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10.3280/QPC2017-040003

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Campbell L.E., McCabe K.L., Melville J.L., Strutt P.A., Schall U. (2015). Social cognition dysfunction in adolescents with 22q11.2 deletion syndrome (velo-cardio-facial syndrome): relationship with executive functioning and social competence/functioning. J. Intellect. Disabil. Res., 59: 845-59.

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2010.01.094

Unstructured Zitierung

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Gerdes M., Solot C., Wang P.P., Moss E., LaRossa D., Randall P., Goldmuntz E., Clark B.J., Driscoll D.A., Jawad A., Emanuel B.S., McDonald-McGinn D.M., Batshaw M.L., Zackai E.H. (1999). Cognitive and Behavior Profile of Preschool Children With Chromosome 22q11.2 Deletion. American Journal of Medical Genetics, 85: 127-133.

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Unstructured Zitierung

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Unstructured Zitierung

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Unstructured Zitierung

Jolinn E.M., Weller R.A., Jessani N.R., Zackai E.H., McDonald-McGinn D.M., Weller E.B. (2009). Affective disorders and other psychiatric diagnoses in children and adolescents with 22q11.2 Deletion Syndrome. J. of Affective Disorders, 9, 119: 177-180.

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Unstructured Zitierung

Kates W.R., Antshel K.M., AbdulSabur N., Colgan D., Funke B., Fremont W., Higgins A.M., Kucherlapati R., Shprintzen R.J. (2006). A Gender-Moderated Effect of a Functional COMT Polymorphism on Prefrontal Brain Morphology and Function in Velo-cardio-facial Syndrome (22q11.2 Deletion Syndrome). Am. J. Med. Genet. B. Neuropsychiatr. Genet., 141B(3): 274-280.

Unstructured Zitierung

Kates W.R., Krauss B.R., AbdulSabur N., Colgan D., Antshel K.M., Higgins A.M., Shprintzen R.J. (2007) The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome). Neuropsychologia, 45(12): 2863-2873.

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Unstructured Zitierung

Kates W.R, Antshel K.M., Faraone S.V., Fremont W.P., Higgins A.M., Shprintzen R.J., Botti J., Kelchner L., McCarthy C. (2011). Neuroanatomic predictors to prodomal psychosis in Velocardiofacial syndrome (22q11.2 deletion syndrome): A longitudinal study. Biol. Psychiatry, 69: 945-952

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Unstructured Zitierung

Kinouchi A., Mori K., Ando M., Takao A. (1976). Facial appearance of patients with conotruncal anomalies. Pediatr. Jpn., 17: 84.

Unstructured Zitierung

Kringelbach M.L., O’Doherty J., Rolls E.T., Andrews C. (2003). Activation of the human orbitofrontal cortex to a liquid food stimulus is correlated with its subjective pleasantness. Cereb. Cortex, 13: 1064-1071.

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Unstructured Zitierung

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Unstructured Zitierung

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Unstructured Zitierung

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Unstructured Zitierung

Marino B., Digilio M.C., Toscano A., Giannotti A., Dallapiccola B. (1999). Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del 22q11. Genetic Counseling, 10: 25-33.

Unstructured Zitierung

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Unstructured Zitierung

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Unstructured Zitierung

Rolls E.T. (1999b). The functions of the orbitofrontal cortex. Neurocase, 5: 301-312.

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Unstructured Zitierung

Rolls E.T. (2000). The orbitofrontal cortex and reward. Cereb. Cortex., 10: 284-294.

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Unstructured Zitierung

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Unstructured Zitierung

Shaikh T.H., Kurahashi H., Saitta S.C., O’Hare A.M., Hu P., Roe B.A., Driscoll D.A., McDonald-McGinn D.M., Zackai E.H., Budarf M.L. et al. (2000). Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: Genomic organization and deletion endpoint analysis. Hum. Mol. Genet., 9: 489-501.

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Unstructured Zitierung

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Unstructured Zitierung

Simon T.J. (2008). A New Account of the Neurocognitive Foundations of Impairments in Space, Time and Number Processing in Children with Chromosome 22q11.2 Deletion Syndrome. Dev. Disabil. Res. Rev., 14(1): 52-58.

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Unstructured Zitierung

Sobin C., Kiley-Brabeck K., Karayiorgou M. (2005). Lower Prepulse Inhibition in Children With the 22q11 Deletion Syndrome. Am. J. Psychiatry, 162: 1090-1099.

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Unstructured Zitierung

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