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1                                              Ophthalmoscopic abnormalities were generally confined to
2 ivided into 2 groups, those with and without ophthalmoscopic alterations, for comparison.
3 seven eyes (46.3%) of 22 infants (55.0%) had ophthalmoscopic alterations.
4                                              Ophthalmoscopic and histologic analyses documented patho
5 to the clinical history, and on the basis of ophthalmoscopic and imaging examinations diabetic macula
6                         RECENT FINDINGS: The ophthalmoscopic and location differences between grouped
7 rim, and disc margin confocal scanning laser ophthalmoscopic (CSLO) parameters, using odds ratios at
8 tudy based on 3 masked expert labels and the ophthalmoscopic diagnosis.
9                                              Ophthalmoscopic evaluation did not show any substantial
10 tinal fluid was identified by EDI OCT (16%), ophthalmoscopic examination (8%), and ultrasonographic e
11                                     Detailed ophthalmoscopic examination and FA were recommended for
12 between traditional zone diagnosis (based on ophthalmoscopic examination and image review) compared w
13                                              Ophthalmoscopic examination features included macular ed
14 ader were compared with those of an indirect ophthalmoscopic examination from an experienced on-site
15 ent in the majority of patients with IP, and ophthalmoscopic examination is less sensitive than FA fo
16                                              Ophthalmoscopic examination of mice homozygous for rd6 r
17                                              Ophthalmoscopic examination of the left eye showed a geo
18 with a PVD diagnosis and history of extended ophthalmoscopic examination on presentation were identif
19 initiated by an examining physician based on ophthalmoscopic examination results.
20                                              Ophthalmoscopic examination revealed a decreased calibre
21                                              Ophthalmoscopic examination revealed an abnormal tangle
22          During infancy and early childhood, ophthalmoscopic examination should be performed frequent
23                                              Ophthalmoscopic examination showed completely unilateral
24 rticipants underwent refracted BCVA testing, ophthalmoscopic examination, and fundus photography at b
25 best-corrected visual acuity (BCVA) testing, ophthalmoscopic examination, and multimodal imaging.
26 rticipants underwent refracted BCVA testing, ophthalmoscopic examination, and stereoscopic color fund
27 proaches, including slit-lamp biomicroscopy, ophthalmoscopic examination, ultrasound backscatter micr
28 ination with the clinical diagnosis based on ophthalmoscopic examination.
29 the silicone droplets still being present on ophthalmoscopic examination.
30 ination with the clinical diagnosis based on ophthalmoscopic examination.
31 ria and retinopathy on the basis of indirect ophthalmoscopic examination; matching was then changed t
32                                              Ophthalmoscopic examinations were performed on aged norm
33 ase, and normal slit lamp biomicroscopic and ophthalmoscopic examinations.
34 rable fraction of isolated patients with the ophthalmoscopic features of Best disease are probably af
35         Familiarity with the morphologic and ophthalmoscopic features of pigmented and de-POFLs is es
36        No growth or change in echographic or ophthalmoscopic features were found in 307 nevi with a m
37 14 of 22 infants (63.6%) from the group with ophthalmoscopic findings and 10 of 18 infants (55.6%) fr
38                    No significant changes in ophthalmoscopic findings and electroretinographic respon
39                                              Ophthalmoscopic findings and FA images were graded for s
40 ed were measured, using examination date and ophthalmoscopic findings as a reference standard.
41           Identification of risk factors for ophthalmoscopic findings in infants born with microcepha
42 ka virus (ZIKV) might cause microcephaly and ophthalmoscopic findings in infants of mothers infected
43  disease, and 57 unrelated probands with the ophthalmoscopic findings of Best disease but no family h
44 of 18 infants (55.6%) from the group without ophthalmoscopic findings.
45 a-bpck/J mice and evaluated their retinas by ophthalmoscopic, histologic, and ultrastructural examina
46 uired from four AMD experts who examined 100 ophthalmoscopic images.
47                                 In addition, ophthalmoscopic signs were more frequent in children (42
48                                              Ophthalmoscopic thresholds, indicating onset of thermal