Sickle Cell Disease

Valrie, C. R., Gil, K. M., Redding-Lallinger, R., & Daeschner, C. (2008).  Daily mood as a mediator or moderator of the pain-sleep relationship in children with sickle cell disease.  Journal of Pediatric Psychology, 32, 857-861.

Valrie, C. R., Gil, K. M., Redding-Lallinger, R., & Dashcner, C. (2007).  The influence of pain and stress on sleep in children with sickle cell disease.  Children’s Health Care, 36, 335-353.

Pence, L.B., Valrie, C. R., Gil, K. M., Redding-Lallinger, R., & Daeschner, C.  (2007).  Optimism predicting daily pain medication use in adolescents with sickle cell disease.  Journal of Pain and Symptom Management, 33, 302-309.

Gil, K. M., Carson, J. W., Porter, L. S., Scipio, C, Bediako, S. M., & Orringer, E.  (2004).  Daily mood and stress predict pain, health care use, and work activity in African American adults with sickle cell disease. Health Psychology, 23, 267–274.

Gil, K. M., Carson, J. W., Porter, L. S., Ready, J., Valrie, C., Redding-Lallinger, R., & Daeschner, C. (2003).  Daily stress and mood and their association with pain, health care use, and school activity in adolescents with sickle cell disease.  Journal of Pediatric Psychology, 28, 363-373.

Gil, K. M., Anthony, K. K., Carson, J, W., Redding-Lallinger, R., Daeschner, C. W., & Ware, R. E. (2001).  Daily coping practice predicts treatment effects in children with sickle cell disease.  Journal of Pediatric Psychology, 26, 163-173.

Gil, K. M., Carson, J. W., Sedway, J. A., Porter, L. S., Wilson Schaeffer, J. J., & Orringer, E.  (2000). Follow-up of coping skills training in adults with sickle cell disease: Analysis of daily pain and coping practice diaries. Health Psychology, 19, 85-90.

Gil, K. M., Porter, L. S., Ready, J., Workman, E., Sedway, J., & Anthony, K. (2000). Pain in children and adolescents with sickle cell disease: An analysis of daily pain diaries. Children’s Health Care, 29, 225-241.

Grant, M., M., Gil, K. M., Floyd, M. Y., & Abrams, M. (2000). Depression and functioning in relation to health care use in sickle cell disease.  Annals of Behavioral Medicine, 22, 149-157.