Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Desirée A, White"'
Autor:
Zoë W. Hawks, Alexandre Todorov, Natasha Marrus, Tomoyuki Nishino, Muhamed Talovic, Mary Beth Nebel, Jessica B. Girault, Savannah Davis, Scott Marek, Benjamin A. Seitzman, Adam T. Eggebrecht, Jed Elison, Stephen Dager, Matthew W. Mosconi, Lawrence Tychsen, Abraham Z. Snyder, Kelly Botteron, Annette Estes, Alan Evans, Guido Gerig, Heather C. Hazlett, Robert C. McKinstry, Juhi Pandey, Robert T. Schultz, Martin Styner, Jason J. Wolff, Lonnie Zwaigenbaum, Lori Markson, Steven E. Petersen, John N. Constantino, Desirée A. White, Joseph Piven, John R. Pruett, Jr.
Publikováno v:
Biological Psychiatry Global Open Science, Vol 3, Iss 1, Pp 149-161 (2023)
Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder diagnosed based on social impairment, restricted interests, and repetitive behaviors. Contemporary theories posit that cerebellar pathology contributes causally to ASD by dis
Externí odkaz:
https://doaj.org/article/ac5eafd8c82d43cc8d1fdb5a74b53ef1
Autor:
Kristina Aldridge, Kimberly K. Cole, Amanda J. Moffitt Gunn, Dawn Peck, Desirée A. White, Shawn E. Christ
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100647- (2020)
Past murine studies of phenylketonuria (PKU) have documented significant effects on cerebellum at both the gross and cellular levels. The profile of neurocognitive and motor difficulties associated with early-treated PKU (ETPKU) is also consistent wi
Externí odkaz:
https://doaj.org/article/51acef2a21e540b586c870bf86d3f51b
Autor:
Zoë Hawks, Joshua Shimony, Jerrel Rutlin, Dorothy K. Grange, Shawn E. Christ, Desirée A. White
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 8-13 (2017)
Sapropterin dihydrochloride (BH4) reduces phenylalanine (Phe) levels and improves white matter integrity in a subset of individuals with phenylketonuria (PKU) known as “responders.” Although prior research has identified biochemical and genotypic
Externí odkaz:
https://doaj.org/article/ab8317c1c00a4f3c88ab34c6b0b96482
Autor:
Zoë Hawks, Anna M. Hood, Dov B. Lerman-Sinkoff, Joshua S. Shimony, Jerrel Rutlin, Daniel Lagoni, Dorothy K. Grange, Desirée A. White
Publikováno v:
NeuroImage: Clinical, Vol 23, Iss , Pp - (2019)
Phenylketonuria (PKU) is a recessive disorder characterized by disruption in the metabolism of the amino acid phenylalanine (Phe). Prior research indicates that individuals with PKU have substantial white matter (WM) compromise. Much less is known ab
Externí odkaz:
https://doaj.org/article/4a0004033ef044bc95ce911cd45509c2
Autor:
Shawn E. Christ, Christopher Saville, Deborah A. Bilder, Mitzie Grant, Susan E. Waisbren, Desirée A. White, Barbara K. Burton, Marie Claire Paulin, Hayley E. Clocksin
Publikováno v:
Neuropsychology. 34:456-466
Objective Previous research has documented executive function (EF) impairments in individuals with early treated phenylketonuria (ETPKU). It remains unclear, however, whether some aspects of EF may be more affected than others. A number of factors, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a63f229ea2aa9d4288801893ed4cb4f2
https://doi.org/10.1037/neu0000625
https://doi.org/10.1037/neu0000625
Publikováno v:
Behavioural Neurology, Vol 24, Iss 3, Pp 177-185 (2011)
The Trail Making Test and Digit Span are neuropsychological tests widely used to assess executive abilities following stroke. The Trails B and Digits Backward conditions of these tests are thought to be more sensitive to executive impairment related
Externí odkaz:
https://doaj.org/article/fe0790cf73ef47d7937a9fc554e551bb
Publikováno v:
Molecular genetics and metabolism. 132(1)
Even with early and continuous treatment, individuals with phenylketonuria (PKU) may exhibit abnormalities of cortical white matter (WM). The present study utilizes a new analysis approach called Automated Fiber-Tract Quantification (AFQ) to advance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776fd6882a02e90188ba0285e0bd8bfe
https://pubmed.ncbi.nlm.nih.gov/33334682
https://pubmed.ncbi.nlm.nih.gov/33334682
Publikováno v:
Developmental Neuropsychology. 43:207-218
Phenylketonuria (PKU) is a hereditary disorder characterized by disrupted phenylalanine metabolism and cognitive impairment. However, the precise nature and developmental trajectory of this cognitive impairment remains unclear. The present study used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a446695381ee7e7380715c45ee326d6f
https://doi.org/10.1080/87565641.2018.1438439
https://doi.org/10.1080/87565641.2018.1438439
Autor:
Dorothy K. Grange, Zoë Hawks, Desirée A. White, Jerrel Rutlin, Shawn E. Christ, Joshua S. Shimony
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 8-13 (2017)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Sapropterin dihydrochloride (BH4) reduces phenylalanine (Phe) levels and improves white matter integrity in a subset of individuals with phenylketonuria (PKU) known as “responders.” Although prior research has identified biochemical and genotypic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93d2033deb3d24a5e4678b04e89ae37b
Publikováno v:
J Clin Psychol Med Settings
Children with sickle cell disease (SCD) experience disproportionately high rates of psychological problems. Our goal was to examine the clinical utility of psychological screening measures to identify children with such problems in medical settings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2843d6951355d6187513b9aaa2028ed6
https://pubmed.ncbi.nlm.nih.gov/31463865
https://pubmed.ncbi.nlm.nih.gov/31463865