Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ling, M"'
Autor:
Nina F. Schor, Ling M. Wong, Jill A. Morris, Beverly L. Davidson, Guangping Gao, Chris H. Boshoff
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 29(12)
The National Institute of Neurological Disorders and Stroke (NINDS) held a workshop titled "Next generation strategies for gene-targeted therapies of central nervous system (CNS) disorders" in September 2019 in Bethesda, MD, USA. The meeting brought
Autor:
Michele Amato, Nicole Tartaglia, Kathryn McCabe, Ling M. Wong, Danielle J Harvey, Abbie Popa, Joshua Cruz, Courtney A. Durdle, Tony J. Simon, Margarita H Cabaral
Publikováno v:
Journal of neurodevelopmental disorders, vol 11, iss 1
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-12 (2019)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-12 (2019)
Journal of Neurodevelopmental Disorders
Objectives Our ability to generate mental representation of magnitude from sensory information affects how we perceive and experience the world. Reduced resolution of the mental representations formed from sensory inputs may generate impairment in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adab0e28f50165cfd8968c3691053b16
https://escholarship.org/uc/item/79q8511r
https://escholarship.org/uc/item/79q8511r
Autor:
Koraly Perez-Edgar, Ingrid N. Leckliter, Tony J. Simon, Ling M. Wong, Danielle J Harvey, Joshua Cruz, Abbie Popa, Kathleen Angkustsiri
Publikováno v:
American journal on intellectual and developmental disabilities, vol 124, iss 6
Individuals with 22q11.2 deletion syndrome (22q11DS) show high rates of anxiety associated with their increased risk of developing schizophrenia. Biased attention is associated with anxiety and is important to investigate in those with 22q11DS given
Veganism is an increasingly popular lifestyle within Western societies. However, there is no consistent definition of veganism across published research or used by vegan advocacy groups. This has implications for measurement and coherence of the rese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e3a6ec8f5a85451b950319aeead140f
https://psyarxiv.com/mkqn4
https://psyarxiv.com/mkqn4
Publikováno v:
Journal of clinical and experimental neuropsychology. 39(10)
The aim of the study was to uncover inhibitory control dynamics and assess antisaccade eye-tracking tasks for relevance in a veteran posttraumatic stress disorder (PTSD) population.Participants were 36 veterans enrolled at the Washington DC Veterans
Autor:
Susan M. Rivera, Tony J. Simon, Ling M. Wong, Yingratana A. McLennan, Danielle J Harvey, Naomi J. Goodrich-Hunsaker, Flora Tassone
Publikováno v:
Journal of the International Neuropsychological Society. 17:746-750
A previous study reported preliminary results of enhanced processing of simple visual information in the form of faster reaction times, in female fragile X premutation carriers (fXPCs). In this study, we assessed manual and oral motor reaction times
Autor:
Melody Zhang, Tony J. Simon, Flora Tassone, Naomi J. Goodrich-Hunsaker, Susan M. Rivera, Yingratana A. McLennan, Ling M. Wong
Publikováno v:
Neuropsychology, vol 28, iss 4
Wong, LM; Goodrich-Hunsaker, NJ; McLennan, Y; Tassone, F; Zhang, M; Rivera, SM; et al.(2014). Eye movements reveal impaired inhibitory control in adult male fragile X premutation carriers asymptomatic for FXTAS. Neuropsychology, 28(4), 571-584. doi: 10.1037/neu0000066. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/74f2r5mg
Wong, LM; Goodrich-Hunsaker, NJ; McLennan, Y; Tassone, F; Zhang, M; Rivera, SM; et al.(2014). Eye movements reveal impaired inhibitory control in adult male fragile X premutation carriers asymptomatic for FXTAS. Neuropsychology, 28(4), 571-584. doi: 10.1037/neu0000066. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/74f2r5mg
Objective: Fragile X premutation carriers (fXPCs) have an expansion of 55 -200 CGG repeats in the FMR1 gene. Male fXPCs are at risk for developing a neurodegenerative motor disorder (FXTAS) often accompanied by inhibitory control impairments, even in
Publikováno v:
Wong, LM; Riggins, T; Harvey, D; Cabaral, M; & Simon, TJ. (2014). Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory. American Journal on Intellectual and Developmental Disabilities, 119(2), 115-132. doi: 10.1352/1944-7558-119.2.115. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/142964tw
American journal on intellectual and developmental disabilities, vol 119, iss 2
American journal on intellectual and developmental disabilities, vol 119, iss 2
Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have impairments in processing spatiotemporal information. The authors examined whether children with 22q11.2DS exhibit impairments in spatial working memory perform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cc4519ba1b044e95a2d6dc58541c1a9
https://europepmc.org/articles/PMC4036086/
https://europepmc.org/articles/PMC4036086/
Publikováno v:
Frontiers in Psychiatry
Frontiers in Psychiatry, Vol 4 (2013)
Frontiers in Psychiatry, Vol 4 (2013)
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is a neurogenetic disorder that is associated with cognitive impairments and significantly elevated risk for developing schizophrenia. While impairments in response inhibition are central to executive
Autor:
Danielle J Harvey, Susan M. Rivera, Ling M. Wong, Yingratana A. McLennan, Flora Tassone, Naomi J. Goodrich-Hunsaker, Tony J. Simon
Publikováno v:
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 4, Iss 1, p 26 (2012)
Wong, Ling M; Goodrich-Hunsaker, Naomi J; McLennan, Yingratana; Tassone, Flora; Harvey, Danielle; Rivera, Susan M; et al.(2012). Young adult male carriers of the Fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed. Journal of Neurodevelopmental Disorders, 4(1), 26. doi: http://dx.doi.org/10.1186/1866-1955-4-26. Retrieved from: http://www.escholarship.org/uc/item/2cd1t5s0
Journal of Neurodevelopmental Disorders, Vol 4, Iss 1, p 26 (2012)
Wong, Ling M; Goodrich-Hunsaker, Naomi J; McLennan, Yingratana; Tassone, Flora; Harvey, Danielle; Rivera, Susan M; et al.(2012). Young adult male carriers of the Fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed. Journal of Neurodevelopmental Disorders, 4(1), 26. doi: http://dx.doi.org/10.1186/1866-1955-4-26. Retrieved from: http://www.escholarship.org/uc/item/2cd1t5s0
Background A previous study reported enhanced psychomotor speed, and subtle but significant cognitive impairments, modulated by age and by mutations in the fragile X mental retardation 1 (FMR1) gene in adult female fragile X premutation carriers (fXP