Rojer R.A., Brandjes D.P. Sickle cell disease; a general overview. Neth J Med 2004, 62:364-374.
-
(2004)
Neth J Med
, vol.62
, pp. 364-374
-
-
Schnog, J.B.1
Duits, A.J.2
Muskiet, F.A.3
ten Cate, H.4
Rojer, R.A.5
Brandjes, D.P.6
-
2
-
-
0242552237
-
Managing sickle cell disease
-
Claster S., Vichinsky E.P. Managing sickle cell disease. BMJ 2003, 327:1151-1155.
-
(2003)
BMJ
, vol.327
, pp. 1151-1155
-
-
Claster, S.1
Vichinsky, E.P.2
-
3
-
-
44949128064
-
Global epidemiology of haemoglobin disorders and derived service indicators
-
Modell B., Darlison M. Global epidemiology of haemoglobin disorders and derived service indicators. Bull World Health Organ 2008, 86:480-487.
-
(2008)
Bull World Health Organ
, vol.86
, pp. 480-487
-
-
Modell, B.1
Darlison, M.2
-
4
-
-
77953952024
-
The inherited diseases of hemoglobin are an emerging global health burden
-
Weatherall D.J. The inherited diseases of hemoglobin are an emerging global health burden. Blood 2010, 115:4331-4336.
-
(2010)
Blood
, vol.115
, pp. 4331-4336
-
-
Weatherall, D.J.1
-
6
-
-
33846005515
-
National evaluation of US newborn screening system components
-
Therrell B.L., Hannon W.H. National evaluation of US newborn screening system components. Ment Retard Dev Disabil Res Rev 2006, 12:236-245.
-
(2006)
Ment Retard Dev Disabil Res Rev
, vol.12
, pp. 236-245
-
-
Therrell, B.L.1
Hannon, W.H.2
-
7
-
-
74049150729
-
The number of people with sickle-cell disease in the United States: national and state estimates
-
Brousseau D.C., Panepinto J.A., Nimmer M., Hoffmann R.G. The number of people with sickle-cell disease in the United States: national and state estimates. Am J Hematol 2010, 85:77-78.
-
(2010)
Am J Hematol
, vol.85
, pp. 77-78
-
-
Brousseau, D.C.1
Panepinto, J.A.2
Nimmer, M.3
Hoffmann, R.G.4
-
8
-
-
77949482609
-
Population estimates of sickle cell disease in the U.S
-
Hassell K.L. Population estimates of sickle cell disease in the U.S. Am J Prev Med 2010, 38:S512-S521.
-
(2010)
Am J Prev Med
, vol.38
-
-
Hassell, K.L.1
-
9
-
-
77951712618
-
Improved survival of children and adolescents with sickle cell disease
-
Quinn C.T., Rogers Z.R., McCavit T.L., Buchanan G.R. Improved survival of children and adolescents with sickle cell disease. Blood 2010, 115:3447-3452.
-
(2010)
Blood
, vol.115
, pp. 3447-3452
-
-
Quinn, C.T.1
Rogers, Z.R.2
McCavit, T.L.3
Buchanan, G.R.4
-
10
-
-
0022628893
-
Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial
-
Gaston M.H., Verter J.I., Woods G., Pegelow C., Kelleher J., Presbury G., et al. Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. N Engl J Med 1986, 314:1593-1599.
-
(1986)
N Engl J Med
, vol.314
, pp. 1593-1599
-
-
Gaston, M.H.1
Verter, J.I.2
Woods, G.3
Pegelow, C.4
Kelleher, J.5
Presbury, G.6
-
11
-
-
58349102500
-
Implementation of universal newborn bloodspot screening for sickle cell disease and other clinically significant haemoglobinopathies in England: screening results for 2005-7
-
Streetly A., Latinovic R., Hall K., Henthorn J. Implementation of universal newborn bloodspot screening for sickle cell disease and other clinically significant haemoglobinopathies in England: screening results for 2005-7. J Clin Pathol 2009, 62:26-30.
-
(2009)
J Clin Pathol
, vol.62
, pp. 26-30
-
-
Streetly, A.1
Latinovic, R.2
Hall, K.3
Henthorn, J.4
-
12
-
-
62649144053
-
Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002
-
Yanni E., Grosse S.D., Yang Q., Olney R.S. Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002. J Pediatr 2009, 154:541-545.
-
(2009)
J Pediatr
, vol.154
, pp. 541-545
-
-
Yanni, E.1
Grosse, S.D.2
Yang, Q.3
Olney, R.S.4
-
13
-
-
40949107353
-
Effectiveness of the 7-valent pneumococcal conjugate vaccine in children with sickle cell disease in the first decade of life
-
Adamkiewicz T.V., Silk B.J., Howgate J., Baughman W., Strayhorn G., Sullivan K., et al. Effectiveness of the 7-valent pneumococcal conjugate vaccine in children with sickle cell disease in the first decade of life. Pediatrics 2008, 121:562-569.
-
(2008)
Pediatrics
, vol.121
, pp. 562-569
-
-
Adamkiewicz, T.V.1
Silk, B.J.2
Howgate, J.3
Baughman, W.4
Strayhorn, G.5
Sullivan, K.6
-
14
-
-
81355163446
-
Sickle cell disease in Africa: a neglected cause of early childhood mortality
-
Grosse S.D., Odame I., Atrash H.K., Amendah D.D., Piel F.B., Williams T.N. Sickle cell disease in Africa: a neglected cause of early childhood mortality. Am J Prev Med 2011, 41:S398-S405.
-
(2011)
Am J Prev Med
, vol.41
-
-
Grosse, S.D.1
Odame, I.2
Atrash, H.K.3
Amendah, D.D.4
Piel, F.B.5
Williams, T.N.6
-
15
-
-
84887611971
-
Managing the acutely ill adult with sickle cell disease
-
90-2
-
Brown M. Managing the acutely ill adult with sickle cell disease. Br J Nurs 2012, 21(90-2):5-6.
-
(2012)
Br J Nurs
, vol.21
, pp. 5-6
-
-
Brown, M.1
-
16
-
-
80455132476
-
Pathophysiological insights in sickle cell disease
-
Odièvre M.H., Verger E., Silva-Pinto A.C., Elion J. Pathophysiological insights in sickle cell disease. Indian J Med Res 2011, 134:532-537.
-
(2011)
Indian J Med Res
, vol.134
, pp. 532-537
-
-
Odièvre, M.H.1
Verger, E.2
Silva-Pinto, A.C.3
Elion, J.4
-
17
-
-
64149099554
-
Neutrophil sandwiches injure the microcirculation
-
Looney M.R., Matthay M.A. Neutrophil sandwiches injure the microcirculation. Nat Med 2009, 15:364-366.
-
(2009)
Nat Med
, vol.15
, pp. 364-366
-
-
Looney, M.R.1
Matthay, M.A.2
-
18
-
-
84876571521
-
-
Available at, [accessed July 18, 2013] Novartis AG Iron Health Alliance
-
Novartis AG Iron Health Alliance Sickle cell disease Available at, [accessed July 18, 2013]. http://www.ironhealthalliance.com/disease-states/sickle-cell-disease.jsp.
-
Sickle cell disease
-
-
-
19
-
-
54349103017
-
Growth and nutritional status of children with homozygous sickle cell disease
-
Al-Saqladi A.W., Cipolotti R., Fijnvandraat K., Brabin B.J. Growth and nutritional status of children with homozygous sickle cell disease. Ann Trop Paediatr 2008, 28:165-189.
-
(2008)
Ann Trop Paediatr
, vol.28
, pp. 165-189
-
-
Al-Saqladi, A.W.1
Cipolotti, R.2
Fijnvandraat, K.3
Brabin, B.J.4
-
20
-
-
80053374132
-
Asthma morbidity and treatment in children with sickle cell disease
-
Anim S.O., Strunk R.C., DeBaun M.R. Asthma morbidity and treatment in children with sickle cell disease. Expert Rev Respir Med 2011, 5:635-645.
-
(2011)
Expert Rev Respir Med
, vol.5
, pp. 635-645
-
-
Anim, S.O.1
Strunk, R.C.2
DeBaun, M.R.3
-
21
-
-
36348959032
-
Management of vasoocclusive pain events in sickle cell disease
-
quiz 8-41
-
Ellison A.M., Shaw K. Management of vasoocclusive pain events in sickle cell disease. Pediatr Emerg Care 2007, 23:832-838. quiz 8-41.
-
(2007)
Pediatr Emerg Care
, vol.23
, pp. 832-838
-
-
Ellison, A.M.1
Shaw, K.2
-
22
-
-
34147223415
-
Anxiety and depression in children and adolescents with sickle cell disease
-
Benton T.D., Ifeagwu J.A., Smith-Whitley K. Anxiety and depression in children and adolescents with sickle cell disease. Curr Psychiatry Rep 2007, 9:114-121.
-
(2007)
Curr Psychiatry Rep
, vol.9
, pp. 114-121
-
-
Benton, T.D.1
Ifeagwu, J.A.2
Smith-Whitley, K.3
-
23
-
-
2542455639
-
Survival of children with sickle cell disease
-
Quinn C.T., Rogers Z.R., Buchanan G.R. Survival of children with sickle cell disease. Blood 2004, 103:4023-4027.
-
(2004)
Blood
, vol.103
, pp. 4023-4027
-
-
Quinn, C.T.1
Rogers, Z.R.2
Buchanan, G.R.3
-
24
-
-
34548753905
-
Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London
-
Telfer P., Coen P., Chakravorty S., Wilkey O., Evans J., Newell H., et al. Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London. Haematologica 2007, 92:905-912.
-
(2007)
Haematologica
, vol.92
, pp. 905-912
-
-
Telfer, P.1
Coen, P.2
Chakravorty, S.3
Wilkey, O.4
Evans, J.5
Newell, H.6
-
25
-
-
69649101810
-
The excess burden of stroke in hospitalized adults with sickle cell disease
-
Strouse J.J., Jordan L.C., Lanzkron S., Casella J.F. The excess burden of stroke in hospitalized adults with sickle cell disease. Am J Hematol 2009, 84:548-552.
-
(2009)
Am J Hematol
, vol.84
, pp. 548-552
-
-
Strouse, J.J.1
Jordan, L.C.2
Lanzkron, S.3
Casella, J.F.4
-
26
-
-
34247108061
-
The pathophysiology, prevention, and treatment of stroke in sickle cell disease
-
Wang W.C. The pathophysiology, prevention, and treatment of stroke in sickle cell disease. Curr Opin Hematol 2007, 14:191-197.
-
(2007)
Curr Opin Hematol
, vol.14
, pp. 191-197
-
-
Wang, W.C.1
-
27
-
-
84860328824
-
Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure
-
DeBaun M.R., Sarnaik S.A., Rodeghier M.J., Minniti C.P., Howard T.H., Iyer R.V., et al. Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure. Blood 2012, 119:3684-3690.
-
(2012)
Blood
, vol.119
, pp. 3684-3690
-
-
DeBaun, M.R.1
Sarnaik, S.A.2
Rodeghier, M.J.3
Minniti, C.P.4
Howard, T.H.5
Iyer, R.V.6
-
28
-
-
0031775847
-
Cognitive screening examinations for silent cerebral infarcts in sickle cell disease
-
DeBaun M.R., Schatz J., Siegel M.J., Koby M., Craft S., Resar L., et al. Cognitive screening examinations for silent cerebral infarcts in sickle cell disease. Neurology 1998, 50:1678-1682.
-
(1998)
Neurology
, vol.50
, pp. 1678-1682
-
-
DeBaun, M.R.1
Schatz, J.2
Siegel, M.J.3
Koby, M.4
Craft, S.5
Resar, L.6
-
29
-
-
0032474692
-
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography
-
Adams R.J., McKie V.C., 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 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
Files, B.4
Vichinsky, E.5
Pegelow, C.6
-
30
-
-
65349103931
-
Utilization of TCD screening for primary stroke prevention in children with sickle cell disease
-
Armstrong-Wells J., Grimes B., Sidney S., Kronish D., Shiboski S.C., Adams R.J., et al. Utilization of TCD screening for primary stroke prevention in children with sickle cell disease. Neurology 2009, 72:1316-1321.
-
(2009)
Neurology
, vol.72
, pp. 1316-1321
-
-
Armstrong-Wells, J.1
Grimes, B.2
Sidney, S.3
Kronish, D.4
Shiboski, S.C.5
Adams, R.J.6
-
31
-
-
85044805921
-
Healthcare provision for sickle cell disease: challenges for the African context
-
Dennis-Antwi J.A., Dyson S.M., Ohene-Frempong K. Healthcare provision for sickle cell disease: challenges for the African context. Divers. Health Soc. Care 2008, 5:241-254.
-
(2008)
Divers. Health Soc. Care
, vol.5
, pp. 241-254
-
-
Dennis-Antwi, J.A.1
Dyson, S.M.2
Ohene-Frempong, K.3
-
32
-
-
64549106465
-
Asthma management: reinventing the wheel in sickle cell disease
-
Morris C.R. Asthma management: reinventing the wheel in sickle cell disease. Am J Hematol 2009, 84:234-241.
-
(2009)
Am J Hematol
, vol.84
, pp. 234-241
-
-
Morris, C.R.1
-
33
-
-
35748980612
-
Asthma is associated with increased mortality in individuals with sickle cell anemia
-
Boyd J.H., Macklin E.A., Strunk R.C., DeBaun M.R. Asthma is associated with increased mortality in individuals with sickle cell anemia. Haematologica 2007, 92:1115-1118.
-
(2007)
Haematologica
, vol.92
, pp. 1115-1118
-
-
Boyd, J.H.1
Macklin, E.A.2
Strunk, R.C.3
DeBaun, M.R.4
-
34
-
-
18044397307
-
Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significance
-
Ballas S.K., 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
-
35
-
-
0142215534
-
Causes of death in sickle cell disease: an autopsy study
-
Manci E.A., Culberson D.E., Yang Y.M., Gardner T.M., Powell R., Haynes J., et al. Causes of death in sickle cell disease: an autopsy study. Br J Haematol 2003, 123:359-365.
-
(2003)
Br J Haematol
, vol.123
, pp. 359-365
-
-
Manci, E.A.1
Culberson, D.E.2
Yang, Y.M.3
Gardner, T.M.4
Powell, R.5
Haynes, J.6
-
36
-
-
0031035337
-
Acute chest syndrome in sickle cell disease: clinical presentation and course. Cooperative Study of Sickle Cell Disease
-
Vichinsky E.P., Styles L.A., Colangelo L.H., Wright E.C., Castro O., Nickerson B. Acute chest syndrome in sickle cell disease: clinical presentation and course. Cooperative Study of Sickle Cell Disease. Blood 1997, 89:1787-1792.
-
(1997)
Blood
, vol.89
, pp. 1787-1792
-
-
Vichinsky, E.P.1
Styles, L.A.2
Colangelo, L.H.3
Wright, E.C.4
Castro, O.5
Nickerson, B.6
-
37
-
-
0025770390
-
Pain in sickle cell disease. Rates and risk factors
-
Platt O.S., Thorington B.D., Brambilla D.J., Milner P.F., Rosse W.F., Vichinsky E., et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med 1991, 325:11-16.
-
(1991)
N Engl J Med
, vol.325
, 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
-
38
-
-
33645643438
-
Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project
-
McClish D.K., Levenson J.L., Penberthy L.T., Roseff S.D., Bovbjerg V.E., Roberts J.D., et al. Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project. J Womens Health (Larchmt) 2006, 15:146-154.
-
(2006)
J Womens Health (Larchmt)
, vol.15
, pp. 146-154
-
-
McClish, D.K.1
Levenson, J.L.2
Penberthy, L.T.3
Roseff, S.D.4
Bovbjerg, V.E.5
Roberts, J.D.6
-
39
-
-
81255210779
-
The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease
-
Strouse J.J., Lanzkron S., Urrutia V. The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease. Expert Rev Hematol 2011, 4:597-606.
-
(2011)
Expert Rev Hematol
, vol.4
, pp. 597-606
-
-
Strouse, J.J.1
Lanzkron, S.2
Urrutia, V.3
-
40
-
-
84856155504
-
Evidence-based management of sickle cell disease in the emergency department
-
[quiz]
-
Glassberg J. Evidence-based management of sickle cell disease in the emergency department. Emerg Med Pract 2011, 13:1-20. [quiz].
-
(2011)
Emerg Med Pract
, vol.13
, pp. 1-20
-
-
Glassberg, J.1
-
41
-
-
51949116346
-
Management of sickle cell disease
-
de Montalembert M. Management of sickle cell disease. BMJ 2008, 337:a1397.
-
(2008)
BMJ
, vol.337
-
-
de Montalembert, M.1
-
42
-
-
0029005136
-
Risk of recurrent stroke in patients with sickle cell disease treated with erythrocyte transfusions
-
Pegelow C.H., Adams R.J., McKie V., Abboud M., Berman B., Miller S.T., 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
Abboud, M.4
Berman, B.5
Miller, S.T.6
-
43
-
-
0037167227
-
New therapies in sickle cell disease
-
Vichinsky E. New therapies in sickle cell disease. Lancet 2002, 360:629-631.
-
(2002)
Lancet
, vol.360
, pp. 629-631
-
-
Vichinsky, E.1
-
44
-
-
84862254136
-
Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children
-
Strouse J.J., Heeney M.M. Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children. Pediatr Blood Cancer 2012, 59:365-371.
-
(2012)
Pediatr Blood Cancer
, vol.59
, pp. 365-371
-
-
Strouse, J.J.1
Heeney, M.M.2
-
45
-
-
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 M.L., Moore R.D., Dover G.J., Barton F.B., Eckert S.V., 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, 332:1317-1322.
-
(1995)
N Engl J Med
, vol.332
, 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
-
46
-
-
0029845949
-
Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial
-
Ferster A., Vermylen C., Cornu G., Buyse M., Corazza F., Devalck C., et al. Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial. Blood 1996, 88:1960-1964.
-
(1996)
Blood
, vol.88
, pp. 1960-1964
-
-
Ferster, A.1
Vermylen, C.2
Cornu, G.3
Buyse, M.4
Corazza, F.5
Devalck, C.6
-
47
-
-
84864917063
-
Effect of hydroxyurea treatment on renal function parameters: results from the multi-center placebo-controlled BABY HUG clinical trial for infants with sickle cell anemia
-
Alvarez O., Miller S.T., Wang W.C., Luo Z., McCarville M.B., Schwartz G.J., et al. Effect of hydroxyurea treatment on renal function parameters: results from the multi-center placebo-controlled BABY HUG clinical trial for infants with sickle cell anemia. Pediatr Blood Cancer 2012, 59:668-674.
-
(2012)
Pediatr Blood Cancer
, vol.59
, pp. 668-674
-
-
Alvarez, O.1
Miller, S.T.2
Wang, W.C.3
Luo, Z.4
McCarville, M.B.5
Schwartz, G.J.6
-
48
-
-
84861094707
-
Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: results from the BABY-HUG phase III clinical trial
-
McGann P.T., Flanagan J.M., Howard T.A., Dertinger S.D., He J., Kulharya A.S., et al. Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: results from the BABY-HUG phase III clinical trial. Pediatr Blood Cancer 2012, 59:254-257.
-
(2012)
Pediatr Blood Cancer
, vol.59
, pp. 254-257
-
-
McGann, P.T.1
Flanagan, J.M.2
Howard, T.A.3
Dertinger, S.D.4
He, J.5
Kulharya, A.S.6
-
49
-
-
84869803950
-
Impact of hydroxyurea on clinical events in the BABY HUG trial
-
[quiz 448]
-
Thornburg C.D., Files B.A., Luo Z., Miller S.T., Kalpatthi R., Iyer R., et al. Impact of hydroxyurea on clinical events in the BABY HUG trial. Blood 2012, 120:4304-4310. [quiz 448].
-
(2012)
Blood
, vol.120
, pp. 4304-4310
-
-
Thornburg, C.D.1
Files, B.A.2
Luo, Z.3
Miller, S.T.4
Kalpatthi, R.5
Iyer, R.6
-
50
-
-
0028046507
-
Effects of a long-term transfusion regimen on sickle cell-related illnesses
-
Styles L.A., Vichinsky E. Effects of a long-term transfusion regimen on sickle cell-related illnesses. J Pediatr 1994, 125:909-911.
-
(1994)
J Pediatr
, vol.125
, pp. 909-911
-
-
Styles, L.A.1
Vichinsky, E.2
-
51
-
-
78651378996
-
Iron-chelating therapy for transfusional iron overload
-
Brittenham G.M. Iron-chelating therapy for transfusional iron overload. N Engl J Med 2011, 364:146-156.
-
(2011)
N Engl J Med
, vol.364
, pp. 146-156
-
-
Brittenham, G.M.1
-
52
-
-
77955971228
-
Deferasirox for managing transfusional iron overload in people with sickle cell disease
-
Meerpohl J.J., Antes G., Rücker G., Fleeman N., Niemeyer C., Bassler D. Deferasirox for managing transfusional iron overload in people with sickle cell disease. Cochrane Database Syst Rev 2010, CD007477.
-
(2010)
Cochrane Database Syst Rev
-
-
Meerpohl, J.J.1
Antes, G.2
Rücker, G.3
Fleeman, N.4
Niemeyer, C.5
Bassler, D.6
-
53
-
-
0036220398
-
Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke
-
Scothorn D.J., Price C., Schwartz D., Terrill C., Buchanan G.R., Shurney W., et al. Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke. J Pediatr 2002, 140:348-354.
-
(2002)
J Pediatr
, vol.140
, pp. 348-354
-
-
Scothorn, D.J.1
Price, C.2
Schwartz, D.3
Terrill, C.4
Buchanan, G.R.5
Shurney, W.6
-
54
-
-
78751697297
-
Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
-
Hulbert M.L., McKinstry R.C., Lacey J.L., Moran C.J., Panepinto J.A., Thompson A.A., et al. Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease. Blood 2011, 117:772-779.
-
(2011)
Blood
, vol.117
, pp. 772-779
-
-
Hulbert, M.L.1
McKinstry, R.C.2
Lacey, J.L.3
Moran, C.J.4
Panepinto, J.A.5
Thompson, A.A.6
-
55
-
-
84860348352
-
Stroke With Transfusions Changing to Hydroxyurea (SWiTCH)
-
Ware R.E., Helms R.W., Investigators S.W. Stroke With Transfusions Changing to Hydroxyurea (SWiTCH). Blood 2012, 119:3925-3932.
-
(2012)
Blood
, vol.119
, pp. 3925-3932
-
-
Ware, R.E.1
Helms, R.W.2
Investigators, S.W.3
-
56
-
-
77953461487
-
Current strategies for the management of children with sickle cell disease
-
de Montalembert M. Current strategies for the management of children with sickle cell disease. Expert Rev Hematol 2009, 2:455-463.
-
(2009)
Expert Rev Hematol
, vol.2
, pp. 455-463
-
-
de Montalembert, M.1
-
57
-
-
84859412957
-
Primary prophylaxis in sickle cell disease: is it feasible? Is it effective?
-
Thompson A.A. Primary prophylaxis in sickle cell disease: is it feasible? Is it effective?. Hematology Am Soc Hematol Educ Program 2011, 2011:434-439.
-
(2011)
Hematology Am Soc Hematol Educ Program
, vol.2011
, pp. 434-439
-
-
Thompson, A.A.1
-
58
-
-
79959244335
-
Stem-cell transplantation in children and adults with sickle cell disease: an update
-
Khoury R., Abboud M.R. Stem-cell transplantation in children and adults with sickle cell disease: an update. Expert Rev Hematol 2011, 4:343-351.
-
(2011)
Expert Rev Hematol
, vol.4
, pp. 343-351
-
-
Khoury, R.1
Abboud, M.R.2
-
59
-
-
70249132888
-
Hematopoietic stem cell transplantation for children with sickle cell disease
-
Oringanje C., Nemecek E., Oniyangi O. Hematopoietic stem cell transplantation for children with sickle cell disease. Cochrane Database Syst Rev 2009, CD007001.
-
(2009)
Cochrane Database Syst Rev
-
-
Oringanje, C.1
Nemecek, E.2
Oniyangi, O.3
-
60
-
-
38949178118
-
Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: an educational void
-
Solomon L.R. Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: an educational void. Blood 2008, 111:997-1003.
-
(2008)
Blood
, vol.111
, pp. 997-1003
-
-
Solomon, L.R.1
-
61
-
-
0036360040
-
Clinical significance of RBC alloantibodies and autoantibodies in sickle cell patients who received transfusions
-
Aygun B., Padmanabhan S., Paley C., Chandrasekaran V. Clinical significance of RBC alloantibodies and autoantibodies in sickle cell patients who received transfusions. Transfusion 2002, 42:37-43.
-
(2002)
Transfusion
, vol.42
, pp. 37-43
-
-
Aygun, B.1
Padmanabhan, S.2
Paley, C.3
Chandrasekaran, V.4
-
62
-
-
77956419792
-
A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease
-
Taylor L.E., Stotts N.A., Humphreys J., Treadwell M.J., Miaskowski C. A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease. J Pain Symptom Manage 2010, 40:416-435.
-
(2010)
J Pain Symptom Manage
, vol.40
, pp. 416-435
-
-
Taylor, L.E.1
Stotts, N.A.2
Humphreys, J.3
Treadwell, M.J.4
Miaskowski, C.5
-
63
-
-
63449117520
-
Barriers to effective pain management in sickle cell disease
-
Wright K., Adeosum O. Barriers to effective pain management in sickle cell disease. Br J Nurs 2009, 18:158-161.
-
(2009)
Br J Nurs
, vol.18
, pp. 158-161
-
-
Wright, K.1
Adeosum, O.2
-
64
-
-
0037288007
-
Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease
-
Telfair J., Haque A., Etienne M., Tang S., Strasser S. Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease. Public Health Rep 2003, 118:27-36.
-
(2003)
Public Health Rep
, vol.118
, pp. 27-36
-
-
Telfair, J.1
Haque, A.2
Etienne, M.3
Tang, S.4
Strasser, S.5
-
65
-
-
0033931159
-
Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina
-
Haque A., Telfair J. Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina. J Rural Health 2000, 16:43-55.
-
(2000)
J Rural Health
, vol.16
, pp. 43-55
-
-
Haque, A.1
Telfair, J.2
-
66
-
-
0036898681
-
Implementing transitions for youth with complex chronic conditions using the medical home model
-
Kelly A.M., Kratz B., Bielski M., Rinehart P.M. Implementing transitions for youth with complex chronic conditions using the medical home model. Pediatrics 2002, 110:1322-1327.
-
(2002)
Pediatrics
, vol.110
, pp. 1322-1327
-
-
Kelly, A.M.1
Kratz, B.2
Bielski, M.3
Rinehart, P.M.4
-
67
-
-
77951619147
-
Sickle cell disease in the United States: looking back and forward at 100years of progress in management and survival
-
Prabhakar H., Haywood C., Molokie R. Sickle cell disease in the United States: looking back and forward at 100years of progress in management and survival. Am J Hematol 2010, 85:346-353.
-
(2010)
Am J Hematol
, vol.85
, pp. 346-353
-
-
Prabhakar, H.1
Haywood, C.2
Molokie, R.3
-
68
-
-
78650383011
-
Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research
-
Treadwell M., Telfair J., Gibson R.W., Johnson S., Osunkwo I. Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research. Am J Hematol 2011, 86:116-120.
-
(2011)
Am J Hematol
, vol.86
, pp. 116-120
-
-
Treadwell, M.1
Telfair, J.2
Gibson, R.W.3
Johnson, S.4
Osunkwo, I.5
-
69
-
-
77950478131
-
Acute care utilization and rehospitalizations for sickle cell disease
-
Brousseau D.C., Owens P.L., Mosso A.L., Panepinto J.A., Steiner C.A. Acute care utilization and rehospitalizations for sickle cell disease. JAMA 2010, 303:1288-1294.
-
(2010)
JAMA
, vol.303
, pp. 1288-1294
-
-
Brousseau, D.C.1
Owens, P.L.2
Mosso, A.L.3
Panepinto, J.A.4
Steiner, C.A.5
-
70
-
-
0036483674
-
A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services
-
Wojciechowski E.A., Hurtig A., Dorn L. A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services. J Pediatr Nurs 2002, 17:18-27.
-
(2002)
J Pediatr Nurs
, vol.17
, pp. 18-27
-
-
Wojciechowski, E.A.1
Hurtig, A.2
Dorn, L.3
-
71
-
-
77649243106
-
From cradle to commencement: transitioning pediatric sickle cell disease patients to adult providers
-
Doulton D.M. From cradle to commencement: transitioning pediatric sickle cell disease patients to adult providers. J Pediatr Oncol Nurs 2010, 27:119-123.
-
(2010)
J Pediatr Oncol Nurs
, vol.27
, pp. 119-123
-
-
Doulton, D.M.1
-
72
-
-
77955959056
-
Moving young people with sickle cell disease from paediatric to adult services
-
Howard J., Woodhead T., Musumadi L., Martell A., Inusa B.P. Moving young people with sickle cell disease from paediatric to adult services. Br J Hosp Med (Lond) 2010, 71:310-314.
-
(2010)
Br J Hosp Med (Lond)
, vol.71
, pp. 310-314
-
-
Howard, J.1
Woodhead, T.2
Musumadi, L.3
Martell, A.4
Inusa, B.P.5
-
73
-
-
34147141453
-
Sickle cell disease: old discoveries, new concepts, and future promise
-
Frenette P.S., Atweh G.F. Sickle cell disease: old discoveries, new concepts, and future promise. J Clin Invest 2007, 117:850-858.
-
(2007)
J Clin Invest
, vol.117
, pp. 850-858
-
-
Frenette, P.S.1
Atweh, G.F.2
-
74
-
-
33646779583
-
Recent advances in globin gene transfer for the treatment of beta-thalassemia and sickle cell anemia
-
Sadelain M. Recent advances in globin gene transfer for the treatment of beta-thalassemia and sickle cell anemia. Curr Opin Hematol 2006, 13:142-148.
-
(2006)
Curr Opin Hematol
, vol.13
, pp. 142-148
-
-
Sadelain, M.1
-
75
-
-
72449211881
-
A systems biology consideration of the vasculopathy of sickle cell anemia: the need for multi-modality chemo-prophylaxsis
-
Hebbel R.P., Vercellotti G., Nath K.A. A systems biology consideration of the vasculopathy of sickle cell anemia: the need for multi-modality chemo-prophylaxsis. Cardiovasc Hematol Disord Drug Targets 2009, 9:271-292.
-
(2009)
Cardiovasc Hematol Disord Drug Targets
, vol.9
, pp. 271-292
-
-
Hebbel, R.P.1
Vercellotti, G.2
Nath, K.A.3
-
76
-
-
18844446494
-
Platelet-vessel wall interactions in the microcirculation
-
Tailor A., Cooper D., Granger D.N. Platelet-vessel wall interactions in the microcirculation. Microcirculation 2005, 12:275-285.
-
(2005)
Microcirculation
, vol.12
, pp. 275-285
-
-
Tailor, A.1
Cooper, D.2
Granger, D.N.3
-
77
-
-
56749163948
-
Pulmonary complications of sickle cell disease
-
Gladwin M.T., Vichinsky E. Pulmonary complications of sickle cell disease. N Engl J Med 2008, 359:2254-2265.
-
(2008)
N Engl J Med
, vol.359
, pp. 2254-2265
-
-
Gladwin, M.T.1
Vichinsky, E.2
|