Home > Publications Database > Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease. > print

001     140900
005     20240321220909.0
024 7 _ |a 10.1093/brain/awz050
|2 doi
024 7 _ |a pmid:30897203
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024 7 _ |a pmc:PMC6735903
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024 7 _ |a 0006-8950
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024 7 _ |a 1460-2156
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037 _ _ |a DZNE-2020-07222
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Vöglein, Jonathan
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245 _ _ |a Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease.
260 _ _ |a Oxford
|c 2019
|b Oxford Univ. Press
264 _ 1 |3 online
|2 Crossref
|b Oxford University Press (OUP)
|c 2019-03-20
264 _ 1 |3 print
|2 Crossref
|b Oxford University Press (OUP)
|c 2019-05-01
336 7 _ |a article
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336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
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520 _ _ |a Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
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536 _ _ |a 344 - Clinical and Health Care Research (POF3-344)
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542 _ _ |i 2019-03-21
|2 Crossref
|u https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 2 |a Adult
|2 MeSH
650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Alzheimer Disease: epidemiology
|2 MeSH
650 _ 2 |a Alzheimer Disease: genetics
|2 MeSH
650 _ 2 |a Alzheimer Disease: physiopathology
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Heterozygote
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Middle Aged
|2 MeSH
650 _ 2 |a Motor Disorders: epidemiology
|2 MeSH
650 _ 2 |a Motor Disorders: genetics
|2 MeSH
650 _ 2 |a Motor Disorders: physiopathology
|2 MeSH
650 _ 2 |a Mutation: genetics
|2 MeSH
700 1 _ |a Paumier, Katrina
|b 1
700 1 _ |a Jucker, Mathias
|0 P:(DE-2719)2000010
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700 1 _ |a Preische, Oliver
|0 P:(DE-2719)2811828
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700 1 _ |a McDade, Eric
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700 1 _ |a Hassenstab, Jason
|b 5
700 1 _ |a Benzinger, Tammie L
|b 6
700 1 _ |a Noble, James M
|b 7
700 1 _ |a Berman, Sarah B
|b 8
700 1 _ |a Graff-Radford, Neill R
|b 9
700 1 _ |a Ghetti, Bernardino
|b 10
700 1 _ |a Farlow, Martin R
|b 11
700 1 _ |a Chhatwal, Jasmeer
|b 12
700 1 _ |a Salloway, Stephen
|b 13
700 1 _ |a Xiong, Chengjie
|b 14
700 1 _ |a Karch, Celeste M
|b 15
700 1 _ |a Cairns, Nigel
|b 16
700 1 _ |a Mori, Hiroshi
|b 17
700 1 _ |a Schofield, Peter R
|b 18
700 1 _ |a Masters, Colin L
|b 19
700 1 _ |a Goate, Alison
|b 20
700 1 _ |a Buckles, Virginia
|b 21
700 1 _ |a Fox, Nick
|b 22
700 1 _ |a Rossor, Martin
|b 23
700 1 _ |a Chrem, Patricio
|b 24
700 1 _ |a Allegri, Ricardo
|b 25
700 1 _ |a Ringman, John M
|b 26
700 1 _ |a Höglinger, Günter
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700 1 _ |a Steiner, Harald
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700 1 _ |a Dieterich, Marianne
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700 1 _ |a Haass, Christian
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700 1 _ |a Laske, Christoph
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700 1 _ |a Morris, John C
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700 1 _ |a Bateman, Randall J
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700 1 _ |a Danek, Adrian
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700 1 _ |a Levin, Johannes
|0 P:(DE-2719)2811659
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|e Last author
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700 1 _ |a Network, Dominantly Inherited Alzheimer
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773 1 8 |a 10.1093/brain/awz050
|b : Oxford University Press (OUP), 2019-03-20
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773 _ _ |a 10.1093/brain/awz050
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