7.0 T MRI在中枢神经系统疾病中的研究进展被引量：1

Research progress of 7.0 T MRI in the central nervous system diseases

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摘要中枢神经系统疾病复杂多样,易造成不可逆的损伤,预后较差,早期干预可明显改善预后。7.0 T磁共振成像(7.0 tesla magnetic resonance imaging,7.0 T MRI)可以提供较常规MRI更优质的神经影像,尤其在微小及早期病变方面有着显著优势,为中枢神经系统疾病的早期诊断和临床研究开辟了一条广阔的道路。笔者纳入了国内外最新文献,论述7.0 T MRI在中枢神经系统疾病中的最新进展。 The central nervous system diseases are complex and diverse,easily cause irreversible damage,and the prognosis is poor.Early intervention can significantly improve the prognosis.7.0 T MRI(7.0 tesla magnetic resonance imaging)can provide better neuroimaging than conventional MRI,especially in small and early lesions,opening up a new broad road in diagnosis and clinical study of central nervous system diseases.This article incorporates the latest literature at home and abroad to discuss the latest advances in 7.0 T MRI in central nervous system diseases.

作者何静王敏刘旭张进蔚洪恩 HE Jing;WANG Min;LIU Xu;ZHANG Jin;WEI Hong'en(Department of Medical Imaging,Shanxi Medical University,Taiyuan 030001,China;Department of Neurology,Shanxi Provincial People’s Hospital,Affiliate of Shanxi Medical University,Taiyuan 030001,China;Department of Radiology,Second Hospital of Shanxi Medical University,Taiyuan 030001,China)

机构地区山西医科大学医学影像学系山西医科大学附属人民医院/山西省人民医院神经内科山西医科大学第二医院放射科

出处《磁共振成像》 CAS 2019年第12期928-932,共5页 Chinese Journal of Magnetic Resonance Imaging

基金国家自然科学基金面上项目(编号：81671364) 中国博士后科学基金面上资助项目(编号：2017M611195) 山西省青年拔尖人才支持计划(编号：2015009) 山西省应用基础研究项目(编号：201801D211010)~~

关键词磁共振成像脑血管疾病运动障碍性疾病癫痫多发性硬化孤独症痴呆 magnetic resonance imaging cerebrovascular disease movement disorders epilepsy multiple sclerosis autism dementia

分类号 R445.2 [医药卫生—影像医学与核医学] R742 [医药卫生—神经病学与精神病学]

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1蔚洪恩,胡风云.BTBR小鼠动物模型在孤独症研究中的作用[J].中华实用儿科临床杂志,2015,30(24):1918-1920. 被引量：4
2蔚洪恩,于欣.脑微梗死的研究进展[J].中国卒中杂志,2018,13(4):409-414. 被引量：4

二级参考文献38

1Wei H,Alberts I,Li X.The apoptotic perspective of autism[J].Int J Dev Neurosci,2014,36:13-18.
2Bhat S,Acharya UR,Adeli H,et al.Autism:cause factors,early diagnosis and therapies[J].Rev Neurosci,2014,25(6):841-850.
3Volkmar FR,McPartland JC.From Kanner to DSM-5:autism as an evol- ving diagnostic concept[J].Annu Rev Clin Psychol,2014,10:193-212.
4Blumberg SJ,Bramlett MD,Kogan MD,et al.Changes in prevalence of parent-reported autism spectrum disorder in school-aged U.S.children:2007 to 2011-2012[R].National Health Statistics Reports No 65 Hyattsville,MD:National Center for Health Statistics,2013.
5Abrahams BS,Geschwind DH.Connecting genes to brain in the autism spectrum disorders[J].Arch Neurol,2010,67(4):395-399.
6Mcfarlane HG,Kusek GK,Yang M,et al.Autism-like behavioral pheno- types in BTBR T + tf/J mice[J].Genes Brain Behav,2008,7(2);152-163.
7Blanchard DC,Defensor EB,Meyza KZ,et al.BTBR T + tf/J mice:au- tism-relevant behaviors and reduced fractone-associated heparan sulfate[J].Neurosci Biobehav Rev,2012,36(1):285-296.
8Clee SM,Nadler ST,.Attie AD.Genetic and genomic studies of the BTBR ob/ob mouse model of type 2 diabetes[J].Am J Ther,2005,12(6):491-498.
9Bolivar VJ,Walters SR,Phoenix JL.Assessing autism-like behavior in mice:variations in social interactions among inbred strains[J].Behav -Brain Res,2007,176(1):21-26.
10Moy SS,Nadler JJ,Young NB,et al.Mouse behavioral tasks relevant to autism:phenotypes of 10 inbred strains[J].Behav Brain Res,2007,176(1):4-20.'.