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Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks

机译：SPAST基因突变导致遗传性痉挛性截瘫与脑功能网络的整体拓扑变化有关

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摘要

AimOur aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.

机译：目的我们的目的是描述与SPAST基因中的基因突变有关的大脑活动的重排。

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期刊名称 Springer Open Choice
作者
Rosaria Rucco; Marianna Liparoti; Francesca Jacini; Fabio Baselice; Antonella Antenora; Giuseppe De Michele; Chiara Criscuolo; Antonio Vettoliere; Laura Mandolesi; Giuseppe Sorrentino; Pierpaolo Sorrentino;
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作者单位

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年(卷),期 -1(40),5
年度 -1
页码 979–984
总页数 6
原文格式 PDF
正文语种
中图分类外科学 ;
关键词
Hereditary spastic paraplegia Motoneuron disease Magnetoencephalography Magnetic source imaging Brain network Neural synchronization;

机译：遗传性痉挛性截瘫;单动神经疾病;脑磁图;磁源成像;脑网络;神经同步;

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专利

1. Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks [J] . Rucco Rosaria, Liparoti Marianna, Jacini Francesca, Neurological sciences . 2019 ,第5期

机译：导致遗传性痉挛性截瘫患者的孢子基因的突变与脑功能网络的全球拓扑改变有关
2. Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males. [J] . Proukakis C, Moore D, Labrum R, Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2011 ,第1a2期

机译：新突变的检测和公开数据的审查表明，由spastin（SPAST）突变引起的遗传性痉挛性截瘫在男性中更为常见。
3. Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia [J] . V. A. Kadnikova, G. E. Rudenskaya, A. A. Stepanova, Scientific reports. . 2019 ,第1期

机译：俄罗斯痉挛性痉挛性截瘫患者的副盐（SPG4）和ATL1（SPG3A）基因的突变谱
4. Analysis of Test-Retest Repeatability of Gait Analysis Parameters in Hereditary Spastic Paraplegia [C] . Armando Coccia, Federica Amitrano, Pietro Balbi, IEEE International Symposium on Medical Measurements and Applications . 2021

机译：遗传痉挛性截瘫术中的步态分析参数的试验 - 重复性分析
5. Development and Manipulation of a Drosophila Model for Toxic Effects of Mutated M1 Spastin in Hereditary Spastic Paraplegia Treatment [D] . Yiantsos, Ioanna. 2019

机译：果蝇突变M1 Spastin在遗传性痉挛性截瘫治疗中毒性作用的果蝇模型的开发和操纵。
6. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia [O] . Victoria Álvarez, Elena Sánchez-Ferrero, Christian Beetz, 2010

机译：西班牙遗传性痉挛性截瘫患者中SPG4（SPAST）和SPG3A（ATL1）基因的突变谱
7. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia [O] . Victoria Álvarez, null null, Elena Sánchez-Ferrero, 2016

机译：西班牙遗传性痉挛性截瘫患者中SPG4（SPAST）和SPG3A（ATL1）基因的突变谱
8. Quantitative and Functional Analyses of Spastin in the Nervous System: Implications for Hereditary Spastic Paraplegia [R] . Solowska, J. M., Morfini, G., Falnikar, A., 2008

机译：神经系统中spastin的定量和功能分析：对遗传性痉挛性截瘫的影响

Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks

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