戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 the sclera subjects to vigorous clearance by episcleral and choroidal circulation; in addition, the p
2                             The left eye had episcleral and conjunctival injection, clear cornea, a d
3 P) was elevated by laser photocoagulation of episcleral and limbal veins.
4 ace, measured 9 x 6 x 3 mm, and exhibited no episcleral attachment or ocular involvement.
5 s a novel technique for quantifying absolute episcleral blood flow in humans.
6 oma treated with iodine 125 or ruthenium 106 episcleral brachytherapy between January 1, 2004, and De
7             A total of 375 eyes treated with episcleral brachytherapy for posterior uveal melanoma fr
8                        Vision loss following episcleral brachytherapy for uveal melanoma is difficult
9  melanoma from 1995 to 2016 and treated with episcleral brachytherapy were included.
10 s developed to predict vision loss following episcleral brachytherapy.
11  counseling for patients being evaluated for episcleral brachytherapy.
12 ing brachytherapy are uncommon 5 years after episcleral brachytherapy.
13 t were secured by suturing, to form a sealed episcleral chamber that was filled with a fluorescein so
14               These results suggest that the episcleral circulation is under tonic neural control and
15                                          The episcleral cyclosporine implant shows promise in reducin
16  This preclinical evaluation showed that the episcleral cyclosporine implant was safe, delivered pote
17                                              Episcleral cyclosporine implants were manufactured with
18                                           An episcleral exoplant facilitates diffusion of fluorescein
19 dium fluorescein (fluorescein, 376 Da) or an episcleral exoplant loaded with fluorescein.
20                         More than 34% of the episcleral hydrogel explants developed symptomatic swell
21                            The ability of an episcleral implant at the equator of the eye to deliver
22  assess the toxicity of a cyclosporine (CsA) episcleral implant for the prevention of high-risk kerat
23 ysis of the ocular drug distribution from an episcleral implant showed that the elimination rate cons
24 porine in the subconjunctival space with the episcleral implant was an effective means of delivering
25                                              Episcleral implants are safe and effective at delivering
26                                     In vivo, episcleral implants at the equator of the eye did not de
27                                              Episcleral implants in vivo delivered a mean total of 2.
28                                          CsA episcleral implants were made with a high (implant A) or
29 patients with unilateral anterior scleral or episcleral inflammation.
30 leading to optic nerve damage was induced by episcleral injection of hypertonic saline, which caused
31 racterized by corneal haze, conjunctival and episcleral injection, corneal infiltrates, and neovascul
32 en 1 and 3 months, at the CAG and underlying episcleral levels, respectively.
33                               The three-vein episcleral/limbal vein occlusion model for inducing glau
34 male Wistar rats (150-180 g) by cautery of 3 episcleral/limbal veins.
35 t surgical removal of a symptomatic, swollen episcleral MIRAgel (MIRA Inc., Waltham, MA) explant at t
36 with equine recurrent uveitis (ERU) received episcleral or deep scleral lamellar CsA implants and wer
37                         There was no case of episcleral or orbital retinoblastoma extension or remote
38 ic Resonance Imaging revealed a left lateral episcleral orbital mass and an incisional biopsy confirm
39 hotocoagulation may be considered only after episcleral pigmentation has become less so as to avoid t
40    I(125) brachytherapy was administered via episcleral plaque according to a standard protocol.
41 ye retention in patients treated with repeat episcleral plaque brachytherapy (EPBT) for locally recur
42                                              Episcleral plaque brachytherapy (EPBT) provides effectiv
43 r high-risk UM (tumors deemed unsuitable for episcleral plaque brachytherapy).
44                    In cases where intratumor/episcleral plaque edema or hemorrhage shifted the dose t
45  were 11 patients (47.8%) who received prior episcleral plaque.
46 ; meibomian glands; skin; retina-choroid; or episcleral regions.
47 mors were commonly dome shaped (75%) with an episcleral sentinel vessel (75%).
48 t barriers to the movement of drugs from the episcleral space into the vitreous in vivo.
49  Diffusion of CsA across the sclera from the episcleral space was not a feasible method of drug deliv
50  depot of drug (100 microl) was added to the episcleral surface while perfusing an irrigating solutio
51 vivo studies before subtenon TA injection or episcleral TA-film implantation.
52 y conjunctivae bilaterally, having undergone episcleral tattooing 7 weeks previously.
53  the few people in Britain to have undergone episcleral tattooing for cosmetic purposes.
54                                              Episcleral tattooing is carried out by individuals with
55 ribing the first forays into the practice of episcleral tattooing.
56 n exterior eye tissues including the cornea, episcleral tissue, and sclera.
57 . 4%) or ciliary body (30% vs. 8%) lymphoma, episcleral vascular congestion (40% vs. 16%), anterior c
58  hours) was a near complete blanching of the episcleral vasculature, and a poorly defined wave was mi
59 o provide a more reliable approach to assess episcleral vasculature.
60  by injection of hypertonic saline solution, episcleral vein cauterization, or optic nerve transectio
61 Hypertonic saline was injected into a single episcleral vein in 17 animals and awake IOP measured in
62 duced by hypertonic saline injection into an episcleral vein in 20 adult male Brown-Norway rats.
63 cular pressure (IOP) was produced in rats by episcleral vein injection of hypertonic saline (N = 30).
64                                              Episcleral vein injection of hypertonic saline is more l
65 own Norway rats (N = 16) received unilateral episcleral vein injection of hypertonic saline to elevat
66                                     A single episcleral vein injection of hypertonic saline was used
67 ateral IOP elevation was produced in rats by episcleral vein injection of hypertonic saline.
68 monitor chronically elevated IOP produced by episcleral vein injection of hypertonic saline.
69 own Norway rats were-administered unilateral episcleral vein injections of hypertonic saline to produ
70 induced in the left eye by hypertonic saline episcleral vein injections.
71  to optic nerve damage was induced using the episcleral vein occlusion model.
72  elevated by injecting 1.9 M saline into the episcleral vein, as previously described in Brown Norway
73  532 nm aimed at the trabecular meshwork and episcleral veins (combination treatment group) or only a
74 mice by laser photocoagulation of limbal and episcleral veins 270 degrees to 300 degrees circumferent
75 DTPA from the subconjunctival space into the episcleral veins and conjunctival lymphatics was 3-log u
76       Diode laser treatment of ICG saturated episcleral veins causes a chronic elevation of IOP and s
77 ser cauterization of trabecular meshwork and episcleral veins in rat eyes.
78         Laser photocoagulation of limbal and episcleral veins induces transient ocular hypertension i
79 sive eye in which cauterizing limbal derived episcleral veins leads to increase in the intraocular pr
80 onal area (CSA) of the aqueous column within episcleral veins was correlated with intraocular pressur
81 flow pathway, preventing flow to the visible episcleral veins.
82 in rats by hypertonic saline injections into episcleral veins.
83 d by injection of hypertonic saline into the episcleral veins.
84 s with 2- to 3-microm tips used to cannulate episcleral veins.
85 mice by laser photocoagulation of limbal and episcleral veins.
86 e (12.5-14.5 mmHg) by cauterization of three episcleral veins.
87  rapid, non-invasive delineation of abnormal episcleral venous plexus secondary to dural CCF.
88 iotz tonography, IOP by pneumotonometry, and episcleral venous pressure (EVP) by automated venomanome
89                                              Episcleral venous pressure (EVP) was measured by gradual
90                         Measurements of IOP, episcleral venous pressure (EVP), conventional outflow f
91 acute elevations in IOP, suggesting elevated episcleral venous pressure (EVP).
92 of the variation in IOP is due to changes in episcleral venous pressure (EVP).
93 etermined by multiple flow-rate infusion and episcleral venous pressure (Pe) measured by manometry.
94 d be reconciled only if nocturnal changes in episcleral venous pressure and/or uveoscleral flow occur
95                      Current measurements of episcleral venous pressure are either invasive or provid
96  mechanisms are exertion-related increase in episcleral venous pressure or ocular compression from sl
97 stigate whether changes in outflow facility, episcleral venous pressure, or uveoscleral flow at night
98 ique altered tonographic outflow facility or episcleral venous pressure.
99  choroidal hemangioma, and signs of elevated episcleral venous pressure.
100 cy, any iridocorneal angle malformation, and episcleral vessel patency in normal eyes vs all other ey
101        After total outflow was measured, the episcleral vessels were blocked with cyanoacrylate to el
102 IOP was produced in rats by cautery of three episcleral vessels.
103 ry to anterior segment dysgenesis had patent episcleral vessels.

 
Page Top