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Neural Plasticity and Compensation for Human Brain Damage
Masahiro Mishina
Department of Neurological Science, Graduate School of Medicine, Nippon Medical School

We previously believed that brain disorders could not be treated. However, brain-imaging techniques have demonstrated functional localization and the recovery of damaged areas of the brain. Through the use of various radiopharmaceuticals, positron emission tomography (PET) allows in vivo imaging of regional cerebral functions, including cerebral blood flow, molecular metabolism, and receptor binding capacity. In addition, PET demonstrates neural plasticity and compensation for brain damage. This paper discusses the plasticity and compensation of the brain revealed by our PET studies.
ϊγεγο 2014; 10(2), 101-105
Key words
positron emission tomography, γ-aminobutyric acid, aphasia, sigma1 receptor, adenosine A2A receptor
Correspondence to
Masahiro Mishina, Department of Neurological Science, Graduate School of Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113-8602, Japan
E-mailFmishina@nms.ac.jp
σtF2014N16ϊ@σF2014N123ϊ |