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1 th a minimum of 2 CSF samples from Alzheimer Centrum Amsterdam cohorts across the AD clinical spectru
3 The camellate pattern found in the vertebral centrum (ce) of this taxon and other titanosaurs shows d
4 early work suggests that ascoma ontogeny and centrum characters are not in conflict with the molecula
12 vessel pathology: those in the white matter centrum semi-ovale have been associated with cerebral am
13 ty of MRI-visible perivascular spaces in the centrum semi-ovale was independently associated with cli
14 that MRI-visible perivascular spaces in the centrum semi-ovale would be associated with a clinical d
15 that MRI-visible perivascular spaces in the centrum semi-ovale would be associated with brain amyloi
17 brainstem, grey- white matters on levels of centrum semiovale (CS), high convexity (HC), and cerebel
18 ity index within perforating arteries of the centrum semiovale (mean difference - 0.09 cm/s, p = 0.03
19 tter lesion load (p < 0.05), more PVS in the centrum semiovale (p < 0.05) and had higher overall PVS
23 y distributions, we hypothesised that severe centrum semiovale EPVS are more common in lobar ICH attr
24 =76) had a higher prevalence of severe (>40) centrum semiovale EPVS compared with other ICH patients
27 rity; only age was associated with increased centrum semiovale EPVS severity (OR: 1.50; 95% CI 1.08 t
28 eatine (tCr) was observed in the NAWM of the centrum semiovale of all MS subgroups, including partici
29 c (ie, severe visible perivascular spaces in centrum semiovale or white matter hyperintensities in a
30 unction measures included: basal ganglia and centrum semiovale perforating artery blood flow velocity
31 microbleeds, cortical superficial siderosis, centrum semiovale perivascular spaces, and white matter
32 microbleeds, cortical superficial siderosis, centrum semiovale perivascular spaces, and white matter
33 different associations for basal ganglia and centrum semiovale PVS might indicate different underlyin
34 subtype) were independently associated with centrum semiovale PVS severity (OR: 1.19; p=0.013 and OR
38 erebral blood flow (CBF) at the level of the centrum semiovale was evaluated by using the Jonckheere-
43 nstem, caudate, thalamus, lentiform nucleus, centrum semiovale, and from frontal, parietal, precentra
44 cts, had significantly reduced NA/Cre in the centrum semiovale, and significantly reduced NA/Cho in t
45 interest chosen in the cortical gray matter, centrum semiovale, caudate nuclei, lentiform nuclei, tha
46 ed bilaterally in regions of interest in the centrum semiovale, corona radiata, internal capsule, cor
47 er white matter regions, particularly in the centrum semiovale, diffusion anisotropy was low, and cyl
48 gnificantly reduced NA/Cre in the brainstem, centrum semiovale, frontal and precentral cortex, and si
49 the region of the corticospinal tract in the centrum semiovale, in the posterior limb of the internal
50 tational age only in the white matter of the centrum semiovale, in which A sigma values increase shar
51 sed FA in the genu, cingulum cingulate gyri, centrum semiovale, inferior longitudinal fasciculi, limb
53 Early lesions affect corpus callosum and centrum semiovale, with or without cerebellar or cord in
61 rial testing multivitamin use (multivitamin [Centrum Silver] or placebo daily) among US male physicia