Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Stephanie M. Sansone"'
Autor:
Rebecca H. Shields, Aaron Kaat, Stephanie M. Sansone, Claire Michalak, Jeanine Coleman, Talia Thompson, Forrest J. McKenzie, Andrew Dakopolos, Karen Riley, Elizabeth Berry-Kravis, Keith F. Widaman, Richard C. Gershon, David Hessl
Publikováno v:
Neurology, vol 100, iss 8
Background and ObjectiveIndividuals with intellectual disability (ID) experience protracted cognitive development compared with typical youth. Sensitive measurement of cognitive change in this population is a critical need for clinical trials and oth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::849406ce02f5162aa2a8691f7a9b7c1c
https://escholarship.org/uc/item/2t6009z9
https://escholarship.org/uc/item/2t6009z9
Autor:
Talia Thompson, Laurel A. Snider, Londi J. Howard, Stephanie M. Sansone, Jeanine Coleman, David R Hessl, Karen Riley
Publikováno v:
Contemporary School Psychology. 22:443-457
Standardized cognitive and educational assessments of individuals with intellectual disability (ID) provide crucial information for parents, researchers, and educators. Understanding the unique developmental strengths and challenges of an individual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e89aefbe08ddb0bc0c994725c4a3824b
https://doi.org/10.1007/s40688-018-0171-4
https://doi.org/10.1007/s40688-018-0171-4
Autor:
Richard Gershon, Claire Michalak, Elizabeth Berry-Kravis, Keith F. Widaman, Forrest J. McKenzie, Jeanine Coleman, David R Hessl, Rebecca H. Shields, Karen Riley, Stephanie M. Sansone, Aaron J. Kaat, Andrea Drayton
Publikováno v:
Neurology
Neurology, vol 94, iss 12
Neurology, vol 94, iss 12
ObjectiveTo advance the science of cognitive outcome measurement for individuals with intellectual disability (ID), we established administration guidelines and evaluated the psychometric properties of the NIH-Toolbox Cognitive Battery (NIHTB-CB) for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::453dad0e44d2180615116ee0755aed0f
https://pubmed.ncbi.nlm.nih.gov/32094243
https://pubmed.ncbi.nlm.nih.gov/32094243
Autor:
Elizabeth Berry-Kravis, Randi J Hagerman, Reshma Joshi, Crystal Crestodina, Danielle J Harvey, Stephanie M. Sansone, Jamie Chin, David R Hessl
Publikováno v:
PloS one, vol 14, iss 1
PLoS ONE
PLoS ONE, Vol 14, Iss 1, p e0209984 (2019)
PLoS ONE
PLoS ONE, Vol 14, Iss 1, p e0209984 (2019)
Author(s): Hessl, David; Harvey, Danielle; Sansone, Stephanie; Crestodina, Crystal; Chin, Jamie; Joshi, Reshma; Hagerman, Randi J; Berry-Kravis, Elizabeth | Abstract: BackgroundNumerous preclinical studies have supported the theory that enhanced acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3398706ff40dfb97ee3430c5097c60da
https://escholarship.org/uc/item/0tk3h1pb
https://escholarship.org/uc/item/0tk3h1pb
Autor:
Susan M. Rivera, Andrea Schneider, David R Hessl, Stephanie M. Sansone, Flora Tassone, Randi J Hagerman, Cindy Johnston, Amy Gossett, Andreea L. Seritan
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 171:1139-1147
Several studies have demonstrated increased rates of anxiety and depressive disorders among female carriers of the fragile X premutation. However, the majority of these studies focused on mothers of children with fragile X syndrome, who experience hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c2eadf066a1067760da656a010cddf6
https://doi.org/10.1002/ajmg.b.32496
https://doi.org/10.1002/ajmg.b.32496
Autor:
Susan M. Rivera, Emilio Ferrer, Andrea Schneider, David R Hessl, Stephanie M. Sansone, Flora Tassone, Randi J Hagerman, Cindy Johnston
Publikováno v:
The Clinical Neuropsychologist. 30:929-943
Objective: Clinical observations and a limited number of research studies provide evidence that the fragile X premutation may confer risk for autism, executive dysfunction, and psychopathology. The link to autism spectrum symptoms and social cognitio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d528da3184acba4f814328b73848cd81
https://doi.org/10.1080/13854046.2016.1189536
https://doi.org/10.1080/13854046.2016.1189536
Autor:
Elizabeth Berry-Kravis, Keith F. Widaman, Jeanine Coleman, Stephanie M. Sansone, Leonard J Abbeduto, Andrea Schneider, Richard Gershon, Kelly C. Rhodes, David R Hessl, Karen Riley, Dena Oaklander
Publikováno v:
Journal of neurodevelopmental disorders, vol 8, iss 1
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
BackgroundRecent advances in understanding molecular and synaptic mechanisms of intellectual disabilities (ID) in fragile X syndrome (FXS) and Down syndrome (DS) through animal models have led to targeted controlled trials with pharmacological agents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c873ce6871c949a27babea8280d55d
https://escholarship.org/uc/item/01w4j926
https://escholarship.org/uc/item/01w4j926
Autor:
Elaine C. Brown, Walter E. Kaufmann, David R Hessl, Scott S. Hall, Elizabeth Berry-Kravis, Stephanie M. Sansone, Keith F. Widaman, Ave M. Lachiewicz, Allan L. Reiss, Amy A. Lightbody
Publikováno v:
Journal of autism and developmental disorders, vol 42, iss 7
Animal studies elucidating the neurobiology of fragile X syndrome (FXS) have led to multiple controlled trials in humans, with the Aberrant Behavior Checklist-Community (ABC-C) commonly adopted as a primary outcome measure. A multi-site collaboration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40a6117e9f3ce0801d2250f1b207bde2
https://pubmed.ncbi.nlm.nih.gov/21972117
https://pubmed.ncbi.nlm.nih.gov/21972117
Autor:
Evan James, Lindsey Jones, Margaret Devany, Kinzie Kiser, Joan Lee, Christine Kim, Laura Borgenheimer, Nicole M. Yanjanin, Mary Kearns, Brianna McSorley, Emily Kolbus, Bryce Ramos, Jenny Shin, Gregory Klazura, Abbey Moon, Catherine Tan, Omar Veloz, Anne Horst, Erin Brennan, Stephanie M. Sansone, Rani Gallardo, Olimpia Gutierrez, Catherine M. Miller, Teresa Raya, Timothy Spear, Mary Howard, Andrew Luttrell, Katherine McKeough, Chris Knoedler, Edwin Siu, Frannie Rudolf, Michael Clark, Shane O'Brien, Aaron Patzwahl, Lindsay Schwartz, Paula Olivieri, Allison Herschel, Stephen Riney, Kevin Moser, Emily Ly, Marie Pereira, Lauren Gabriel, Mary Kelly, Melissa Cheng, Kasturi Haldar, Mairaj Uddin, Elizabeth White, Courtney Ensslin, Daniel Castellanos, Craig Pymento, Nina Farivari, Lauren Lange, Jennifer VanTrieste, Moriah Castleman, Sean M. Mitchell, Ryan Shay, Jennifer Albus, Sarah Hodge, Katrina Epperson, Forbes D. Porter, Shanik Fernando, Samuel S. C. Rund, Eileena Li, Wei Lu, Erin Ramelb, Geoff Roberts, Marisa Truong, Natalie Bott, Mark Robertshaw
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e23666 (2011)
PLoS ONE
PLoS ONE
Niemann-Pick Disease, type C (NPC) is a fatal, neurodegenerative, lysosomal storage disorder. It is a rare disease with broad phenotypic spectrum and variable age of onset. These issues make it difficult to develop a universally accepted clinical out
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8636c8892cecb5f8d5a48698b55bffb5
http://europepmc.org/articles/PMC3184943?pdf=render
http://europepmc.org/articles/PMC3184943?pdf=render
Autor:
Andrea Schneider, Christina Prescott, Elizabeth Berry-Kravis, David R Hessl, Erika S. Bickel, Stephanie M. Sansone
Publikováno v:
Journal of Neurodevelopmental Disorders
Journal of neurodevelopmental disorders, vol 6, iss 1
Journal of neurodevelopmental disorders, vol 6, iss 1
Background Intellectual disability (ID) is characterized by global cognitive deficits, yet the very IQ tests used to assess ID have limited range and precision in this population, especially for more impaired individuals. Methods We describe the deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::033f434ad55e41dae4736feadc3b7e63