Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Stacey Lurie"'
Autor:
Teresa Tavassoli, Christina Layton, Tess Levy, Mikaela Rowe, Julia George-Jones, Jessica Zweifach, Stacey Lurie, Joseph D. Buxbaum, Alexander Kolevzon, Paige M. Siper
Publikováno v:
Genes, Vol 12, Iss 7, p 977 (2021)
Phelan–McDermid syndrome (PMS) is one of the most common genetic forms of autism spectrum disorder (ASD). While sensory reactivity symptoms are widely reported in idiopathic ASD (iASD), few studies have examined sensory symptoms in PMS. The current
Externí odkaz:
https://doaj.org/article/90306f34e30a4a72962dedfae3fcae00
Autor:
Paige M. Siper, Christina Layton, Tess Levy, Stacey Lurie, Nurit Benrey, Jessica Zweifach, Mikaela Rowe, Lara Tang, Sylvia Guillory, Danielle Halpern, Ivy Giserman-Kiss, Maria Del Pilar Trelles, Jennifer H. Foss-Feig, Silvia De Rubeis, Teresa Tavassoli, Joseph D. Buxbaum, Alexander Kolevzon
Publikováno v:
Genes, Vol 12, Iss 3, p 351 (2021)
Background: Activity dependent neuroprotective protein (ADNP) syndrome is one of the most common single-gene causes of autism spectrum disorder (ASD) and intellectual disability, however, the phenotypes remain poorly described. Here we examine the se
Externí odkaz:
https://doaj.org/article/056837a52bc34151a51e862ffc2d6f4f
Autor:
Paige M Siper, Vance Zemon, James Gordon, Julia George-Jones, Stacey Lurie, Jessica Zweifach, Teresa Tavassoli, A Ting Wang, Jesslyn Jamison, Joseph D Buxbaum, Alexander Kolevzon
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0164422 (2016)
OBJECTIVE:There is a critical need to identify biomarkers and objective outcome measures that can be used to understand underlying neural mechanisms in autism spectrum disorder (ASD). Visual evoked potentials (VEPs) offer a noninvasive technique to e
Externí odkaz:
https://doaj.org/article/5f13835e2c404860b051531a6193ddbe
Autor:
Christina Layton, Julia George-Jones, Mikaela Rowe, Stacey Lurie, Jessica Zweifach, Tess Levy, Alexander Kolevzon, Paige M. Siper, Joseph D. Buxbaum, Teresa Tavassoli
Publikováno v:
Genes, Vol 12, Iss 977, p 977 (2021)
Genes
Volume 12
Issue 7
Genes
Volume 12
Issue 7
Phelan–McDermid syndrome (PMS) is one of the most common genetic forms of autism spectrum disorder (ASD). While sensory reactivity symptoms are widely reported in idiopathic ASD (iASD), few studies have examined sensory symptoms in PMS. The current
Autor:
Maureen Mulhern, Jessica Zweifach, Paige M. Siper, Danielle Halpern, M. Pilar Trelles, Chloe Brittenham, Joseph D. Buxbaum, Julia George-Jones, Vance Zemon, Sylvia Guillory, Stacey Lurie, Jordana Weissman, James Gordon, Jennifer H. Foss-Feig, Alexander Kolevzon, Teresa Tavassoli, Audrey Rouhandeh, Mikaela Rowe
Publikováno v:
J Am Acad Child Adolesc Psychiatry
OBJECTIVE: The current study utilized visual evoked potentials (VEPs) to examine excitatory and inhibitory postsynaptic activity in children with Phelan-McDermid syndrome (PMS) and the association with genetic factors. PMS is caused by haploinsuffici
Autor:
Ivy Giserman-Kiss, Nurit Benrey, Teresa Tavassoli, Sylvia Guillory, Maria del Pilar Trelles, Alexander Kolevzon, Joseph D. Buxbaum, Jessica Zweifach, Christina Layton, Mikaela Rowe, Silvia De Rubeis, Stacey Lurie, Lara Tang, Jennifer H. Foss-Feig, Danielle Halpern, Paige M. Siper, Tess Levy
Publikováno v:
Genes, Vol 12, Iss 351, p 351 (2021)
Genes
Volume 12
Issue 3
Genes
Volume 12
Issue 3
Background: Activity dependent neuroprotective protein (ADNP) syndrome is one of the most common single-gene causes of autism spectrum disorder (ASD) and intellectual disability, however, the phenotypes remain poorly described. Here we examine the se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b225b00ace7a862da731532d95230845
https://centaur.reading.ac.uk/96599/1/genes-12-00351.pdf
https://centaur.reading.ac.uk/96599/1/genes-12-00351.pdf
For many professionals, patients, and relatives of individuals with autism spectrum disorder (ASD), the co-occurrence with addiction to alcohol or drugs seems unimaginable. How could autism be hidden behind addiction and how could someone diagnosed w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daa127636c6f81479a5beb09692882a6
https://doi.org/10.1093/oxfordhb/9780190910761.013.4
https://doi.org/10.1093/oxfordhb/9780190910761.013.4
Autor:
Paige M. Siper, Stacey Lurie, Emily Fourie, Hillary Rieger, A. Ting Wang, Joseph D. Buxbaum, Alexander Kolevzon, Erin Li, Jacquelin Rankine
Publikováno v:
Journal of Autism and Developmental Disorders. 47:1605-1617
Phelan-McDermid syndrome (PMS) is a single-locus cause of developmental delay, autism spectrum disorder, and minimal verbal abilities. There is an urgent need to identify objective outcome measures of expressive language for use in this and other min
Autor:
Alexander Kolevzon, Teresa Tavassoli, Paige M. Siper, E. Li, Stacey Lurie, A. M. Mieses, A. T. Wang, Latha Soorya
Publikováno v:
Journal of autism and developmental disorders. 46(7)
Phelan-McDermid syndrome (PMS), a monogenic form of autism spectrum disorder (ASD), results from deletion or mutation of the SHANK3 gene. Atypical sensory reactivity is now included in the diagnostic criteria for ASD. Examining the sensory phenotype
Autor:
Julia George-Jones, Alexander Kolevzon, Allison Durkin, Paige M. Siper, Audrey Rouhandeh, Kristin Meyering, Jordana Weissman, Joseph D. Buxbaum, Stacey Lurie, Mikaela Rowe
Publikováno v:
Biological Psychiatry. 83:S9