Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease

Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer's dis...

Full description

Saved in:
Bibliographic Details
Published inJournal of clinical neurology (Seoul, Korea) Vol. 13; no. 4; pp. 387 - 393
Main Authors Park, Kee Hyung, Noh, Young, Choi, Eun-Jung, Kim, Hyungsik, Chun, Sohyun, Son, Young-Don
Format Journal Article
LanguageEnglish
Published Korea (South) Korean Neurological Association 01.10.2017
대한신경과학회
Subjects
Online AccessGet full text
ISSN1738-6586
2005-5013
DOI10.3988/jcn.2017.13.4.387

Cover

Abstract Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer's disease. We therefore investigated the functional connectivity between the hippocampus and other brain regions using resting-state fMRI and compared the findings between EOAD and LOAD. We recruited 13 patients with EOAD and 19 patients with LOAD at the early disease stage. Twenty-one young controls and ten old controls were also recruited. Each participant completed a standardized neuropsychological battery of tests and underwent T1-weighted structural MRI. fMRI data were acquired during the resting state using 3-T MRI. The functional connectivity to the hippocampus was calculated based on automated anatomical labeling templates. The functional connectivity from the hippocampus to other brain regions differed between patients with EOAD and LOAD. The LOAD patients showed decreased hippocampal connectivity to cortical regions, such as to the middle temporal cortex, orbitofrontal cortex, postcentral cortex, supramarginal cortex, and rolandic operculum. In contrast, EOAD patients showed smaller functional changes of the cortical regions connected to the hippocampus, such as the middle frontal cortex. EOAD and LOAD patients exhibited different hippocampal connectivity. The memory decline in EOAD may be due to brain areas other than the hippocampus.
AbstractList Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer's disease. We therefore investigated the functional connectivity between the hippocampus and other brain regions using resting-state fMRI and compared the findings between EOAD and LOAD.BACKGROUND AND PURPOSEEarly-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer's disease. We therefore investigated the functional connectivity between the hippocampus and other brain regions using resting-state fMRI and compared the findings between EOAD and LOAD.We recruited 13 patients with EOAD and 19 patients with LOAD at the early disease stage. Twenty-one young controls and ten old controls were also recruited. Each participant completed a standardized neuropsychological battery of tests and underwent T1-weighted structural MRI. fMRI data were acquired during the resting state using 3-T MRI. The functional connectivity to the hippocampus was calculated based on automated anatomical labeling templates.METHODSWe recruited 13 patients with EOAD and 19 patients with LOAD at the early disease stage. Twenty-one young controls and ten old controls were also recruited. Each participant completed a standardized neuropsychological battery of tests and underwent T1-weighted structural MRI. fMRI data were acquired during the resting state using 3-T MRI. The functional connectivity to the hippocampus was calculated based on automated anatomical labeling templates.The functional connectivity from the hippocampus to other brain regions differed between patients with EOAD and LOAD. The LOAD patients showed decreased hippocampal connectivity to cortical regions, such as to the middle temporal cortex, orbitofrontal cortex, postcentral cortex, supramarginal cortex, and rolandic operculum. In contrast, EOAD patients showed smaller functional changes of the cortical regions connected to the hippocampus, such as the middle frontal cortex.RESULTSThe functional connectivity from the hippocampus to other brain regions differed between patients with EOAD and LOAD. The LOAD patients showed decreased hippocampal connectivity to cortical regions, such as to the middle temporal cortex, orbitofrontal cortex, postcentral cortex, supramarginal cortex, and rolandic operculum. In contrast, EOAD patients showed smaller functional changes of the cortical regions connected to the hippocampus, such as the middle frontal cortex.EOAD and LOAD patients exhibited different hippocampal connectivity. The memory decline in EOAD may be due to brain areas other than the hippocampus.CONCLUSIONSEOAD and LOAD patients exhibited different hippocampal connectivity. The memory decline in EOAD may be due to brain areas other than the hippocampus.
Background and Purpose Early-onset Alzheimer’s disease (EOAD) and late-onset Alzheimer’s disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer’s disease. We therefore investigated the functional connectivity between the hippocampus and other brain regions using resting-state fMRI and compared the findings between EOAD and LOAD. Methods We recruited 13 patients with EOAD and 19 patients with LOAD at the early disease stage. Twenty-one young controls and ten old controls were also recruited. Each participant completed a standardized neuropsychological battery of tests and underwent T1-weighted structural MRI. fMRI data were acquired during the resting state using 3-T MRI. The functional connectivity to the hippocampus was calculated based on automated anatomical labeling templates. Results The functional connectivity from the hippocampus to other brain regions differed between patients with EOAD and LOAD. The LOAD patients showed decreased hippocampal connectivity to cortical regions, such as to the middle temporal cortex, orbitofrontal cortex, postcentral cortex, supramarginal cortex, and rolandic operculum. In contrast, EOAD patients showed smaller functional changes of the cortical regions connected to the hippocampus, such as the middle frontal cortex. Conclusions EOAD and LOAD patients exhibited different hippocampal connectivity. The memory decline in EOAD may be due to brain areas other than the hippocampus. KCI Citation Count: 3
Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer's disease. We therefore investigated the functional connectivity between the hippocampus and other brain regions using resting-state fMRI and compared the findings between EOAD and LOAD. We recruited 13 patients with EOAD and 19 patients with LOAD at the early disease stage. Twenty-one young controls and ten old controls were also recruited. Each participant completed a standardized neuropsychological battery of tests and underwent T1-weighted structural MRI. fMRI data were acquired during the resting state using 3-T MRI. The functional connectivity to the hippocampus was calculated based on automated anatomical labeling templates. The functional connectivity from the hippocampus to other brain regions differed between patients with EOAD and LOAD. The LOAD patients showed decreased hippocampal connectivity to cortical regions, such as to the middle temporal cortex, orbitofrontal cortex, postcentral cortex, supramarginal cortex, and rolandic operculum. In contrast, EOAD patients showed smaller functional changes of the cortical regions connected to the hippocampus, such as the middle frontal cortex. EOAD and LOAD patients exhibited different hippocampal connectivity. The memory decline in EOAD may be due to brain areas other than the hippocampus.
Author Chun, Sohyun
Park, Kee Hyung
Choi, Eun-Jung
Kim, Hyungsik
Noh, Young
Son, Young-Don
AuthorAffiliation a Department of Neurology, Gachon University Gil Medical Center, Incheon, Korea
c Department of Family Medicine, Gachon University Gil Medical Center, Incheon, Korea
b Neuroscience Research Institute, Gachon University, Incheon, Korea
d Department of Radiology, Gachon University Gil Medical Center, Incheon, Korea
e Department of Biomedical Engineering, College of Health Science, Gachon University, Incheon, Korea
AuthorAffiliation_xml – name: d Department of Radiology, Gachon University Gil Medical Center, Incheon, Korea
– name: a Department of Neurology, Gachon University Gil Medical Center, Incheon, Korea
– name: e Department of Biomedical Engineering, College of Health Science, Gachon University, Incheon, Korea
– name: c Department of Family Medicine, Gachon University Gil Medical Center, Incheon, Korea
– name: b Neuroscience Research Institute, Gachon University, Incheon, Korea
Author_xml – sequence: 1
  givenname: Kee Hyung
  surname: Park
  fullname: Park, Kee Hyung
  organization: Department of Neurology, Gachon University Gil Medical Center, Incheon, Korea
– sequence: 2
  givenname: Young
  surname: Noh
  fullname: Noh, Young
  organization: Department of Neurology, Gachon University Gil Medical Center, Incheon, Korea., Neuroscience Research Institute, Gachon University, Incheon, Korea
– sequence: 3
  givenname: Eun-Jung
  surname: Choi
  fullname: Choi, Eun-Jung
  organization: Neuroscience Research Institute, Gachon University, Incheon, Korea
– sequence: 4
  givenname: Hyungsik
  surname: Kim
  fullname: Kim, Hyungsik
  organization: Department of Family Medicine, Gachon University Gil Medical Center, Incheon, Korea
– sequence: 5
  givenname: Sohyun
  surname: Chun
  fullname: Chun, Sohyun
  organization: Department of Radiology, Gachon University Gil Medical Center, Incheon, Korea
– sequence: 6
  givenname: Young-Don
  surname: Son
  fullname: Son, Young-Don
  organization: Neuroscience Research Institute, Gachon University, Incheon, Korea., Department of Biomedical Engineering, College of Health Science, Gachon University, Incheon, Korea
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29057631$$D View this record in MEDLINE/PubMed
https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002270714$$DAccess content in National Research Foundation of Korea (NRF)
BookMark eNp9kc1u1DAURi1URKeFB2CDvAMWCf6JHWeDNBpaWmmkSqisWFiOc824TZzBTkYanh5Pp1TAgtWV5fN91_I5QydhDIDQa0pK3ij14c6GkhFal5SXVclV_QwtGCGiEITyE7SgNVeFFEqeorOU7giRNVH0BTplDRG15HSBvl3OwU5-DKbHqzEEyIedn_Z4dHjaAL7y2-1ozbCdE_YBX5jY7wtsQod3qcRrM0FxExJMeNn_3IAfIL5N-JNPYBK8RM-d6RO8epzn6Ovlxe3qqljffL5eLdeFrTifCqZa6CqiRGPb1jnrqKVguk4ArwyrWqZc46RthRCUuabjlSSWUBCdqZnrFD9H74-9ITp9b70ejX-Y30d9H_Xyy-21ZpLUlLLMfjyy27kdoLMQpmh6vY1-MHH_kPz7JvhN7tlpIQWXrM4F7x4L4vhjhjTpwScLfW8CjHPStBEVV7LiMqNv_tz1tOT372eAHgEbx5QiuCeEEn0wrLNhfTCsKdeVzoZzpv4nY_1kDgbzc33_n-Qvy62sxQ
CitedBy_id crossref_primary_10_1007_s00415_021_10851_9
crossref_primary_10_3389_fnagi_2021_789099
crossref_primary_10_3923_ajb_2020_21_27
crossref_primary_10_1038_s41380_019_0404_6
crossref_primary_10_1016_j_clinph_2021_05_012
crossref_primary_10_3390_ijms232214417
crossref_primary_10_3233_JAD_220745
crossref_primary_10_1016_j_jad_2020_12_049
crossref_primary_10_1097_WCO_0000000000000570
crossref_primary_10_1212_CON_0000000000000687
crossref_primary_10_3390_biomedicines10030611
crossref_primary_10_1089_brain_2020_0847
crossref_primary_10_3390_md20110662
Cites_doi 10.1093/brain/awh539
10.3233/JAD-121927
10.1111/jon.12252
10.1177/1533317512459798
10.1212/WNL.0b013e31825dce28
10.3346/jkms.2010.25.7.1071
10.1097/WAD.0000000000000027
10.1016/S1474-4422(12)70200-4
10.3233/JAD-130461
10.1016/j.neurobiolaging.2013.01.004
10.1016/S1474-4422(10)70306-9
10.1016/S1474-4422(11)70156-9
10.1212/WNL.34.7.939
10.1212/01.wnl.0000344568.09360.31
10.1007/s10072-012-1225-4
10.1016/j.neuroimage.2005.12.033
10.1016/j.neurobiolaging.2005.09.012
10.1016/j.neurobiolaging.2008.01.010
10.1016/j.neurobiolaging.2014.03.009
10.3233/JAD-2011-0001
10.1159/000116984
10.1016/j.neurobiolaging.2013.01.001
10.1212/WNL.0000000000001003
10.2174/1567205053585783
10.1002/hbm.20324
10.1093/brain/awl377
ContentType Journal Article
Copyright Copyright © 2017 Korean Neurological Association
Copyright © 2017 Korean Neurological Association 2017 Korean Neurological Association
Copyright_xml – notice: Copyright © 2017 Korean Neurological Association
– notice: Copyright © 2017 Korean Neurological Association 2017 Korean Neurological Association
DBID AAYXX
CITATION
NPM
7X8
5PM
ACYCR
DOI 10.3988/jcn.2017.13.4.387
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
Korean Citation Index
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

PubMed
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
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2005-5013
EndPage 393
ExternalDocumentID oai_kci_go_kr_ARTI_2607112
PMC5653627
29057631
10_3988_jcn_2017_13_4_387
Genre Journal Article
GrantInformation_xml – fundername: ;
  grantid: 2013-45
– fundername: ;
  grantid: NRF-2012M3A9B6055379
GroupedDBID 29K
2WC
5-W
5GY
8JR
8XY
9ZL
AAKDD
AAYXX
ACYCR
ADBBV
ADRAZ
AENEX
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
CITATION
D-I
DIK
DU5
E3Z
EF.
F5P
GROUPED_DOAJ
HYE
KQ8
M48
OK1
PGMZT
RPM
M~E
NPM
7X8
5PM
ID FETCH-LOGICAL-c433t-28bed40859cbbffcf1c1eadd5e34a24b28f9f6cb55512f9d3460c01e5da72fd83
IEDL.DBID M48
ISSN 1738-6586
IngestDate Tue Nov 21 21:27:01 EST 2023
Thu Aug 21 18:23:48 EDT 2025
Fri Jul 11 15:49:06 EDT 2025
Wed Feb 19 02:44:02 EST 2025
Tue Jul 01 03:10:48 EDT 2025
Thu Apr 24 23:05:34 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords early-onset Alzheimer's disease
functional connectivity
hippocampus
late-onset Alzheimer's disease
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c433t-28bed40859cbbffcf1c1eadd5e34a24b28f9f6cb55512f9d3460c01e5da72fd83
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These authors contributed equally to this work.
https://doi.org/10.3988/jcn.2017.13.4.387
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.3988/jcn.2017.13.4.387
PMID 29057631
PQID 1954386436
PQPubID 23479
PageCount 7
ParticipantIDs nrf_kci_oai_kci_go_kr_ARTI_2607112
pubmedcentral_primary_oai_pubmedcentral_nih_gov_5653627
proquest_miscellaneous_1954386436
pubmed_primary_29057631
crossref_primary_10_3988_jcn_2017_13_4_387
crossref_citationtrail_10_3988_jcn_2017_13_4_387
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2017-10-01
PublicationDateYYYYMMDD 2017-10-01
PublicationDate_xml – month: 10
  year: 2017
  text: 2017-10-01
  day: 01
PublicationDecade 2010
PublicationPlace Korea (South)
PublicationPlace_xml – name: Korea (South)
PublicationTitle Journal of clinical neurology (Seoul, Korea)
PublicationTitleAlternate J Clin Neurol
PublicationYear 2017
Publisher Korean Neurological Association
대한신경과학회
Publisher_xml – name: Korean Neurological Association
– name: 대한신경과학회
References Whitwell (10.3988/jcn.2017.13.4.387_ref26) 2012; 11
Ridgway (10.3988/jcn.2017.13.4.387_ref12) 2012; 79
Sohn (10.3988/jcn.2017.13.4.387_ref23) 2014; 28
Ahn (10.3988/jcn.2017.13.4.387_ref22) 2010; 25
McKhann (10.3988/jcn.2017.13.4.387_ref20) 1984; 34
Cho (10.3988/jcn.2017.13.4.387_ref11) 2013; 34
Kim (10.3988/jcn.2017.13.4.387_ref15) 2005; 128
Rombouts (10.3988/jcn.2017.13.4.387_ref7) 2005; 2
Scheff (10.3988/jcn.2017.13.4.387_ref4) 2006; 27
Cho (10.3988/jcn.2017.13.4.387_ref13) 2013; 34
Noh (10.3988/jcn.2017.13.4.387_ref21) 2014; 40
Cavedo (10.3988/jcn.2017.13.4.387_ref25) 2014; 35
Cho (10.3988/jcn.2017.13.4.387_ref17) 2013; 35
van der Flier (10.3988/jcn.2017.13.4.387_ref10) 2011; 10
Hong (10.3988/jcn.2017.13.4.387_ref6) 2013; 34
Fellgiebel (10.3988/jcn.2017.13.4.387_ref5) 2011; 26
Henneman (10.3988/jcn.2017.13.4.387_ref2) 2009; 72
Barnes (10.3988/jcn.2017.13.4.387_ref3) 2009; 30
Wang (10.3988/jcn.2017.13.4.387_ref9) 2006; 31
Murray (10.3988/jcn.2017.13.4.387_ref18) 2011; 10
Moon (10.3988/jcn.2017.13.4.387_ref14) 2015; 25
Frisoni (10.3988/jcn.2017.13.4.387_ref24) 2007; 130
Braak (10.3988/jcn.2017.13.4.387_ref1) 1993; 33
Wang (10.3988/jcn.2017.13.4.387_ref8) 2007; 28
Noh (10.3988/jcn.2017.13.4.387_ref19) 2014; 83
Kaiser (10.3988/jcn.2017.13.4.387_ref16) 2012; 27
23507771 - J Alzheimers Dis. 2013;35(4):813-21
15888536 - Brain. 2005 Aug;128(Pt 8):1790-801
16473024 - Neuroimage. 2006 Jun;31(2):496-504
16289476 - Neurobiol Aging. 2006 Oct;27(10):1372-84
15974906 - Curr Alzheimer Res. 2005 Apr;2(2):115-6
23394958 - Neurobiol Aging. 2013 Jul;34(7):1740-7
6610841 - Neurology. 1984 Jul;34(7):939-44
24577457 - J Alzheimers Dis. 2014;40(4):877-86
25344382 - Neurology. 2014 Nov 18;83(21):1936-44
17293358 - Brain. 2007 Mar;130(Pt 3):720-30
22722624 - Neurology. 2012 Jul 3;79(1):80-4
21802369 - Lancet Neurol. 2011 Sep;10(9):785-96
17133390 - Hum Brain Mapp. 2007 Oct;28(10):967-78
21185234 - Lancet Neurol. 2011 Mar;10(3):280-8
21971465 - J Alzheimers Dis. 2011;26 Suppl 3:257-62
18346820 - Neurobiol Aging. 2009 Nov;30(11):1711-23
23109096 - Neurol Sci. 2013 Jul;34(7):1215-21
20592901 - J Korean Med Sci. 2010 Jul;25(7):1071-6
8307060 - Eur Neurol. 1993;33(6):403-8
25940587 - J Neuroimaging. 2015 Sep-Oct;25(5):728-37
22951070 - Lancet Neurol. 2012 Oct;11(10):868-77
19289740 - Neurology. 2009 Mar 17;72(11):999-1007
22990206 - Am J Alzheimers Dis Other Demen. 2012 Nov;27(7):520-9
23391426 - Neurobiol Aging. 2013 Jul;34(7):1921.e9-1921.e15
24614267 - Alzheimer Dis Assoc Disord. 2014 Jul-Sep;28(3):239-46
24721821 - Neurobiol Aging. 2014 Sep;35(9):2004-12
References_xml – volume: 128
  start-page: 1790
  year: 2005
  ident: 10.3988/jcn.2017.13.4.387_ref15
  publication-title: Brain
  doi: 10.1093/brain/awh539
– volume: 35
  start-page: 813
  year: 2013
  ident: 10.3988/jcn.2017.13.4.387_ref17
  publication-title: J Alzheimers Dis
  doi: 10.3233/JAD-121927
– volume: 25
  start-page: 728
  year: 2015
  ident: 10.3988/jcn.2017.13.4.387_ref14
  publication-title: J Neuroimaging
  doi: 10.1111/jon.12252
– volume: 27
  start-page: 520
  year: 2012
  ident: 10.3988/jcn.2017.13.4.387_ref16
  publication-title: Am J Alzheimers Dis Other Demen
  doi: 10.1177/1533317512459798
– volume: 79
  start-page: 80
  year: 2012
  ident: 10.3988/jcn.2017.13.4.387_ref12
  publication-title: Neurology
  doi: 10.1212/WNL.0b013e31825dce28
– volume: 25
  start-page: 1071
  year: 2010
  ident: 10.3988/jcn.2017.13.4.387_ref22
  publication-title: J Korean Med Sci
  doi: 10.3346/jkms.2010.25.7.1071
– volume: 28
  start-page: 239
  year: 2014
  ident: 10.3988/jcn.2017.13.4.387_ref23
  publication-title: Alzheimer Dis Assoc Disord
  doi: 10.1097/WAD.0000000000000027
– volume: 11
  start-page: 868
  year: 2012
  ident: 10.3988/jcn.2017.13.4.387_ref26
  publication-title: Lancet Neurol
  doi: 10.1016/S1474-4422(12)70200-4
– volume: 40
  start-page: 877
  year: 2014
  ident: 10.3988/jcn.2017.13.4.387_ref21
  publication-title: J Alzheimers Dis
  doi: 10.3233/JAD-130461
– volume: 34
  start-page: 1921.e9
  year: 2013
  ident: 10.3988/jcn.2017.13.4.387_ref11
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2013.01.004
– volume: 10
  start-page: 280
  year: 2011
  ident: 10.3988/jcn.2017.13.4.387_ref10
  publication-title: Lancet Neurol
  doi: 10.1016/S1474-4422(10)70306-9
– volume: 10
  start-page: 785
  year: 2011
  ident: 10.3988/jcn.2017.13.4.387_ref18
  publication-title: Lancet Neurol
  doi: 10.1016/S1474-4422(11)70156-9
– volume: 34
  start-page: 939
  year: 1984
  ident: 10.3988/jcn.2017.13.4.387_ref20
  publication-title: Neurology
  doi: 10.1212/WNL.34.7.939
– volume: 72
  start-page: 999
  year: 2009
  ident: 10.3988/jcn.2017.13.4.387_ref2
  publication-title: Neurology
  doi: 10.1212/01.wnl.0000344568.09360.31
– volume: 34
  start-page: 1215
  year: 2013
  ident: 10.3988/jcn.2017.13.4.387_ref6
  publication-title: Neurol Sci
  doi: 10.1007/s10072-012-1225-4
– volume: 31
  start-page: 496
  year: 2006
  ident: 10.3988/jcn.2017.13.4.387_ref9
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2005.12.033
– volume: 27
  start-page: 1372
  year: 2006
  ident: 10.3988/jcn.2017.13.4.387_ref4
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2005.09.012
– volume: 30
  start-page: 1711
  year: 2009
  ident: 10.3988/jcn.2017.13.4.387_ref3
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2008.01.010
– volume: 35
  start-page: 2004
  year: 2014
  ident: 10.3988/jcn.2017.13.4.387_ref25
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2014.03.009
– volume: 26
  start-page: 257
  issue: Suppl 3
  year: 2011
  ident: 10.3988/jcn.2017.13.4.387_ref5
  publication-title: J Alzheimers Dis
  doi: 10.3233/JAD-2011-0001
– volume: 33
  start-page: 403
  year: 1993
  ident: 10.3988/jcn.2017.13.4.387_ref1
  publication-title: Eur Neurol
  doi: 10.1159/000116984
– volume: 34
  start-page: 1740
  year: 2013
  ident: 10.3988/jcn.2017.13.4.387_ref13
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2013.01.001
– volume: 83
  start-page: 1936
  year: 2014
  ident: 10.3988/jcn.2017.13.4.387_ref19
  publication-title: Neurology
  doi: 10.1212/WNL.0000000000001003
– volume: 2
  start-page: 115
  year: 2005
  ident: 10.3988/jcn.2017.13.4.387_ref7
  publication-title: Curr Alzheimer Res
  doi: 10.2174/1567205053585783
– volume: 28
  start-page: 967
  year: 2007
  ident: 10.3988/jcn.2017.13.4.387_ref8
  publication-title: Hum Brain Mapp
  doi: 10.1002/hbm.20324
– volume: 130
  start-page: 720
  year: 2007
  ident: 10.3988/jcn.2017.13.4.387_ref24
  publication-title: Brain
  doi: 10.1093/brain/awl377
– reference: 17293358 - Brain. 2007 Mar;130(Pt 3):720-30
– reference: 20592901 - J Korean Med Sci. 2010 Jul;25(7):1071-6
– reference: 25940587 - J Neuroimaging. 2015 Sep-Oct;25(5):728-37
– reference: 23391426 - Neurobiol Aging. 2013 Jul;34(7):1921.e9-1921.e15
– reference: 8307060 - Eur Neurol. 1993;33(6):403-8
– reference: 16289476 - Neurobiol Aging. 2006 Oct;27(10):1372-84
– reference: 21971465 - J Alzheimers Dis. 2011;26 Suppl 3:257-62
– reference: 22990206 - Am J Alzheimers Dis Other Demen. 2012 Nov;27(7):520-9
– reference: 24721821 - Neurobiol Aging. 2014 Sep;35(9):2004-12
– reference: 23507771 - J Alzheimers Dis. 2013;35(4):813-21
– reference: 18346820 - Neurobiol Aging. 2009 Nov;30(11):1711-23
– reference: 15974906 - Curr Alzheimer Res. 2005 Apr;2(2):115-6
– reference: 23109096 - Neurol Sci. 2013 Jul;34(7):1215-21
– reference: 17133390 - Hum Brain Mapp. 2007 Oct;28(10):967-78
– reference: 25344382 - Neurology. 2014 Nov 18;83(21):1936-44
– reference: 6610841 - Neurology. 1984 Jul;34(7):939-44
– reference: 23394958 - Neurobiol Aging. 2013 Jul;34(7):1740-7
– reference: 22951070 - Lancet Neurol. 2012 Oct;11(10):868-77
– reference: 24614267 - Alzheimer Dis Assoc Disord. 2014 Jul-Sep;28(3):239-46
– reference: 22722624 - Neurology. 2012 Jul 3;79(1):80-4
– reference: 21802369 - Lancet Neurol. 2011 Sep;10(9):785-96
– reference: 24577457 - J Alzheimers Dis. 2014;40(4):877-86
– reference: 15888536 - Brain. 2005 Aug;128(Pt 8):1790-801
– reference: 21185234 - Lancet Neurol. 2011 Mar;10(3):280-8
– reference: 16473024 - Neuroimage. 2006 Jun;31(2):496-504
– reference: 19289740 - Neurology. 2009 Mar 17;72(11):999-1007
SSID ssj0067081
Score 2.1648815
Snippet Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline...
Background and Purpose Early-onset Alzheimer’s disease (EOAD) and late-onset Alzheimer’s disease (LOAD) have different clinical and neuroimaging...
SourceID nrf
pubmedcentral
proquest
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 387
SubjectTerms Original
신경과학
Title Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease
URI https://www.ncbi.nlm.nih.gov/pubmed/29057631
https://www.proquest.com/docview/1954386436
https://pubmed.ncbi.nlm.nih.gov/PMC5653627
https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002270714
Volume 13
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
ispartofPNX Journal of Clinical Neurology, 2017, 13(4), , pp.387-393
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1bi9QwFA67K4gv4t26ukQRBCFlcuklDyKLOozi6osDCz6E5rZbdzYz286I-us9aTuDI6NPfWia0HxJzndyDt9B6LnOvaiA15JIl4lwMiOaW0mEd0zCmcyF7bItPuWTqfhwmp3uoXV5q2EC252uXawnNW1m6Y-rn69hw7-KHqcEB-6biUKmtEgpT0XKy2IfXQPDlEdf7ERsggp5MepqltIC9jgY3rwPcu7uIooES-AyOadbFms_NH4XGf07p_IPIzW-hW4O7BIf98vhNtpz4Q66fjLEz--ir2MwY_3tH-5SXExfPALPPQYmiCf1YgHG7XKxanEdcKd-THAVLP7epvgj8FLyObRuiY9nv85dfemaFy1-28d47qHp-N2XNxMylFcgRnC-JKzUznYCZ0Zr742nhsK6spnjomJCs9JLnxudAaliXgJs-ciMqMtsVTBvS34fHYR5cA8RrqQpfAySSi0FnAnSZtJqFuXxuKycT9BoPYXKDNrjsQTGTIEPEgFQAICKACjKlVAAQIJebj5Z9MIb_2v8DHBRF6ZWUS47Ps_m6qJR4BS8Vyxq6FGWoKdr2BTsoRgYqYKbr1oVVe94CdwsT9CDHsbNmOtVkKBiC-BNgzjg9ptQn3c63cCVgR4Uj_7Z5yG6EX-jzw18jA6Wzco9AY6z1Efd3cBRt35_A9JD98w
linkProvider Scholars Portal
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=Functional+Connectivity+of+the+Hippocampus+in+Early-+and+vs.+Late-Onset+Alzheimer%27s+Disease&rft.jtitle=Journal+of+clinical+neurology+%28Seoul%2C+Korea%29&rft.au=Park%2C+Kee+Hyung&rft.au=Noh%2C+Young&rft.au=Choi%2C+Eun+Jung&rft.au=Kim%2C+Hyungsik&rft.date=2017-10-01&rft.issn=1738-6586&rft.volume=13&rft.issue=4&rft.spage=387&rft_id=info:doi/10.3988%2Fjcn.2017.13.4.387&rft_id=info%3Apmid%2F29057631&rft.externalDocID=29057631
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1738-6586&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1738-6586&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1738-6586&client=summon