The Behavioural Dysfunction Questionnaire discriminates behavioural variant frontotemporal dementia from Alzheimer’s disease dementia and major depressive disorder
Background and objectives Early-stage behavioural variant frontotemporal dementia (bvFTD) is often misdiagnosed, highlighting the need for new diagnostic instruments. Based on the revised diagnostic criteria for bvFTD, we developed the Behavioural Dysfunction Questionnaire (BDQ). In this explorative...
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Veröffentlicht in: | Journal of neurology 2023-07, Vol.270 (7), p.3433-3441 |
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creator | Semenkova, Anna Piguet, Olivier Johnen, Andreas Schroeter, Matthias L. Godulla, Jannis Linnemann, Christoph Mühlhauser, Markus Sauer, Thomas Baumgartner, Markus Anderl-Straub, Sarah Otto, Markus Felbecker, Ansgar Kressig, Reto W. Berres, Manfred Sollberger, Marc |
description | Background and objectives
Early-stage behavioural variant frontotemporal dementia (bvFTD) is often misdiagnosed, highlighting the need for new diagnostic instruments. Based on the revised diagnostic criteria for bvFTD, we developed the Behavioural Dysfunction Questionnaire (BDQ). In this explorative study, we aimed to determine the best scoring and analytical method for the BDQ to discriminate between bvFTD and non-bvFTD patients.
Materials and methods
34 patients with early-stage bvFTD, 56 with early-stage Alzheimer's disease dementia (ADD) and 41 with major depressive disorder (MDD) were recruited. We calculated BDQ-items with or without inclusion of a time criterion: (a) without time criterion, (b) with 10 years’ time criterion (symptom presence less than 10 years), and (c) with 3 years’ time criterion (symptom presentation within the first 3 years). Using these three differently calculated items, we generated six variables, i.e. 3*2 [BDQ-Global Score (BDQ-GS; domains average score); BDQ-Global Domain Score (BDQ-GDS; domains categorical score)]. Then, we performed univariate and bivariate (BDQ-GS and BDQ-GDS combined) ROC analyses.
Results
Models including BDQ-GS, BDQ-GDS or both variables combined discriminated similarly between groups. In contrast, models without time criterion or with 10 years’ time criterion discriminated better than models including variables with 3 years’ time criterion. These models discriminated highly (AUC = 85.98–87.78) between bvFTD and MDD and bvFTD and ADD, respectively.
Conclusion
BDQ-scores without any time criterion discriminated highly between early-stage bvFTD and non-bvFTD groups, which could improve the early diagnosis of bvFTD. With its standardised procedure, the BDQ is also appropriate for repeated assessments. |
doi_str_mv | 10.1007/s00415-023-11666-6 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10267256</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2825641366</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-d6f757a8287e0d0187db9914bfa0345c08f196459d6d9863f63c8c7432aa083d3</originalsourceid><addsrcrecordid>eNp9Ustu1DAUtRAVHQo_wAJFYsMm7bUd28kKteVRpEoIqawtT3zT8SixBzsZqaz4jX5Af4wvwemUtrBgZevec8_1OT6EvKJwSAHUUQKoqCiB8ZJSKWUpn5AFrTgraSWap2QBvIJScFHtk-cprQGgzo1nZJ_LRjCgdEFuLlZYnODKbF2YoumL91epm3w7uuCLrxOm-eKNi1hYl9roBufNiKlYPprZmuiMH4suBj-GEYdNmMsWB_SjM3N9KI77Hyt0A8ZfP6_TTIYm4QPGeFsMZh1iLm0ipuS2tytDtBhfkL3O9Alf3p0H5NvHDxenZ-X5l0-fT4_Py7ZSYiyt7JRQpma1QrBAa2WXTUOrZWeyFaKFuqONzBZYaZta8k7ytm5VdswYqLnlB-TdjnczLQe0bX5aFqI3WbaJVzoYp__ueLfSl2GrKTCpmJCZ4e0dQwzfZ_v0kG3Dvjcew5Q0Uw2AAEZn6Jt_oOtsp8_6NKszV0W5nFFsh2pjSClid_8aCnqOgd7FQOcY6NsY6Hno9WMd9yN__j0D-A6QcstfYnzY_R_a3zSPw9A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2825641366</pqid></control><display><type>article</type><title>The Behavioural Dysfunction Questionnaire discriminates behavioural variant frontotemporal dementia from Alzheimer’s disease dementia and major depressive disorder</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Semenkova, Anna ; Piguet, Olivier ; Johnen, Andreas ; Schroeter, Matthias L. ; Godulla, Jannis ; Linnemann, Christoph ; Mühlhauser, Markus ; Sauer, Thomas ; Baumgartner, Markus ; Anderl-Straub, Sarah ; Otto, Markus ; Felbecker, Ansgar ; Kressig, Reto W. ; Berres, Manfred ; Sollberger, Marc</creator><creatorcontrib>Semenkova, Anna ; Piguet, Olivier ; Johnen, Andreas ; Schroeter, Matthias L. ; Godulla, Jannis ; Linnemann, Christoph ; Mühlhauser, Markus ; Sauer, Thomas ; Baumgartner, Markus ; Anderl-Straub, Sarah ; Otto, Markus ; Felbecker, Ansgar ; Kressig, Reto W. ; Berres, Manfred ; Sollberger, Marc</creatorcontrib><description>Background and objectives
Early-stage behavioural variant frontotemporal dementia (bvFTD) is often misdiagnosed, highlighting the need for new diagnostic instruments. Based on the revised diagnostic criteria for bvFTD, we developed the Behavioural Dysfunction Questionnaire (BDQ). In this explorative study, we aimed to determine the best scoring and analytical method for the BDQ to discriminate between bvFTD and non-bvFTD patients.
Materials and methods
34 patients with early-stage bvFTD, 56 with early-stage Alzheimer's disease dementia (ADD) and 41 with major depressive disorder (MDD) were recruited. We calculated BDQ-items with or without inclusion of a time criterion: (a) without time criterion, (b) with 10 years’ time criterion (symptom presence less than 10 years), and (c) with 3 years’ time criterion (symptom presentation within the first 3 years). Using these three differently calculated items, we generated six variables, i.e. 3*2 [BDQ-Global Score (BDQ-GS; domains average score); BDQ-Global Domain Score (BDQ-GDS; domains categorical score)]. Then, we performed univariate and bivariate (BDQ-GS and BDQ-GDS combined) ROC analyses.
Results
Models including BDQ-GS, BDQ-GDS or both variables combined discriminated similarly between groups. In contrast, models without time criterion or with 10 years’ time criterion discriminated better than models including variables with 3 years’ time criterion. These models discriminated highly (AUC = 85.98–87.78) between bvFTD and MDD and bvFTD and ADD, respectively.
Conclusion
BDQ-scores without any time criterion discriminated highly between early-stage bvFTD and non-bvFTD groups, which could improve the early diagnosis of bvFTD. With its standardised procedure, the BDQ is also appropriate for repeated assessments.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-023-11666-6</identifier><identifier>PMID: 36952011</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Alzheimer Disease - diagnosis ; Alzheimer's disease ; Dementia ; Dementia disorders ; Depressive Disorder, Major - diagnosis ; Diagnosis, Differential ; Frontotemporal dementia ; Frontotemporal Dementia - diagnosis ; Humans ; Medicine ; Medicine & Public Health ; Mental depression ; Neurodegenerative diseases ; Neurology ; Neuropsychological Tests ; Neuroradiology ; Neurosciences ; Original Communication ; Questionnaires</subject><ispartof>Journal of neurology, 2023-07, Vol.270 (7), p.3433-3441</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-d6f757a8287e0d0187db9914bfa0345c08f196459d6d9863f63c8c7432aa083d3</citedby><cites>FETCH-LOGICAL-c475t-d6f757a8287e0d0187db9914bfa0345c08f196459d6d9863f63c8c7432aa083d3</cites><orcidid>0000-0001-8863-3731 ; 0000-0003-0409-8554 ; 0000-0002-6696-1440 ; 0000-0002-6034-5911 ; 0000-0001-9073-6617 ; 0000-0002-6995-9442 ; 0000-0002-3215-7681</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00415-023-11666-6$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00415-023-11666-6$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36952011$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Semenkova, Anna</creatorcontrib><creatorcontrib>Piguet, Olivier</creatorcontrib><creatorcontrib>Johnen, Andreas</creatorcontrib><creatorcontrib>Schroeter, Matthias L.</creatorcontrib><creatorcontrib>Godulla, Jannis</creatorcontrib><creatorcontrib>Linnemann, Christoph</creatorcontrib><creatorcontrib>Mühlhauser, Markus</creatorcontrib><creatorcontrib>Sauer, Thomas</creatorcontrib><creatorcontrib>Baumgartner, Markus</creatorcontrib><creatorcontrib>Anderl-Straub, Sarah</creatorcontrib><creatorcontrib>Otto, Markus</creatorcontrib><creatorcontrib>Felbecker, Ansgar</creatorcontrib><creatorcontrib>Kressig, Reto W.</creatorcontrib><creatorcontrib>Berres, Manfred</creatorcontrib><creatorcontrib>Sollberger, Marc</creatorcontrib><title>The Behavioural Dysfunction Questionnaire discriminates behavioural variant frontotemporal dementia from Alzheimer’s disease dementia and major depressive disorder</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Background and objectives
Early-stage behavioural variant frontotemporal dementia (bvFTD) is often misdiagnosed, highlighting the need for new diagnostic instruments. Based on the revised diagnostic criteria for bvFTD, we developed the Behavioural Dysfunction Questionnaire (BDQ). In this explorative study, we aimed to determine the best scoring and analytical method for the BDQ to discriminate between bvFTD and non-bvFTD patients.
Materials and methods
34 patients with early-stage bvFTD, 56 with early-stage Alzheimer's disease dementia (ADD) and 41 with major depressive disorder (MDD) were recruited. We calculated BDQ-items with or without inclusion of a time criterion: (a) without time criterion, (b) with 10 years’ time criterion (symptom presence less than 10 years), and (c) with 3 years’ time criterion (symptom presentation within the first 3 years). Using these three differently calculated items, we generated six variables, i.e. 3*2 [BDQ-Global Score (BDQ-GS; domains average score); BDQ-Global Domain Score (BDQ-GDS; domains categorical score)]. Then, we performed univariate and bivariate (BDQ-GS and BDQ-GDS combined) ROC analyses.
Results
Models including BDQ-GS, BDQ-GDS or both variables combined discriminated similarly between groups. In contrast, models without time criterion or with 10 years’ time criterion discriminated better than models including variables with 3 years’ time criterion. These models discriminated highly (AUC = 85.98–87.78) between bvFTD and MDD and bvFTD and ADD, respectively.
Conclusion
BDQ-scores without any time criterion discriminated highly between early-stage bvFTD and non-bvFTD groups, which could improve the early diagnosis of bvFTD. With its standardised procedure, the BDQ is also appropriate for repeated assessments.</description><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer's disease</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Depressive Disorder, Major - diagnosis</subject><subject>Diagnosis, Differential</subject><subject>Frontotemporal dementia</subject><subject>Frontotemporal Dementia - diagnosis</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mental depression</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Questionnaires</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9Ustu1DAUtRAVHQo_wAJFYsMm7bUd28kKteVRpEoIqawtT3zT8SixBzsZqaz4jX5Af4wvwemUtrBgZevec8_1OT6EvKJwSAHUUQKoqCiB8ZJSKWUpn5AFrTgraSWap2QBvIJScFHtk-cprQGgzo1nZJ_LRjCgdEFuLlZYnODKbF2YoumL91epm3w7uuCLrxOm-eKNi1hYl9roBufNiKlYPprZmuiMH4suBj-GEYdNmMsWB_SjM3N9KI77Hyt0A8ZfP6_TTIYm4QPGeFsMZh1iLm0ipuS2tytDtBhfkL3O9Alf3p0H5NvHDxenZ-X5l0-fT4_Py7ZSYiyt7JRQpma1QrBAa2WXTUOrZWeyFaKFuqONzBZYaZta8k7ytm5VdswYqLnlB-TdjnczLQe0bX5aFqI3WbaJVzoYp__ueLfSl2GrKTCpmJCZ4e0dQwzfZ_v0kG3Dvjcew5Q0Uw2AAEZn6Jt_oOtsp8_6NKszV0W5nFFsh2pjSClid_8aCnqOgd7FQOcY6NsY6Hno9WMd9yN__j0D-A6QcstfYnzY_R_a3zSPw9A</recordid><startdate>20230701</startdate><enddate>20230701</enddate><creator>Semenkova, Anna</creator><creator>Piguet, Olivier</creator><creator>Johnen, Andreas</creator><creator>Schroeter, Matthias L.</creator><creator>Godulla, Jannis</creator><creator>Linnemann, Christoph</creator><creator>Mühlhauser, Markus</creator><creator>Sauer, Thomas</creator><creator>Baumgartner, Markus</creator><creator>Anderl-Straub, Sarah</creator><creator>Otto, Markus</creator><creator>Felbecker, Ansgar</creator><creator>Kressig, Reto W.</creator><creator>Berres, Manfred</creator><creator>Sollberger, Marc</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8863-3731</orcidid><orcidid>https://orcid.org/0000-0003-0409-8554</orcidid><orcidid>https://orcid.org/0000-0002-6696-1440</orcidid><orcidid>https://orcid.org/0000-0002-6034-5911</orcidid><orcidid>https://orcid.org/0000-0001-9073-6617</orcidid><orcidid>https://orcid.org/0000-0002-6995-9442</orcidid><orcidid>https://orcid.org/0000-0002-3215-7681</orcidid></search><sort><creationdate>20230701</creationdate><title>The Behavioural Dysfunction Questionnaire discriminates behavioural variant frontotemporal dementia from Alzheimer’s disease dementia and major depressive disorder</title><author>Semenkova, Anna ; Piguet, Olivier ; Johnen, Andreas ; Schroeter, Matthias L. ; Godulla, Jannis ; Linnemann, Christoph ; Mühlhauser, Markus ; Sauer, Thomas ; Baumgartner, Markus ; Anderl-Straub, Sarah ; Otto, Markus ; Felbecker, Ansgar ; Kressig, Reto W. ; Berres, Manfred ; Sollberger, Marc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-d6f757a8287e0d0187db9914bfa0345c08f196459d6d9863f63c8c7432aa083d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alzheimer Disease - diagnosis</topic><topic>Alzheimer's disease</topic><topic>Dementia</topic><topic>Dementia disorders</topic><topic>Depressive Disorder, Major - diagnosis</topic><topic>Diagnosis, Differential</topic><topic>Frontotemporal dementia</topic><topic>Frontotemporal Dementia - diagnosis</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mental depression</topic><topic>Neurodegenerative diseases</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Original Communication</topic><topic>Questionnaires</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Semenkova, Anna</creatorcontrib><creatorcontrib>Piguet, Olivier</creatorcontrib><creatorcontrib>Johnen, Andreas</creatorcontrib><creatorcontrib>Schroeter, Matthias L.</creatorcontrib><creatorcontrib>Godulla, Jannis</creatorcontrib><creatorcontrib>Linnemann, Christoph</creatorcontrib><creatorcontrib>Mühlhauser, Markus</creatorcontrib><creatorcontrib>Sauer, Thomas</creatorcontrib><creatorcontrib>Baumgartner, Markus</creatorcontrib><creatorcontrib>Anderl-Straub, Sarah</creatorcontrib><creatorcontrib>Otto, Markus</creatorcontrib><creatorcontrib>Felbecker, Ansgar</creatorcontrib><creatorcontrib>Kressig, Reto W.</creatorcontrib><creatorcontrib>Berres, Manfred</creatorcontrib><creatorcontrib>Sollberger, Marc</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Semenkova, Anna</au><au>Piguet, Olivier</au><au>Johnen, Andreas</au><au>Schroeter, Matthias L.</au><au>Godulla, Jannis</au><au>Linnemann, Christoph</au><au>Mühlhauser, Markus</au><au>Sauer, Thomas</au><au>Baumgartner, Markus</au><au>Anderl-Straub, Sarah</au><au>Otto, Markus</au><au>Felbecker, Ansgar</au><au>Kressig, Reto W.</au><au>Berres, Manfred</au><au>Sollberger, Marc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Behavioural Dysfunction Questionnaire discriminates behavioural variant frontotemporal dementia from Alzheimer’s disease dementia and major depressive disorder</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2023-07-01</date><risdate>2023</risdate><volume>270</volume><issue>7</issue><spage>3433</spage><epage>3441</epage><pages>3433-3441</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>Background and objectives
Early-stage behavioural variant frontotemporal dementia (bvFTD) is often misdiagnosed, highlighting the need for new diagnostic instruments. Based on the revised diagnostic criteria for bvFTD, we developed the Behavioural Dysfunction Questionnaire (BDQ). In this explorative study, we aimed to determine the best scoring and analytical method for the BDQ to discriminate between bvFTD and non-bvFTD patients.
Materials and methods
34 patients with early-stage bvFTD, 56 with early-stage Alzheimer's disease dementia (ADD) and 41 with major depressive disorder (MDD) were recruited. We calculated BDQ-items with or without inclusion of a time criterion: (a) without time criterion, (b) with 10 years’ time criterion (symptom presence less than 10 years), and (c) with 3 years’ time criterion (symptom presentation within the first 3 years). Using these three differently calculated items, we generated six variables, i.e. 3*2 [BDQ-Global Score (BDQ-GS; domains average score); BDQ-Global Domain Score (BDQ-GDS; domains categorical score)]. Then, we performed univariate and bivariate (BDQ-GS and BDQ-GDS combined) ROC analyses.
Results
Models including BDQ-GS, BDQ-GDS or both variables combined discriminated similarly between groups. In contrast, models without time criterion or with 10 years’ time criterion discriminated better than models including variables with 3 years’ time criterion. These models discriminated highly (AUC = 85.98–87.78) between bvFTD and MDD and bvFTD and ADD, respectively.
Conclusion
BDQ-scores without any time criterion discriminated highly between early-stage bvFTD and non-bvFTD groups, which could improve the early diagnosis of bvFTD. With its standardised procedure, the BDQ is also appropriate for repeated assessments.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36952011</pmid><doi>10.1007/s00415-023-11666-6</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8863-3731</orcidid><orcidid>https://orcid.org/0000-0003-0409-8554</orcidid><orcidid>https://orcid.org/0000-0002-6696-1440</orcidid><orcidid>https://orcid.org/0000-0002-6034-5911</orcidid><orcidid>https://orcid.org/0000-0001-9073-6617</orcidid><orcidid>https://orcid.org/0000-0002-6995-9442</orcidid><orcidid>https://orcid.org/0000-0002-3215-7681</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - diagnosis Alzheimer's disease Dementia Dementia disorders Depressive Disorder, Major - diagnosis Diagnosis, Differential Frontotemporal dementia Frontotemporal Dementia - diagnosis Humans Medicine Medicine & Public Health Mental depression Neurodegenerative diseases Neurology Neuropsychological Tests Neuroradiology Neurosciences Original Communication Questionnaires |
title | The Behavioural Dysfunction Questionnaire discriminates behavioural variant frontotemporal dementia from Alzheimer’s disease dementia and major depressive disorder |
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