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Small gray matter volume in orbitofrontal cortex in Prader‐Willi syndrome: A voxel‐based MRI study

Prader‐Willi syndrome (PWS) is a genetically determined neurodevelopmental disorder presenting with behavioral symptoms including hyperphagia, disinhibition, and compulsive behavior. The behavioral problems in individuals with PWS are strikingly similar to those in patients with frontal pathologies,...

詳細記述

保存先:
書誌詳細
出版年:Hum Brain Mapp
主要な著者: Ogura, Kaeko, Fujii, Toshikatsu, Abe, Nobuhito, Hosokai, Yoshiyuki, Shinohara, Mayumi, Takahashi, Shoki, Mori, Etsuro
フォーマット: Artigo
言語:Inglês
出版事項: Wiley Subscription Services, Inc., A Wiley Company 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6869908/
https://ncbi.nlm.nih.gov/pubmed/20669168
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.21089
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