-
1
-
-
0025770390
-
Pain in sickle cell disease. Rates and risk factors
-
O.S. Platt, B.D. Thorington, D.J. Brambilla, P.F. Milner, W.F. Rosse, and E. Vichinsky Pain in sickle cell disease. Rates and risk factors N Engl J Med 325 1991 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
-
2
-
-
38749109710
-
Daily assessment of pain in adults with sickle cell disease
-
W.R. Smith, L.T. Penberthy, V.E. Bovbjerg, D.K. McClish, J.D. Roberts, and B. Dahman Daily assessment of pain in adults with sickle cell disease Ann Intern Med 148 2008 94 101 (Pubitemid 351651552)
-
(2008)
Annals of Internal Medicine
, 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
Aisiku, I.P.7
Levenson, J.L.8
Roseff, S.D.9
-
3
-
-
0023180585
-
The painful crisis of homozygous sickle cell disease. A study of risk factors
-
DOI 10.1001/archinte.147.7.1231
-
K.F. Baum, D.T. Dunn, G.H. Maude, and G.R. Serjeant The painful crisis of homozygous sickle cell disease. A study of the risk factors Arch Intern Med 147 1987 1231 1234 (Pubitemid 17102149)
-
(1987)
Archives of Internal Medicine
, vol.147
, Issue.7
, pp. 1231-1234
-
-
Baum, K.F.1
Dunn, D.T.2
Maude, G.H.3
Serjeant, G.R.4
-
4
-
-
0028810664
-
Paradoxical increase of painful crises in sickle cell patients with alpha-thalassemia
-
H.H. Billett, R.L. Nagel, and M.E. Fabry Paradoxical increase of painful crises in sickle cell patients with alpha-thalassemia Blood 86 1995 4382
-
(1995)
Blood
, vol.86
, pp. 4382
-
-
Billett, H.H.1
Nagel, R.L.2
Fabry, M.E.3
-
5
-
-
0029017748
-
Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease
-
F.M. Gill, L.A. Sleeper, S.J. Weiner, A.K. Brown, R. Bellevue, and R. Grover Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease Blood 86 1995 776 783
-
(1995)
Blood
, vol.86
, 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
-
6
-
-
47749090563
-
Chronic hyper-hemolysis in sickle cell anemia: Association of vascular complications and mortality with less frequent vasoocclusive pain
-
JGt Taylor, V.G. Nolan, L. Mendelsohn, G.J. Kato, M.T. Gladwin, and M.H. Steinberg Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain PLoS One 3 2008 e2095
-
(2008)
PLoS One
, vol.3
, pp. 2095
-
-
Taylor, J.1
Nolan, V.G.2
Mendelsohn, L.3
Kato, G.J.4
Gladwin, M.T.5
Steinberg, M.H.6
-
7
-
-
0034642592
-
Prediction of adverse outcomes in children with sickle cell disease
-
DOI 10.1056/NEJM200001133420203
-
S.T. Miller, L.A. Sleeper, C.H. Pegelow, L.E. Enos, W.C. Wang, and S.J. Weiner Prediction of adverse outcomes in children with sickle cell disease N Engl J Med 342 2000 83 89 (Pubitemid 30036599)
-
(2000)
New England Journal of Medicine
, vol.342
, Issue.2
, pp. 83-89
-
-
Miller, S.T.1
Sleeper, L.A.2
Pegelow, C.H.3
Enos, L.E.4
Wang, W.C.5
Weiner, S.J.6
Wethers, D.L.7
Smith, J.8
Kinney, T.R.9
-
8
-
-
38349193738
-
Prediction of adverse outcomes in children with sickle cell anemia: A study of the Dallas Newborn Cohort
-
C.T. Quinn, N.J. Lee, E.P. Shull, N. Ahmad, Z.R. Rogers, and G.R. Buchanan Prediction of adverse outcomes in children with sickle cell anemia: a study of the Dallas Newborn Cohort Blood 111 2008 544 548
-
(2008)
Blood
, vol.111
, pp. 544-548
-
-
Quinn, C.T.1
Lee, N.J.2
Shull, E.P.3
Ahmad, N.4
Rogers, Z.R.5
Buchanan, G.R.6
-
9
-
-
11144279969
-
Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease
-
DOI 10.1002/pbc.20180
-
J.A. Panepinto, D.C. Brousseau, C.A. Hillery, and J.P. Scott Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease Pediatr Blood Cancer 44 2005 182 186 (Pubitemid 40041536)
-
(2005)
Pediatric Blood and Cancer
, vol.44
, Issue.2
, pp. 182-186
-
-
Panepinto, J.A.1
Brousseau, D.C.2
Hillery, C.A.3
Scott, J.P.4
-
10
-
-
62949183515
-
Elevated tricuspid regurgitant jet velocity in children and adolescents with sickle cell disease: Association with hemolysis and hemoglobin oxygen desaturation
-
C.P. Minniti, C. Sable, A. Campbell, S. Rana, G. Ensing, and N. Dham Elevated tricuspid regurgitant jet velocity in children and adolescents with sickle cell disease: association with hemolysis and hemoglobin oxygen desaturation Haematologica 94 2009 340 347
-
(2009)
Haematologica
, vol.94
, pp. 340-347
-
-
Minniti, C.P.1
Sable, C.2
Campbell, A.3
Rana, S.4
Ensing, G.5
Dham, N.6
-
11
-
-
0035412399
-
A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia
-
A.S. Tan, T.C. Quah, P.S. Low, and S.S. Chong A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia Blood 98 2001 250 251
-
(2001)
Blood
, vol.98
, pp. 250-251
-
-
Tan, A.S.1
Quah, T.C.2
Low, P.S.3
Chong, S.S.4
-
12
-
-
0035659821
-
Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia
-
DOI 10.1067/mpd.2001.119593
-
S.T. Miller, E. Wright, M. Abboud, B. Berman, B. Files, and C.D. Scher Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia J Pediatr 139 2001 785 789 (Pubitemid 34014456)
-
(2001)
Journal of Pediatrics
, vol.139
, Issue.6
, pp. 785-789
-
-
Miller, S.T.1
Wright, E.2
Abboud, M.3
Berman, B.4
Files, B.5
Scher, C.D.6
Styles, L.7
Adams, R.J.8
-
13
-
-
0034702282
-
Causes and outcomes of the acute chest syndrome in sickle cell disease
-
DOI 10.1056/NEJM200006223422502
-
E.P. Vichinsky, L.D. Neumayr, A.N. Earles, R. Williams, E.T. Lennette, and D. Dean Causes and outcomes of the acute chest syndrome in sickle cell disease. National Acute Chest Syndrome Study Group N Engl J Med 342 2000 1855 1865 (Pubitemid 30419049)
-
(2000)
New England Journal of Medicine
, vol.342
, Issue.25
, pp. 1855-1865
-
-
Vichinsky, E.P.1
Neumayr, L.D.2
Earles, A.N.3
Williams, R.4
Lennette, E.T.5
Dean, D.6
Nickerson, B.7
Orringer, E.8
McKie, V.9
Bellevue, R.10
Daeschner, C.11
Manci, E.A.12
Abboud, M.13
Moncino, M.14
Ballas, S.15
Ware, R.16
-
14
-
-
0242266583
-
Hypoxaemia in sickle cell disease: Biomarker modulation and relevance to pathophysiology
-
DOI 10.1016/S0140-6736(03)14689-2
-
B.N. Setty, M.J. Stuart, C. Dampier, D. Brodecki, and J.L. Allen Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology Lancet 362 2003 1450 1455 (Pubitemid 37352882)
-
(2003)
Lancet
, vol.362
, Issue.9394
, pp. 1450-1455
-
-
Setty, B.N.Y.1
Stuart, M.J.2
Dampier, C.3
Brodecki, D.4
Allen, J.L.5
-
15
-
-
49149105638
-
Elevated urinary leukotriene E4 levels are associated with hospitalization for pain in children with sickle cell disease
-
J.E. Jennings, T. Ramkumar, J. Mao, J. Boyd, M. Castro, and J.J. Field Elevated urinary leukotriene E4 levels are associated with hospitalization for pain in children with sickle cell disease Am J Hematol 83 2008 640 643
-
(2008)
Am J Hematol
, vol.83
, pp. 640-643
-
-
Jennings, J.E.1
Ramkumar, T.2
Mao, J.3
Boyd, J.4
Castro, M.5
Field, J.J.6
-
16
-
-
77949436543
-
Asthma and sickle cell disease: Two distinct diseases or part of the same process?
-
J.J. Field, and M.R. DeBaun Asthma and sickle cell disease: two distinct diseases or part of the same process? Hematology Am Soc Hematol Educ Program 2009 45 53
-
(2009)
Hematology Am Soc Hematol Educ Program
, pp. 45-53
-
-
Field, J.J.1
Debaun, M.R.2
-
17
-
-
64549155231
-
Urinary cysteinyl leukotriene E4 significantly increases during pain in children and adults with sickle cell disease
-
J.J. Field, R.C. Strunk, J.E. Knight-Perry, M.A. Blinder, R.R. Townsend, and M.R. DeBaun Urinary cysteinyl leukotriene E4 significantly increases during pain in children and adults with sickle cell disease Am J Hematol 84 2009 231 233
-
(2009)
Am J Hematol
, vol.84
, pp. 231-233
-
-
Field, J.J.1
Strunk, R.C.2
Knight-Perry, J.E.3
Blinder, M.A.4
Townsend, R.R.5
Debaun, M.R.6
-
18
-
-
57349158830
-
Asthma is associated with acute chest syndrome, but not with an increased rate of hospitalization for pain among children in France with sickle cell anemia: A retrospective cohort study
-
F. Bernaudin, R.C. Strunk, A. Kamdem, C. Arnaud, P. An, and M. Torres Asthma is associated with acute chest syndrome, but not with an increased rate of hospitalization for pain among children in France with sickle cell anemia: a retrospective cohort study Haematologica 93 2008 1917 1918
-
(2008)
Haematologica
, vol.93
, pp. 1917-1918
-
-
Bernaudin, F.1
Strunk, R.C.2
Kamdem, A.3
Arnaud, C.4
An, P.5
Torres, M.6
-
19
-
-
33747479576
-
Asthma is associated with acute chest syndrome and pain in children with sickle cell anemia
-
J.H. Boyd, E.A. Macklin, R.C. Strunk, and M.R. DeBaun Asthma is associated with acute chest syndrome and pain in children with sickle cell anemia Blood 108 2006 2923 2927
-
(2006)
Blood
, vol.108
, pp. 2923-2927
-
-
Boyd, J.H.1
MacKlin, E.A.2
Strunk, R.C.3
Debaun, M.R.4
-
20
-
-
0021894845
-
The interaction of coexistent α-thalassemia and sickle cell anemia: A model for the clinical and cellular results of diminished polymerization?
-
S.H. Embury The interaction of coexistent alpha-thalassemia and sickle cell anemia: a model for the clinical and cellular results of diminished polymerization? Ann N Y Acad Sci 445 1985 37 44 (Pubitemid 15246508)
-
(1985)
Annals of the New York Academy of Sciences
, vol.445
, pp. 37-44
-
-
Embury, S.H.1
-
21
-
-
0026631318
-
Hydroxyurea: Effects on hemoglobin F production in patients with sickle cell anemia
-
S. Charache, G.J. Dover, R.D. Moore, S. Eckert, S.K. Ballas, and M. Koshy Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia Blood 79 1992 2555 2565
-
(1992)
Blood
, vol.79
, pp. 2555-2565
-
-
Charache, S.1
Dover, G.J.2
Moore, R.D.3
Eckert, S.4
Ballas, S.K.5
Koshy, M.6
-
22
-
-
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
-
S. Charache, M.L. Terrin, R.D. Moore, G.J. Dover, F.B. Barton, and S.V. Eckert 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 332 1995 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
-
23
-
-
54849433162
-
The presence of alpha-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell disease
-
N. Vasavda, S. Badiger, D. Rees, S. Height, J. Howard, and S.L. Thein The presence of alpha-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell disease Br J Haematol 143 2008 589 592
-
(2008)
Br J Haematol
, vol.143
, pp. 589-592
-
-
Vasavda, N.1
Badiger, S.2
Rees, D.3
Height, S.4
Howard, J.5
Thein, S.L.6
-
24
-
-
0026774086
-
Red blood cell changes during the evolution of the sickle cell painful crisis
-
S.K. Ballas, and E.D. Smith Red blood cell changes during the evolution of the sickle cell painful crisis Blood 79 1992 2154 2163
-
(1992)
Blood
, vol.79
, pp. 2154-2163
-
-
Ballas, S.K.1
Smith, E.D.2
-
25
-
-
0014558319
-
Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease
-
C.L. Neely, T. Wajima, A.P. Kraus, L.W. Diggs, and L. Barreras Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease Am J Clin Pathol 52 1969 167 169
-
(1969)
Am J Clin Pathol
, vol.52
, pp. 167-169
-
-
Neely, C.L.1
Wajima, T.2
Kraus, A.P.3
Diggs, L.W.4
Barreras, L.5
-
26
-
-
33644775612
-
Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease
-
DOI 10.1182/blood-2005-06-2373
-
G.J. Kato, V. McGowan, R.F. Machado, J.A. Little, J.T. Taylor, and C.R. Morris 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 107 2006 2279 2285 (Pubitemid 43345545)
-
(2006)
Blood
, vol.107
, Issue.6
, pp. 2279-2285
-
-
Kato, G.J.1
McGowan, V.2
Machado, R.F.3
Little, J.A.4
Taylor VI, J.5
Morris, C.R.6
Nichols, J.S.7
Wang, X.8
Poljakovic, M.9
Morris Jr., S.M.10
Gladwin, M.T.11
-
27
-
-
0025969263
-
Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells
-
S.K. Ballas Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells Am J Hematol 36 1991 122 130
-
(1991)
Am J Hematol
, vol.36
, pp. 122-130
-
-
Ballas, S.K.1
-
28
-
-
4143132048
-
Are there clinical phenotypes of homozygous sickle cell disease?
-
DOI 10.1111/j.1365-2141.2004.05025.x
-
N. Alexander, D. Higgs, G. Dover, and G.R. Serjeant Are there clinical phenotypes of homozygous sickle cell disease? Br J Haematol 126 2004 606 611 (Pubitemid 39093105)
-
(2004)
British Journal of Haematology
, vol.126
, Issue.4
, pp. 606-611
-
-
Alexander, N.1
Higgs, D.2
Dover, G.3
Serjeant, G.R.4
-
29
-
-
33750683974
-
GTP cyclohydrolase and tetrahydrobiopterin regulate pain sensitivity and persistence
-
DOI 10.1038/nm1490, PII NM1490
-
I. Tegeder, M. Costigan, R.S. Griffin, A. Abele, I. Belfer, and H. Schmidt GTP cyclohydrolase and tetrahydrobiopterin regulate pain sensitivity and persistence Nat Med 12 2006 1269 1277 (Pubitemid 44706929)
-
(2006)
Nature Medicine
, vol.12
, Issue.11
, pp. 1269-1277
-
-
Tegeder, I.1
Costigan, M.2
Griffin, R.S.3
Abele, A.4
Belfer, I.5
Schmidt, H.6
Ehnert, C.7
Nejim, J.8
Marian, C.9
Scholz, J.10
Wu, T.11
Allchorne, A.12
Diatchenko, L.13
Binshtok, A.M.14
Goldman, D.15
Adolph, J.16
Sama, S.17
Atlas, S.J.18
Carlezon, W.A.19
Parsegian, A.20
Lotsch, J.21
Fillingim, R.B.22
Maixner, W.23
Geisslinger, G.24
Max, M.B.25
Woolf, C.J.26
more..
-
30
-
-
0029618383
-
Design of the multicenter study of hydroxyurea in sickle cell anemia
-
DOI 10.1016/S0197-2456(95)00098-4
-
S. Charache, M.L. Terrin, R.D. Moore, G.J. Dover, R.P. McMahon, and F.B. Barton Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea Control Clin Trials 16 1995 432 446 (Pubitemid 26035810)
-
(1995)
Controlled Clinical Trials
, vol.16
, Issue.6
, pp. 432-446
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
Dover, G.J.4
McMahon, R.P.5
Barton, F.B.6
Waclawiw, M.7
Eckert, S.V.8
|