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Molecular Imaging of Huntington's Disease

机译:亨廷顿氏舞蹈症的分子成像

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The onset and the clinical progression of Huntington Disease (HD) is influenced by several events prompted by a genetic mutation that affects several organs tissues including different regions of the brain. In the last decades years, Positron Emission Tomography (PET) and Magnetic Resonance Imaging (MRI) helped to deepen the knowledge of neurodegenerative mechanisms that guide to clinical symptoms. Brain imaging with PET represents a tool to investigate the physiopathology occurring in the brain and it has been used to predict the age of onset of the disease and to evaluate the therapeutic efficacy of new drugs. This article reviews the contribution of PET and MRI in the research field on Huntington's disease, focusing in particular on some most relevant achievements that have helped recognize the molecular changes, the clinical symptoms and evolution of the disease. J. Cell. Physiol. 232: 1988-1993, 2017. (c) 2016 Wiley Periodicals, Inc.
机译:发病的临床进展亨廷顿病(HD)是受到一些影响事件引起的基因突变影响等器官组织大脑的不同区域。几十年来,正电子发射断层扫描(PET)和磁共振成像(MRI)帮助深化神经退行性的知识机制,指导临床症状。成像与宠物代表一个工具进行调查大脑的生理病理学发生和它已经被用于预测的发病的年龄吗疾病和评价治疗效果的新药物。PET和MRI研究领域的贡献在亨廷顿氏舞蹈症,尤其是聚焦在一些最相关的成就帮助识别的分子变化,疾病的临床症状和演化。j .细胞。威利期刊公司。

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