Zobrazeno 1 - 10 of 38 pro vyhledávání: '"Andrew M Heitzer"'
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Akademický článek
Hydroxyurea maintains working memory function in pediatric sickle cell disease.
Autor: Jesyin Lai, Ping Zou, Josue L Dalboni da Rocha, Andrew M Heitzer, Tushar Patni, Yimei Li, Matthew A Scoggins, Akshay Sharma, Winfred C Wang, Kathleen J Helton, Ranganatha Sitaram
Publikováno v: PLoS ONE, Vol 19, Iss 6, p e0296196 (2024)
Sickle cell disease (SCD) decreases the oxygen-carrying capacity of red blood cells. Children with SCD have reduced/restricted cerebral blood flow, resulting in neurocognitive deficits. Hydroxyurea is the standard treatment for SCD; however, whether
Externí odkaz: https://doaj.org/article/05d95e82c38841618da7990cc2ad9ead
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2
Akademický článek
Academic Performance of Children With Sickle Cell Disease in the United States: A Meta-Analysis
Autor: Andrew M. Heitzer, Latacha Hamilton, Claire Stafford, Jeffrey Gossett, Lara Ouellette, Ana Trpchevska, Allison A. King, Guolian Kang, Jane S. Hankins
Publikováno v: Frontiers in Neurology, Vol 12 (2021)
Background: Students with sickle cell disease are at risk for poor academic performance due to the combined and/or interactive effects of environmental, psychosocial, and disease-specific factors. Poor academic performance has significant social and
Externí odkaz: https://doaj.org/article/cffa53f689464ea694e5061ee8509518
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7
Working memory and school readiness in preschool children with sickle cell disease compared to demographically matched controls
Autor: Andrew M. Heitzer, Jane E. Schreiber, Xiaomeng Yuan, Fang Wang, Haitao Pan, J. Carolyn Graff, Laura Murphy, Rebecca Rupff, Kathryn Russell, Winfred Wang, Jeremie H. Estepp, Jane S. Hankins, Jerlym S. Porter, Lisa M. Jacola
Publikováno v: British journal of haematologyREFERENCES.
Children diagnosed with sickle cell disease (SCD) are at risk of the development of neurobehavioural problems early in life. Specific impairments in executive function skills, including working memory, have been documented in school-aged children wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::406cdf47be6b0199e92bacbb66097d07
https://pubmed.ncbi.nlm.nih.gov/36264030
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8
Progression of central nervous system disease from pediatric to young adulthood in sickle cell anemia
Autor: Grace Champlin, Winfred C. Wang, Jeremie H. Estepp, Andrew M. Heitzer, Robert F. Davis, Kenneth I. Ataga, Jane S. Hankins, Curtis L. Owens, Guolian Kang, Scott N. Hwang, Allison A. King, Lisa M. Jacola, Juan Ding, Justin Newman
Publikováno v: Exp Biol Med (Maywood)
Silent cerebral infarcts and arteriopathy are common and progressive in individuals with sickle cell anemia. However, most data describing brain lesions in sickle cell anemia are cross-sectional or derive from pediatric cohorts with short follow-up.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc76fb49bbcf03dd1e55655b3ef5304c
https://doi.org/10.1177/15353702211035778
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9
Developmental screening of three‐year‐old children with sickle cell disease compared to controls
Autor: Molly Beth Freeman, Banu Aygun, Matthew P. Smeltzer, Yvonne Carroll, Jeremie H. Estepp, Guolian Kang, Latacha Hamilton, Winfred C. Wang, Joseph Moen, Jane E. Schreiber, Andrew M. Heitzer
Publikováno v: British Journal of Haematology. 195:621-628
We previously found that neurodevelopmental deficits commonly occurred in three-year-olds with sickle cell disease (SCD), but clinical significance was uncertain because a comparison group was lacking. Our objective in the current study was to prospe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb6a7de588851cf714f6fefdfa860be2
https://doi.org/10.1111/bjh.17780
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10
Internalizing Symptoms in Adolescents With Sickle Cell Disease
Autor: Andrew M Heitzer, Jennifer Longoria, Jerlym S Porter, Erin MacArthur, Brian Potter, Juan Ding, Jeffrey Gossett, Guolian Kang, Jane S Hankins
Publikováno v: J Pediatr Psychol
Objective Sickle cell disease (SCD) is a genetic blood disorder that may affect patients’ mood and behavior. However, measuring the prevalence of internalizing symptoms (anxiety and depression) in patients with SCD has been elusive. We assessed int
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9674c9712fc467129c8afaa3dc78b48c
https://europepmc.org/articles/PMC10120839/
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