{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Hoch MJ"],"funding":["NIBIB NIH HHS","NIA NIH HHS","NINDS NIH HHS","National Institute of Biomedical Imaging and Bioengineering","National Institute on Aging"],"pagination":["1437-1443"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8367627"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["42(8)"],"pubmed_abstract":["<h4>Background and purpose</h4>Diffusion MR imaging sequences essential for clinical neuroradiology imaging protocols may be accelerated with simultaneous multislice acquisitions. We tested whether simultaneous multislice-accelerated diffusion data were clinically equivalent to standard acquisitions.<h4>Materials and methods</h4>In this retrospective study, clinical diffusion sequences obtained before and after implementation of 2-slice simultaneous multislice acceleration and an altered diffusion gradient sampling scheme using the same 3T MRI scanner and 20-channel coil (<i>n</i> = 25 per group) were independently and blindly evaluated by 2 neuroradiologists for perceived quality, artifacts, and overall diagnostic utility. Diffusion tractography was performed in 13 patients both with and "],"journal":["AJNR. American journal of neuroradiology"],"pubmed_title":["Simultaneous Multislice for Accelerating Diffusion MRI in Clinical Neuroradiology Protocols."],"pmcid":["PMC8367627"],"funding_grant_id":["K23 AG048622","R01 NS088040","P41 EB017183","P30 AG066512","R01 NS039135","AG048622-01","P41EB017183"],"pubmed_authors":["Pacione D","Bruno M","Hoch MJ","Fieremans E","Lui YW","Shepherd TM"],"additional_accession":[]},"is_claimable":false,"name":"Simultaneous Multislice for Accelerating Diffusion MRI in Clinical Neuroradiology Protocols.","description":"<h4>Background and purpose</h4>Diffusion MR imaging sequences essential for clinical neuroradiology imaging protocols may be accelerated with simultaneous multislice acquisitions. We tested whether simultaneous multislice-accelerated diffusion data were clinically equivalent to standard acquisitions.<h4>Materials and methods</h4>In this retrospective study, clinical diffusion sequences obtained before and after implementation of 2-slice simultaneous multislice acceleration and an altered diffusion gradient sampling scheme using the same 3T MRI scanner and 20-channel coil (<i>n</i> = 25 per group) were independently and blindly evaluated by 2 neuroradiologists for perceived quality, artifacts, and overall diagnostic utility. Diffusion tractography was performed in 13 patients both with and ","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Aug","modification":"2025-04-26T16:36:30.55Z","creation":"2025-04-06T15:13:16.905Z"},"accession":"S-EPMC8367627","cross_references":{"pubmed":["33985946"],"doi":["10.3174/ajnr.a7140","10.3174/ajnr.A7140"]}}