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 RECENT FINDINGS: The
ophthalmoscopic and location differences between grouped
6 rim, and disc margin confocal scanning laser
ophthalmoscopic (
CSLO) parameters, using odds ratios at
7 tinal fluid was identified by EDI OCT (16%),
ophthalmoscopic examination (8%), and ultrasonographic e
8 between traditional zone diagnosis (based on
ophthalmoscopic examination and image review) compared w
9 Ophthalmoscopic examination features included macular ed
10 ader were compared with those of an indirect
ophthalmoscopic examination from an experienced on-site
11 Ophthalmoscopic examination of mice homozygous for rd6 r
12 Ophthalmoscopic examination of the left eye showed a geo
13 Ophthalmoscopic examination revealed a decreased calibre
14 Ophthalmoscopic examination revealed an abnormal tangle
15 During infancy and early childhood,
ophthalmoscopic examination should be performed frequent
16 best-corrected visual acuity (BCVA) testing,
ophthalmoscopic examination, and multimodal imaging.
17 proaches, including slit-lamp biomicroscopy,
ophthalmoscopic examination, ultrasound backscatter micr
18 the silicone droplets still being present on
ophthalmoscopic examination.
19 ination with the clinical diagnosis based on
ophthalmoscopic examination.
20 ination with the clinical diagnosis based on
ophthalmoscopic examination.
21 ria and retinopathy on the basis of indirect
ophthalmoscopic examination; matching was then changed t
22 Ophthalmoscopic examinations were performed on aged norm
23 ase, and normal slit lamp biomicroscopic and
ophthalmoscopic examinations.
24 rable fraction of isolated patients with the
ophthalmoscopic features of Best disease are probably af
25 Familiarity with the morphologic and
ophthalmoscopic features of pigmented and de-POFLs is es
26 No growth or change in echographic or
ophthalmoscopic features were found in 307 nevi with a m
27 14 of 22 infants (63.6%) from the group with
ophthalmoscopic findings and 10 of 18 infants (55.6%) fr
28 No significant changes in
ophthalmoscopic findings and electroretinographic respon
29 ed were measured, using examination date and
ophthalmoscopic findings as a reference standard.
30 Identification of risk factors for
ophthalmoscopic findings in infants born with microcepha
31 ka virus (ZIKV) might cause microcephaly and
ophthalmoscopic findings in infants of mothers infected
32 disease, and 57 unrelated probands with the
ophthalmoscopic findings of Best disease but no family h
33 of 18 infants (55.6%) from the group without
ophthalmoscopic findings.
34 a-bpck/J mice and evaluated their retinas by
ophthalmoscopic,
histologic, and ultrastructural examina
35 uired from four AMD experts who examined 100
ophthalmoscopic images.
36 In addition,
ophthalmoscopic signs were more frequent in children (42
37 Ophthalmoscopic thresholds, indicating onset of thermal