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Crosby, L. E., Joffe, N., Dunseath, L. & Lee, R. (under review). Design joins the battle against sickle-cell disease. Design Management Review.
Crosby L.E., Smith T., Parr W.D., Mitchell M.J. The community engagement and translational research speaker series: An innovative model of health education. Community Medicine and Health Education, 3(5), 1-5. 2013.
Valenzuela, J., Vaughn, L., Crosby, L., Strong, H., Kissling, A. & Mitchell, M. Understanding the experiences of youth living with sickle cell disease: A photovoice pilot. Family and Community Health, 36(2), 97-108. 2013.
Crosby, L. E., Parr, W., Smith, T., & Mitchell, M.J. The Community Leaders Institute: An innovative program to train community leaders in health research. Academic Medicine, 88(3), 335-342. 2013.
Crosby, L.E., Barach, I., McGrady, M.E., Kalinyak, K.A., Eastin, A.E., & Mitchell, M.J. Integrating interactive web-based technology to assess adherence and clinical outcomes in pediatric sickle cell disease. Anemia, 2012. doi:10.1155/2012/492428. 2012.
Modi, A.C., Crosby, L.E., Hines, J., Drotar, D., & Mitchell, M.J. Feasibility of web-based technology to assess adherence to clinic appointments in youth with sickle cell disease. Journal of Pediatric Hematology / Oncology, 34(3):e93-96. 2012.
Daly, B., Kral, M., Brown, R., Elkin, D., Madan-Swain, A., Mitchell, M., Crosby, L., DeMatteo, D., LaRosa, A., & Jackson, S. Ameliorating attention problems in children with sickle cell disease: Randomized, double-blind, placebo-controlled trials of methylphenidate. Journal of Developmental and Behavioral Pediatrics. 33(3), 244-251. 2012.
Vaughn, L., McLinden, D., Jacquez, F., Crosby, L., Slater, S., & Mitchell, M. Understanding the social networks of parents of children with sickle cell disease. Journal of the Health Care for the Poor and Underserved, 22(3),1014-1029. 2011.
Brinkman, B., Sherman, S., Zmitrovich, A., Visscher, M., Crosby, L., Phelan, K., & Donovan, E. In their own words: Adolescent views on ADHD and their evolving role managing medication. Academic Pediatrics, 12, 53-61. 2011.
Oliver-Carpenter, G., Barach, I., Crosby, L. E., Valenzuela, J., Mitchell, M. J. Disease management, coping, and functional disability in pediatric sickle cell disease. J Natl Med Assoc,103, 131-137. 2011.
Neal-Barnett, A. M., Stadulis, R., Payne, M. R., Crosby, L., Mitchell, M., Williams, L., & Williams-Costa, C. In the company of my sisters: Sister circles as an anxiety intervention for professional African-American women. Journal of Affective Disorders, 129(1-3), 213-218. 2011.
Hines, J., Mitchell, M. J., Crosby, L. E., Johnson, A., Valenzuela, J. M., Kalinyak, K., et al. Engaging patients with sickle cell disease and their families in disease education, research, and community awareness. Journal of Prevention & Intervention in the Community, 39(3), 256-272. 2011.
Hines J, Crosby LE, Davis O, Harris A, Mitchell M. Youth Engagement in Sickle Cell Disease. Health Education and Behavior. [in press].
Herzer M, Godiwala N, Hommel KA, Driscoll K, Mitchell M, Crosby LE, Piazza-Waggoner C, Zeller MH, Modi AC. Family functioning in the context of pediatric chronic conditions. J Dev Behav Pediatr. 31(1):26-34. Jan, 2010.
Alfano C, Pina A, Villata I, Beidel D, Ammerman R, Crosby L. Mediators and moderators of outcome in the behavioral treatment of childhood social phobia. Journal of the American Academy of Child and Adolescent Psychiatry. Jul 21, 2009.
Brinkman WB, Sherman SN, Zmitrovich AR, Visscher MO, Crosby LE, Phelan KJ, Donovan EF. Parental angst making and revisiting decisions about treatment of attention-deficit/hyperactivity disorder. Pediatrics. 124(2):580-9. Aug, 2009.
Crosby L, Modi A, Lemanek K, Guilfoyle S, Kalinyak K, Mitchell M. Perceived barriers to clinic appointments for adolescents with sickle cell disease. Journal of Pediatric Hematology/Oncology. 31(8):571-6. Aug, 2009.
Modi A, Crosby L, Guilfoyle S, Lemanek K, Witherspoon D, Mitchell M. Barriers to Treatment Adherence for Pediatric Patients with Sickle Cell Disease and their Families. Children’s Health Care. 2009.
Bolling C, Crosby LE, Stark L, Boles R. How pediatricians can improve diet and activity for overweight preschoolers: A qualitative study of parental attitudes. Ambulatory Pediatrics. 2009.
Lynch-Jordan A, Kashikar-Zuck S, Crosby L, Lopez W, Smolyansky B, Parkins I, Luzader C, Hartman A, Guilfoyle S, Powers S. Applying quality improvement methods to implement a measurement system for chronic pain-related disability. Journal of Pediatric Psychology. 2009.
Mitchell M, Carpenter O, Crosby L, Bishop C, Hines J, Noll J. Growth status in children and adolescents with sickle cell disease. Journal of Pediatric Hematology and Oncology. 2009.
Beidel DC, Turner SM, Young BJ, Ammerman RT, Sallee FR, Crosby LE. Psychopathology of adolescent social phobia. Journal of Psychopathology and Behavioral Assessment. 29:47-54. 2007.
Mitchell M, Lemanek K, Palermo T, Crosby L, Nichols A, Powers S. Parent perspectives on pain management, coping, and family functioning in pediatric sickle cell disease. Clinical Pediatrics. 46: 311-319. 2007.
Rao P, Beidel DC, Turner SM, Ammerman RT, Crosby LE, Sallee FR. Developmental differences in social anxiety disorder. Behaviour Research and Therapy. 45:1181-1191. 2007.
Beidel D, Turner S, Sallee R, Ammerman R, Crosby L,Pathak S. SET-C vs. fluoxetine in the Treatment of Childhood Social Phobia. Journal of the American Academy of Child and Adolescent Psychiatry. 46: 1622-1632. 2007.
Crosby L, Hines J, Peek L, Kalinyak K, Modi A, Seid M, Mitchell M. Barriers to Care, Health-Related Quality of Life and Healthcare Satisfaction in Pediatric Sickle Cell Disease [Abstract]. Journal of Hematology. [in press].
Crosby L, Leace L, Coleman P, Mitchell M, Shook L, Kalinyak K, Webb T. Transition Modules for Adolescents and Young Adults with Sickle Cell Disease [Abstract]. Journal of Hematology. [in press].
Eber P, Mitchell M, Davis O, Crosby L. Coordination and Collaboration of School-Based Services: Roles, Responsibilities, and Outcomes [Abstract]. In Newman C, Liberton C, Kutash K, Friedman RM, eds, The 20th Annual Research Conference Proceedings: A System of Care for Children’s Mental Health: Expanding the Research Base. Tampa: University of South Florida, Louis de la Parte Florida Mental Health Institute, Research and Training Center for Children’s Mental Health. 2010.
Crosby L, Nichols A, Davis O, Shrimplin K. A Collaborative Effort to Disseminate Evidenced-Based Research on Children Who Witness Domestic Violence [Abstract]. In Newman C, Liberton C, Kutash K, Friedman RM, eds, The 19th Annual Research Conference Proceedings: A System of Care for Children’s Mental Health: Expanding the Research Base (pp. 357-360). Tampa: University of South Florida, Louis de la Parte Florida Mental Health Institute, Research and Training Center for Children’s Mental Health. 2007.
Valenzuela J, Crosby L, Mitchell M. PhotoVoice Project and Photo Exhibit Gives Voice to Youth with Sickle Cell Disease. CenterTALK. Winter, 2010.
Crosby L, Hines J, Mitchell M. 8th Annual Research Day Features Pain Management and Youth Empowerment Activities. Winter, 2010.
Crosby L, Nortz M. How Can A Neuropsychological Evaluation Help My Child With Sickle Cell Disease? CenterTALK. Summer, 2009.
Crosby L, Hines J, Mitchell M. 7th Annual SCD Research and Education Day Teaches Parents and Youth Ways to Manage Stress. CenterTALK. Winter 2009.
Mitchell MJ, Crosby L. Research and Education Day 2006: Promoting Sickle Cell Disease Research, Education and Awareness. CenterTALK. 2007.
Mitchell MJ, Crosby L. Integrating Research, Education and Awareness for Children with Sickle Cell Disease. Society for Pediatric Psychology Newsletter. 2007.
Lori E. Crosby, PsyD
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