Subthreshold Psychotic Symptoms in 22q11.2 Deletion Syndrome

OBJECTIVE: Chromosome 22q11.2 deletion syndrome (22q11DS) confers 25% risk for psychosis and is an invaluable window for understanding the neurobiological substrate of psychosis risk. The Structured Interview for Prodromal Syndromes (SIPS) is well validated in non-deleted populations for detecting c...

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Hlavní autoři: Tang, Sunny X., Yi, James J., Moore, Tyler M., Calkins, Monica E., Kohler, Christian G., Whinna, Daneen A., Souders, Margaret C., Zackai, Elaine H., McDonald-McGinn, Donna M., Emanuel, Beverly S., Bilker, Warren B., Gur, Ruben C., Gur, Raquel E.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2014
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4159384/
https://ncbi.nlm.nih.gov/pubmed/25151422
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaac.2014.05.009
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