000 01487 a2200481 4500
005 20250518003456.0
264 0 _c20190826
008 201908s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/WNL.0000000000006503
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGroot, Colin
245 0 0 _aClinical phenotype, atrophy, and small vessel disease in
_h[electronic resource]
260 _bNeurology
_c11 2018
300 _ae1851-e1859 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAged
650 0 4 _aAlzheimer Disease
_xgenetics
650 0 4 _aApolipoprotein E2
_xgenetics
650 0 4 _aAtrophy
650 0 4 _aBrain
_xpathology
650 0 4 _aCross-Sectional Studies
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMicrovessels
_xpathology
650 0 4 _aMiddle Aged
650 0 4 _aPhenotype
700 1 _aSudre, Carole H
700 1 _aBarkhof, Frederik
700 1 _aTeunissen, Charlotte E
700 1 _avan Berckel, Bart N M
700 1 _aSeo, Sang Won
700 1 _aOurselin, Sébastien
700 1 _aScheltens, Philip
700 1 _aCardoso, M Jorge
700 1 _avan der Flier, Wiesje M
700 1 _aOssenkoppele, Rik
773 0 _tNeurology
_gvol. 91
_gno. 20
_gp. e1851-e1859
856 4 0 _uhttps://doi.org/10.1212/WNL.0000000000006503
_zAvailable from publisher's website
999 _c28958740
_d28958740