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1 opathy lesions (retinal blot hemorrhages and microaneurysms).
2 els and penetrating arterioles with numerous microaneurysms.
3 l Neural Network (Mask-RCNN) for quantifying microaneurysms.
4 r to those seen in human DR including ME and microaneurysms.
5 tailed characterization of perfused diabetic microaneurysms.
6 n sensitivities of new, static and regressed microaneurysms.
7 infiltrated with macrophages, forming pseudo-microaneurysms.
8 hemosiderin deposits, vessel tortuosity, and microaneurysms.
9 ppearance of pericyte ghosts or formation of microaneurysms.
10 ntrol) and was preceded by mesangiolysis and microaneurysms.
11 ll death, leukocyte plugging of vessels, and microaneurysms.
12 etic retinopathy of both eyes with scattered microaneurysms.
13 ers (15/173; 9%) and the outermost extent of microaneurysms (113/173; 68%) were localized to the oute
14 dataset comprising 148 images annotated with microaneurysms, 118 (75%) and 30 (25%) of which were use
15 0) for any retinopathy, 3.11 (1.71-5.65) for microaneurysms, 3.08 (1.42-6.68) for soft exudates, 2.55
16                          Over half of closed microaneurysms (45/86, 52.3%) left hyperreflective spots
17 as able to identify a mean (SD) of 6.4 (4.0) microaneurysms (95% CI, 4.4-8.5), while FA identified a
18  while FA identified a mean (SD) of 10 (6.9) microaneurysms (95% CI, 6.4-13.5).
19 cantly inhibiting the development of retinal microaneurysms, acellular capillaries, and pericyte ghos
20 examination revealed multiple mid-peripheral microaneurysms and a wreath-like type 3 arteriovenous an
21 ng clinical pathologic fundus lesions (e.g., microaneurysms and focal edema), were markedly delayed (
22 ading of secondary vascular effects, such as microaneurysms and hemorrhages, by clinical examination
23 lar to those observed in diabetes, including microaneurysms and increased vascular permeability, sugg
24                 Zonal assessments of macular microaneurysms and macular leakage index values revealed
25 bx3 in ECs results in glomerular hypoplasia, microaneurysms and regressed fenestrations leading to fi
26 a significant decrease in the mean number of microaneurysms and retinal hemorrhages on UWF CFP at M3
27                                      Smaller microaneurysms and those with heterogeneous lumen were p
28 as significantly correlated to the number of microaneurysms and to the FAZ surface.
29 n nodular glomerulosclerosis, mesangiolysis, microaneurysms, and arteriolar hyalinosis associated wit
30 tivity, manifesting as dilation, tortuosity, microaneurysms, and decreased cerebral blood flow, as ob
31 sangial matrix expansion, mesangiolysis with microaneurysms, and Kimmelstiel-Wilson nodules.
32 illary length, width, density, the number of microaneurysms, and the percent of capillary length invo
33                                              Microaneurysms are biomarkers of microvascular injury in
34 e superior field than in the inferior field, microaneurysms are more frequent in the superior than in
35                                              Microaneurysms are the key hallmark of the early stage o
36                    Retinal thickness through microaneurysms as well as the presence of adjacent hypor
37                         External diameter of microaneurysms averaged 104 mum (range 43-266 mum).
38                              Closure rate of microaneurysms by both FA and SD-OCT was 69.9% (84/123),
39 iabetic retinopathy (DR) is characterized by microaneurysms, capillary nonperfusion, and ischemia wit
40                                         Some microaneurysm centers (15/173; 9%) and the outermost ext
41 reflectivity were positively associated with microaneurysm closure at 12 months (P < .0001, P < .001,
42                                              Microaneurysm closure rate increased at 6 and 12 months
43 eneous lumen were positively associated with microaneurysm closure.
44 or DRIL extent, cysts, hyperreflective foci, microaneurysms, cone outer segment tip visibility, and e
45 f DME with macular leakage index and macular microaneurysm count (P < 0.01).
46 ith macular leakage index and posterior pole microaneurysm count (P = 0.0002 and P = 0.03, respective
47  eyes with DME showed a significantly higher microaneurysm count (P = 0.001) and leakage index (P < 0
48 (mean = 9.53%); P<2x10(-16)], and panretinal microaneurysm count [mild NPDR (mean = 36), moderate NPD
49                                Additionally, microaneurysm count and ischemic index were quantified i
50 x, panretinal ischemic index, and panretinal microaneurysm count are associated with DR severity.
51   Quantitative measures of leakage index and microaneurysm count in the posterior pole on UWFA images
52                    Panretinal leakage index, microaneurysm count, and ischemic index were not signifi
53 addition to posterior pole leakage index and microaneurysm count, DME was associated with older age (
54 anretinal leakage index, ischemic index, and microaneurysm count.
55            Down-trending leakage indices and microaneurysm counts were demonstrated over 1 year of an
56                                              Microaneurysm dimensions, percent depth within the retin
57 ing of atheromatous plaques, atherosclerotic microaneurysms extending into periaortic vascular channe
58                          Characterization of microaneurysms following focal laser photocoagulation re
59 ce of pericyte ghosts, vascular leakage, and microaneurysm formation.
60                                              Microaneurysms found in regions without nonperfusion wer
61 tworks using ensembling for the detection of microaneurysms from OCT angiography en face images from
62 of ensembled U-nets to automatically segment microaneurysms from OCT angiography fundus projections.
63 ejection with glomerulitis, microthrombosis, microaneurysms, glomerular hypertrophy, podocyte loss, g
64   To evaluate detection of hemorrhage and/or microaneurysm (H/Ma) using ultrawide field (UWF) retinal
65                                         Most microaneurysms had an internal lumen with homogeneous re
66 d from another 15 dogs after 31 months, when microaneurysms had previously been observed to develop.
67              For retinal hemorrhages and/ or microaneurysms, hard exudates, new vessels, fibrous prol
68 with diabetes and without signs of DR (e.g., microaneurysms, hemorrhages), plus three control eyes an
69 presence of pathologic conditions, including microaneurysms, hemorrhages, exudates, neovascularizatio
70              On UWF-CF images, the number of microaneurysms, hemorrhages, neovascularizations, and ar
71 tio [OR] 2.47 [95% CI 1.42-4.31]) or retinal microaneurysms/hemorrhages (2.28 [1.24-4.18]) were signi
72 r narrowing, arteriovenous (AV) nicking, and microaneurysms/hemorrhages were evaluated on digital ret
73 etinal microvascular lesions (AV nicking and microaneurysms/hemorrhages) are more likely to have mult
74 orithms determined VRA and hemorrhage and/or microaneurysm (HMA) counts.
75 , and histological analysis showed incipient microaneurysms in retinas of gal-fed marmosets.
76  significantly correlated with the number of microaneurysms in the DCP, the surface of capillary non
77 sms in the superficial vascular complex, and microaneurysms in the deep vascular complex (DVC) (p = 0
78                 SSPiM may be correlated with microaneurysms in the DVC and a poor anatomical response
79        After multivariate logistic analysis, microaneurysms in the DVC were the only different factor
80 pared to the non-DME eyes, DME eyes had more microaneurysms in the SCP and the DCP (p = 0,039 and p =
81 se-free duration, previous injection number, microaneurysms in the superficial vascular complex, and
82                                              Microaneurysms, intraretinal microvascular abnormalities
83                                              Microaneurysms, intraretinal microvascular abnormalities
84 lammation was not a significant predictor of microaneurysm leakage.
85 tion at month 1 and again every 3 months for microaneurysm leakage.
86 signaling leads to the formation of abundant microaneurysms, leaky capillaries, and retinal hemorrhag
87        The worst changes histologically were microaneurysms, leukocyte and platelet plugging of aneur
88 FA metrics, including leakage, ischemia, and microaneurysm (MA) burden.
89   An automated system for the measurement of microaneurysm (MA) turnover was developed and compared w
90   All individual DR lesions (hemorrhage [H], microaneurysm [ma], cotton wool spot [CWS], intraretinal
91                                              Microaneurysms (MAs) are one of the earliest clinically
92                                              Microaneurysms (MAs) have distinct, oval-shaped, hyperre
93               To correlate the appearance of microaneurysms (MAs) on structural spectral-domain optic
94 rochannels designed to mimic saccular-shaped microaneurysms (microaneurysm-on-a-chip, or MAOAC), whic
95 haracterized by microangiopathies, including microaneurysms, microhemorrhages, and nerve layer infarc
96                                      Leaking microaneurysms (n = 123) were analyzed in eyes (n = 29)
97 s manifested by an increase in the number of microaneurysms, neovascular tufts, and preretinal nuclei
98              The exact intraretinal depth of microaneurysms on OCTA was localized in all cases (100%)
99 ned to mimic saccular-shaped microaneurysms (microaneurysm-on-a-chip, or MAOAC), which signify common
100 nal hemorrhages only, 3) presence of retinal microaneurysms only, and 4) presence of moderate or wors
101 nts with diabetes had retinal defects (e.g., microaneurysms or exudates or both) within the field of
102 age, larger haemorrhage, fibrinoid necrosis, microaneurysms, perivascular space dilation, perivascula
103             Increased FA leakage of diabetic microaneurysms positively correlated with perianeurysm f
104                                   The DR and microaneurysm scores from the first nonreferable DR (NRD
105                          Furthermore, DR and microaneurysm scores generated from low- and high-resolu
106                                     Perfused microaneurysms seen by SD-OCT were localized deeper than
107                                              Microaneurysms showed relatively slower flow, IRMAs show
108 here was not complete correspondence between microaneurysms shown on FA and PV-OCT images.
109    It also mitigated vascular remodeling and microaneurysms significantly.
110 erfusion, inflammation, and pericyte loss on microaneurysm size and leakage in DR through three-dimen
111                                 In addition, microaneurysm size was a significant predictor of leakag
112 s were found to be independent predictors of microaneurysm size.
113                                   Almost all microaneurysms spanned more than 1 retinal layer (157/17
114  layers (DRIL), cysts, epiretinal membranes, microaneurysms, subretinal fluid, and outer layer disrup
115                          It identified fewer microaneurysms than FA, but located their exact intraret
116 l vascular integrity regarding the number of microaneurysms, the number of IRMA, the surface of capil
117 ted system to investigate some properties of microaneurysm turnover, in particular the differing dete
118 DR through three-dimensional analysis of 636 microaneurysms using high-resolution confocal scanning l
119                          Closure of diabetic microaneurysms was characterized in detail following foc
120 and F1-score values for detecting individual microaneurysms were 0.786, 0.615, and 0.690, respectivel
121                               A total of 173 microaneurysms were analyzed in 50 eyes (14 mild nonprol
122 inal microvascular abnormalities (IRMAs) and microaneurysms were associated with the areas of nonperf
123                       The characteristics of microaneurysms were evaluated by 2 masked observers usin
124                                              Microaneurysms were first classified as perfused if flow
125 blocked the development of mesangiolysis and microaneurysms, whereas tubulointerstitial injury was no
126 teriopathy include the "string of beads" and microaneurysms which are indistinguishable from those of
127 es were segmented for ischemia, leakage, and microaneurysms with manual correction as needed.

 
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