Zobrazeno 1 - 10
of 230
pro vyhledávání: '"Ursula Bellugi"'
Autor:
Chun Chieh Fan, Timothy T. Brown, Hauke Bartsch, Joshua M. Kuperman, Donald J. Hagler, Jr, Andrew Schork, Yvonne Searcy, Ursula Bellugi, Eric Halgren, Anders M. Dale
Publikováno v:
NeuroImage: Clinical, Vol 15, Iss , Pp 343-347 (2017)
Williams Syndrome (WS) is a rare genetic disorder with unique behavioral features. Yet the rareness of WS has limited the number and type of studies that can be conducted in which inferences are made about how neuroanatomical abnormalities mediate be
Externí odkaz:
https://doaj.org/article/fc0ddf2c5e6644eca92a4758e21ab3fc
Autor:
Branka Hrvoj-Mihic, Kari L. Hanson, Caroline H. Lew, Lisa Stefanacci, Bob Jacobs, Ursula Bellugi, Katerina Semendeferi
Publikováno v:
Frontiers in Neuroscience, Vol 11 (2017)
Williams syndrome (WS) is a unique neurodevelopmental disorder with a specific behavioral and cognitive profile, which includes hyperaffiliative behavior, poor social judgment, and lack of social inhibition. Here we examined the morphology of basal d
Externí odkaz:
https://doaj.org/article/024268f5e4b54e5fa94d9810b8a6def1
Publikováno v:
Brain Sciences, Vol 8, Iss 12, p 209 (2018)
Williams Syndrome (WS) is a neurodevelopmental disorder caused by a deletion of 25⁻28 genes on chromosome 7 and characterized by a specific behavioral phenotype, which includes hypersociability and anxiety. Here, we examined the density of neurons
Externí odkaz:
https://doaj.org/article/a2fe5e49554d4718a8898e1cd0996f30
Autor:
Fumiko Hoeft, Li Dai, Brian W Haas, Kristen Sheau, Masaru Mimura, Debra Mills, Albert Galaburda, Ursula Bellugi, Julie R Korenberg, Allan L Reiss
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e104088 (2014)
In this study of eight rare atypical deletion cases with Williams-Beuren syndrome (WS; also known as 7q11.23 deletion syndrome) consisting of three different patterns of deletions, compared to typical WS and typically developing (TD) individuals, we
Externí odkaz:
https://doaj.org/article/f67f43341046480a807d0360caf59faf
Autor:
Li Dai, C Sue Carter, Jian Ying, Ursula Bellugi, Hossein Pournajafi-Nazarloo, Julie R Korenberg
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e38513 (2012)
The molecular and neural mechanisms regulating human social-emotional behaviors are fundamentally important but largely unknown; unraveling these requires a genetic systems neuroscience analysis of human models. Williams Syndrome (WS), a condition ca
Externí odkaz:
https://doaj.org/article/4d64cc7f9b704b8682d1568a86104876
Autor:
Michael C Gao, Ursula Bellugi, Li Dai, Debra L Mills, Eric M Sobel, Kenneth Lange, Julie R Korenberg
Publikováno v:
PLoS ONE, Vol 5, Iss 4, p e10292 (2010)
Although genetics is the most significant known determinant of human intelligence, specific gene contributions remain largely unknown. To accelerate understanding in this area, we have taken a new approach by studying the relationship between quantit
Externí odkaz:
https://doaj.org/article/ce1c3068170249c8afc636bf038cb8c6
Autor:
Gregory Hickok, Ursula Bellugi
Publikováno v:
The Routledge International Handbook of Psycholinguistic and Cognitive Processes ISBN: 9781003204213
The Handbook of Psycholinguistic and Cognitive Processes ISBN: 9780203848005
The Handbook of Psycholinguistic and Cognitive Processes ISBN: 9780203848005
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27d70602e9c18821cb42b7160352eb3c
https://doi.org/10.4324/9781003204213-37
https://doi.org/10.4324/9781003204213-37
Publikováno v:
Spatial Cognition ISBN: 9781315785462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66be48bc898d1f475ca8025239bfdd87
https://doi.org/10.4324/9781315785462-16
https://doi.org/10.4324/9781315785462-16
Autor:
Laura A. Petitto, Ursula Bellugi
Publikováno v:
Spatial Cognition ISBN: 9781315785462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b538978b724cdf0737cbc14ab9143e4d
https://doi.org/10.4324/9781315785462-17
https://doi.org/10.4324/9781315785462-17