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1 d venular diameter, and markers for cerebral small vessel disease.
2 EPVS) are a promising neuroimaging marker of small vessel disease.
3 rns of brain injury supported both large and small vessel disease.
4 dase pathway in the pathogenesis of cerebral small vessel disease.
5 ascular risk factors known to cause sporadic small vessel disease.
6 neuroimaging and genetic markers of cerebral small vessel disease.
7 Disease-type disease rather than to cerebral small vessel disease.
8 , which belongs to the continuum of cerebral small vessel disease.
9 whole brain atrophy in symptomatic cerebral small vessel disease.
10 finding appears to be related to underlying small vessel disease.
11 ibutions to quality of life in patients with small vessel disease.
12 (MRI) are a neuroimaging marker of cerebral small vessel disease.
13 ld identify a homogeneous subpopulation with small vessel disease.
14 r spaces may reflect the underlying cerebral small vessel disease.
15 ebrovascular diseases secondary to large and small vessel disease.
16 bnormalities, resemble symptoms and signs of small vessel disease.
17 function over time in patients with cerebral small vessel disease.
18 the brain are important markers of aging and small-vessel disease.
19 ent type of stroke caused mainly by cerebral small-vessel disease.
20 ied a COL4A1 mutation in a human family with small-vessel disease.
21 tify CTEPH patients with significant distal, small-vessel disease.
22 n the settings of vascular calcification and small-vessel disease.
23 l large-vessel disease compared with that of small-vessel disease.
24 resting-state CBF is a marker of CMB-related small-vessel disease.
25 other magnetic resonance imaging markers of small-vessel disease.
26 bal brain atrophy and an increased burden of small-vessel disease.
27 arge-vessel and cardioembolic stroke but not small-vessel disease.
28 inding and may be a useful endophenotype for small vessel diseases.
30 7.2% versus 24.1+/-15.9%, P<0.0001; and mean small-vessel disease, 11.7+/-14.6 versus 14.1+/-8.7, P=0
31 coma is associated with evidence of cerebral small vessel disease; 2) that imaging biomarkers of cere
33 for precisely how amyloid-beta and cerebral small vessel disease affect cognitive impairment remain
34 amyloid angiopathy is a common, well-defined small vessel disease and a largely untreatable cause of
35 we scored the severity of arteriolosclerotic small vessel disease and cerebral amyloid angiopathy, an
36 investigations into the connections between small vessel disease and delayed seizures are warranted.
39 non-demyelinating disorders such as chronic small vessel disease and other inflammatory, granulomato
40 ear if and how associations between cerebral small-vessel disease and Alzheimer disease (AD) patholog
41 ebral amyloid angiopathy is a common form of small-vessel disease and an important risk factor for co
42 CADASIL and their mechanistic connection to small-vessel disease and GOM accumulation remain enigmat
43 , hypertension, lacunar stroke and ischaemic small vessel disease, and have generated interest as a m
44 validated mutations that cause porencephaly, small vessel disease, and hereditary angiopathy, nephrop
45 sights into the longitudinal pathogenesis of small vessel disease, and imply that therapies aimed at
46 abetes, dyslipidemia, smoking, infarcts from small-vessel disease, and "other definite" causes and wo
47 neuroimaging and genetic markers of cerebral small vessel disease: APOE variants epsilon2/epsilon4, c
48 ion, white matter microstructural changes in small vessel disease are associated with apathy but not
49 Y ON THIS ARTICLE: Amyloid-beta and cerebral small vessel disease are the two major causes of cogniti
51 atter lesions (WMLs)-an imaging surrogate of small vessel disease-are associated with a higher rate o
52 pathy and depression can be distinguished in small vessel disease both in terms of their relative rel
55 bidities, cognition, hippocampal volume, and small-vessel disease but not on gait speed (0.85 vs 0.92
56 e potential neuroimaging markers of cerebral small vessel disease, but their functional significance
58 CADASIL is a genetic paradigm of cerebral small vessel disease caused by NOTCH3 mutations that ste
59 e severity of structural vascular pathology (small vessel disease, cerebral amyloid angiopathy or VWF
61 pathy (CAA) is a common age related cerebral small vessel disease, characterised by progressive depos
62 patients, 33% of stroke was due to cerebral small vessel disease compared with 14% in the white stro
65 pression hypothesis postulates that cerebral small vessel disease (CSVD) leads to depressive symptoms
68 us early and late manifestations of cerebral small vessel disease (eg, microbleeds and white matter h
69 appears aggravated in patients with cerebral small-vessel disease, especially in apolipoprotein E eps
70 nt membrane and COL4A1 mutations cause adult small vessel disease, familial porencephaly and heredita
71 cts of cerebrovascular disease, particularly small vessel disease, from those of Alzheimer's disease
73 alent CMBs, and markers of cerebral ischemic small-vessel disease, heavy alcohol consumption (vs ligh
74 imaging markers of the severity and type of small-vessel disease (hypertensive arteriopathy or cereb
75 kely harbor a more advanced form of cerebral small vessel disease in need of efficacious therapeutic
76 ease; 2) that imaging biomarkers of cerebral small vessel disease in POAG and NTG will show different
79 gnitive impairment, and other MRI markers of small vessel disease, in a patient cohort of ischaemic s
80 and to magnetic resonance imaging markers of small-vessel disease including increased white matter hy
81 nce of magnetic resonance imaging markers of small vessel disease, including cerebral microbleeds and
86 suggest that apathy, but not depression, in small vessel disease is related to damage to cortical-su
89 of frontal-subcortical circuits by cerebral small-vessel disease is thought to predispose to depress
90 antineutrophil cytoplasmic antibody-positive small vessel diseases, is largely restricted to case rep
91 lopathy (CADASIL), the most common inherited small-vessel disease, is associated with vascular aggreg
92 thy (CARASIL), an inherited form of cerebral small vessel disease leading to early-onset stroke and p
96 we hypothesized that CSF markers related to small vessel disease may also be applicable as biomarker
101 e lowest in cortex from patients with severe small vessel disease or cerebral amyloid angiopathy, nei
103 rs than the large artery disease (p<0.0001), small vessel disease (p=0.001), and cardioembolic (p=0.0
104 with SVS, we assessed its influence on other small vessel disease phenotypes, as well as on messenger
105 bnormal vascular development, which triggers small-vessel disease, recurrent hemorrhagic strokes, and
106 thrombotic material or coexistent intrinsic small-vessel disease, remains a major determinant of poo
108 corporated into a prespecified ordinal total small vessel disease score, ranging from 0 to 6 points.
110 e gave a higher estimate of the frequency of small vessel disease stroke, particularly in white patie
115 tients with late-onset AD have more comorbid small vessel disease (SVD) contributing to clinical seve
122 to assess whether and how single markers of small vessel disease (SVD) or a combination thereof expl
123 arterioles (PAs), a major target of cerebral small vessel disease (SVD), and determined whether relax
124 aneous intracerebral hemorrhage (ICH) due to small vessel disease (SVD), but the association between
125 is a neurological syndrome characterized by small vessel disease (SVD), stroke, and vascular cogniti
126 association is possibly mediated by cerebral small vessel disease (SVD), which has been associated wi
127 lacunar strokes are associated with cerebral small vessel disease (SVD), which is the commonest vascu
133 oke and is a major manifestation of cerebral small vessel disease, the primary cause of vascular cogn
134 ith the hypothesis that PVS reflect cerebral small vessel disease; the different associations for bas
137 y, percentage of fibrosis, and percentage of small-vessel disease were correlated with the genotype.
139 hy and magnetic resonance imaging markers of small vessel disease (white matter hyperintensities or l
140 dinal cohort of 99 subjects with symptomatic small vessel disease, who were followed-up for >/=1 year
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