Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome

OBJECTIVE: Phelan-McDermid syndrome (PMS) is caused by haploinsufficiency of SHANK3 on terminal chromosome 22. Knowledge about altered neuroanatomical circuitry in PMS comes from mouse models showing striatal hypertrophy in the basal ganglia, and from humans with evidence of cerebellar atrophy. To d...

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Bibliografske podrobnosti
izdano v:Pediatr Neurol
Main Authors: Srivastava, Siddharth, Scherrer, Benoit, Prohl, Anna K., Filip-Dhima, Rajna, Kapur, Kush, Kolevzon, Alexander, Buxbaum, Joseph D., Berry-Kravis, Elizabeth, Soorya, Latha, Thurm, Audrey, Powell, Craig M., Bernstein, Jonathan A, Warfield, Simon K., Sahin, Mustafa
Format: Artigo
Jezik:Inglês
Izdano: 2018
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6309632/
https://ncbi.nlm.nih.gov/pubmed/30396833
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pediatrneurol.2018.09.008
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