176 related articles for article (PubMed ID: 11573035)
21. Psychological Predictors of Pain in Children and Adolescents With Sickle Cell Disease: A Scoping Review.
Donohoe C; Smith EL
J Pediatr Oncol Nurs; 2019; 36(2):150-159. PubMed ID: 30565483
[No Abstract] [Full Text] [Related]
22. Parent perspectives on pain management, coping, and family functioning in pediatric sickle cell disease.
Mitchell MJ; Lemanek K; Palermo TM; Crosby LE; Nichols A; Powers SW
Clin Pediatr (Phila); 2007 May; 46(4):311-9. PubMed ID: 17475988
[TBL] [Abstract][Full Text] [Related]
23. Psychological adjustment of children with sickle cell disease: stability and change over a 10-month period.
Thompson RJ; Gil KM; Keith BR; Gustafson KE; George LK; Kinney TR
J Consult Clin Psychol; 1994 Aug; 62(4):856-6. PubMed ID: 7962891
[TBL] [Abstract][Full Text] [Related]
24. Factors that influence adolescent adaptation to sickle cell disease.
Burlew K; Telfair J; Colangelo L; Wright EC
J Pediatr Psychol; 2000; 25(5):287-99. PubMed ID: 10880059
[TBL] [Abstract][Full Text] [Related]
25. Daily mood and stress predict pain, health care use, and work activity in African American adults with sickle-cell disease.
Gil KM; Carson JW; Porter LS; Scipio C; Bediako SM; Orringer E
Health Psychol; 2004 May; 23(3):267-74. PubMed ID: 15099167
[TBL] [Abstract][Full Text] [Related]
26. Predictors of coping with pain in mothers and their children with sickle cell syndrome.
Sharpe JN; Brown RT; Thompson NJ; Eckman J
J Am Acad Child Adolesc Psychiatry; 1994; 33(9):1246-55. PubMed ID: 7995790
[TBL] [Abstract][Full Text] [Related]
27. Sickle cell disease pain: relation of coping strategies to adjustment.
Gil KM; Abrams MR; Phillips G; Keefe FJ
J Consult Clin Psychol; 1989 Dec; 57(6):725-31. PubMed ID: 2600243
[TBL] [Abstract][Full Text] [Related]
28. Evaluation of a disease-specific self-efficacy instrument in adolescents with sickle cell disease and its relationship to adjustment.
Clay OJ; Telfair J
Child Neuropsychol; 2007 Mar; 13(2):188-203. PubMed ID: 17364574
[TBL] [Abstract][Full Text] [Related]
29. A family-based randomized controlled trial of pain intervention for adolescents with sickle cell disease.
Barakat LP; Schwartz LA; Salamon KS; Radcliffe J
J Pediatr Hematol Oncol; 2010 Oct; 32(7):540-7. PubMed ID: 20686425
[TBL] [Abstract][Full Text] [Related]
30. Appraisal and coping with vaso-occlusive crisis in adolescents with sickle cell disease.
Fletcher C
Pediatr Nurs; 2000; 26(3):319-24. PubMed ID: 12026399
[TBL] [Abstract][Full Text] [Related]
31. Increased Patient Activation Is Associated with Fewer Emergency Room Visits and Hospitalizations for Pain in Adults with Sickle Cell Disease.
Cronin RM; Dorner TL; Utrankar A; Allen W; Rodeghier M; Kassim AA; Jackson GP; DeBaun MR
Pain Med; 2019 Aug; 20(8):1464-1471. PubMed ID: 30329108
[TBL] [Abstract][Full Text] [Related]
32. The association of optimism and perceived discrimination with health care utilization in adults with sickle cell disease.
Stanton MV; Jonassaint CR; Bartholomew FB; Edwards C; Richman L; DeCastro L; Williams R
J Natl Med Assoc; 2010 Nov; 102(11):1056-63. PubMed ID: 21141295
[TBL] [Abstract][Full Text] [Related]
33. Self-efficacy and pain catastrophizing in systemic lupus erythematosus: relationship to pain, stiffness, fatigue, and psychological distress.
Somers TJ; Kurakula PC; Criscione-Schreiber L; Keefe FJ; Clowse ME
Arthritis Care Res (Hoboken); 2012 Sep; 64(9):1334-40. PubMed ID: 22505314
[TBL] [Abstract][Full Text] [Related]
34. Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease.
Haywood C; Diener-West M; Strouse J; Carroll CP; Bediako S; Lanzkron S; Haythornthwaite J; Onojobi G; Beach MC; ;
J Pain Symptom Manage; 2014 Nov; 48(5):934-43. PubMed ID: 24742787
[TBL] [Abstract][Full Text] [Related]
35. Sickle cell disease pain in children and adolescents: change in pain frequency and coping strategies over time.
Gil KM; Thompson RJ; Keith BR; Tota-Faucette M; Noll S; Kinney TR
J Pediatr Psychol; 1993 Oct; 18(5):621-37. PubMed ID: 8295083
[TBL] [Abstract][Full Text] [Related]
36. The role of catastrophizing in sickle cell disease--the PiSCES project.
Citero Vde A; Levenson JL; McClish DK; Bovbjerg VE; Cole PL; Dahman BA; Penberthy LT; Aisiku IP; Roseff SD; Smith WR
Pain; 2007 Dec; 133(1-3):39-46. PubMed ID: 17408858
[TBL] [Abstract][Full Text] [Related]
37. Coping and health service utilisation in a UK study of paediatric sickle cell pain.
Anie KA; Steptoe A; Ball S; Dick M; Smalling BM
Arch Dis Child; 2002 May; 86(5):325-9. PubMed ID: 11970920
[TBL] [Abstract][Full Text] [Related]
38. Adaptation and coping: a look at a sickle cell patient population over age 30--an integral phase of the life long developmental process.
Abrams MR; Phillips G; Whitworth E
J Health Soc Policy; 1994; 5(3-4):141-60. PubMed ID: 10138756
[TBL] [Abstract][Full Text] [Related]
39. Symptoms of depression and anxiety in adolescents with sickle cell disease: the role of intrapersonal characteristics and stress processing variables.
Simon K; Barakat LP; Patterson CA; Dampier C
Child Psychiatry Hum Dev; 2009 Jun; 40(2):317-30. PubMed ID: 19169810
[TBL] [Abstract][Full Text] [Related]
40. Parent Perspectives on Pain Management in Preschool-Age Children With Sickle Cell Disease.
Smith K; Reinman L; Schatz J; Roberts CW
J Pediatr Oncol Nurs; 2018; 35(1):16-24. PubMed ID: 29094643
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
