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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

238 related items for PubMed ID: 28602692

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  • 2. Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell Disease.
    Brandow AM, Panepinto JA.
    J Pediatr Hematol Oncol; 2016 May; 38(4):288-93. PubMed ID: 26907660
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  • 3. How sickle cell disease patients experience, understand and explain their pain: An Interpretative Phenomenological Analysis study.
    Coleman B, Ellis-Caird H, McGowan J, Benjamin MJ.
    Br J Health Psychol; 2016 Feb; 21(1):190-203. PubMed ID: 26333530
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  • 4. Disease-Related, Nondisease-Related, and Situational Catastrophizing in Sickle Cell Disease and Its Relationship With Pain.
    Mathur VA, Kiley KB, Carroll CP, Edwards RR, Lanzkron S, Haythornthwaite JA, Campbell CM.
    J Pain; 2016 Nov; 17(11):1227-1236. PubMed ID: 27555427
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  • 5. Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia.
    Darbari DS, Vaughan KJ, Roskom K, Seamon C, Diaw L, Quinn M, Conrey A, Schechter AN, Haythornthwaite JA, Waclawiw MA, Wallen GR, Belfer I, Taylor JG.
    Scand J Pain; 2017 Oct; 17():279-286. PubMed ID: 28969994
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  • 8. 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
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  • 10. Thermal pain and sensory processing in children with sickle cell disease.
    O'Leary JD, Crawford MW, Odame I, Shorten GD, McGrath PA.
    Clin J Pain; 2014 Mar; 30(3):244-50. PubMed ID: 23629596
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  • 13. Quantitative sensory testing and pain-evoked cytokine reactivity: comparison of patients with sickle cell disease to healthy matched controls.
    Campbell CM, Carroll CP, Kiley K, Han D, Haywood C, Lanzkron S, Swedberg L, Edwards RR, Page GG, Haythornthwaite JA.
    Pain; 2016 Apr; 157(4):949-956. PubMed ID: 26713424
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  • 14. Patients with sickle cell disease have increased sensitivity to cold and heat.
    Brandow AM, Stucky CL, Hillery CA, Hoffmann RG, Panepinto JA.
    Am J Hematol; 2013 Jan; 88(1):37-43. PubMed ID: 23115062
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  • 15. Emotional reactions to pain predict psychological distress in adult patients with Sickle Cell Disease (SCD).
    Edwards CL, Killough A, Wood M, Doyle T, Feliu M, Barker CS, Uppal P, DeCastro L, Wellington C, Whitfield KE, O'Garo KG, Morgan K, Edwards Alesii LY, Byrd GS, McCabe M, Goli V, Keys A, Hill L, Collins-McNeil J, Trambadia J, Guinyard D, Muhammad M, McDonald P, Schmechel DE, Robinson E.
    Int J Psychiatry Med; 2014 Jan; 47(1):1-16. PubMed ID: 24956913
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  • 16. Multiple Levels of Suffering: Discrimination in Health-Care Settings is Associated With Enhanced Laboratory Pain Sensitivity in Sickle Cell Disease.
    Mathur VA, Kiley KB, Haywood C, Bediako SM, Lanzkron S, Carroll CP, Buenaver LF, Pejsa M, Edwards RR, Haythornthwaite JA, Campbell CM.
    Clin J Pain; 2016 Dec; 32(12):1076-1085. PubMed ID: 26889615
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  • 17. Pediatric Sickle Cell Disease and Parent and Child Catastrophizing.
    Sil S, Dampier C, Cohen LL.
    J Pain; 2016 Sep; 17(9):963-71. PubMed ID: 27263990
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  • 20. Neurocognitive and psychological effects of persistent pain in pediatric sickle cell disease.
    Connolly ME, Bills SE, Hardy SJ.
    Pediatr Blood Cancer; 2019 Sep; 66(9):e27823. PubMed ID: 31131984
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