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Diffusion tensor imaging study in Duchenne muscular dystrophy

  
@article{ATM9639,
	author = {Ya Fu and Yuru Dong and Chao Zhang and Yu Sun and Shu Zhang and Xuetao Mu and Hong Wang and Weihai Xu and Shiwen Wu},
	title = {Diffusion tensor imaging study in Duchenne muscular dystrophy},
	journal = {Annals of Translational Medicine},
	volume = {4},
	number = {6},
	year = {2016},
	keywords = {},
	abstract = {Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disorder associated with an intellectual deficit which is non-progressive. The aim of this study was to investigate brain microstructural changes in DMD and to explore the relationship between such changes and cognitive impairment.	
Methods: All participants (12 DMD patients, 14 age-matched healthy boys), intelligence quotients (IQs) [both full (FIQ) and verbal (VIQ)] were evaluated using the Wechsler intelligence scale for children China revised (WISC-CR) edition, and brain gray matter (GM) and white matter (WM) changes were mapped using diffusion tensor imaging (DTI) with fractional anisotropy (FA). The differences between groups were analyzed using the t-test and the association of cognition with neuroimaging parameters was evaluated using Pearson’s correlation coefficient.	
Results: Compared to the normal controls, the DMD group had lower FIQ (82.0±15.39 vs. 120.21±16.06) and significantly lower splenium of corpus callosum (CC) FA values (P},
	issn = {2305-5847},	url = {https://atm.amegroups.org/article/view/9639}
}