Testing a convolutional neural network‐based hippocampal segmentation method in a stroke population
As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long‐term quality of life for stroke survivors. Hippocampal volume may be an important neuroimaging biomarker in poststroke dementia, as it has been associated with many other forms of...
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Published in | Human brain mapping Vol. 43; no. 1; pp. 234 - 243 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Hoboken, USA
John Wiley & Sons, Inc
01.01.2022
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Abstract | As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long‐term quality of life for stroke survivors. Hippocampal volume may be an important neuroimaging biomarker in poststroke dementia, as it has been associated with many other forms of dementia. However, studying hippocampal volume using MRI requires hippocampal segmentation. Advances in automated segmentation methods have allowed for studying the hippocampus on a large scale, which is important for robust results in the heterogeneous stroke population. However, most of these automated methods use a single atlas‐based approach and may fail in the presence of severe structural abnormalities common in stroke. Hippodeep, a new convolutional neural network‐based hippocampal segmentation method, does not rely solely on a single atlas‐based approach and thus may be better suited for stroke populations. Here, we compared quality control and the accuracy of segmentations generated by Hippodeep and two well‐accepted hippocampal segmentation methods on stroke MRIs (FreeSurfer 6.0 whole hippocampus and FreeSurfer 6.0 sum of hippocampal subfields). Quality control was performed using a stringent protocol for visual inspection of the segmentations, and accuracy was measured as volumetric correlation with manual segmentations. Hippodeep performed significantly better than both FreeSurfer methods in terms of quality control. All three automated segmentation methods had good correlation with manual segmentations and no one method was significantly more correlated than the others. Overall, this study suggests that both Hippodeep and FreeSurfer may be useful for hippocampal segmentation in stroke rehabilitation research, but Hippodeep may be more robust to stroke lesion anatomy.
In this study, we compared three automated hippocampal segmentation methods in a large stroke population in terms of quality control and segmentation accuracy compared to manual segmentations. While all three methods yielded similar volumes, new convolutional neural network based segmentation method Hippodeep had the lowest method‐wise quality control fail rate, suggesting it may be the most robust to post‐stroke anatomical distortions. |
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AbstractList | As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long‐term quality of life for stroke survivors. Hippocampal volume may be an important neuroimaging biomarker in poststroke dementia, as it has been associated with many other forms of dementia. However, studying hippocampal volume using MRI requires hippocampal segmentation. Advances in automated segmentation methods have allowed for studying the hippocampus on a large scale, which is important for robust results in the heterogeneous stroke population. However, most of these automated methods use a single atlas‐based approach and may fail in the presence of severe structural abnormalities common in stroke. Hippodeep, a new convolutional neural network‐based hippocampal segmentation method, does not rely solely on a single atlas‐based approach and thus may be better suited for stroke populations. Here, we compared quality control and the accuracy of segmentations generated by Hippodeep and two well‐accepted hippocampal segmentation methods on stroke MRIs (FreeSurfer 6.0 whole hippocampus and FreeSurfer 6.0 sum of hippocampal subfields). Quality control was performed using a stringent protocol for visual inspection of the segmentations, and accuracy was measured as volumetric correlation with manual segmentations. Hippodeep performed significantly better than both FreeSurfer methods in terms of quality control. All three automated segmentation methods had good correlation with manual segmentations and no one method was significantly more correlated than the others. Overall, this study suggests that both Hippodeep and FreeSurfer may be useful for hippocampal segmentation in stroke rehabilitation research, but Hippodeep may be more robust to stroke lesion anatomy.
In this study, we compared three automated hippocampal segmentation methods in a large stroke population in terms of quality control and segmentation accuracy compared to manual segmentations. While all three methods yielded similar volumes, new convolutional neural network based segmentation method Hippodeep had the lowest method‐wise quality control fail rate, suggesting it may be the most robust to post‐stroke anatomical distortions. As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long-term quality of life for stroke survivors. Hippocampal volume may be an important neuroimaging biomarker in poststroke dementia, as it has been associated with many other forms of dementia. However, studying hippocampal volume using MRI requires hippocampal segmentation. Advances in automated segmentation methods have allowed for studying the hippocampus on a large scale, which is important for robust results in the heterogeneous stroke population. However, most of these automated methods use a single atlas-based approach and may fail in the presence of severe structural abnormalities common in stroke. Hippodeep, a new convolutional neural network-based hippocampal segmentation method, does not rely solely on a single atlas-based approach and thus may be better suited for stroke populations. Here, we compared quality control and the accuracy of segmentations generated by Hippodeep and two well-accepted hippocampal segmentation methods on stroke MRIs (FreeSurfer 6.0 whole hippocampus and FreeSurfer 6.0 sum of hippocampal subfields). Quality control was performed using a stringent protocol for visual inspection of the segmentations, and accuracy was measured as volumetric correlation with manual segmentations. Hippodeep performed significantly better than both FreeSurfer methods in terms of quality control. All three automated segmentation methods had good correlation with manual segmentations and no one method was significantly more correlated than the others. Overall, this study suggests that both Hippodeep and FreeSurfer may be useful for hippocampal segmentation in stroke rehabilitation research, but Hippodeep may be more robust to stroke lesion anatomy. As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long-term quality of life for stroke survivors. Hippocampal volume may be an important neuroimaging biomarker in poststroke dementia, as it has been associated with many other forms of dementia. However, studying hippocampal volume using MRI requires hippocampal segmentation. Advances in automated segmentation methods have allowed for studying the hippocampus on a large scale, which is important for robust results in the heterogeneous stroke population. However, most of these automated methods use a single atlas-based approach and may fail in the presence of severe structural abnormalities common in stroke. Hippodeep, a new convolutional neural network-based hippocampal segmentation method, does not rely solely on a single atlas-based approach and thus may be better suited for stroke populations. Here, we compared quality control and the accuracy of segmentations generated by Hippodeep and two well-accepted hippocampal segmentation methods on stroke MRIs (FreeSurfer 6.0 whole hippocampus and FreeSurfer 6.0 sum of hippocampal subfields). Quality control was performed using a stringent protocol for visual inspection of the segmentations, and accuracy was measured as volumetric correlation with manual segmentations. Hippodeep performed significantly better than both FreeSurfer methods in terms of quality control. All three automated segmentation methods had good correlation with manual segmentations and no one method was significantly more correlated than the others. Overall, this study suggests that both Hippodeep and FreeSurfer may be useful for hippocampal segmentation in stroke rehabilitation research, but Hippodeep may be more robust to stroke lesion anatomy.As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long-term quality of life for stroke survivors. Hippocampal volume may be an important neuroimaging biomarker in poststroke dementia, as it has been associated with many other forms of dementia. However, studying hippocampal volume using MRI requires hippocampal segmentation. Advances in automated segmentation methods have allowed for studying the hippocampus on a large scale, which is important for robust results in the heterogeneous stroke population. However, most of these automated methods use a single atlas-based approach and may fail in the presence of severe structural abnormalities common in stroke. Hippodeep, a new convolutional neural network-based hippocampal segmentation method, does not rely solely on a single atlas-based approach and thus may be better suited for stroke populations. Here, we compared quality control and the accuracy of segmentations generated by Hippodeep and two well-accepted hippocampal segmentation methods on stroke MRIs (FreeSurfer 6.0 whole hippocampus and FreeSurfer 6.0 sum of hippocampal subfields). Quality control was performed using a stringent protocol for visual inspection of the segmentations, and accuracy was measured as volumetric correlation with manual segmentations. Hippodeep performed significantly better than both FreeSurfer methods in terms of quality control. All three automated segmentation methods had good correlation with manual segmentations and no one method was significantly more correlated than the others. Overall, this study suggests that both Hippodeep and FreeSurfer may be useful for hippocampal segmentation in stroke rehabilitation research, but Hippodeep may be more robust to stroke lesion anatomy. |
Author | Tubi, Meral A. Jahanshad, Neda Braskie, Meredith N. Liew, Sook‐Lei Zavaliangos‐Petropulu, Artemis Zhu, Alyssa Thompson, Paul M. Haddad, Elizabeth |
AuthorAffiliation | 2 Imaging Genetics Center, Mark & Mary Stevens Institute for Neuroimaging & Informatics Keck School of Medicine of USC Marina del Rey California USA 1 Neural Plasticity and Neurorehabilitation Laboratory University of Southern California Los Angeles California USA 3 Chan Division of Occupational Science and Occupational Therapy Ostrow School of Dentistry, University of Southern California Los Angeles California USA |
AuthorAffiliation_xml | – name: 1 Neural Plasticity and Neurorehabilitation Laboratory University of Southern California Los Angeles California USA – name: 3 Chan Division of Occupational Science and Occupational Therapy Ostrow School of Dentistry, University of Southern California Los Angeles California USA – name: 2 Imaging Genetics Center, Mark & Mary Stevens Institute for Neuroimaging & Informatics Keck School of Medicine of USC Marina del Rey California USA |
Author_xml | – sequence: 1 givenname: Artemis orcidid: 0000-0003-1953-8663 surname: Zavaliangos‐Petropulu fullname: Zavaliangos‐Petropulu, Artemis organization: Keck School of Medicine of USC – sequence: 2 givenname: Meral A. surname: Tubi fullname: Tubi, Meral A. organization: Keck School of Medicine of USC – sequence: 3 givenname: Elizabeth surname: Haddad fullname: Haddad, Elizabeth organization: Keck School of Medicine of USC – sequence: 4 givenname: Alyssa surname: Zhu fullname: Zhu, Alyssa organization: Keck School of Medicine of USC – sequence: 5 givenname: Meredith N. surname: Braskie fullname: Braskie, Meredith N. organization: Keck School of Medicine of USC – sequence: 6 givenname: Neda surname: Jahanshad fullname: Jahanshad, Neda organization: Keck School of Medicine of USC – sequence: 7 givenname: Paul M. surname: Thompson fullname: Thompson, Paul M. organization: Keck School of Medicine of USC – sequence: 8 givenname: Sook‐Lei orcidid: 0000-0001-5935-4215 surname: Liew fullname: Liew, Sook‐Lei email: sliew@chan.usc.edu organization: Ostrow School of Dentistry, University of Southern California |
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Cites_doi | 10.1002/hipo.22717 10.1016/j.media.2017.11.004 10.1038/mp.2015.69 10.1016/S1474-4422(05)70221-0 10.1007/BF00308809 10.1016/j.neuroimage.2010.09.025 10.1038/ncomms13624 10.1002/hbm.25015 10.1093/cercor/bhy109 10.1161/STROKEAHA.108.536144 10.1161/CIRCRESAHA.116.308413 10.1016/j.jalz.2014.05.1756 10.1037/0033-2909.86.2.420 10.1177/1545968316662708 10.1016/j.biopsych.2013.11.020 10.1016/j.neuroimage.2006.01.021 10.1016/j.neuroimage.2019.116485 10.1097/NEN.0000000000000054 10.18632/aging.101931 10.1016/j.nicl.2019.102008 10.1161/STROKEAHA.111.636498 10.1212/WNL.0000000000004086 10.1038/mp.2015.63 10.1016/j.jcm.2016.02.012 10.1111/ijs.12301 10.1038/sdata.2018.11 10.1016/S1474-4422(18)30497-6 10.1016/j.neuroimage.2019.05.017 10.1016/j.nicl.2018.10.019 10.3389/fninf.2019.00013 10.1016/S0896-6273(02)00569-X 10.1016/S1474-4422(17)30343-5 10.1016/j.dadm.2019.04.001 10.3233/JAD-180676 10.1016/j.jalz.2013.03.001 10.1016/j.nicl.2019.101904 10.1037/a0032837 10.1016/j.neuroimage.2006.01.015 10.1016/j.neuroimage.2015.04.042 10.1016/j.dadm.2016.10.006 10.1155/2018/4303161 10.1038/nrneurol.2017.16 10.1002/hbm.23559 10.1016/j.nicl.2012.08.002 10.1016/j.neuroimage.2012.01.021 10.1093/oso/9780195125894.001.0001 |
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Keywords | hippocampus MRI image segmentation stroke convolutional neural network lesion |
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References | 2017; 7 2017; 8 2018; 28 2006; 31 2009; 40 2013; 27 2019; 11 2017; 27 2019; 13 2015; 11 2002; 33 2017; 89 1991; 82 2011; 54 2019; 18 2003 2018; 66 2018; 43 2016; 15 2020; 208 2019a; 21 2017; 31 2018; 2018 2018; 5 2012; 1 2015; 115 2019b; 24 2016; 9968 2017; 16 2020 2017; 38 2019; 23 2017; 13 2016; 21 2005; 4 2017; 120 2014; 9 1979; 86 2014; 73 2012; 43 2019; 197 2014; 75 2012; 62 e_1_2_9_30_1 e_1_2_9_31_1 e_1_2_9_11_1 e_1_2_9_34_1 e_1_2_9_10_1 e_1_2_9_35_1 e_1_2_9_13_1 e_1_2_9_12_1 e_1_2_9_33_1 Yang X. (e_1_2_9_45_1) 2016; 9968 e_1_2_9_15_1 e_1_2_9_38_1 e_1_2_9_14_1 e_1_2_9_39_1 e_1_2_9_17_1 e_1_2_9_36_1 e_1_2_9_16_1 e_1_2_9_37_1 e_1_2_9_19_1 e_1_2_9_18_1 e_1_2_9_41_1 e_1_2_9_42_1 e_1_2_9_20_1 e_1_2_9_40_1 e_1_2_9_22_1 e_1_2_9_21_1 e_1_2_9_46_1 e_1_2_9_24_1 e_1_2_9_43_1 e_1_2_9_23_1 e_1_2_9_44_1 e_1_2_9_8_1 Nelson J. S. (e_1_2_9_32_1) 2003 e_1_2_9_7_1 e_1_2_9_6_1 e_1_2_9_5_1 e_1_2_9_4_1 e_1_2_9_3_1 e_1_2_9_2_1 e_1_2_9_9_1 e_1_2_9_26_1 e_1_2_9_25_1 e_1_2_9_28_1 e_1_2_9_47_1 e_1_2_9_27_1 e_1_2_9_48_1 e_1_2_9_29_1 |
References_xml | – volume: 54 start-page: 2033 issue: 3 year: 2011 end-page: 2044 article-title: A reproducible evaluation of ANTs similarity metric performance in brain image registration publication-title: NeuroImage – volume: 23 year: 2019 article-title: Hippocampal volume across age: Nomograms derived from over 19,700 people in UKBiobank publication-title: NeuroImage: Clinical – volume: 31 start-page: 3 issue: 1 year: 2017 end-page: 24 article-title: Can neurological biomarkers of brain impairment be used to predict poststroke motor recovery? A systematic review publication-title: Neurorehabilitation and Neural Repair – volume: 11 start-page: 184 issue: 2 year: 2015 end-page: 194 article-title: Operationalizing protocol differences for EADC‐ADNI manual hippocampal segmentation publication-title: Alzheimer's and Dementia – volume: 1 start-page: 1 issue: 1 year: 2012 end-page: 17 article-title: Neuroimaging of structural pathology and connectomics in traumatic brain injury: Toward personalized outcome prediction publication-title: NeuroImage: Clinical – volume: 9968 start-page: 97 year: 2016 end-page: 107 article-title: Registration of pathological images publication-title: Synthesis in Medical Imaging – volume: 8 year: 2017 article-title: Novel genetic loci associated with hippocampal volume publication-title: Nature Communications – volume: 21 start-page: 547 issue: 4 year: 2016 end-page: 553 article-title: Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium publication-title: Molecular Psychiatry – volume: 7 start-page: 11 year: 2017 end-page: 23 article-title: STROKOG (stroke and cognition consortium): An international consortium to examine the epidemiology, diagnosis, and treatment of neurocognitive disorders in relation to cerebrovascular disease publication-title: Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring – year: 2003 – volume: 27 start-page: 481 issue: 5 year: 2017 end-page: 494 article-title: Hippocampal subfields at ultra high field MRI: An overview of segmentation and measurement methods publication-title: Hippocampus – volume: 13 year: 2019 article-title: Trajectories of the hippocampal subfields atrophy in the Alzheimer's disease: A structural imaging study publication-title: Frontiers in Neuroinformatics – volume: 18 start-page: 223 issue: 3 year: 2019 end-page: 225 article-title: Dementia risk after transient ischaemic attack and stroke publication-title: The Lancet Neurology – volume: 208 start-page: 116485 year: 2020 article-title: Hippocampal diaschisis contributes to anosognosia for hemiplegia: Evidence from lesion network‐symptom‐mapping publication-title: NeuroImage – volume: 75 start-page: 527 issue: 7 year: 2014 end-page: 533 article-title: A focus on structural brain imaging in the Alzheimer's disease Neuroimaging Initiative publication-title: Biological Psychiatry – volume: 120 start-page: 439 issue: 3 year: 2017 end-page: 448 article-title: Stroke compendium global burden of stroke effects of neurologic injury on cardiovascular function vascular cognitive impairment publication-title: Circulation Research – volume: 24 year: 2019b article-title: Assessment of longitudinal hippocampal atrophy in the first year after ischemic stroke using automate segmentation techniques publication-title: Neuroimage: Clinical – volume: 73 start-page: 305 issue: 4 year: 2014 end-page: 311 article-title: Neuron volumes in hippocampal subfields in delayed poststroke and aging‐related dementias publication-title: Journal of Neuropathology & Experimental Neurology – volume: 82 start-page: 239 issue: 4 year: 1991 end-page: 259 article-title: Neuropathological stageing of Alzheimer‐related changes publication-title: Acta Neuropathologica – volume: 62 start-page: 774 year: 2012 end-page: 781 article-title: FreeSurfer publication-title: NeuroImage – volume: 86 start-page: 420 issue: 2 year: 1979 end-page: 428 article-title: Intraclass correlations: Uses in assessing rater reliability publication-title: Psychological Bulletin – volume: 40 start-page: 2042 issue: 6 year: 2009 end-page: 2045 article-title: Hippocampal lesion patterns in acute posterior cerebral artery stroke: Clinical and MRI findings publication-title: Stroke – volume: 11 start-page: 2542 issue: 9 year: 2019 end-page: 2544 article-title: Aging and ischemic stroke publication-title: Aging – volume: 2018 start-page: 1 year: 2018 end-page: 13 article-title: Brain midline shift measurement and its automation: A review of techniques and algorithms publication-title: International Journal of Biomedical Imaging – volume: 43 start-page: 808 issue: 3 year: 2012 end-page: 814 article-title: Hippocampal neuronal atrophy and cognitive function in delayed poststroke and aging‐related dementias publication-title: Stroke – volume: 15 start-page: 155 issue: 2 year: 2016 end-page: 163 article-title: A guideline of selecting and reporting intraclass correlation coefficients for reliability research publication-title: Journal of Chiropractic Medicine – volume: 197 start-page: 589 year: 2019 end-page: 597 article-title: Testing a deep convolutional neural network for automated hippocampus segmentation in a longitudinal sample of healthy participants publication-title: NeuroImage – volume: 9 start-page: 824 issue: 6 year: 2014 end-page: 828 article-title: Charting cognitive and volumetric trajectories after stroke: Protocol for the cognition and neocortical volume after stroke (CANVAS) study publication-title: International Journal of Stroke – volume: 11 start-page: 439 year: 2019 end-page: 449 article-title: Progress update from the hippocampal subfields group publication-title: Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring – year: 2020 article-title: The ENIGMA Stroke Recovery Working Group: Big data neuroimaging to study brain‐behavior relationships after stroke publication-title: Human Brain Mapping – volume: 5 year: 2018 article-title: A large, open source dataset of stroke anatomical brain images and manual lesion segmentations publication-title: Scientific Data – volume: 38 start-page: 2875 issue: 6 year: 2017 end-page: 2896 article-title: Your algorithm might think the hippocampus grows in Alzheimer's disease: Caveats of longitudinal automated hippocampal volumetry publication-title: Human Brain Mapping – volume: 4 start-page: 752 issue: 11 year: 2005 end-page: 759 article-title: Poststroke dementia publication-title: The Lancet Neurology – volume: 11 start-page: 111 issue: 2 year: 2015 end-page: 125 article-title: The EADC‐ADNI harmonized protocol for manual hippocampal segmentation on magnetic resonance: Evidence of validity publication-title: Alzheimer's and Dementia – volume: 115 start-page: 117 year: 2015 end-page: 137 article-title: A computational atlas of the hippocampal formation using ex vivo, ultra‐high resolution MRI: Application to adaptive segmentation of in vivo MRI publication-title: NeuroImage – volume: 66 start-page: 811 issue: 2 year: 2018 end-page: 823 article-title: Alzheimer's disease biomarkers have distinct associations with specific hippocampal subfield volumes publication-title: Journal of Alzheimer's Disease – volume: 31 start-page: 968 issue: 3 year: 2006 end-page: 980 article-title: An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest publication-title: NeuroImage – volume: 21 start-page: 806 issue: 6 year: 2016 end-page: 812 article-title: Subcortical brain alterations in major depressive disorder: Findings from the ENIGMA Major Depressive Disorder working group publication-title: Molecular Psychiatry – volume: 33 start-page: 341 issue: 3 year: 2002 end-page: 355 article-title: Whole brain segmentation: Neurotechnique automated labeling of neuroanatomical structures in the human brain publication-title: Neuron – volume: 13 start-page: 148 issue: 3 year: 2017 end-page: 159 article-title: Early‐onset and delayed‐onset poststroke dementia‐revisiting the mechanisms publication-title: Nature Reviews Neurology – volume: 89 start-page: 116 issue: 2 year: 2017 end-page: 124 article-title: Structural MRI markers of brain aging early after ischemic stroke publication-title: Neurology – volume: 28 start-page: 2959 issue: 8 year: 2018 end-page: 2975 article-title: Sex differences in the adult human brain: Evidence from 5216 UKbiobank participants publication-title: Cerebral Cortex – volume: 21 year: 2019a article-title: A comparison of automated segmentation and manual tracing in estimating hippocampal volume in ischemic stroke and healthy control participants publication-title: NeuroImage: Clinical – volume: 27 start-page: 438 issue: 4 year: 2013 end-page: 451 article-title: Heterogeneity of brain lesions in pediatric traumatic brain injury publication-title: Neuropsychology – volume: 43 start-page: 214 year: 2018 end-page: 228 article-title: Segmentation of the hippocampus by transferring algorithmic knowledge for large cohort processing publication-title: Medical Image Analysis – volume: 31 start-page: 1116 issue: 3 year: 2006 end-page: 1128 article-title: User‐guided 3D active contour segmentation of anatomical structures: Significantly improved efficiency and reliability publication-title: NeuroImage – volume: 16 start-page: 862 issue: 11 year: 2017 end-page: 864 article-title: Pathology and hippocampal atrophy in Alzheimer's disease publication-title: The Lancet Neurology – ident: e_1_2_9_16_1 doi: 10.1002/hipo.22717 – ident: e_1_2_9_42_1 doi: 10.1016/j.media.2017.11.004 – ident: e_1_2_9_39_1 doi: 10.1038/mp.2015.69 – ident: e_1_2_9_26_1 doi: 10.1016/S1474-4422(05)70221-0 – ident: e_1_2_9_5_1 doi: 10.1007/BF00308809 – ident: e_1_2_9_2_1 doi: 10.1016/j.neuroimage.2010.09.025 – ident: e_1_2_9_18_1 doi: 10.1038/ncomms13624 – ident: e_1_2_9_29_1 doi: 10.1002/hbm.25015 – ident: e_1_2_9_36_1 doi: 10.1093/cercor/bhy109 – ident: e_1_2_9_41_1 doi: 10.1161/STROKEAHA.108.536144 – ident: e_1_2_9_10_1 doi: 10.1161/CIRCRESAHA.116.308413 – ident: e_1_2_9_13_1 doi: 10.1016/j.jalz.2014.05.1756 – ident: e_1_2_9_40_1 doi: 10.1037/0033-2909.86.2.420 – ident: e_1_2_9_23_1 doi: 10.1177/1545968316662708 – ident: e_1_2_9_6_1 doi: 10.1016/j.biopsych.2013.11.020 – ident: e_1_2_9_8_1 doi: 10.1016/j.neuroimage.2006.01.021 – ident: e_1_2_9_24_1 doi: 10.1016/j.neuroimage.2019.116485 – ident: e_1_2_9_15_1 doi: 10.1097/NEN.0000000000000054 – ident: e_1_2_9_46_1 doi: 10.18632/aging.101931 – ident: e_1_2_9_22_1 doi: 10.1016/j.nicl.2019.102008 – ident: e_1_2_9_14_1 doi: 10.1161/STROKEAHA.111.636498 – ident: e_1_2_9_44_1 doi: 10.1212/WNL.0000000000004086 – ident: e_1_2_9_43_1 doi: 10.1038/mp.2015.63 – ident: e_1_2_9_25_1 doi: 10.1016/j.jcm.2016.02.012 – ident: e_1_2_9_7_1 doi: 10.1111/ijs.12301 – ident: e_1_2_9_28_1 doi: 10.1038/sdata.2018.11 – ident: e_1_2_9_9_1 doi: 10.1016/S1474-4422(18)30497-6 – ident: e_1_2_9_34_1 doi: 10.1016/j.neuroimage.2019.05.017 – ident: e_1_2_9_21_1 doi: 10.1016/j.nicl.2018.10.019 – ident: e_1_2_9_48_1 doi: 10.3389/fninf.2019.00013 – ident: e_1_2_9_12_1 doi: 10.1016/S0896-6273(02)00569-X – ident: e_1_2_9_17_1 doi: 10.1016/S1474-4422(17)30343-5 – ident: e_1_2_9_35_1 doi: 10.1016/j.dadm.2019.04.001 – ident: e_1_2_9_31_1 doi: 10.3233/JAD-180676 – ident: e_1_2_9_4_1 doi: 10.1016/j.jalz.2013.03.001 – ident: e_1_2_9_33_1 doi: 10.1016/j.nicl.2019.101904 – ident: e_1_2_9_3_1 doi: 10.1037/a0032837 – ident: e_1_2_9_47_1 doi: 10.1016/j.neuroimage.2006.01.015 – ident: e_1_2_9_19_1 doi: 10.1016/j.neuroimage.2015.04.042 – ident: e_1_2_9_37_1 doi: 10.1016/j.dadm.2016.10.006 – volume: 9968 start-page: 97 year: 2016 ident: e_1_2_9_45_1 article-title: Registration of pathological images publication-title: Synthesis in Medical Imaging – ident: e_1_2_9_27_1 doi: 10.1155/2018/4303161 – ident: e_1_2_9_30_1 doi: 10.1038/nrneurol.2017.16 – ident: e_1_2_9_38_1 doi: 10.1002/hbm.23559 – ident: e_1_2_9_20_1 doi: 10.1016/j.nicl.2012.08.002 – ident: e_1_2_9_11_1 doi: 10.1016/j.neuroimage.2012.01.021 – volume-title: Principles and practice of neuropathology year: 2003 ident: e_1_2_9_32_1 doi: 10.1093/oso/9780195125894.001.0001 |
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Snippet | As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long‐term quality of life for stroke... As stroke mortality rates decrease, there has been a surge of effort to study poststroke dementia (PSD) to improve long-term quality of life for stroke... |
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SubjectTerms | Abnormalities Accuracy Aging Alzheimer's disease Artificial neural networks Atrophy Automation Biomarkers Cognition & reasoning Consortia convolutional neural network Datasets as Topic Dementia Dementia disorders Hippocampus Hippocampus - diagnostic imaging Hippocampus - pathology Humans Image processing Image Processing, Computer-Assisted - methods Image Processing, Computer-Assisted - standards Image segmentation Inspection lesion Magnetic resonance imaging Magnetic Resonance Imaging - methods Magnetic Resonance Imaging - standards Medical imaging Methods MRI Neural networks Neural Networks, Computer Neuroimaging Neuroimaging - methods Neuroimaging - standards Pathology Quality Control Quality of life Rehabilitation Robustness Scanners Stroke Stroke - diagnostic imaging Stroke - pathology |
Title | Testing a convolutional neural network‐based hippocampal segmentation method in a stroke population |
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