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Perceived Emergency Department Care and Disease Status in Pediatric Sickle Cell Patients
(East Carolina University, 2011)
The present study described the overall emergency department (ED) experiences of children with SCD, and examined the relationship between characteristics of care (waiting time, communication/interaction with the health ...
Establishing Validity for Measures of Executive Functioning and Behavior in Children and Adolescents with Sickle Cell Disease
(East Carolina University, 2013)
This study examined the criterion validity of the Behavior Rating Inventory for Executive Functioning (BRIEF; Gioia, Isquith, Guy, & Kenworthy, 2000) and the Behavior Assessment System for Children, 2nd Edition (BASC-2; ...
Knowledge of Sickle Cell Trait and Disease among African-American College Students
(East Carolina University, 2011)
The term sickle cell disease (SCD) refers to a collection of hemoglobinopathies (inherited blood disorders) characterized by abnormal hemoglobin and produced through the homozygous inheritance of a sickle cell allele. ...
Predictors of Grade Retention in Children and Adolescents with Sickle Cell Disease
(East Carolina University, 2013)
This study examined the predictive value of sex, socioeconomic status (SES), disease severity, family achievement-orientation, and family relationship quality for predicting grade retention in children and adolescents with ...
The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease
(East Carolina University, 2013)
Sickle cell disease (SCD) is a complex group of genetic blood disorders that currently affects 90,000-100,000 Americans primarily of African descent. SCD leads to physiological and psychosocial distress. In relation to ...