C9ORF72 hexanucleotide repeat expansion with Alzheimer's disease‐like clinical phenotype: A case report with results from neuropsychology, CSF, FDG‐PET, and PiB‐PET. Issue 12 (27th October 2020)

Record Type:: Journal Article
Title:: C9ORF72 hexanucleotide repeat expansion with Alzheimer's disease‐like clinical phenotype: A case report with results from neuropsychology, CSF, FDG‐PET, and PiB‐PET. Issue 12 (27th October 2020)
Main Title:: C9ORF72 hexanucleotide repeat expansion with Alzheimer's disease‐like clinical phenotype: A case report with results from neuropsychology, CSF, FDG‐PET, and PiB‐PET
Authors:: Filikci, Zuhal
Gustafsson, Moa Anna Kristina
Henriksen, Otto Mølby
Marner, Lisbeth
Høgh, Peter
Abstract:: Abstract: A thorough family history and relevant investigation program are essential to settle accurate diagnosis when clinical presentation is atypical or with a mixed picture. Abstract : A thorough family history and relevant investigation program are essential to settle accurate diagnosis when clinical presentation is atypical or with a mixed picture.
Is Part Of:: Clinical case reports. Volume 8:Issue 12(2020)
Journal:: Clinical case reports
Issue:: Volume 8:Issue 12(2020)
Issue Display:: Volume 8, Issue 12 (2020)
Year:: 2020
Volume:: 8
Issue:: 12
Issue Sort Value:: 2020-0008-0012-0000
Page Start:: 3415
Page End:: 3419
Publication Date:: 2020-10-27
Subjects:: Alzheimer's disease -- C9Orf72 gene mutation -- frontotemporal dementia -- genetic testing
Medicine -- Periodicals
616.09
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2050-0904 ↗
DOI:: 10.1002/ccr3.3417 ↗
Languages:: English
ISSNs:: 2050-0904
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 23378.xml