296 related articles for article (PubMed ID: 24300219)
21. Development, Content Validity, and User Review of a Web-based Multidimensional Pain Diary for Adolescent and Young Adults With Sickle Cell Disease.
Bakshi N; Stinson JN; Ross D; Lukombo I; Mittal N; Joshi SV; Belfer I; Krishnamurti L
Clin J Pain; 2015 Jun; 31(6):580-90. PubMed ID: 25565585
[TBL] [Abstract][Full Text] [Related]
22. Preliminary construct validity of patient-reported outcomes to assess chronic pain in adults with sickle cell disease.
Mucalo L; Field JJ; Highland J; Khan H; Hankins JS; Singh A; Brandow AM
Blood Adv; 2023 Jul; 7(14):3658-3665. PubMed ID: 37058480
[TBL] [Abstract][Full Text] [Related]
23. Adherence to hydroxyurea, health-related quality of life domains, and patients' perceptions of sickle cell disease and hydroxyurea: a cross-sectional study in adolescents and young adults.
Badawy SM; Thompson AA; Lai JS; Penedo FJ; Rychlik K; Liem RI
Health Qual Life Outcomes; 2017 Jul; 15(1):136. PubMed ID: 28679417
[TBL] [Abstract][Full Text] [Related]
24. Fatigue in Children With Sickle Cell Disease: Association With Neurocognitive and Social-Emotional Functioning and Quality of Life.
Anderson LM; Allen TM; Thornburg CD; Bonner MJ
J Pediatr Hematol Oncol; 2015 Nov; 37(8):584-9. PubMed ID: 26479993
[TBL] [Abstract][Full Text] [Related]
25. Living with sickle cell disease and depression in Lagos, Nigeria: A mixed methods study.
Ola BA; Yates SJ; Dyson SM
Soc Sci Med; 2016 Jul; 161():27-36. PubMed ID: 27239705
[TBL] [Abstract][Full Text] [Related]
26. Stigma and quality of life in adults with sickle cell disease in Jamaica and the United States.
Bulgin D; Asnani M; Vorderstrasse A; Royal C; Pan W; Tanabe P
Psychol Health Med; 2023 Jun; 28(5):1133-1147. PubMed ID: 34957879
[TBL] [Abstract][Full Text] [Related]
27. Keys to Recruiting and Retaining Seriously Ill African Americans With Sickle Cell Disease in Longitudinal Studies: Respectful Engagement and Persistence.
Suarez ML; Schlaeger JM; Angulo V; Shuey DA; Carrasco J; Roach KL; Ezenwa MO; Yao Y; Wang ZJ; Molokie RE; Wilkie DJ
Am J Hosp Palliat Care; 2020 Feb; 37(2):123-128. PubMed ID: 31394904
[TBL] [Abstract][Full Text] [Related]
28. Vaso-occlusive painful events in sickle cell disease: impact on child well-being.
Brandow AM; Brousseau DC; Pajewski NM; Panepinto JA
Pediatr Blood Cancer; 2010 Jan; 54(1):92-7. PubMed ID: 19653296
[TBL] [Abstract][Full Text] [Related]
29. The lives of adults over 30 living with sickle cell disorder.
Caird H; Camic PM; Thomas V
Br J Health Psychol; 2011 Sep; 16(3):542-58. PubMed ID: 21722275
[TBL] [Abstract][Full Text] [Related]
30. Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain.
Sil S; Cohen LL; Dampier C
Clin J Pain; 2016 Jun; 32(6):527-33. PubMed ID: 26379074
[TBL] [Abstract][Full Text] [Related]
31. Daily functioning and quality of life in children with sickle cell disease pain: relationship with family and neighborhood socioeconomic distress.
Palermo TM; Riley CA; Mitchell BA
J Pain; 2008 Sep; 9(9):833-40. PubMed ID: 18550443
[TBL] [Abstract][Full Text] [Related]
32. Examining Biopsychosocial Factors in Relation to Multiple Pain Features in Pediatric Sickle Cell Disease.
Schlenz AM; Schatz J; Roberts CW
J Pediatr Psychol; 2016 Sep; 41(8):930-40. PubMed ID: 26869665
[TBL] [Abstract][Full Text] [Related]
33. Examining the influence of pain and fatigue on neurocognitive functioning in adolescents and young adults with sickle cell disease.
Semko JH; Longoria J; Porter J; Potter B; Bhatia S; Pan H; Hankins JS; Heitzer AM
Pediatr Blood Cancer; 2023 Nov; 70(11):e30621. PubMed ID: 37561401
[TBL] [Abstract][Full Text] [Related]
34. Sickle cell disease in Grenada: Quality of life and barriers to care.
Grygiel A; Ikolo F; Stephen R; Bleasdille D; Robbins-Furman P; Nelson B; Sobering AK; Elsea SH
Mol Genet Genomic Med; 2021 Jan; 9(1):e1567. PubMed ID: 33332776
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Use of the new pediatric PROMIS measures of pain and physical experiences for children with sickle cell disease.
Singh A; DasGupta M; Simpson PM; Panepinto JA
Pediatr Blood Cancer; 2019 May; 66(5):e27633. PubMed ID: 30688017
[TBL] [Abstract][Full Text] [Related]
37. Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life.
Chin N; Asnani M
Hemoglobin; 2024 Mar; 48(2):87-93. PubMed ID: 38616298
[TBL] [Abstract][Full Text] [Related]
38. Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project.
McClish DK; Levenson JL; Penberthy LT; Roseff SD; Bovbjerg VE; Roberts JD; Aisiku IP; Smith WR
J Womens Health (Larchmt); 2006 Mar; 15(2):146-54. PubMed ID: 16536678
[TBL] [Abstract][Full Text] [Related]
39. Depression and anxiety in adults with sickle cell disease: the PiSCES project.
Levenson JL; McClish DK; Dahman BA; Bovbjerg VE; de A Citero V; Penberthy LT; Aisiku IP; Roberts JD; Roseff SD; Smith WR
Psychosom Med; 2008 Feb; 70(2):192-6. PubMed ID: 18158366
[TBL] [Abstract][Full Text] [Related]
40. Daily stress and mood and their association with pain, health-care use, and school activity in adolescents with sickle cell disease.
Gil KM; Carson JW; Porter LS; Ready J; Valrie C; Redding-Lallinger R; Daeschner C
J Pediatr Psychol; 2003; 28(5):363-73. PubMed ID: 12808013
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
