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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,...
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| Publicat a: | Hum Brain Mapp |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wiley Subscription Services, Inc., A Wiley Company
2010
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| Matèries: | |
| Accés en línia: | 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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