search www.ncbi.nlm.nih.gov.

Journal Articles

  1. Edwards, CL; Raynor, RD; Feliu, M; McDougald, C; Johnson, S; Schmechel, D; Wood, M; Bennett, GG; Saurona, P; Bonner, M; Wellington, C; DeCastro, LM; Whitworth, E; Abrams, M; Logue, P; Edwards, L; Martinez, S; Whitfield, KE, Neuropsychological assessment, neuroimaging, and neuropsychiatric evaluation in pediatric and adult patients with sickle cell disease (SCD)., Neuropsychiatr Dis Treat, vol. 3 no. 6 (December, 2007), pp. 705-709, ISSN 1176-6328 [19300604], [doi]
    (last updated on 2024/04/24)

    Abstract:
    Traditionally, neuropsychological deficits due to Sickle Cell Disease (SCD) have been understudied in adults. We have begun to suspect, however, that symptomatic and asymptomatic Cerebrovascular Events (CVE) may account for an alarming number of deficits in this population. In the current brief review, we critically evaluated the pediatric and adult literatures on the neurocognitive effects of SCD. We highlighted the studies that have been published on this topic and posit that early detection of CVE via neurocognitive testing, neuropsychiatric evaluations, and neuroimaging may significantly reduce adult cognitive and functional morbidities.

    Keywords:
    Adult • African Americans • Aged • Computers • Hispanic Americans • Humans • Middle Aged • Ownership • Poverty • Public Housing • Social Environment* • Urban Population • statistics & numerical data • statistics & numerical data* • utilization*


©2013 Duke Global Health Institute | Contact Us | Employment | Make a Gift | Duke University | Duke Medicine | Interdisciplinary Studies