Literature DB >> 16139469

Short-term memory in children with sickle cell disease: executive versus modality-specific processing deficits.

Jeffrey Schatz1, Carla W Roberts.   

Abstract

Prior research has identified a number of areas of cognitive deficit among children with sickle cell disease (SCD), including decrements in memory span and working memory. The present study examined short-term memory span and working memory performance among children with SCD (n = 25) and demographically matched comparison children (n = 25) using digit span, spatial span, and the self-ordered pointing test. Children with SCD showed difficulties only for digit span-backward. Additional cognitive ability measures administered indicated auditory processing was an area of deficit related to digit span-backward performance. The study suggests that modality specific deficits are one factor in short-term memory span for children with SCD. The cause of this deficit is unclear, but may involve both central and peripheral components of auditory processing.

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Year:  2005        PMID: 16139469     DOI: 10.1016/j.acn.2005.06.008

Source DB:  PubMed          Journal:  Arch Clin Neuropsychol        ISSN: 0887-6177            Impact factor:   2.813


  4 in total

1.  Working Memory in Children With Neurocognitive Effects From Sickle Cell Disease: Contributions of the Central Executive and Processing Speed.

Authors:  Kelsey E Smith; Jeffrey Schatz
Journal:  Dev Neuropsychol       Date:  2016-10-19       Impact factor: 2.253

2.  Children's higher order cognitive abilities and the development of secondary memory.

Authors:  Duneesha De Alwis; Joel Myerson; Tamara Hershey; Sandra Hale
Journal:  Psychon Bull Rev       Date:  2009-10

3.  Cognitive Function, Coping, and Depressive Symptoms in Children and Adolescents with Sickle Cell Disease.

Authors:  Kemar V Prussien; Michael R DeBaun; Janet Yarboi; Heather Bemis; Colleen McNally; Ellen Williams; Bruce E Compas
Journal:  J Pediatr Psychol       Date:  2018-06-01

4.  PedsQL™ Multidimensional Fatigue Scale in sickle cell disease: feasibility, reliability, and validity.

Authors:  Julie A Panepinto; Sylvia Torres; Cristiane B Bendo; Timothy L McCavit; Bogdan Dinu; Sandra Sherman-Bien; Christy Bemrich-Stolz; James W Varni
Journal:  Pediatr Blood Cancer       Date:  2013-09-13       Impact factor: 3.167

  4 in total

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