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pro vyhledávání: '"Leah M. Mattiaccio"'
Autor:
Leah M. Mattiaccio, Ioana L. Coman, Carlie A. Thompson, Wanda P. Fremont, Kevin M. Antshel, Wendy R. Kates
Publikováno v:
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-11 (2018)
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a neurodevelopmental syndrome associated with deficits in cognitive and emotional processing. This syndrome represents one of the highest risk factors for the development of schizophrenia. Pr
Externí odkaz:
https://doaj.org/article/e9a40ef5493848ab98a540b0e3be5f60
Autor:
Leah M. Mattiaccio, Kevin M. Antshel, Wendy R. Kates, Frank A. Middleton, Wanda Fremont, David Berhanu
Publikováno v:
Psychiatry Research: Neuroimaging. 259:10-15
Dysfunction of cortical circuitry involving prefrontal cortex, cingulate gyrus and mesial temporal lobe has been implicated in the pathophysiology of psychotic symptoms. 22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that comports a 2
Autor:
Ioana L. Coman, Carlie A. Thompson, Wendy R. Kates, Leah M. Mattiaccio, Wanda Fremont, Kevin M. Antshel
Publikováno v:
Behavioral and Brain Functions : BBF
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-11 (2018)
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-11 (2018)
Background 22q11.2 deletion syndrome (22q11DS) is a neurodevelopmental syndrome associated with deficits in cognitive and emotional processing. This syndrome represents one of the highest risk factors for the development of schizophrenia. Previous st
Autor:
Ioana L. Coman, Leah M. Mattiaccio, Wanda Fremont, Seetha Ramanathan, Kevin M. Antshel, Wendy R. Kates, Stephen V. Faraone
Publikováno v:
European Neuropsychopharmacology. 27:S481
We conducted a twelve-year longitudinal study of neuroanatomic, neurofunctional and neuropsychological development in youth with 22q11.2 deletion syndrome (22q11DS). Participants, consisting of 88 youth with 22q11DS, 33 unaffected siblings, and 32 co
Autor:
Kevin M. Antshel, Wanda Fremont, Leah M. Mattiaccio, Ioana L. Coman, Carrie E. Bearden, Matthew J. Schreiner, Wendy R. Kates
Publikováno v:
Journal of neurodevelopmental disorders, vol 8, iss 1
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
Background 22q11.2 deletion syndrome (22q11DS) is a neurogenetic condition associated with deficits in neuropsychological functioning and psychiatric disorders. This deletion confers a high risk for the development of psychosis, as approximately 30