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Found 6 results
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van Swieten, John C
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2022
Holstege H
,
Hulsman M
,
Charbonnier C
,
Grenier-Boley B
,
Quenez O
,
Grozeva D
,
van Rooij JGJ
,
Sims R
,
Ahmad S
,
Amin N
et al.
. 2022.
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease.
.
Nat Genet. 54(12):1786-1794.
2017
Höglinger GU
,
Respondek G
,
Stamelou M
,
Kurz C
,
Josephs KA
,
Lang AE
,
Mollenhauer B
,
Müller U
,
Nilsson C
,
Whitwell JL
et al.
. 2017.
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.
.
Mov Disord. 32(6):853-864.
2012
Majounie E
,
Renton AE
,
Mok K
,
Dopper EGP
,
Waite A
,
Rollinson S
,
Chiò A
,
Restagno G
,
Nicolaou N
,
Simon-Sanchez J
et al.
. 2012.
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
.
Lancet Neurol. 11(4):323-30.
2011
Chen-Plotkin AS
,
Martinez-Lage M
,
Sleiman PMA
,
Hu W
,
Greene R
,
Wood EMcCarty
,
Bing S
,
Grossman M
,
Schellenberg GD
,
Hatanpaa KJ
et al.
. 2011.
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
.
Arch Neurol. 68(4):488-97.
Höglinger GU
,
Melhem NM
,
Dickson DW
,
Sleiman PMA
,
San Wang L-
,
Klei L
,
Rademakers R
,
de Silva R
,
Litvan I
,
Riley DE
et al.
. 2011.
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
.
Nat Genet. 43(7):699-705.
2010
Van Deerlin VM
,
Sleiman PMA
,
Martinez-Lage M
,
Chen-Plotkin A
,
San Wang L-
,
Graff-Radford NR
,
Dickson DW
,
Rademakers R
,
Boeve BF
,
Grossman M
et al.
. 2010.
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
.
Nat Genet. 42(3):234-9.