Association between fully automated MRI-based volumetry of different brain regions and neuropsychological test performance in patients with amnestic mild cognitive impairment and Alzheimer’s disease
Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance...
Saved in:
Published in | European archives of psychiatry and clinical neuroscience Vol. 263; no. 4; pp. 335 - 344 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer-Verlag
01.06.2013
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0940-1334 1433-8491 1433-8491 |
DOI | 10.1007/s00406-012-0350-7 |
Cover
Loading…
Abstract | Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance in amnestic MCI and patients with mild dementia due to Alzheimer’s disease (AD) in a cross-sectional and longitudinal study. In order to assess a possible prognostic value of fully automated MRI-based volumetry for future cognitive performance, the rate of change of neuropsychological test performance over time was also tested for its correlation with fully automated MRI-based volumetry at baseline. In 50 subjects, 18 with amnestic MCI, 21 with mild AD, and 11 controls, neuropsychological testing and T1-weighted MRI were performed at baseline and at a mean follow-up interval of 2.1 ± 0.5 years (
n
= 19). Fully automated MRI volumetry of the grey matter volume (GMV) was performed using a combined stereotactic normalisation and segmentation approach as provided by SPM8 and a set of pre-defined binary lobe masks. Left and right hippocampus masks were derived from probabilistic cytoarchitectonic maps. Volumes of the inner and outer liquor space were also determined automatically from the MRI. Pearson’s test was used for the correlation analyses. Left hippocampal GMV was significantly correlated with performance in memory tasks, and left temporal GMV was related to performance in language tasks. Bilateral frontal, parietal and occipital GMVs were correlated to performance in neuropsychological tests comprising multiple domains. Rate of GMV change in the left hippocampus was correlated with decline of performance in the Boston Naming Test (BNT), Mini-Mental Status Examination, and trail making test B (TMT-B). The decrease of BNT and TMT-A performance over time correlated with the loss of grey matter in multiple brain regions. We conclude that fully automated MRI-based volumetry allows detection of regional grey matter volume loss that correlates with neuropsychological performance in patients with amnestic MCI or mild AD. Because of the high level of automation, MRI-based volumetry may easily be integrated into clinical routine to complement the current diagnostic procedure. |
---|---|
AbstractList | Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance in amnestic MCI and patients with mild dementia due to Alzheimer's disease (AD) in a cross-sectional and longitudinal study. In order to assess a possible prognostic value of fully automated MRI-based volumetry for future cognitive performance, the rate of change of neuropsychological test performance over time was also tested for its correlation with fully automated MRI-based volumetry at baseline. In 50 subjects, 18 with amnestic MCI, 21 with mild AD, and 11 controls, neuropsychological testing and T1-weighted MRI were performed at baseline and at a mean follow-up interval of 2.1 plus or minus 0.5 years (n = 19). Fully automated MRI volumetry of the grey matter volume (GMV) was performed using a combined stereotactic normalisation and segmentation approach as provided by SPM8 and a set of pre-defined binary lobe masks. Left and right hippocampus masks were derived from probabilistic cytoarchitectonic maps. Volumes of the inner and outer liquor space were also determined automatically from the MRI. Pearson's test was used for the correlation analyses. Left hippocampal GMV was significantly correlated with performance in memory tasks, and left temporal GMV was related to performance in language tasks. Bilateral frontal, parietal and occipital GMVs were correlated to performance in neuropsychological tests comprising multiple domains. Rate of GMV change in the left hippocampus was correlated with decline of performance in the Boston Naming Test (BNT), Mini-Mental Status Examination, and trail making test B (TMT-B). The decrease of BNT and TMT-A performance over time correlated with the loss of grey matter in multiple brain regions. We conclude that fully automated MRI-based volumetry allows detection of regional grey matter volume loss that correlates with neuropsychological performance in patients with amnestic MCI or mild AD. Because of the high level of automation, MRI-based volumetry may easily be integrated into clinical routine to complement the current diagnostic procedure. Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance in amnestic MCI and patients with mild dementia due to Alzheimer's disease (AD) in a cross-sectional and longitudinal study. In order to assess a possible prognostic value of fully automated MRI-based volumetry for future cognitive performance, the rate of change of neuropsychological test performance over time was also tested for its correlation with fully automated MRI-based volumetry at baseline. In 50 subjects, 18 with amnestic MCI, 21 with mild AD, and 11 controls, neuropsychological testing and T1-weighted MRI were performed at baseline and at a mean follow-up interval of 2.1 ± 0.5 years (n = 19). Fully automated MRI volumetry of the grey matter volume (GMV) was performed using a combined stereotactic normalisation and segmentation approach as provided by SPM8 and a set of pre-defined binary lobe masks. Left and right hippocampus masks were derived from probabilistic cytoarchitectonic maps. Volumes of the inner and outer liquor space were also determined automatically from the MRI. Pearson's test was used for the correlation analyses. Left hippocampal GMV was significantly correlated with performance in memory tasks, and left temporal GMV was related to performance in language tasks. Bilateral frontal, parietal and occipital GMVs were correlated to performance in neuropsychological tests comprising multiple domains. Rate of GMV change in the left hippocampus was correlated with decline of performance in the Boston Naming Test (BNT), Mini-Mental Status Examination, and trail making test B (TMT-B). The decrease of BNT and TMT-A performance over time correlated with the loss of grey matter in multiple brain regions. We conclude that fully automated MRI-based volumetry allows detection of regional grey matter volume loss that correlates with neuropsychological performance in patients with amnestic MCI or mild AD. Because of the high level of automation, MRI-based volumetry may easily be integrated into clinical routine to complement the current diagnostic procedure.[PUBLICATION ABSTRACT] Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance in amnestic MCI and patients with mild dementia due to Alzheimer’s disease (AD) in a cross-sectional and longitudinal study. In order to assess a possible prognostic value of fully automated MRI-based volumetry for future cognitive performance, the rate of change of neuropsychological test performance over time was also tested for its correlation with fully automated MRI-based volumetry at baseline. In 50 subjects, 18 with amnestic MCI, 21 with mild AD, and 11 controls, neuropsychological testing and T1-weighted MRI were performed at baseline and at a mean follow-up interval of 2.1 ± 0.5 years ( n = 19). Fully automated MRI volumetry of the grey matter volume (GMV) was performed using a combined stereotactic normalisation and segmentation approach as provided by SPM8 and a set of pre-defined binary lobe masks. Left and right hippocampus masks were derived from probabilistic cytoarchitectonic maps. Volumes of the inner and outer liquor space were also determined automatically from the MRI. Pearson’s test was used for the correlation analyses. Left hippocampal GMV was significantly correlated with performance in memory tasks, and left temporal GMV was related to performance in language tasks. Bilateral frontal, parietal and occipital GMVs were correlated to performance in neuropsychological tests comprising multiple domains. Rate of GMV change in the left hippocampus was correlated with decline of performance in the Boston Naming Test (BNT), Mini-Mental Status Examination, and trail making test B (TMT-B). The decrease of BNT and TMT-A performance over time correlated with the loss of grey matter in multiple brain regions. We conclude that fully automated MRI-based volumetry allows detection of regional grey matter volume loss that correlates with neuropsychological performance in patients with amnestic MCI or mild AD. Because of the high level of automation, MRI-based volumetry may easily be integrated into clinical routine to complement the current diagnostic procedure. Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance in amnestic MCI and patients with mild dementia due to Alzheimer's disease (AD) in a cross-sectional and longitudinal study. In order to assess a possible prognostic value of fully automated MRI-based volumetry for future cognitive performance, the rate of change of neuropsychological test performance over time was also tested for its correlation with fully automated MRI-based volumetry at baseline. In 50 subjects, 18 with amnestic MCI, 21 with mild AD, and 11 controls, neuropsychological testing and T1-weighted MRI were performed at baseline and at a mean follow-up interval of 2.1 ± 0.5 years (n = 19). Fully automated MRI volumetry of the grey matter volume (GMV) was performed using a combined stereotactic normalisation and segmentation approach as provided by SPM8 and a set of pre-defined binary lobe masks. Left and right hippocampus masks were derived from probabilistic cytoarchitectonic maps. Volumes of the inner and outer liquor space were also determined automatically from the MRI. Pearson's test was used for the correlation analyses. Left hippocampal GMV was significantly correlated with performance in memory tasks, and left temporal GMV was related to performance in language tasks. Bilateral frontal, parietal and occipital GMVs were correlated to performance in neuropsychological tests comprising multiple domains. Rate of GMV change in the left hippocampus was correlated with decline of performance in the Boston Naming Test (BNT), Mini-Mental Status Examination, and trail making test B (TMT-B). The decrease of BNT and TMT-A performance over time correlated with the loss of grey matter in multiple brain regions. We conclude that fully automated MRI-based volumetry allows detection of regional grey matter volume loss that correlates with neuropsychological performance in patients with amnestic MCI or mild AD. Because of the high level of automation, MRI-based volumetry may easily be integrated into clinical routine to complement the current diagnostic procedure.Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance in amnestic MCI and patients with mild dementia due to Alzheimer's disease (AD) in a cross-sectional and longitudinal study. In order to assess a possible prognostic value of fully automated MRI-based volumetry for future cognitive performance, the rate of change of neuropsychological test performance over time was also tested for its correlation with fully automated MRI-based volumetry at baseline. In 50 subjects, 18 with amnestic MCI, 21 with mild AD, and 11 controls, neuropsychological testing and T1-weighted MRI were performed at baseline and at a mean follow-up interval of 2.1 ± 0.5 years (n = 19). Fully automated MRI volumetry of the grey matter volume (GMV) was performed using a combined stereotactic normalisation and segmentation approach as provided by SPM8 and a set of pre-defined binary lobe masks. Left and right hippocampus masks were derived from probabilistic cytoarchitectonic maps. Volumes of the inner and outer liquor space were also determined automatically from the MRI. Pearson's test was used for the correlation analyses. Left hippocampal GMV was significantly correlated with performance in memory tasks, and left temporal GMV was related to performance in language tasks. Bilateral frontal, parietal and occipital GMVs were correlated to performance in neuropsychological tests comprising multiple domains. Rate of GMV change in the left hippocampus was correlated with decline of performance in the Boston Naming Test (BNT), Mini-Mental Status Examination, and trail making test B (TMT-B). The decrease of BNT and TMT-A performance over time correlated with the loss of grey matter in multiple brain regions. We conclude that fully automated MRI-based volumetry allows detection of regional grey matter volume loss that correlates with neuropsychological performance in patients with amnestic MCI or mild AD. Because of the high level of automation, MRI-based volumetry may easily be integrated into clinical routine to complement the current diagnostic procedure. Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or dementia. We aimed at investigating the relation between fully automated MRI-based volumetric measures and neuropsychological test performance in amnestic MCI and patients with mild dementia due to Alzheimer's disease (AD) in a cross-sectional and longitudinal study. In order to assess a possible prognostic value of fully automated MRI-based volumetry for future cognitive performance, the rate of change of neuropsychological test performance over time was also tested for its correlation with fully automated MRI-based volumetry at baseline. In 50 subjects, 18 with amnestic MCI, 21 with mild AD, and 11 controls, neuropsychological testing and T1-weighted MRI were performed at baseline and at a mean follow-up interval of 2.1 ± 0.5 years (n = 19). Fully automated MRI volumetry of the grey matter volume (GMV) was performed using a combined stereotactic normalisation and segmentation approach as provided by SPM8 and a set of pre-defined binary lobe masks. Left and right hippocampus masks were derived from probabilistic cytoarchitectonic maps. Volumes of the inner and outer liquor space were also determined automatically from the MRI. Pearson's test was used for the correlation analyses. Left hippocampal GMV was significantly correlated with performance in memory tasks, and left temporal GMV was related to performance in language tasks. Bilateral frontal, parietal and occipital GMVs were correlated to performance in neuropsychological tests comprising multiple domains. Rate of GMV change in the left hippocampus was correlated with decline of performance in the Boston Naming Test (BNT), Mini-Mental Status Examination, and trail making test B (TMT-B). The decrease of BNT and TMT-A performance over time correlated with the loss of grey matter in multiple brain regions. We conclude that fully automated MRI-based volumetry allows detection of regional grey matter volume loss that correlates with neuropsychological performance in patients with amnestic MCI or mild AD. Because of the high level of automation, MRI-based volumetry may easily be integrated into clinical routine to complement the current diagnostic procedure. |
Author | Spies, Lothar Lehmbeck, Jan T. Eichenlaub, Martin Arlt, Sönke Jahn, Holger Buchert, Ralph |
Author_xml | – sequence: 1 givenname: Sönke surname: Arlt fullname: Arlt, Sönke email: arlt@uke.de, arlt@uke.uni-hamburg.de organization: Department of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf – sequence: 2 givenname: Ralph surname: Buchert fullname: Buchert, Ralph organization: Department of Nuclear Medicine – sequence: 3 givenname: Lothar surname: Spies fullname: Spies, Lothar organization: jung diagnostics GmbH – sequence: 4 givenname: Martin surname: Eichenlaub fullname: Eichenlaub, Martin organization: Department of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf – sequence: 5 givenname: Jan T. surname: Lehmbeck fullname: Lehmbeck, Jan T. organization: Department of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf – sequence: 6 givenname: Holger surname: Jahn fullname: Jahn, Holger organization: Department of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22940716$$D View this record in MEDLINE/PubMed |
BookMark | eNqNks1u1DAUhSNURKeFB2CDLLFhE7j-STJZjioolYqQEKwjx7mecRXbwXZaDStegzfqc_AkOEwroUogVrbk7xwf-56T4sh5h0XxnMJrCtC8iQAC6hIoK4FXUDaPihUVnJdr0dKjYgWtgJJyLo6LkxivAIBWDJ4Ux4zlk4bWq-J2E6NXRibjHekx3SA6oudx3BM5J29lwoF8-HRR9jLm3bUfZ4sp7InXZDBaY0CXSB-kcSTgNrtEIt1AHM7BT3Gvdn70W6PkSBLGRCYM2gcrnUKSJVO-OBtEcmPSjkjrMmMUsWYciPJbZ5K5zqCdpAl2uWnx3ozfdmgshp_ff8ScImLO9rR4rOUY8dndelp8eff289n78vLj-cXZ5rJUAqpU9kqouhZ6EOtK1Fzzng2SrkG1TCo2sJYLvhZDpVqQXPWy1_nPWmw0HTgD1Py0eHXwnYL_Oue4nTVR4ThKh36OHeUNg6puG_EfaNWIDDZNRl8-QK_8HFx-yELVLWUAPFMv7qi5tzh0UzBWhn13P84MNAdABR9jQN0pk37PNuUJjR2FbilOdyhOl4vTLcXplgD0gfLe_F8adtDEzLothj9C_1X0C7F_2kE |
CitedBy_id | crossref_primary_10_1016_j_jneumeth_2014_01_033 crossref_primary_10_1097_WNN_0000000000000295 crossref_primary_10_1371_journal_pone_0162889 crossref_primary_10_1186_s13195_015_0147_9 crossref_primary_10_3233_JAD_230206 crossref_primary_10_1016_j_bbr_2016_05_061 crossref_primary_10_1016_j_nicl_2013_08_006 crossref_primary_10_1093_arclin_acu012 crossref_primary_10_1159_000517822 crossref_primary_10_1097_TGR_0000000000000286 crossref_primary_10_1016_j_nicl_2019_102158 crossref_primary_10_3233_JAD_142280 crossref_primary_10_3233_JAD_220877 crossref_primary_10_7717_peerj_8178 crossref_primary_10_1007_s00406_013_0409_0 crossref_primary_10_1080_24754269_2022_2064611 crossref_primary_10_3233_JAD_240150 crossref_primary_10_14412_2074_2711_2019_4_28_32 crossref_primary_10_1016_j_neurol_2024_02_394 crossref_primary_10_2174_1567205019666220418155130 crossref_primary_10_1016_j_neuroimage_2015_10_056 crossref_primary_10_2174_1871527322666230519113201 crossref_primary_10_1159_000479149 crossref_primary_10_1159_000455832 crossref_primary_10_1177_09622802211022404 crossref_primary_10_1111_cns_12317 crossref_primary_10_1016_j_neulet_2014_02_034 crossref_primary_10_3389_fnins_2023_1089134 crossref_primary_10_1007_s00429_024_02873_6 crossref_primary_10_12963_csd_14177 crossref_primary_10_3390_brainsci13050806 crossref_primary_10_1186_1465_9921_14_140 crossref_primary_10_3389_fnagi_2023_1052783 crossref_primary_10_1007_s12264_014_1490_8 crossref_primary_10_1016_j_psychres_2024_116103 crossref_primary_10_1590_1806_9282_66_4_512 crossref_primary_10_1016_j_pscychresns_2020_111043 crossref_primary_10_1038_s41598_024_67389_9 crossref_primary_10_1017_S1355617721000564 crossref_primary_10_31887_DCNS_2013_15_4_hjahn crossref_primary_10_1093_cercor_bhaa208 crossref_primary_10_1016_j_neurobiolaging_2013_02_002 crossref_primary_10_1080_13854046_2021_1900399 |
Cites_doi | 10.1097/WAD.0b013e318192e745 10.1016/j.neuroimage.2005.02.018 10.1007/s00429-005-0025-5 10.1007/s00415-004-0390-7 10.1016/j.neulet.2003.12.072 10.1016/S1053-8119(02)00026-5 10.1016/j.neuroimage.2005.02.042 10.1016/S1053-8119(09)70884-5 10.1016/j.pscychresns.2006.01.007 10.1002/hbm.20905 10.1159/000017133 10.1016/j.neuroimage.2009.12.125 10.1016/j.neuroimage.2004.12.034 10.1016/j.pscychresns.2010.03.003 10.1017/S003329179600431X 10.1002/hbm.20708 |
ContentType | Journal Article |
Copyright | Springer-Verlag 2012 Springer-Verlag Berlin Heidelberg 2013 |
Copyright_xml | – notice: Springer-Verlag 2012 – notice: Springer-Verlag Berlin Heidelberg 2013 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7TK 7X7 7XB 88E 88G 8AO 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH GNUQQ K9. M0S M1P M2M PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQQKQ PQUKI PRINS PSYQQ Q9U 7X8 |
DOI | 10.1007/s00406-012-0350-7 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Neurosciences Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Psychology Database (Alumni) ProQuest Pharma Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials Proquest Central ProQuest One ProQuest Central Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student ProQuest Health & Medical Complete (Alumni) ProQuest Health & Medical Collection Medical Database Psychology Database ProQuest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest One Psychology ProQuest Central Basic MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest One Psychology ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing ProQuest Pharma Collection ProQuest Central China ProQuest Central ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Health & Medical Research Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Central Basic ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Psychology Journals (Alumni) Neurosciences Abstracts ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest Psychology Journals ProQuest One Academic UKI Edition ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | Neurosciences Abstracts ProQuest One Psychology MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1433-8491 |
EndPage | 344 |
ExternalDocumentID | 2983864871 22940716 10_1007_s00406_012_0350_7 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GroupedDBID | --- -53 -5E -5G -BR -EM -Y2 -~C .86 .GJ .VR 06C 06D 0R~ 0VY 1N0 2.D 203 28- 29G 29~ 2J2 2JN 2JY 2KG 2KM 2LR 2P1 2VQ 2~H 30V 36B 3O- 3V. 4.4 406 408 409 40D 40E 53G 5GY 5QI 5RE 5VS 67Z 6NX 7X7 88E 8AO 8FI 8FJ 8UJ 95- 95. 95~ 96X AAAVM AABHQ AACDK AAHNG AAIAL AAJBT AAJKR AANXM AANZL AARHV AARTL AASML AATNV AATVU AAUYE AAWCG AAYIU AAYQN AAYTO AAYZH ABAKF ABBBX ABBXA ABDBF ABDZT ABECU ABFTV ABHLI ABHQN ABIPD ABIVO ABJNI ABJOX ABKCH ABKTR ABLJU ABMNI ABMQK ABNWP ABPLI ABQBU ABQSL ABSXP ABTEG ABTKH ABTMW ABULA ABUWG ABWNU ABXPI ACAOD ACBXY ACDTI ACGFS ACHSB ACHXU ACKNC ACMDZ ACMLO ACOKC ACOMO ACPIV ACPRK ACUDM ACUHS ACZOJ ADBBV ADHIR ADINQ ADJJI ADKNI ADKPE ADRFC ADTPH ADURQ ADYFF ADZKW AEBTG AEFIE AEFQL AEGAL AEGNC AEJHL AEJRE AEKMD AEMSY AENEX AEOHA AEPYU AESKC AETLH AEVLU AEXYK AFBBN AFEXP AFFNX AFKRA AFLOW AFQWF AFWTZ AFZKB AGAYW AGDGC AGGDS AGJBK AGMZJ AGQEE AGQMX AGRTI AGWIL AGWZB AGYKE AHAVH AHBYD AHIZS AHKAY AHMBA AHSBF AHYZX AIAKS AIGIU AIIXL AILAN AITGF AJBLW AJRNO AJZVZ AKMHD ALIPV ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AOCGG ARMRJ AXYYD AZFZN AZQEC B-. B0M BA0 BBWZM BDATZ BENPR BGNMA BPHCQ BSONS BVXVI CAG CCPQU COF CS3 CSCUP DDRTE DL5 DNIVK DPUIP DU5 DWQXO EAD EAP EBC EBD EBLON EBS EIOEI EJD EMB EMK EMOBN EN4 EPL EPS ESBYG ESX F5P FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRRFC FSGXE FWDCC FYUFA G-Y G-Z GGCAI GGRSB GJIRD GNUQQ GNWQR GQ6 GQ7 GQ8 GRRUI GXS H13 HF~ HG5 HG6 HMCUK HMJXF HQYDN HRMNR HVGLF HZ~ IAO IHE IHR IJ- IKXTQ IMOTQ IPY ITC ITM IWAJR IXC IZIGR IZQ I~X I~Z J-C J0Z JBSCW JCJTX JZLTJ KDC KOV KOW KPH LAS LLZTM M1P M2M M4Y MA- N2Q N9A NB0 NDZJH NPVJJ NQJWS NU0 O9- O93 O9G O9I O9J OAM P19 P9S PF0 PQQKQ PROAC PSQYO PSYQQ PT4 PT5 Q2X QOK QOR QOS R89 R9I RHV RIG RNI ROL RPX RRX RSV RZK S16 S1Z S26 S27 S28 S37 S3B SAP SCLPG SDE SDH SDM SHX SISQX SJYHP SMD SNE SNPRN SNX SOHCF SOJ SPISZ SRMVM SSLCW SSXJD STPWE SV3 SZ9 SZN T13 T16 TSG TSK TSV TT1 TUC TUS U2A U9L UG4 UKHRP UOJIU UTJUX UZXMN VC2 VFIZW W23 W48 WJK WK8 YLTOR Z45 Z7U Z7W Z82 Z87 Z8O Z8Q Z8V Z91 ZMTXR ZOVNA ZXP ~8M ~EX AAPKM AAYXX ABBRH ABDBE ABFSG ACSTC ADHKG AEZWR AFDZB AFHIU AFOHR AGQPQ AHPBZ AHWEU AIXLP ATHPR AYFIA CITATION PHGZM PHGZT CGR CUY CVF ECM EIF NPM 7TK 7XB 8FK ABRTQ K9. PJZUB PKEHL PPXIY PQEST PQUKI PRINS PUEGO Q9U 7X8 |
ID | FETCH-LOGICAL-c405t-bc4c664fd485463f3b2da180c92ac2d2934384d5c90a3cbabf0159e7f1d320ef3 |
IEDL.DBID | BENPR |
ISSN | 0940-1334 1433-8491 |
IngestDate | Fri Sep 05 06:21:53 EDT 2025 Fri Sep 05 06:27:02 EDT 2025 Sat Aug 23 14:51:39 EDT 2025 Thu Apr 03 07:07:27 EDT 2025 Thu Apr 24 23:11:03 EDT 2025 Tue Jul 01 04:31:13 EDT 2025 Fri Feb 21 02:36:13 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Keywords | Neuropsychology Alzheimer’s disease Mild cognitive impairment MRI volumetry Dementia |
Language | English |
License | http://www.springer.com/tdm |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c405t-bc4c664fd485463f3b2da180c92ac2d2934384d5c90a3cbabf0159e7f1d320ef3 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
PMID | 22940716 |
PQID | 1356912003 |
PQPubID | 47319 |
PageCount | 10 |
ParticipantIDs | proquest_miscellaneous_1372056974 proquest_miscellaneous_1357497477 proquest_journals_1356912003 pubmed_primary_22940716 crossref_citationtrail_10_1007_s00406_012_0350_7 crossref_primary_10_1007_s00406_012_0350_7 springer_journals_10_1007_s00406_012_0350_7 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 20130600 2013-6-00 2013-Jun 20130601 |
PublicationDateYYYYMMDD | 2013-06-01 |
PublicationDate_xml | – month: 6 year: 2013 text: 20130600 |
PublicationDecade | 2010 |
PublicationPlace | Berlin/Heidelberg |
PublicationPlace_xml | – name: Berlin/Heidelberg – name: Germany – name: Heidelberg |
PublicationTitle | European archives of psychiatry and clinical neuroscience |
PublicationTitleAbbrev | Eur Arch Psychiatry Clin Neurosci |
PublicationTitleAlternate | Eur Arch Psychiatry Clin Neurosci |
PublicationYear | 2013 |
Publisher | Springer-Verlag Springer Nature B.V |
Publisher_xml | – name: Springer-Verlag – name: Springer Nature B.V |
References | Kovacevic, Rafii, Brewer (CR3) 2009; 23 Basso, Yang, Warren, MacAvoy, Varma, Bronen, van Dyck (CR14) 2006; 146 Chetelat, Baron (CR1) 2003; 18 Amunts, Kedo, Kindler, Pieperhoff, Mohlberg, Shah, Habel, Schneider, Zilles (CR11) 2005; 210 Lemaitre, Crivello, Grassiot, Alperovitch, Tzourio, Mazoyer (CR8) 2005; 26 Morra, Tu, Apostolova, Green, Avedissian, Madsen, Parikshak, Hua, Toga, Jack, Schuff, Weiner, Thompson (CR4) 2009; 30 Fonov, Evans, McKinstry, Almli, Collins (CR9) 2009; 47 Apostolova, Morra, Green, Hwang, Avedissian, Woo, Cummings, Toga, Jack, Weiner, Thompson (CR12) 2010; 51 Pantel, Schroder, Schad, Friedlinger, Knopp, Schmitt, Geissler, Bluml, Essig, Sauer (CR16) 1997; 27 Golebiowski, Barcikowska, Pfeffer (CR2) 1999; 10 Eickhoff, Stephan, Mohlberg, Grefkes, Fink, Amunts, Zilles (CR10) 2005; 25 Pantel, Schonknecht, Essig, Schroder (CR15) 2004; 361 Teipel, Ewers, Wolf, Jessen, Kolsch, Arlt, Luckhaus, Schonknecht, Schmidtke, Heuser, Frolich, Ende, Pantel, Wiltfang, Rakebrandt, Peters, Born, Kornhuber, Hampel (CR6) 2010; 182 Ashburner, Friston (CR7) 2005; 26 van der Flier, van Buchem, Weverling-Rijnsburger, Mutsaers, Bollen, Admiraal-Behloul, Westendorp, Middelkoop (CR13) 2004; 251 Apostolova, Thompson, Green, Hwang, Zoumalan, Jack, Harvey, Petersen, Thal, Aisen, Toga, Cummings, Decarli (CR5) 2010; 31 K Amunts (350_CR11) 2005; 210 JH Morra (350_CR4) 2009; 30 G Chetelat (350_CR1) 2003; 18 J Pantel (350_CR16) 1997; 27 WM Flier van der (350_CR13) 2004; 251 M Golebiowski (350_CR2) 1999; 10 M Basso (350_CR14) 2006; 146 J Ashburner (350_CR7) 2005; 26 VS Fonov (350_CR9) 2009; 47 LG Apostolova (350_CR12) 2010; 51 SJ Teipel (350_CR6) 2010; 182 S Kovacevic (350_CR3) 2009; 23 H Lemaitre (350_CR8) 2005; 26 LG Apostolova (350_CR5) 2010; 31 SB Eickhoff (350_CR10) 2005; 25 J Pantel (350_CR15) 2004; 361 19474571 - Alzheimer Dis Assoc Disord. 2009 Apr-Jun;23(2):139-45 16524704 - Psychiatry Res. 2006 Apr 30;146(3):251-61 19172649 - Hum Brain Mapp. 2009 Sep;30(9):2766-88 10364646 - Dement Geriatr Cogn Disord. 1999 Jul-Aug;10(4):284-8 15311341 - J Neurol. 2004 Jun;251(6):671-5 16208455 - Anat Embryol (Berl). 2005 Dec;210(5-6):343-52 9122303 - Psychol Med. 1997 Jan;27(1):221-9 15955500 - Neuroimage. 2005 Jul 1;26(3):900-11 15955494 - Neuroimage. 2005 Jul 1;26(3):839-51 20143386 - Hum Brain Mapp. 2010 May;31(5):786-97 20493672 - Psychiatry Res. 2010 Jun 30;182(3):244-50 12595205 - Neuroimage. 2003 Feb;18(2):525-41 15850749 - Neuroimage. 2005 May 1;25(4):1325-35 20083211 - Neuroimage. 2010 May 15;51(1):488-99 15135882 - Neurosci Lett. 2004 May 6;361(1-3):17-20 |
References_xml | – volume: 23 start-page: 139 year: 2009 end-page: 145 ident: CR3 article-title: High-throughput, fully automated volumetry for prediction of Mmse and Cdr decline in mild cognitive impairment publication-title: Alzheimer Dis Assoc Disord doi: 10.1097/WAD.0b013e318192e745 – volume: 26 start-page: 839 year: 2005 end-page: 851 ident: CR7 article-title: Unified segmentation publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.02.018 – volume: 210 start-page: 343 year: 2005 end-page: 352 ident: CR11 article-title: Cytoarchitectonic mapping of the human amygdala, hippocampal region and entorhinal cortex: intersubject variability and probability maps publication-title: Anat Embryol (Berl) doi: 10.1007/s00429-005-0025-5 – volume: 251 start-page: 671 year: 2004 end-page: 675 ident: CR13 article-title: Memory complaints in patients with normal cognition are associated with smaller hippocampal volumes publication-title: J Neurol doi: 10.1007/s00415-004-0390-7 – volume: 361 start-page: 17 year: 2004 end-page: 20 ident: CR15 article-title: Distribution of cerebral atrophy assessed by magnetic resonance imaging reflects patterns of neuropsychological deficits in Alzheimer’s dementia publication-title: Neurosci Lett doi: 10.1016/j.neulet.2003.12.072 – volume: 18 start-page: 525 year: 2003 end-page: 541 ident: CR1 article-title: Early diagnosis of Alzheimer’s disease: contribution of structural neuroimaging publication-title: Neuroimage doi: 10.1016/S1053-8119(02)00026-5 – volume: 26 start-page: 900 year: 2005 end-page: 911 ident: CR8 article-title: Age- and sex-related effects on the neuroanatomy of healthy elderly publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.02.042 – volume: 47 start-page: 102 year: 2009 ident: CR9 article-title: Unbiased nonlinear average age-appropriate brain templates from birth to adulthood publication-title: NeuroImage doi: 10.1016/S1053-8119(09)70884-5 – volume: 146 start-page: 251 year: 2006 end-page: 261 ident: CR14 article-title: Volumetry of amygdala and hippocampus and memory performance in Alzheimer’s disease publication-title: Psychiatry Res doi: 10.1016/j.pscychresns.2006.01.007 – volume: 31 start-page: 786 year: 2010 end-page: 797 ident: CR5 article-title: 3d comparison of low, intermediate, and advanced hippocampal atrophy in Mci publication-title: Hum Brain Mapp doi: 10.1002/hbm.20905 – volume: 10 start-page: 284 year: 1999 end-page: 288 ident: CR2 article-title: Magnetic resonance imaging-based hippocampal volumetry in patients with dementia of the Alzheimer type publication-title: Dement Geriatr Cogn Disord doi: 10.1159/000017133 – volume: 51 start-page: 488 year: 2010 end-page: 499 ident: CR12 article-title: Automated 3d mapping of baseline and 12-month associations between three verbal memory measures and hippocampal atrophy in 490 Adni subjects publication-title: Neuroimage doi: 10.1016/j.neuroimage.2009.12.125 – volume: 25 start-page: 1325 year: 2005 end-page: 1335 ident: CR10 article-title: A new Spm toolbox for combining probabilistic cytoarchitectonic maps and functional imaging data publication-title: Neuroimage doi: 10.1016/j.neuroimage.2004.12.034 – volume: 182 start-page: 244 year: 2010 end-page: 250 ident: CR6 article-title: Multicentre variability of Mri-based medial temporal lobe volumetry in Alzheimer’s disease publication-title: Psychiatry Res doi: 10.1016/j.pscychresns.2010.03.003 – volume: 27 start-page: 221 year: 1997 end-page: 229 ident: CR16 article-title: Quantitative magnetic resonance imaging and neuropsychological functions in dementia of the Alzheimer type publication-title: Psychol Med doi: 10.1017/S003329179600431X – volume: 30 start-page: 2766 year: 2009 end-page: 2788 ident: CR4 article-title: Automated 3d mapping of hippocampal atrophy and its clinical correlates in 400 subjects with Alzheimer’s disease, mild cognitive impairment, and elderly controls publication-title: Hum Brain Mapp doi: 10.1002/hbm.20708 – volume: 26 start-page: 839 year: 2005 ident: 350_CR7 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.02.018 – volume: 51 start-page: 488 year: 2010 ident: 350_CR12 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2009.12.125 – volume: 25 start-page: 1325 year: 2005 ident: 350_CR10 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2004.12.034 – volume: 27 start-page: 221 year: 1997 ident: 350_CR16 publication-title: Psychol Med doi: 10.1017/S003329179600431X – volume: 251 start-page: 671 year: 2004 ident: 350_CR13 publication-title: J Neurol – volume: 18 start-page: 525 year: 2003 ident: 350_CR1 publication-title: Neuroimage doi: 10.1016/S1053-8119(02)00026-5 – volume: 31 start-page: 786 year: 2010 ident: 350_CR5 publication-title: Hum Brain Mapp doi: 10.1002/hbm.20905 – volume: 26 start-page: 900 year: 2005 ident: 350_CR8 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.02.042 – volume: 146 start-page: 251 year: 2006 ident: 350_CR14 publication-title: Psychiatry Res doi: 10.1016/j.pscychresns.2006.01.007 – volume: 10 start-page: 284 year: 1999 ident: 350_CR2 publication-title: Dement Geriatr Cogn Disord doi: 10.1159/000017133 – volume: 361 start-page: 17 year: 2004 ident: 350_CR15 publication-title: Neurosci Lett doi: 10.1016/j.neulet.2003.12.072 – volume: 182 start-page: 244 year: 2010 ident: 350_CR6 publication-title: Psychiatry Res doi: 10.1016/j.pscychresns.2010.03.003 – volume: 47 start-page: 102 year: 2009 ident: 350_CR9 publication-title: NeuroImage doi: 10.1016/S1053-8119(09)70884-5 – volume: 210 start-page: 343 year: 2005 ident: 350_CR11 publication-title: Anat Embryol (Berl) doi: 10.1007/s00429-005-0025-5 – volume: 23 start-page: 139 year: 2009 ident: 350_CR3 publication-title: Alzheimer Dis Assoc Disord doi: 10.1097/WAD.0b013e318192e745 – volume: 30 start-page: 2766 year: 2009 ident: 350_CR4 publication-title: Hum Brain Mapp doi: 10.1002/hbm.20708 – reference: 15955500 - Neuroimage. 2005 Jul 1;26(3):900-11 – reference: 20493672 - Psychiatry Res. 2010 Jun 30;182(3):244-50 – reference: 9122303 - Psychol Med. 1997 Jan;27(1):221-9 – reference: 19474571 - Alzheimer Dis Assoc Disord. 2009 Apr-Jun;23(2):139-45 – reference: 16208455 - Anat Embryol (Berl). 2005 Dec;210(5-6):343-52 – reference: 19172649 - Hum Brain Mapp. 2009 Sep;30(9):2766-88 – reference: 10364646 - Dement Geriatr Cogn Disord. 1999 Jul-Aug;10(4):284-8 – reference: 20143386 - Hum Brain Mapp. 2010 May;31(5):786-97 – reference: 15850749 - Neuroimage. 2005 May 1;25(4):1325-35 – reference: 16524704 - Psychiatry Res. 2006 Apr 30;146(3):251-61 – reference: 15311341 - J Neurol. 2004 Jun;251(6):671-5 – reference: 15955494 - Neuroimage. 2005 Jul 1;26(3):839-51 – reference: 15135882 - Neurosci Lett. 2004 May 6;361(1-3):17-20 – reference: 12595205 - Neuroimage. 2003 Feb;18(2):525-41 – reference: 20083211 - Neuroimage. 2010 May 15;51(1):488-99 |
SSID | ssj0001520 |
Score | 2.2398367 |
Snippet | Fully automated magnetic resonance imaging (MRI)-based volumetry may serve as biomarker for the diagnosis in patients with mild cognitive impairment (MCI) or... |
SourceID | proquest pubmed crossref springer |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 335 |
SubjectTerms | Aged Alzheimer Disease - pathology Alzheimer Disease - psychology Alzheimer's disease Automation Brain - pathology Cognitive Dysfunction - pathology Cognitive Dysfunction - psychology Disease Progression Female Humans Image Processing, Computer-Assisted - methods Longitudinal Studies Magnetic Resonance Imaging - methods Male Medicine Medicine & Public Health Mental Recall - physiology Middle Aged Neuropsychological Tests Neurosciences Original Paper Psychiatry Retrospective Studies Trail Making Test Wechsler Scales |
SummonAdditionalLinks | – databaseName: SpringerLink Journals (ICM) dbid: U2A link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3NitRAEG50BfEi_m_WVUrwpASS7k46OQ7LLqswHsSBvYVO_-DATGaYyRzWk6_hG-1z7JNsVdKJI6sLnnJIdWhS1VVfdf0x9l5aj7hYSfRNEhdLK3VceKFinRljNcdHN85n-iU_n8nPF9lFqOPeDtnuQ0iy09RjsRvJG3m_PKZoWKzuswcZuu6Uxzfjk1H9okHqLlZKCloKIYdQ5t8-8acxuoUwb0VHO6Nz9oQ9DmgRJj17n7J7rnnGHk5DPPw5u9r7uxBSroBu1C9B79oVolFnYfr1U0zGykKvitrNJaw8DKNRWqhpTATQiAYUQdCNha7L5XpfNwJC0hbWv8sMAJeEpqxboNtc0MuGWnYYWM4XFsa8JKBCzPmGbiG7b08WP767-dJtrn_-2kIIEL1gs7PTbyfncZjNEBuEeG1cG2nyXHorC2qo70XNrU6LxJRcG24RREhRSJuZMtHC1Lr2yJjSKZ9awRPnxUt20Kwad8jAl67QLjeqTrx0aV1mEt1OQ_pAai98xJKBSZUJjctpfsaiGlsud3ytkK8V8bVSEfswLln3XTvuIj4eOF-FA7ytUpHlZUqZexF7N77Go0fxFN241a6jUZL8MXUXjeKIMZEqYq96qRp3xHlJ7nQesY-DmO1t4F_bPfov6tfsEe8HeKDYH7ODdrNzbxBGtfXb7tjcALvPGSg priority: 102 providerName: Springer Nature |
Title | Association between fully automated MRI-based volumetry of different brain regions and neuropsychological test performance in patients with amnestic mild cognitive impairment and Alzheimer’s disease |
URI | https://link.springer.com/article/10.1007/s00406-012-0350-7 https://www.ncbi.nlm.nih.gov/pubmed/22940716 https://www.proquest.com/docview/1356912003 https://www.proquest.com/docview/1357497477 https://www.proquest.com/docview/1372056974 |
Volume | 263 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lj9MwELbY9sIFgXgFlmqQkJBAEYnjxMkJtdCygHaFVlQqp8jxQ1Rqk26bHnZ_IL8LT-Jki1b05IPtyMqMx9_M2PMR8oYpY3ExZ9Y3CbTPFBN-aiLui1hKJahtGjqf84vkbM6-LeKFC7jt3LXKziY2hlpVEmPkH8IoTrIQr1J93Fz5yBqF2VVHoXFChtYEp_GADCfTix-XvS22p1MTZckwgxlFrMtrBm0Z0cabpj5m13z-78l0B27eSZU2J9DsIXngoCOMW1k_Ivd0-Zj8Ofi_4C5dAcbUr0Hs68riUa3g_PKrj8eVgtYY1dtrqAx05Cg1FEgUAUjSYJUQRKmgqXO5ObSOYEFpDZvbhwZgp7iyrDvAeC6IdYlFOySslysF_c0kwKeYyy3GIZtvj1c3v_Vyrbdvd-ASRE_IfDb9-enMd9wMvrQQr_YLyWSSMKNYigX1TVRQJcI0kBkVkioLIliUMhXLLBCRLERhrCwyzU2oIhpoEz0lg7Iq9XMCJtOp0InkRWCYDossZtbtlGgPmDCR8UjQySWXrnA58mes8r7kciPK3IoyR1Hm3CPv-imbtmrHscGnnbBzt4F3-a26eeR13223HuZTRKmrfTOGM_TH-LExnFqMaUd55FmrSP2KKM3QnU488r7TrIMF_G-5L44v9yW5T1vGDqvap2RQb_f6lcVNdTEiJ3zBR2Q4nnyezLD98uv7dOS2jO2d0_FfpXAd1g |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEF6V9gAXBOJlKDBIICSQhb1evw4IFWiV0CZCVSv1Ztb7EJESOySOUPhR_Ax-FzN-Nagit5588O5qpZmd-WZmdz7GXgptERfHAmMTz7hCC-kmNohdGSqlJcdPTeczGkeDc_HlIrzYYb-7tzB0rbKzibWh1qWiHPk7Pwij1KerVB_mP1xijaLqakeh0ajFsVn_xJBt-X74GeX7ivOjw7NPA7dlFXAVgpPKzZVQUSSsFgm1grdBzrX0E0-lXCqu0f2JIBE6VKknA5XL3KLHTE1sfR1wz9gA173B9hBmpHiK9j4ejr-e9rYfvWGd1UmpYhoEoqujek3b0jp65y5V89z4X094Bd5eKc3WHu_oDrvdQlU4aHTrLtsxxT32Z0Oe0F7yAsrhr0GuqhLxr9EwOh265B41NMavWqyhtNCRsVSQEzEFECkEKj3IQkPdV3O-aY0BQXAF88uHDYBT2jawS6D8MchZQU1CFMwmUw39TSigp5-TBeU967UPpr--m8nMLF4voS1I3Wfn1yK1B2y3KAvziIFNTSJNpOLcs8L4eRoKDHMV2R8hbWAd5nVyyVTbKJ34OqZZ3-K5FmWGosxIlFnssDf9lHnTJWTb4P1O2FlrMJbZpXo77EX_G4861W9kYcpVPSYWFP_F28bEHDEtjnLYw0aR-h1xnlL4HjnsbadZGxv433Yfb9_uc3ZzcDY6yU6G4-Mn7BZv2EJQzffZbrVYmaeI2ar8WXtQgH277rP5Fz0SVk8 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1baxNBFB5qCuKLVLytVj2CIihLd2dnbw8i1TY01oZSLPRtnZ0LDSSbmGwo8af5A_xdnrO3Rop569M-7Mxy2HOfc-Z8jL0R2mJcHAvMTTzjCi2km9ggdmWolJYcHxWcz8kwOjoXXy_Ciy32u70LQ22VrU2sDLWeKjoj3_ODMEp9aqXas01bxOlB_9Psp0sIUlRpbeE0ahE5NqsrTN8WHwcHyOu3nPcPv385chuEAVdhoFK6uRIqioTVIqGx8DbIuZZ-4qmUS8U1ukIRJEKHKvVkoHKZW_SeqYmtrwPuGRvgd--w7Ri9YtJj258Ph6dnnR9Az1id8KRUPQ0C0dZUvXqEaZXJc5cqe278r1e8EereKNNW3q-_w-43YSvs13L2gG2Z4iH7s8ZbaBq-gH7bCuSynGIsbDScnA1ccpUaakNYzlcwtdACs5SQE0gFEEAEKgDIQkM1Y3O2bpkBA-ISZteXHAC3NCNhF0BnySAnBQ0MUTAZjTV0XVFA10BHczoDrb69P_51aUYTM3-3gKY49Yid3wrXHrNeMS3MUwY2NYk0kYpzzwrj52koMOVVZIuEtIF1mNfyJVPN0HTC7hhn3bjnipUZsjIjVmaxw953W2b1xJBNi3dbZmeN8Vhk16LusNfda1R7quXIwkyX1ZpYUC4Yb1oTc4xvcZXDntSC1FHEeUqpfOSwD61krRHwP3KfbSb3FbuLOpl9GwyPn7N7vAYOQSnfZb1yvjQvMHwr85eNngD7cduq-Rfyq1p7 |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Association+between+fully+automated+MRI-based+volumetry+of+different+brain+regions+and+neuropsychological+test+performance+in+patients+with+amnestic+mild+cognitive+impairment+and+Alzheimer%27s+disease&rft.jtitle=European+archives+of+psychiatry+and+clinical+neuroscience&rft.au=Arlt%2C+S%C3%B6nke&rft.au=Buchert%2C+Ralph&rft.au=Spies%2C+Lothar&rft.au=Eichenlaub%2C+Martin&rft.date=2013-06-01&rft.issn=1433-8491&rft.eissn=1433-8491&rft.volume=263&rft.issue=4&rft.spage=335&rft_id=info:doi/10.1007%2Fs00406-012-0350-7&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0940-1334&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0940-1334&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0940-1334&client=summon |