-
1
-
-
0036842466
-
Home management of pain in sickle cell disease: A daily diary study in children and adolescents
-
C. Dampier, E. Ely, D. Brodecki, and P. O'Neal, "Home management of pain in sickle cell disease: a daily diary study in children and adolescents, " Journal of PediatricHematology/Oncology, vol. 24, no. 8, pp. 643-647, 2002.
-
(2002)
Journal of PediatricHematology/Oncology
, vol.24
, Issue.8
, pp. 643-647
-
-
Dampier, C.1
Ely, E.2
Brodecki, D.3
O'Neal, P.4
-
2
-
-
0036905062
-
Characteristics of painmanaged at home in children and adolescents with sickle cell disease by using diary self-reports
-
C. Dampier, B. Ely, D. Brodecki, and P. O'Neal, "Characteristics of painmanaged at home in children and adolescents with sickle cell disease by using diary self-reports, " Journal of Pain, vol. 3, no. 6, pp. 461-470, 2002.
-
(2002)
Journal of Pain
, vol.3
, Issue.6
, pp. 461-470
-
-
Dampier, C.1
Ely, B.2
Brodecki, D.3
O'Neal, P.4
-
3
-
-
0025770390
-
Pain insickle cell disease. Rates and risk factors
-
O. S. Platt, B. D. Thorington, D. J. Brambilla et al., "Pain insickle cell disease. Rates and risk factors, "The New England Journal of Medicine, vol. 325, no. 1, pp. 11-16, 1991.
-
(1991)
The New England Journal of Medicine
, vol.325
, Issue.1
, pp. 11-16
-
-
Platt, O.S.1
Thorington, B.D.2
Brambilla, D.J.3
-
4
-
-
11144279969
-
Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease
-
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, " Pediatric Blood and Cancer, vol. 44, no. 2, pp. 182-186, 2005.
-
(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
-
5
-
-
45549086734
-
Retrospective evaluation of pain assessment and treatment for acute vasoocclusive episodes in children with sickle cell disease
-
W. T. Zempsky, K. A. Loiselle, K. McKay et al., "Retrospective evaluation of pain assessment and treatment for acute vasoocclusive episodes in children with sickle cell disease, " Pediatric Blood and Cancer, vol. 51, no. 2, pp. 265-268, 2008.
-
(2008)
Pediatric Blood and Cancer
, vol.51
, Issue.2
, pp. 265-268
-
-
Zempsky, W.T.1
Loiselle, K.A.2
McKay, K.3
-
6
-
-
77950478131
-
Acute care utilization and rehospitalizations for sickle cell disease
-
D. C. Brousseau, P. L. Owens, A. L. Mosso, J. A. Panepinto, and C. A. Steiner, "Acute care utilization and rehospitalizations for sickle cell disease, " The Journal of the American Medical Association, vol. 303, no. 13, pp. 1288-1294, 2010.
-
(2010)
The Journal of the American Medical Association
, vol.303
, Issue.13
, pp. 1288-1294
-
-
Brousseau, D.C.1
Owens, P.L.2
Mosso, A.L.3
Panepinto, J.A.4
Steiner, C.A.5
-
7
-
-
77949434989
-
Administrative data sets and health services research on hemoglobinopathies. A review of the literature
-
S. D. Grosse, S. L. Boulet, D. D. Amendah, and S. O. Oyeku, "Administrative data sets and health services research on hemoglobinopathies. A review of the literature, " American Journal of Preventive Medicine, vol. 38, no. 4, pp. S557-S567, 2010.
-
(2010)
American Journal of Preventive Medicine
, vol.38
, Issue.4
, pp. S557-S567
-
-
Grosse, S.D.1
Boulet, S.L.2
Amendah, D.D.3
Oyeku, S.O.4
-
8
-
-
0023644113
-
Consensus conference. Newborn screening for sickle cell disease and other hemoglobinopathies
-
"Consensus conference. Newborn screening for sickle cell disease and other hemoglobinopathies, " The Journal of the American Medical Association, vol. 258, no. 9, pp. 1205-1209, 1987.
-
(1987)
The Journal of the American Medical Association
, vol.258
, Issue.9
, pp. 1205-1209
-
-
-
9
-
-
0022628893
-
Prophylaxis with oral penicillin in children with sickle cell anemia. Arandomized trial
-
M. H. Gaston, J. I. Verter, G. Woods et al., "Prophylaxis with oral penicillin in children with sickle cell anemia. Arandomized trial, " New England Journal of Medicine, vol. 314, no. 25, pp. 1593-1599, 1986.
-
(1986)
New England Journal of Medicine
, vol.314
, Issue.25
, pp. 1593-1599
-
-
Gaston, M.H.1
Verter, J.I.2
Woods, G.3
-
10
-
-
33746594094
-
Stroke Prevention Trial in Sickle Cell Anemia (STOP): Extended follow-up and final results
-
M. T. Lee, S. Piomelli, S. Granger et al., "Stroke Prevention Trial in Sickle Cell Anemia (STOP): extended follow-up and final results, " Blood, vol. 108, no. 3, pp. 847-852, 2006.
-
(2006)
Blood
, vol.108
, Issue.3
, pp. 847-852
-
-
Lee, M.T.1
Piomelli, S.2
Granger, S.3
-
11
-
-
79955909191
-
Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG)
-
W. C. Wang, R. E. Ware, S. T. Miller et al., "Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG), " The Lancet, vol. 377, no. 9778, pp. 1663-1672, 2011.
-
(2011)
The Lancet
, vol.377
, Issue.9778
, pp. 1663-1672
-
-
Wang, W.C.1
Ware, R.E.2
Miller, S.T.3
-
12
-
-
0037414164
-
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Risks and benefits up to 9 years of treatment
-
M. H. Steinberg, F. Barton, O. Castro et al., "Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment, " Journal of the American Medical Association, vol. 289, no. 13, pp. 1645-1651, 2003.
-
(2003)
Journal of the American Medical Association
, vol.289
, Issue.13
, pp. 1645-1651
-
-
Steinberg, M.H.1
Barton, F.2
Castro, O.3
-
13
-
-
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 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, "The New England Journal ofMedicine, vol. 332, no. 20, pp. 1317-1322, 1995.
-
(1995)
The New England Journal OfMedicine
, vol.332
, Issue.20
, pp. 1317-1322
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
-
14
-
-
84957891583
-
Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD with Transfusions Changing to Hydroxyurea (TWiTCH): A multicentre, open-label, phase 3 non-inferiority trial
-
10019
-
R. E. Ware, B. R. Davis, W. H. Schultz et al., "Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD with Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial, " The Lancet, vol. 387, no. 10019, pp. 661-670, 2016.
-
(2016)
The Lancet
, vol.387
, pp. 661-670
-
-
Ware, R.E.1
Davis, B.R.2
Schultz, W.H.3
-
15
-
-
0030745927
-
National trends in the mortality of children with sickle cell disease, 1968 through 1992
-
H. Davis, K. C. Schoendorf, P. J. Gergen, and R. M. Moore Jr., "National trends in the mortality of children with sickle cell disease, 1968 through 1992, " American Journal of Public Health, vol. 87, no. 8, pp. 1317-1322, 1997.
-
(1997)
American Journal of Public Health
, vol.87
, Issue.8
, pp. 1317-1322
-
-
Davis, H.1
Schoendorf, K.C.2
Gergen, P.J.3
Moore, R.M.4
-
16
-
-
0014963910
-
Health care priority and sickle cell anemia
-
R. B. Scott, "Health care priority and sickle cell anemia, " JAMA, vol. 214, no. 4, pp. 731-734, 1970.
-
(1970)
JAMA
, vol.214
, Issue.4
, pp. 731-734
-
-
Scott, R.B.1
-
17
-
-
0028291736
-
Mortality in sickle cell disease. Life expectancy and risk factors for early death
-
O. S. Platt, D. J. Brambilla, W. F. Rosse et al., "Mortality in sickle cell disease. Life expectancy and risk factors for early death, " NewEngland Journal ofMedicine, vol. 330, no. 23, pp. 1639-1644, 1994.
-
(1994)
NewEngland Journal OfMedicine
, vol.330
, Issue.23
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
-
18
-
-
84876435847
-
Mortality rates and age at death from sickle cell disease: U. S., 1979-2005
-
S. Lanzkron, C. Patrick Carroll, and C. Haywood Jr., "Mortality rates and age at death from sickle cell disease: U. S., 1979-2005, " Public Health Reports, vol. 128, no. 2, pp. 110-116, 2013.
-
(2013)
Public Health Reports
, vol.128
, Issue.2
, pp. 110-116
-
-
Lanzkron, S.1
Patrick Carroll, C.2
Haywood, C.3
-
19
-
-
33750600143
-
Circumstances of death in adult sickle cell disease patients
-
D. S. Darbari, P. Kple-Faget, J. Kwagyan, S. Rana, V. R. Gordeuk, and O. Castro, "Circumstances of death in adult sickle cell disease patients, " American Journal of Hematology, vol. 81, no. 11, pp. 858-863, 2006.
-
(2006)
American Journal of Hematology
, vol.81
, Issue.11
, pp. 858-863
-
-
Darbari, D.S.1
Kple-Faget, P.2
Kwagyan, J.3
Rana, S.4
Gordeuk, V.R.5
Castro, O.6
-
20
-
-
84892430495
-
Severe painful vasoocclusive crises and mortality in a contemporary adult sickle cell anemia cohort study
-
D. S. Darbari, Z. Wang, M. Kwak et al., "Severe painful vasoocclusive crises and mortality in a contemporary adult sickle cell anemia cohort study, " PLoS ONE, vol. 8, no. 11, Article ID e79923, 2013.
-
(2013)
PLoS ONE
, vol.8
, Issue.11
-
-
Darbari, D.S.1
Wang, Z.2
Kwak, M.3
-
21
-
-
84907016412
-
Management of sickle cell disease: Summary of the 2014 evidencebased report by expert panel members
-
B. P. Yawn, G. R. Buchanan, A. N. Afenyi-Annan et al., "Management of sickle cell disease: summary of the 2014 evidencebased report by expert panel members, " JAMA, vol. 312, no. 10, pp. 1033-1048, 2014.
-
(2014)
JAMA
, vol.312
, Issue.10
, pp. 1033-1048
-
-
Yawn, B.P.1
Buchanan, G.R.2
Afenyi-Annan, A.N.3
-
22
-
-
84975257632
-
Recent treatment guidelines for managing adult patients with sickle cell disease: Challenges in access to care, social issues, and adherence
-
P. Adams-Graves and L. Bronte-Jordan, "Recent treatment guidelines for managing adult patients with sickle cell disease: challenges in access to care, social issues, and adherence, " Expert Review of Hematology, vol. 9, no. 6, pp. 541-552, 2016.
-
(2016)
Expert Review of Hematology
, vol.9
, Issue.6
, pp. 541-552
-
-
Adams-Graves, P.1
Bronte-Jordan, L.2
-
23
-
-
78851469729
-
Health-related quality of life in adults with sickle cell disease (SCD): A report from the comprehensive sickle cell centers clinical trial consortium
-
C. Dampier, P. LeBeau, S. Rhee et al., "Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium, " American Journal of Hematology, vol. 86, no. 2, pp. 203-205, 2011.
-
(2011)
American Journal of Hematology
, vol.86
, Issue.2
, pp. 203-205
-
-
Dampier, C.1
LeBeau, P.2
Rhee, S.3
-
24
-
-
78650383011
-
Transition from pediatric to adult care in sickle cell disease: Establishing evidence-based practice and directions for research
-
M. Treadwell, J. Telfair, R. W. Gibson, S. Johnson, and I. Osunkwo, "Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research, " American Journal of Hematology, vol. 86, no. 1, pp. 116-120, 2011.
-
(2011)
American Journal of Hematology
, vol.86
, Issue.1
, pp. 116-120
-
-
Treadwell, M.1
Telfair, J.2
Gibson, R.W.3
Johnson, S.4
Osunkwo, I.5
-
25
-
-
84989282834
-
Self-efficacy and readiness for transition from pediatric to adult care in sickle cell disease
-
M. Treadwell, S. Johnson, I. Sisler et al., "Self-efficacy and readiness for transition from pediatric to adult care in sickle cell disease, " International Journal of Adolescent Medicine and Health, vol. 28, no. 4, pp. 381-388, 2016.
-
(2016)
International Journal of Adolescent Medicine and Health
, vol.28
, Issue.4
, pp. 381-388
-
-
Treadwell, M.1
Johnson, S.2
Sisler, I.3
-
26
-
-
84969530854
-
Development of a sickle cell disease readiness for transition assessment
-
M. Treadwell, S. Johnson, I. Sisler et al., "Development of a sickle cell disease readiness for transition assessment, " International Journal ofAdolescentMedicine andHealth, vol. 28, no. 2, pp. 193-201, 2016.
-
(2016)
International Journal OfAdolescentMedicine AndHealth
, vol.28
, Issue.2
, pp. 193-201
-
-
Treadwell, M.1
Johnson, S.2
Sisler, I.3
-
27
-
-
84868624911
-
Transition and sickle cell disease
-
M. R. DeBaun and J. Telfair, "Transition and sickle cell disease, " Pediatrics, vol. 130, no. 5, pp. 926-935, 2012.
-
(2012)
Pediatrics
, vol.130
, Issue.5
, pp. 926-935
-
-
DeBaun, M.R.1
Telfair, J.2
-
28
-
-
84945957913
-
Transitioning adolescents and young adults with sickle cell disease from pediatric to adult health care: Provider perspectives
-
N. B. Stollon, C. W. Paine, M. S. Lucas et al., "Transitioning adolescents and young adults with sickle cell disease from pediatric to adult health care: provider perspectives, " Journal of Pediatric Hematology/Oncology, vol. 37, no. 8, pp. 577-583, 2015.
-
(2015)
Journal of Pediatric Hematology/Oncology
, vol.37
, Issue.8
, pp. 577-583
-
-
Stollon, N.B.1
Paine, C.W.2
Lucas, M.S.3
-
29
-
-
80052883018
-
When children with sickle-cell disease become adults: Lack of outpatient care leads to increased use of the emergency department
-
B. G. Hemker, D. C. Brousseau, K. Yan, R. G. Hoffmann, and J. A. Panepinto, "When children with sickle-cell disease become adults: lack of outpatient care leads to increased use of the emergency department, " American Journal of Hematology, vol. 86, no. 10, pp. 863-865, 2011.
-
(2011)
American Journal of Hematology
, vol.86
, Issue.10
, pp. 863-865
-
-
Hemker, B.G.1
Brousseau, D.C.2
Yan, K.3
Hoffmann, R.G.4
Panepinto, J.A.5
-
30
-
-
84857808941
-
Young adults with SCD in US children's hospitals: Are they different fromadolescents?
-
A. K. Dickerson, J. Klima, M. M. Rhodes, and S. H. O'Brien, "Young adults with SCD in US children's hospitals: are they different fromadolescents?" Pediatric Blood and Cancer, vol. 58, no. 5, pp. 741-745, 2012.
-
(2012)
Pediatric Blood and Cancer
, vol.58
, Issue.5
, pp. 741-745
-
-
Dickerson, A.K.1
Klima, J.2
Rhodes, M.M.3
O'Brien, S.H.4
-
31
-
-
84943580591
-
Age-related emergency department reliance in patients with sickle cell disease
-
M. A. Blinder, M. S. Duh, M. Sasane, A. Trahey, C. Paley, and F. Vekeman, "Age-related emergency department reliance in patients with sickle cell disease, " Journal of EmergencyMedicine, vol. 49, no. 4, pp. 513-522. e1, 2015.
-
(2015)
Journal of EmergencyMedicine
, vol.49
, Issue.4
, pp. 513-522e1
-
-
Blinder, M.A.1
Duh, M.S.2
Sasane, M.3
Trahey, A.4
Paley, C.5
Vekeman, F.6
-
32
-
-
84975029023
-
Improving sickle cell transitions of care through health information technology
-
J. R. Frost, R. K. Cherry, S. O. Oyeku et al., "Improving sickle cell transitions of care through health information technology, " American Journal of Preventive Medicine, vol. 51, supplement 1, pp. S17-S23, 2016.
-
(2016)
American Journal of Preventive Medicine
, vol.51
, pp. S17-S23
-
-
Frost, J.R.1
Cherry, R.K.2
Oyeku, S.O.3
-
33
-
-
84992578444
-
Young adult perspectives on a successful transition from pediatric to adult care in sickle cell disease
-
A. E. Sobota, E. Umeh, and J. W. Mack, "Young adult perspectives on a successful transition from pediatric to adult care in sickle cell disease, " Journal of Hematology Research, vol. 2, no. 1, pp. 17-24, 2015.
-
(2015)
Journal of Hematology Research
, vol.2
, Issue.1
, pp. 17-24
-
-
Sobota, A.E.1
Umeh, E.2
Mack, J.W.3
-
34
-
-
84936928610
-
A biopsychosocial model for the management of patients with sicklecell disease transitioning to adult medical care
-
L. E. Crosby, C. T. Quinn, and K. A. Kalinyak, "A biopsychosocial model for the management of patients with sicklecell disease transitioning to adult medical care, " Advances in Therapy, vol. 32, no. 4, pp. 293-305, 2015.
-
(2015)
Advances in Therapy
, vol.32
, Issue.4
, pp. 293-305
-
-
Crosby, L.E.1
Quinn, C.T.2
Kalinyak, K.A.3
-
35
-
-
85002213611
-
Exploring transition to self-management within the culture of sickle cell disease
-
N. Labore, B. Mawn, J. Dixon, and B. Andemariam, "Exploring transition to self-management within the culture of sickle cell disease, " Journal of Transcultural Nursing, vol. 28, no. 1, pp. 70-78, 2017.
-
(2017)
Journal of Transcultural Nursing
, vol.28
, Issue.1
, pp. 70-78
-
-
Labore, N.1
Mawn, B.2
Dixon, J.3
Andemariam, B.4
-
36
-
-
84973503084
-
Applicability of the SMARTmodel of transition readiness for sickle-cell disease
-
S. S. Mulchan, J. M. Valenzuela, L. E. Crosby, and C. Diaz Pow Sang, "Applicability of the SMARTmodel of transition readiness for sickle-cell disease, " Journal of Pediatric Psychology, vol. 41, no. 5, pp. 543-554, 2016.
-
(2016)
Journal of Pediatric Psychology
, vol.41
, Issue.5
, pp. 543-554
-
-
Mulchan, S.S.1
Valenzuela, J.M.2
Crosby, L.E.3
Diaz Pow Sang, C.4
-
37
-
-
84944449854
-
APHON/ASPHOpolicy statement for the transition of patients with sickle cell disease from pediatric to adult health care
-
R. Bryant, J. S. Porter, and A. Sobota, "APHON/ASPHOpolicy statement for the transition of patients with sickle cell disease from pediatric to adult health care, " Journal of Pediatric Oncology Nursing, vol. 32, no. 6, pp. 355-359, 2015.
-
(2015)
Journal of Pediatric Oncology Nursing
, vol.32
, Issue.6
, pp. 355-359
-
-
Bryant, R.1
Porter, J.S.2
Sobota, A.3
-
38
-
-
0024847804
-
Sickle cell disease pain: Relation of coping strategies to adjustment
-
K. M. Gil, M. R. Abrams, G. Phillips, and F. J. Keefe, "Sickle cell disease pain: relation of coping strategies to adjustment, " Journal of Consulting and Clinical Psychology, vol. 57, no. 6, pp. 725-731, 1989.
-
(1989)
Journal of Consulting and Clinical Psychology
, vol.57
, Issue.6
, pp. 725-731
-
-
Gil, K.M.1
Abrams, M.R.2
Phillips, G.3
Keefe, F.J.4
-
39
-
-
0030828947
-
Psychosocial determinants of health care utilization in sickle cell disease patients
-
F. L. Reese and W. R. Smith, "Psychosocial determinants of health care utilization in sickle cell disease patients, " Annals of Behavioral Medicine, vol. 19, no. 2, pp. 171-178, 1997.
-
(1997)
Annals of Behavioral Medicine
, vol.19
, Issue.2
, pp. 171-178
-
-
Reese, F.L.1
Smith, W.R.2
-
40
-
-
13444252435
-
Understanding pain and improving management of sickle cell disease: The PiSCES study
-
W. R. Smith, V. E. Bovbjerg, L. T. Penberthy et al., "Understanding pain and improving management of sickle cell disease: The PiSCES study, " Journal of the National Medical Association, vol. 97, no. 2, pp. 183-193, 2005.
-
(2005)
Journal of the National Medical Association
, vol.97
, Issue.2
, pp. 183-193
-
-
Smith, W.R.1
Bovbjerg, V.E.2
Penberthy, L.T.3
-
41
-
-
38749109710
-
Daily assessment of pain in adults with sickle cell disease
-
W. R. Smith, L. T. Penberthy, V. E. Bovbjerg et al., "Daily assessment of pain in adults with sickle cell disease, " Annals of Internal Medicine, vol. 148, no. 2, pp. 94-101, 2008.
-
(2008)
Annals of Internal Medicine
, vol.148
, Issue.2
, pp. 94-101
-
-
Smith, W.R.1
Penberthy, L.T.2
Bovbjerg, V.E.3
-
42
-
-
0020575984
-
The use of coping strategies in chronic low back pain patients: Relationship to patient characteristics and current adjustment
-
A. K. Rosenstiel and F. J. Keefe, "The use of coping strategies in chronic low back pain patients: relationship to patient characteristics and current adjustment, " Pain, vol. 17, no. 1, pp. 33-44, 1983.
-
(1983)
Pain
, vol.17
, Issue.1
, pp. 33-44
-
-
Rosenstiel, A.K.1
Keefe, F.J.2
-
43
-
-
0036727446
-
Sickle cell disease: Pain, coping and quality of life in a study of adults in the UK
-
K. A. Anie, A. Steptoe, and D. H. Bevan, "Sickle cell disease: pain, coping and quality of life in a study of adults in the UK, " British Journal of Health Psychology, vol. 7, no. 3, pp. 331-344, 2002.
-
(2002)
British Journal of Health Psychology
, vol.7
, Issue.3
, pp. 331-344
-
-
Anie, K.A.1
Steptoe, A.2
Bevan, D.H.3
-
44
-
-
0026877917
-
The MOS 36-item shortform health survey (Sf-36). I. Conceptual framework and item selection
-
J. E. Ware and C. D. Sherbourne, "The MOS 36-item shortform health survey (Sf-36). I. conceptual framework and item selection, " Medical Care, vol. 30, no. 6, pp. 473-483, 1992.
-
(1992)
Medical Care
, vol.30
, Issue.6
, pp. 473-483
-
-
Ware, J.E.1
Sherbourne, C.D.2
-
45
-
-
0024042879
-
The MOS shortform general health survey. Reliability and validity in a patient population
-
A. L. Stewart, R. D. Hays, and J. E. Ware Jr., "The MOS shortform general health survey. Reliability and validity in a patient population, " Medical Care, vol. 26, no. 7, pp. 724-735, 1988.
-
(1988)
Medical Care
, vol.26
, Issue.7
, pp. 724-735
-
-
Stewart, A.L.1
Hays, R.D.2
Ware, J.E.3
-
46
-
-
2142698685
-
Comparison of the redundancy, reliability, and responsiveness to change among SF-36
-
Oswestry disability index, andmultidimensional pain inventory
-
H. Wittink, D. C. Turk, D. B. Carr, A. Sukiennik, and W. Rogers, "Comparison of the redundancy, reliability, and responsiveness to change among SF-36, Oswestry disability index, andmultidimensional pain inventory, " Clinical Journal of Pain, vol. 20, no. 3, pp. 133-142, 2004.
-
(2004)
Clinical Journal of Pain
, vol.20
, Issue.3
, pp. 133-142
-
-
Wittink, H.1
Turk, D.C.2
Carr, D.B.3
Sukiennik, A.4
Rogers, W.5
-
47
-
-
27344441977
-
Health related quality of life in sickle cell patients: The PiSCES project
-
D. K. McClish, L. T. Penberthy, V. E. Bovbjerg et al., "Health related quality of life in sickle cell patients: the PiSCES project, " Health and Quality of Life Outcomes, vol. 3, article 50, 2005.
-
(2005)
Health and Quality of Life Outcomes
, vol.3
-
-
McClish, D.K.1
Penberthy, L.T.2
Bovbjerg, V.E.3
-
48
-
-
84987485548
-
Dimensions of social support in the MSPSS: Factorial structure, reliability, and theoretical implications
-
S. S. Kazarian and S. B. McCabe, "Dimensions of social support in the MSPSS: factorial structure, reliability, and theoretical implications, " Journal of Community Psychology, vol. 19, no. 2, pp. 150-160, 1991.
-
(1991)
Journal of Community Psychology
, vol.19
, Issue.2
, pp. 150-160
-
-
Kazarian, S.S.1
McCabe, S.B.2
-
49
-
-
0025792301
-
Themultidimensional scale of perceived social support: A confirmation study
-
N. W. Dahlem, G. D. Zimet, and R. R. Walker, "Themultidimensional scale of perceived social support: a confirmation study, " Journal of Clinical Psychology, vol. 47, no. 6, pp. 756-761, 1991.
-
(1991)
Journal of Clinical Psychology
, vol.47
, Issue.6
, pp. 756-761
-
-
Dahlem, N.W.1
Zimet, G.D.2
Walker, R.R.3
-
50
-
-
0033544340
-
Validation and utility of a self-report version of PRIME-MD: The PHQPrimary Care Study
-
R. L. Spitzer, K. Kroenke, and J. B. W. Williams, "Validation and utility of a self-report version of PRIME-MD: The PHQPrimary Care Study, " Journal of the American Medical Association, vol. 282, no. 18, pp. 1737-1744, 1999.
-
(1999)
Journal of the American Medical Association
, vol.282
, Issue.18
, pp. 1737-1744
-
-
Spitzer, R.L.1
Kroenke, K.2
Williams, J.B.W.3
-
51
-
-
39149083377
-
Depression and anxiety in adults with sickle cell disease: The PiSCES project
-
J. L. Levenson, D. K. McClish, B. A. Dahman et al., "Depression and anxiety in adults with sickle cell disease: the PiSCES project, " Psychosomatic Medicine, vol. 70, no. 2, pp. 192-196, 2008.
-
(2008)
Psychosomatic Medicine
, vol.70
, Issue.2
, pp. 192-196
-
-
Levenson, J.L.1
McClish, D.K.2
Dahman, B.A.3
-
52
-
-
34548859568
-
Alcohol abuse in sickle cell disease: The Pisces project
-
J. L. Levenson, D. K. McClish, B. A. Dahman et al., "Alcohol abuse in sickle cell disease: The Pisces project, " American Journal on Addictions, vol. 16, no. 5, pp. 383-388, 2007.
-
(2007)
American Journal on Addictions
, vol.16
, Issue.5
, pp. 383-388
-
-
Levenson, J.L.1
McClish, D.K.2
Dahman, B.A.3
-
53
-
-
77954620459
-
The Patient Health Questionnaire somatic, anxiety, and depressive symptom scales: A systematic review
-
K. Kroenke, R. L. Spitzer, J. B. W. Williams, and B. Löwe, "The Patient Health Questionnaire somatic, anxiety, and depressive symptom scales: a systematic review, " General Hospital Psychiatry, vol. 32, no. 4, pp. 345-359, 2010.
-
(2010)
General Hospital Psychiatry
, vol.32
, Issue.4
, pp. 345-359
-
-
Kroenke, K.1
Spitzer, R.L.2
Williams, J.B.W.3
Löwe, B.4
-
54
-
-
80052894208
-
Somatic symptom burden in adults with sickle cell disease predicts pain, depression, anxiety, health care utilization, and quality of life: The PiSCES Project
-
A. Sogutlu, J. L. Levenson, D. K. McClish, S. D. Rosef, and W. R. Smith, "Somatic symptom burden in adults with sickle cell disease predicts pain, depression, anxiety, health care utilization, and quality of life: the PiSCES Project, " Psychosomatics, vol. 52, no. 3, pp. 272-279, 2011.
-
(2011)
Psychosomatics
, vol.52
, Issue.3
, pp. 272-279
-
-
Sogutlu, A.1
Levenson, J.L.2
McClish, D.K.3
Rosef, S.D.4
Smith, W.R.5
-
55
-
-
0029618383
-
Design of the multicenter study of hydroxyurea in sickle cell anemia
-
S. Charache, M. L. Terrin, R. D. Moore et al., "Design of the multicenter study of hydroxyurea in sickle cell anemia, " Controlled Clinical Trials, vol. 16, no. 6, pp. 432-446, 1995.
-
(1995)
Controlled Clinical Trials
, vol.16
, Issue.6
, pp. 432-446
-
-
Charache, S.1
Terrin, M.L.2
Moore, R.D.3
-
56
-
-
69049109697
-
Pain site frequency and location in sickle cell disease: The PiSCES project
-
D. K. McClish, W. R. Smith, B. A. Dahman et al., "Pain site frequency and location in sickle cell disease: The PiSCES project, " Pain, vol. 145, no. 1-2, pp. 246-251, 2009.
-
(2009)
Pain
, vol.145
, Issue.1-2
, pp. 246-251
-
-
McClish, D.K.1
Smith, W.R.2
Dahman, B.A.3
-
57
-
-
74049106223
-
Emergency department reliance: A discriminatory measure of frequent emergency department users
-
E. L. Kroner, R. G. Hoffmann, and D. C. Brousseau, "Emergency department reliance: a discriminatory measure of frequent emergency department users, " Pediatrics, vol. 125, no. 1, pp. 133-138, 2010.
-
(2010)
Pediatrics
, vol.125
, Issue.1
, pp. 133-138
-
-
Kroner, E.L.1
Hoffmann, R.G.2
Brousseau, D.C.3
-
58
-
-
75149198597
-
Pain, coping and health care utilization in younger and older adults with sickle cell disease
-
K. A. Sanders, S. M. Labott, R. Molokie, S. R. Shelby, and J. Desimone, "Pain, coping and health care utilization in younger and older adults with sickle cell disease, " Journal of Health Psychology, vol. 15, no. 1, pp. 131-137, 2010.
-
(2010)
Journal of Health Psychology
, vol.15
, Issue.1
, pp. 131-137
-
-
Sanders, K.A.1
Labott, S.M.2
Molokie, R.3
Shelby, S.R.4
Desimone, J.5
-
59
-
-
85018627213
-
SCD in Saudi children, teens and adults: A study in health related quality of life
-
A. E. Ahmed, A. S. Alaskar, D. K. McClish et al., "SCD in Saudi children, teens and adults: a study in health related quality of life, " Journal of Blood Disorders, vol. 3, no. 1, article 1036, 2016.
-
(2016)
Journal of Blood Disorders
, vol.3
, Issue.1
-
-
Ahmed, A.E.1
Alaskar, A.S.2
McClish, D.K.3
-
60
-
-
2542607703
-
The older sickle cell patient
-
T. D. H. McKerrell, H. W. Cohen, and H. H. Billett, "The older sickle cell patient, " American Journal of Hematology, vol. 76, no. 2, pp. 101-106, 2004.
-
(2004)
American Journal of Hematology
, vol.76
, Issue.2
, pp. 101-106
-
-
McKerrell, T.D.H.1
Cohen, H.W.2
Billett, H.H.3
-
61
-
-
36249019018
-
The role of catastrophizing in sickle cell disease: The PiSCES project
-
V. D. A. Citero, J. L. Levenson, D. K. McClish et al., "The role of catastrophizing in sickle cell disease: the PiSCES project, " Pain, vol. 133, no. 1-3, pp. 39-46, 2007.
-
(2007)
Pain
, vol.133
, Issue.1-3
, pp. 39-46
-
-
Citero, V.D.A.1
Levenson, J.L.2
McClish, D.K.3
-
62
-
-
33645643438
-
Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES project
-
D. K. McClish, J. L. Levenson, L. T. Penberthy et al., "Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES project, " Journal ofWomen's Health, vol. 15, no. 2, pp. 146-154, 2006.
-
(2006)
Journal OfWomen's Health
, vol.15
, Issue.2
, pp. 146-154
-
-
McClish, D.K.1
Levenson, J.L.2
Penberthy, L.T.3
-
63
-
-
77955486134
-
Health-related quality of life in children with sickle cell disease: A report from the comprehensive sickle cell centers clinical trial consortium
-
C. Dampier, S. Lieff, P. LeBeau et al., "Health-related quality of life in children with sickle cell disease: a report from the comprehensive sickle cell centers clinical trial consortium, " Pediatric Blood and Cancer, vol. 55, no. 3, pp. 485-494, 2010.
-
(2010)
Pediatric Blood and Cancer
, vol.55
, Issue.3
, pp. 485-494
-
-
Dampier, C.1
Lieff, S.2
LeBeau, P.3
-
64
-
-
33750003950
-
Hydroxyurea and sickle cell anemia: Effect on quality of life
-
S. K. Ballas, F. B. Barton, M. A. Waclawiw et al., "Hydroxyurea and sickle cell anemia: effect on quality of life, " Health and Quality of Life Outcomes, vol. 4, article 59, 2006.
-
(2006)
Health and Quality of Life Outcomes
, vol.4
-
-
Ballas, S.K.1
Barton, F.B.2
Waclawiw, M.A.3
-
65
-
-
84966570649
-
The measure of sickle cell stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust Study
-
S. M. Bediako, S. Lanzkron, M. Diener-West, G. Onojobi, M. C. Beach, and C. Haywood, "The measure of sickle cell stigma: initial findings from the Improving Patient Outcomes through Respect and Trust Study, " Journal of Health Psychology, vol. 21, no. 5, pp. 808-820, 2014.
-
(2014)
Journal of Health Psychology
, vol.21
, Issue.5
, pp. 808-820
-
-
Bediako, S.M.1
Lanzkron, S.2
Diener-West, M.3
Onojobi, G.4
Beach, M.C.5
Haywood, C.6
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