ライフサイエンスコーパス: biomicroscopy

1 hinning and flow abnormalities undetected by biomicroscopy.

2 tumor on clinical examination and ultrasound biomicroscopy.

3 rneas (3 +/- 0.4) quantified using slit lamp biomicroscopy.

4 Eyes were examined weekly by slit-lamp biomicroscopy.

5 assessed by ophthalmologists using slit-lamp biomicroscopy.

6 ne, CRB1, and mutations using topography and biomicroscopy.

7 in the rabbit eye was graded with slit lamp biomicroscopy.

8 in a large family were examined by slit lamp biomicroscopy.

9 iac function using high-frequency ultrasound biomicroscopy.

10 AC depth was measured using an ultrasound biomicroscopy.

11 rafts were evaluated clinically by slit lamp biomicroscopy.

12 Graft survival was evaluated by slit lamp biomicroscopy.

13 taract development by conventional slit-lamp biomicroscopy.

14 sure and for as long as 10 days by slit lamp biomicroscopy.

15 sion of cataracts was monitored by slit-lamp biomicroscopy.

16 mechanism of AAC was confirmed by ultrasound biomicroscopy.

17 gated with an ultrahigh-frequency ultrasound biomicroscopy.

18 gic features not visible to the clinician on biomicroscopy.

19 igh-quality color photography and ultrasound biomicroscopy.

20 argin of each eye, confirmed with ultrasound biomicroscopy.

21 ion, indirect ophthalmoscopy, and ultrasound biomicroscopy.

22 8, and 72 hours after treatment by slit-lamp biomicroscopy.

23 oscopy, biometry, pachymetry, and ultrasound biomicroscopy.

24 edia thicknesses were measured by ultrasound biomicroscopy.

25 anterior segment examination with slit-lamp biomicroscopy.

26 ion regarding macular edema than FA (77%) or biomicroscopy (76%).

27 sing standard ultrasonography and ultrasound biomicroscopy, a lack of a transillumination shadow, and

28 r hyaloid membrane observed during slit-lamp biomicroscopy after posterior vitreous detachment and co

29 Ultrasound biomicroscopy allows longitudinal studies of tumor devel

30 determined with stereomicroscopy, slit lamp biomicroscopy, alpha-smooth muscle actin (alphaSMA), fib

31 rafts were evaluated by ophthalmic slit-lamp biomicroscopy and analyzed by Kaplan-Meier survival curv

32 Ultrasound biomicroscopy and anterior segment optical coherence tom

33 d 72 hours and were re-examined by slit-lamp biomicroscopy and by indirect ophthalmoscopy.

34 Slit lamp biomicroscopy and corneal pachymetry were performed week

35 phy (OCT) has become an important adjunct to biomicroscopy and fluorescein angiography.

36 thelial closure was monitored with slit lamp biomicroscopy and fluorescein staining, and corneal neov

37 d corrected (CDVA) distance visual acuities, biomicroscopy and fundus appearance, topography-derived

38 amage was assessed by stereoscopic slit-lamp biomicroscopy and fundus photography and by confocal sca

39 the AC cell response, evaluated by slit-lamp biomicroscopy and graded using a standard grading system

40 ate of the grafts was assessed clinically by biomicroscopy and histologically for 8 weeks postimplant

41 erent soft x-ray sources for applications in biomicroscopy and in chemical spectroscopy.

42 and 72 hours after injection using slit-lamp biomicroscopy and laser flare photometry.

43 ure, best corrected visual acuity, slit lamp biomicroscopy and medical history were obtained by anoth

44 Ultrasound biomicroscopy and more recently anterior segment optical

45 actous stages visually observed by slit lamp biomicroscopy and retroillumination photography.

46 al advances, including diagnostic ultrasound biomicroscopy and small-incision surgery with foldable,

47 oscopy, assessment of IOL centration, fundus biomicroscopy and spectral-domain optical coherence tomo

48 al and optic nerve structure included fundus biomicroscopy and stereophotography.

49 s of each patient were examined by slit-lamp biomicroscopy and white-light IVCM (Confoscan 4; Nidek T

50 At 24 and 72 hours, slit-lamp biomicroscopy (and additionally indirect ophthalmoscopy)

51 t, cumulative dose, Orlando stage (slit-lamp biomicroscopy), and serum concentrations of amiodarone a

52 ce were screened for cataract with slit lamp biomicroscopy, and dissected lenses were examined with d

53 ivo lens changes were monitored by slit lamp biomicroscopy, and enucleated lenses were examined under

54 efects by indirect ophthalmoscopy, slit-lamp biomicroscopy, and ERG to discover new spontaneous mutat

55 Flowmetry, wall strain analyses, biomicroscopy, and histology were completed.

56 ity (CDVA), cycloplegic refraction, slitlamp biomicroscopy, and keratometry (K).

57 easurement, ultrasound pachymetry, slit-lamp biomicroscopy, and laser scanning in vivo confocal micro

58 l acuity recorded in LogMAR units, slit-lamp biomicroscopy, and optical coherence tomography were ana

59 CT) was measured using histology, ultrasound biomicroscopy, and optical coherence tomography.

60 After maximal mydriasis, slit-lamp biomicroscopy, and photography, imaging of the anterior

61 heir ocular surface evaluated with slit-lamp biomicroscopy, and tear production quantified with the S

62 Modern imaging modalities such as ultrasound biomicroscopy, anterior segment optical coherence tomogr

63 Ultrasound biomicroscopy appears to be a valuable tool in confirmin

64 eyes in the study were examined by slit-lamp biomicroscopy at baseline and 6, 9, 24, 48, and 72 hours

65 All eyes were examined by slit-lamp biomicroscopy at baseline, 3, 6, 9, 24, 48, and 72 hours

66 disk hemorrhage was evaluated with slit lamp biomicroscopy at each clinic visit prior to and followin

67 rt defects can be diagnosed using ultrasound biomicroscopy but not with the clinical ultrasound syste

68 22 of 32 SCD eyes (68.8%) had retinopathy on biomicroscopy, by UWFA 4 of 24 (16.7%) SCD eyes had peri

69 specular microscopy, gonioscopy, ultrasound biomicroscopy, central macular thickness, intraocular pr

70 ive errors and best-corrected visual acuity, biomicroscopy, color fundus photography, electroretinogr

71 Ultrasound biomicroscopy confirmed the presence of a 3.8 mm parieta

72 Smartphone ophthalmoscopy and biomicroscopy could not be used to examine the fundus an

73 Best-corrected visual acuity, slit-lamp biomicroscopy, dilated fundus examination, wide-field ph

74 Slit lamp biomicroscopy disclosed the clinical features of LCD in

75 rious times following injection by slit lamp biomicroscopy, electroretinography (ERG), bacterial and

76 assessed bacteriologically and by slit lamp biomicroscopy, electroretinography, histology, and infla

77 Ultrasound biomicroscopy, endoscopy, and contrast agents were used

78 eudophakic patients who underwent ultrasound biomicroscopy examination between May 2009 and February

79 normal in all of the study groups; slit lamp biomicroscopy examinations revealed that no cells or fib

80 phic and clinical characteristics, slit-lamp biomicroscopy findings, and dilated ophthalmoscopy resul

81 hotometry were consistent with the slit-lamp biomicroscopy flare findings up to grade 3+.

82 pared with untreated animals using slit-lamp biomicroscopy, flow cytometry, and ELISA.

83 best-corrected visual acuity (BCVA), fundus biomicroscopy, fluorescein angiography (FA), and SDOCT.

84 ased on best-corrected visual acuity, fundus biomicroscopy, fluorescein angiography, and OCT.

85 Corneal biomicroscopy, fluorescein test, digital tonometry.

86 All eyes were evaluated by slit-lamp biomicroscopy for inflammatory response at 3, 6, 9, 24,

87 xcellent diagnostic capability of ultrasound biomicroscopy for most CHDs.

88 evaluated over 8 weeks in a masked manner by biomicroscopy for signs of rejection.

89 considerable agreement with dilated retinal biomicroscopy for the grading of DR.

90 Biomicroscopy, funduscopy, Pentacam imaging, noncontact

91 and best-corrected visual acuity, slit-lamp biomicroscopy, Goldmann applanation tonometry, gonioscop

92 subjective refraction IOP, anterior segment biomicroscopy, gonioscopy, assessment of IOL centration,

93 and ocular examination, including slit-lamp biomicroscopy, gonioscopy, specular microscopy.

94 edulloblastoma formation, we used ultrasound biomicroscopy-guided in utero injection of a Shh-express

95 Ultrasound biomicroscopy has allowed us to elucidate the anatomic v

96 Ultrasound biomicroscopy has revolutionized the evaluation of the a

97 Ultrasound biomicroscopy has the advantage of being able to illustr

98 mpared throughout the course of infection by biomicroscopy, histology, electroretinography, and bacte

99 Infection courses were analyzed by biomicroscopy, histology, electroretinography, and quant

100 Ultrasound biomicroscopy imaged the entire ciliary body, anterior a

101 Ultrasonic biomicroscopy images of zebrafish eyes were obtained wit

102 thinning/atrophy was detected by ultrasound biomicroscopy in 15% of cases and focal angle closure in

103 tic misplacement was confirmed by ultrasound biomicroscopy in all suspected cases.

104 ic fundus photography (method 1) and dilated biomicroscopy in combination with optical coherence tomo

105 r hyaloid membrane observed during slit-lamp biomicroscopy in patients with posterior vitreous detach

106 This review describes the role of ultrasound biomicroscopy in the measurement of the anatomic structu

107 th a small or large eyecup during ultrasound biomicroscopy, indentation with a gonioscopy lens, and s

108 Visual outcomes, slit lamp biomicroscopy, intraocular pressure (IOP), and posterior

109 view, best-corrected visual acuity, slitlamp biomicroscopy, intraocular pressure measurement, goniosc

110 t of best-corrected visual acuity, slit-lamp biomicroscopy, intraocular pressure measurement, indirec

111 Ultrasonic biomicroscopy is a potential new diagnostic modality for

112 fined as high-grade lens opacity observed by biomicroscopy judged to be the cause of a best-corrected

113 ; ophthalmic examination including slit-lamp biomicroscopy, noncontact tonometry, fundus photography,

114 Clinical follow-up using biomicroscopy of the cornea was performed at days 2, 4,

115 Different approaches, including slit-lamp biomicroscopy, ophthalmoscopic examination, ultrasound b

116 ked grader, applanation tonometry, slit-lamp biomicroscopy, optic nerve evaluation, and A-scan ultras

117 The clinical outcome was monitored by biomicroscopy, optical coherence tomography, confocal mi

118 valuated for signs of rejection by slit lamp biomicroscopy over 8 weeks.

119 Intraoperative ultrasound biomicroscopy performed at the time of the right eye tub

120 Ultrasound biomicroscopy provides objective, high-resolution images

121 aphy measurements, endothelial cell density, biomicroscopy, refraction, and intraoperative and postop

122 Ultrasound biomicroscopy revealed ciliary body cysts in the left ey

123 ptical coherence tomography and stereoscopic biomicroscopy review.

124 ment are slit-lamp biomicroscopy, ultrasound biomicroscopy, scheimpflug imaging, phakometry, optical

125 Biomicroscopy showed conjunctival hyperaemia in the left

126 Slit-lamp biomicroscopy showed refractile, polychromatic crystalli

127 Comparison was made between slit lamp biomicroscopy (SLB) and photographic grading.

128 findings, including visual acuity, slit-lamp biomicroscopy, spectral-domain optical coherence tomogra

129 e was no evidence of macular edema by fundus biomicroscopy, stereo fundus photography, or OCT.

130 On ultrasound biomicroscopy the anterior chamber structures were diffi

131 Compared to biomicroscopy, the sensitivity and specificity of smartp

132 All corneas were examined by using slit-lamp biomicroscopy to determine the severity of FECD versus n

133 A uveitis specialist used slit-lamp biomicroscopy to grade the AC cells on a scale of 0 to 4

134 or cataract, a high grade of lens opacity by biomicroscopy to which best-corrected visual acuity wors

135 day imaging technologies such as ultrasound biomicroscopy (UBM) and more recently, anterior segment

136 facilitate this process, such as ultrasound biomicroscopy (UBM) and the anterior segment OCT (AS-OCT

137 asurements taken with Orbscan II, ultrasound biomicroscopy (UBM) and the Artemis-2 VHF (very-high-fre

138 Ultrasound biomicroscopy (UBM) demonstrated hypotrophy of the cilia

139 Ultrasound biomicroscopy (UBM) images of the anterior chamber were

140 Ultrasound biomicroscopy (UBM) showed that the angle in the right e

141 , we have initiated studies using ultrasound biomicroscopy (UBM) to evaluate the vessel wall thicknes

142 n supine and sitting positions by ultrasound biomicroscopy (UBM) with bag/balloon technology.

143 alitative parameters defined from ultrasound biomicroscopy (UBM), anterior segment optical coherence

144 The techniques covered are: ultrasound biomicroscopy (UBM), microSPECT, microPET, near infrared

145 By means of ultrasound biomicroscopy (UBM), thickened (720 / 700 micron) and de

146 Using in utero ultrasound biomicroscopy (UBM), we studied embryonic day (E) 10.5 t

147 mined in utero with 40- to 50-MHz ultrasound biomicroscopy (UBM)-Doppler, to determine onset of embry

148 All corneas were examined using slit-lamp biomicroscopy, ultrasonic pachymetry, and confocal micro

149 r imaging the anterior segment are slit-lamp biomicroscopy, ultrasound biomicroscopy, scheimpflug ima

150 e incidence of mild to moderate hyperemia by biomicroscopy was 18%, 24%, and 11%, respectively.

151 itus with mild diabetic retinopathy (MDR) on biomicroscopy was analyzed using a custom-built algorith

152 Ultrasound biomicroscopy was performed in 21 eyes of 17 monkeys.

153 Slit lamp biomicroscopy was performed throughout the period and th

154 mography (OCT), infrared fundus imaging, and biomicroscopy were performed at baseline and at week 1,

155 scan, retinoscopy, refraction, and slit-lamp biomicroscopy were performed.

156 photography, ultrasonography, and ultrasonic biomicroscopy were used to evaluate clinical response to

157 photography, ultrasonography, and ultrasonic biomicroscopy were used to locate and evaluate the exten

158 Eyes were examined by slit lamp biomicroscopy with fluorescein solution to assess epithe