ライフサイエンスコーパス: posterior

1 sion (PTV, PTV1, or PTV2) was 0.8 cm (0.6 cm posterior).

2 ur subnuclei (anterior, lateral, medial, and posterior).

3 s, there is nonetheless proliferation in the posterior.

4 rossing commissural axons along the anterior-posterior (A-P) axis.

5 on wild-type BM in vivo reveals an anterior-posterior (A-P) symmetric stiffness gradient, which fail

6 ffecting the anterior (dry eye syndrome) and posterior (age-related macular degeneration, diabetic re

7 inesin 1 transports oskar mRNA to the oocyte posterior along a polarised microtubule cytoskeleton tha

8 a 2- to 4-Hz delta signature that modulated posterior alpha activity and behavior during predictive

9 gether, these findings support the idea that posterior alpha oscillations represent a state of increa

10 For each subject, the posterior alpha power variations were convolved with the

11 intrinsic sensory hyperactivity (suppressed posterior alpha power, source-localized to the visual co

12 e incidence of the recurrence of CAIS in the posterior and anterior circulations to determine if the

13 pendent force and stiffness along the antero-posterior and dorso-ventral axis.

14 l ectoderm was subdivided along the anterior-posterior and medial-lateral axes by microdissections.

15 expressed differentially along the anterior-posterior and medial-lateral axes of the chick tectum us

16 s of intermediate uveitis, and most cases of posterior and panuveitides requiring treatment are treat

17 But how posterior (and other) auditory areas represent acoustic

18 r, 32.5+/-8.8% (range, 6.0%-57.9%) for uncut posterior, and 42.3+/-6.6% (range, 25.5%-65.4%) for midp

19 s to collecting system or sinus, anterior or posterior, and location relative to polar lines (RENAL)

20 herapy for many noninfectious, intermediate, posterior, and panuveitides.

21 tomic subtypes of uveitis included anterior, posterior, and panuveitis in 2, 13, and 6 patients, resp

22 malized neuromelanin volume of the anterior, posterior, and whole SNpc correlated with Unified Parkin

23 that they form a distinct glomerulus in the posterior antennal lobe (PAL).

24 dy provides evidence that the often-reported posterior-anterior shift in aging may not reflect a glob

25 hese results suggest that the often-reported posterior-anterior shift may not reflect the inability o

26 and overlapping cognitive processes along a posterior-anterior vmPFC axis.

27 u(H) regulate gene expression along anterior-posterior (AP) or dorsal-ventral (DV) axes, respectively

28 , where it acts as a mediator of anterior to posterior (AP) patterning, whereas fibroblast growth fac

29 We decomposed the posterior AR in the cortical source space with a 3-way P

30 In primates, posterior auditory cortical areas are thought to be part

31 e body extends to form the complete anterior-posterior axis during the somite-forming stages.

32 BPTF is required for anterior-posterior axis formation of the mouse embryo and was sho

33 olarization of node cells along the anterior-posterior axis of mouse embryos is responsible for left-

34 processes, including gastrulation, anterior-posterior axis specification, organ and tissue developme

35 circular fibres led to a bifurcated anterior-posterior axis with fused heads forming in single anteri

36 es at different positions along the anterior-posterior axis.

37 thalamus, and moderate projections from the posterior bed nucleus of the stria terminalis, mesocorti

38 A1, but not in circumscribed regions of the posterior belt and parabelt cortex.

39 n of cell polarity that defines the anterior-posterior body axis frequently fails.

40 blations of DD04 or DD05 specifically affect posterior body movements, whereas ablations of DD02 or D

41 nterior (internal limiting membrane) and the posterior boundary of the RNFL.

42 ons and increased functional connectivity in posterior brain regions of postweaning social isolation

43 xpressing neurons located in the dorsomedial posterior brain that are sufficient to elicit preference

44 o maintain contiguous air contact across the posterior breathing spiracles.

45 d visual acuity, incidence of macular edema, posterior capsular opacification, epiretinal membrane, a

46 To investigate the risk of posterior capsular rupture (PCR) during cataract surgery

47 urgery (M-SICS), as well as in patients with posterior capsular rupture (PCR).

48 To objectively assess the long-term posterior capsule opacification (PCO) and neodymium-dope

49 srupting complication of cataract surgery is posterior capsule opacification (PCO; secondary cataract

50 Four serious complications were evaluated: posterior capsule rupture, dropped lens fragments, retin

51 systemic anomalies who underwent lensectomy, posterior capsulorrhexis, and anterior vitrectomy combin

52 re the severity of ischemic damage following posterior ciliary artery (PCA) occlusion in old, atheros

53 The observation of reduced perfusion in the posterior cingulate and cuneal cortex, which are regions

54 lusters appeared in the medial occipital and posterior cingulate cortex (each left and right).

55 A reduction in glucose metabolism in the posterior cingulate cortex (PCC) predicts conversion to

56 erent foraging tasks that neurons in primate posterior cingulate cortex (PCC) signal decision salienc

57 We observed directed influence from the posterior cingulate cortex (PCC) to the anterior cingula

58 anterior cingulate cortex (pACC) and ventral posterior cingulate cortex (vPCC)-regions possibly affec

59 to be statistically significant only in the posterior cingulate cortex for the WBN data.

60 uence of the medial prefrontal cortex on the posterior cingulate cortex in depression is a neural cor

61 cortex had a "hyperregulatory" effect on the posterior cingulate cortex in the depressed group, with

62 between the medial prefrontal cortex and the posterior cingulate cortex than in the control group (od

63 ross pedalism in the left pSTS and bilateral posterior cingulate cortex.

64 in the precentral, prefrontal, fusiform, and posterior cingulate cortices before CBT-I.

65 rsolateral-prefrontal activation and reduced posterior cingulate deactivation, whereas OCD patients s

66 Posterior cingulate metabolism decreased when both amylo

67 better with SUVRWM (Pearson r: from 0.63 for posterior cingulate to 0.89 for precuneus, P < 0.0001) t

68 A ratio of metabolism in the posterior cingulate to precuneus plus cuneus was calcula

69 decrease of the T1/T2-weighted ratio in the posterior cingulate was related to performance in attent

70 the orbitofrontal cortex (OFC), anterior and posterior cingulate, insula and temporal lobes (Cohen's

71 ion coefficient, 197.4-275; P < .001) in the posterior cingulate, lateral parietal, hippocampal, and

72 ontal cortex (PFC) but increased GBCr in the posterior cingulate, precuneus, lingual gyrus, and cereb

73 pretectal, parvocellular, and magnocellular posterior commissure and lateral terminal nuclei), JcP (

74 sophila wing disc, Hedgehog (Hh) produced by posterior compartment cells distributes in a concentrati

75 subcellular locations prior to release from posterior compartment cells that express it, and was tak

76 Mesh procedures for anterior and posterior compartment prolapse cannot be recommended for

77 undergoing primary transvaginal anterior or posterior compartment prolapse surgery by 65 gynaecologi

78 for medial wing disc growth, at least in the posterior compartment.

79 K) during laser lens surgery on anterior and posterior corneal astigmatism and total corneal refracti

80 uation of the impact of the altered anterior/posterior corneal curvature relationship.

81 induced a relevant change in the anterior to posterior corneal curvature relationship; this needs to

82 ained stable (0.40 and 0.23 for anterior and posterior corneal surfaces, respectively) in different p

83 Over 12 months, there were changes in posterior corneal tilt, coma, and hexafoil in the PCRI g

84 r/higher structural connectivity in anterior/posterior corpus callosum.

85 illations in the EEG alpha frequency band in posterior cortex can dissociate current from future sear

86 ter pathways and functionally connected more posterior cortical areas could contribute to apathy.

87 onally fulfilled the diagnostic criteria for posterior cortical atrophy and eight for logopenic varia

88 heimer disease and 3 with atypical variants (posterior cortical atrophy, logopenic variant primary pr

89 However, more recent work has implicated posterior cortical regions [9-12], suggesting that PFC e

90 onships seen mainly in gyral regions in more posterior cortices.

91 Kinesin 1 transports dynactin to the oocyte posterior, creating a positive feedback loop that increa

92 ated to occur 478,600 years ago (95% highest posterior density [HPD], 391,000 to 569,600 years ago).

93 A posterior displacement of the femoral head epiphysis wit

94 iated with significant, progressive relative posterior displacement of the temporal peripapillary ret

95 erval (CrI) estimates were obtained from the posterior distribution of the sum of country-specific es

96 ov chain Monte Carlo algorithm that produces posterior distributions of ages for each individual, bas

97 -of-the-art approach for simulating from the posterior distributions of population genetics parameter

98 Specifically, we approximate the posterior distributions of the unknown parameters with a

99 PAR-2 inhibits CDC-42-dependent NMY-2 in the posterior domain by inhibiting PAR-3 and PAR-6.

100 h ventral pathway, the activation profile of posterior dorsal regions was correlated with recognition

101 tors, located at spatially coherent anterior-posterior, dorsal-ventral, and medial-lateral coordinate

102 rent representational similarity between the posterior-dorsal and lateral-ventral regions was corrobo

103 lamic nucleus (PF)-controlled neurons in the posterior dorsomedial striatum (pDMS) are critical for i

104 part of the fan-shaped body primordium, the posterior EB primordium moves forward and merges with th

105 ated by the type II lineages DM1-4, form the posterior EB primordium.

106 Posterior ectodermal activation of Hox is initiated in t

107 one and an antero-inferior inflection of its posterior edge in the Pax7-deficient mice.

108 stiffness and increasing fluidity toward its posterior elongating region.

109 ally in the source attribution of resulting (posterior) emissions, and hence conclusions from such st

110 s the flow and orients extension towards the posterior end.

111 the parahippocampal gyrus, particularly the posterior entorhinal cortex, which in our parcellation i

112 Finally, posterior estimates of cumulative GPP under control and

113 Currently, drug delivery to the posterior eye segment relies on intravitreal injections

114 hibit abnormal eye shape at the anterior and posterior eye segments, but whether the outer coats of t

115 During the anterior-posterior fate specification of insects, anterior fates

116 gating tissue (called the "blastoderm"), and posterior fates arise in an elongating tissue (called th

117 d via DM stripping, most of the cells in the posterior fibrosis tissue did not originate from the cor

118 luorescein angiograms although within a more posterior field of view.

119 lude the preferred use of MRI for diagnosing posterior fossa lesions, the management of basilar arter

120 natomical location (supratentorial region or posterior fossa) and further divided into distinct molec

121 ation, optical tortuosity, flattening of the posterior globe, swelling of the optic disc, and bilater

122 We show that a posterior glycolytic gradient is established in response

123 level rules are encoded along an anterior-to-posterior gradient within PFC.

124 organization revealed the subdivision of the posterior group of the thalamus into four subnuclei (ant

125 12 for each anterior group, n = 13 for each posterior group) for 2 tissue types (enamel and dentine)

126 ) and bottom-up inhibition deficits (reduced posterior-->frontal Granger causality).

127 ressed in the right retrosplenial cortex and posterior HC and was only sensitive to vertical pitch, w

128 entered during navigation of the city, right posterior hippocampal activity indexes the change in the

129 parietal, temporal, occipital, anterior, and posterior hippocampal, parahippocampal, and fusiform reg

130 Posterior hippocampus appears to support context encodin

131 In parallel, the posterior hippocampus became less involved as schema obj

132 Monitoring this posterior 'hot zone' in real time predicted whether an i

133 centromeric TAD subsequently regulates more posterior Hoxd genes in digit cells.

134 rovide immunohistochemical evidence that the posterior hyaloid membrane is a true basement membrane e

135 e is a true basement membrane enveloping the posterior hyaloid surface.

136 to subthalamic (STN), premammillary (PM) and posterior hypothalamic (PH) populations.

137 One such circuit is the posterior hypothalamic histamine (HA) system, implicated

138 Histaminergic (HA) neurons, found in the posterior hypothalamic tuberomammillary nucleus (TMN), e

139 Fifteen subjects with 2 posterior implants and corresponding contralateral teeth

140 ious methods while offering the advantage of posterior inference.

141 In the macaque monkey brain, posterior inferior temporal (PIT) cortex cells contribut

142 ized by the predictive coding model, whereas posterior insula encoded stimulus intensity.

143 caudate/nucleus accumbens, and anterior and posterior insula, 2) to unexpected reward receipt in the

144 nexpected reward receipt in the anterior and posterior insula, and 3) to unexpected reward omission i

145 ontal cortex (OFC), and another was found in posterior insula.

146 eives dense projections from the midline and posterior intralaminar thalamus, and moderate projection

147 e used cortical cooling to silence inputs to posterior IT and compared the findings with an HMAX mode

148 tion of myosin leads to the loss of anterior-posterior junctions before the loss of dorsal-ventral ju

149 was a nonsignificant trend toward a flatter posterior KA and steeper posterior KM and the total corn

150 nd toward a flatter posterior KA and steeper posterior KM and the total corneal Z2(-2) was low at 1 a

151 In PLTR surgery, irregular posterior lamellar incision at the center of the eyelid

152 Here we show that neuromasts of the posterior lateral line in medaka are composed of two ind

153 sers simultaneously, we could scan and sever posterior lateral microtubule neurons [posterior lateral

154 sever posterior lateral microtubule neurons [posterior lateral microtubules (PLMs)] on both sides of

155 lanted into vastus lateralis, biceps femoris posterior, lateral gastrocnemius and tibialis anterior i

156 e hypertensive encephalopathy and reversible posterior leukoencephalopathy syndrome (RPLS), is a neur

157 rest: splenium of corpus callosum (SPCC) and posterior limb of internal capsule (PLIC).

158 l sample of Purkinje cells recorded from the posterior lobe hemisphere in awake cats.

159 hiefly associated with the anterior lobe and posterior lobule HVI.

160 Our results suggest a significant impact of posterior lobules pathology in corticocerebellar loop di

161 Structural alterations in individual posterior lobules, in which cognitive functioning seems

162 supporting fixed partial dentures (FPDs) in posterior mandibular and maxillary jaws.

163 , N+ patients without NAT or VR; (2) R1-0 mm posterior-margin for the NAT group (P = 0.004).

164 s) (<3.3 mm) to restore partially edentulous posterior maxillary and mandibular areas is limited.

165 Similar to LTMLM, LT-Fam is computed from posterior mean liabilities (PML) under a liability thres

166 medial parvicellular portion of the ventral posterior medial division, VPMpc) of mice and the thalam

167 ons in the rodent barrel cortex (BC) and the posterior medial nucleus of the thalamus (POm).

168 in these signals explains fMRI responses in posterior-medial frontal cortex.

169 nths' follow-up) was 0.35 (.05-1.15) year-1 (posterior median and 95% CrI), corresponding to mean inf

170 ic hedgehog (Shh) is expressed in the distal posterior mesenchyme, where it acts as a mediator of ant

171 increases the length and persistence of the posterior microtubules that deliver oskar mRNA to the co

172 Positive connectivity between amygdala and posterior middle cingulate cortex was found in female pa

173 pecial importance within these pathways: the posterior middle temporal gyrus, thought to serve as a l

174 contributes to epithelium remodeling in the posterior midgut and thereby facilitates the trans-epith

175 tween-subject reinstatement effects within a posterior midline core memory retrieval network during a

176 Posterior movement of the lamina (LD-BM increase or LD-A

177 cribed fatty area between cervical spine and posterior muscles.

178 and were characterized by an early (200 ms) posterior negativity and a later (>300 ms) parietal posi

179 pocampal, and fusiform regions, as well as a posterior neocortical VOI composed of average values fro

180 PERSI reference region was 2.22% for a large posterior neocortical VOI, 1.84% for MUBADA, 1.46% for f

181 of the mouse embryo and was shown to promote posterior neuroectodermal fate by enhancing Smad2-activa

182 The localisation of oskar mRNA to the posterior of the Drosophila oocyte defines where the abd

183 sed signatures of reward identity in lateral posterior OFC were modulated after selective devaluation

184 atients 13 years or older with intermediate, posterior, or panuveitis (active within </=60 days) enro

185 The chemokine pathway, in turn, directs the posterior outgrowth of dHb efferents toward the IPN and,

186 Specifically, the posterior P2 component over the parieto-occipital lobe p

187 The most common location is the posterior paraspinal mediastinum, retroperitoneum, neck

188 vity by examining population recordings from posterior parietal (PPC) and prefrontal (PFC) cortices i

189 /hMT+, primary somatosensory cortex (SI) and posterior parietal cortex (PPC; Brodmann areas 7/40).

190 wed sustained alpha/micro suppression in the Posterior Parietal Cortex and Inferior Parietal Lobe, in

191 the signals measured from the monkey medial posterior parietal cortex are valid for correctly decodi

192 tic stimulation (TMS) of human occipital and posterior parietal cortex can give rise to visual sensat

193 Mountcastle and colleagues proposed that the posterior parietal cortex contains a "command apparatus"

194 ct cortical excitability in occipital versus posterior parietal cortex, calling into question the bro

195 decoding reach trajectories from the medial posterior parietal cortex, this highlights the medial pa

196 into anatomically reorganized motor, but not posterior parietal, cortex eliminated behavioral gains f

197 e less frequent in the periphery than in the posterior pole (46% vs. 76%) and negligible in controls.

198 From 13 (31.0%) eyes with a perfused posterior pole (an area encompassing a 5 disc diameter r

199 cornea, equatorial and posterior sclera, and posterior pole containing the optic nerve head.

200 ferior, superior, and central regions of the posterior pole in 83%, 75%, 67%, 54%, and 25% of eyes, r

201 efield angiography, we have ascertained that posterior pole nonperfusion of more than 10 DA remains t

202 ost-treatment scar (55%) or fovea (16%), and posterior pole scanning for new tumors (11%).

203 fusion isolated in the periphery (beyond the posterior pole), only 1 (7.7%) eye developed new vessels

204 rge bullous peripheral schisis involving the posterior pole, vascular abnormalities and haemorrhages.

205 ts (26%) had a combination of lesions in the posterior pole.

206 we show that porcine PGCs originate from the posterior pre-primitive-streak competent epiblast by seq

207 Furthermore, posterior predictive checks showed that a model which as

208 The posterior probabilities of the NBC model are then traine

209 rents and rank the estimated models by their posterior probabilities.

210 lso helps to improve the coupling of the NBC posterior probability and the intrinsic structural featu

211 cording to a prespecified decision rule (ie, posterior probability for comparability >90%).

212 xpressed modules (CEMs), while assigning the posterior probability for each dataset in support of eac

213 sian analysis] for difference, -5.2 to 2.3%; posterior probability of noninferiority, >0.999).

214 increased effective connectivity between the posterior putamen and other areas of the motor circuit d

215 ed prior reports of age-related decreases in posterior recruitment and increases in prefrontal recrui

216 arance of the primitive streak in the future posterior region of a radially symmetric disc.

217 ne end and undergo elongation similar to the posterior region of the embryo, suggesting that they dev

218 Interestingly, many cells in the posterior regions of eye imaginal discs carrying a doubl

219 become localised to the future anterior and posterior regions of the embryo, where they will, respec

220 ping palatal mesenchyme, particularly in the posterior regions of the palatal shelves.

221 illary length) and the ANB angle (the antero-posterior relation of the maxilla to the mandible) seem

222 ed in motor cortex areas that are medial and posterior relative to ALM, including vibrissal motor cor

223 Over two decades have passed since posterior reversible encephalopathy syndrome (PRES) was

224 Posterior reversible encephalopathy syndrome (PRES), als

225 sease, zone, stage, category, and aggressive posterior ROP (AP-ROP).

226 ch as eyes with zone I disease or aggressive posterior ROP), the disadvantages are that the ROP recur

227 hat BMP signaling is required to establish a posterior SATB2+ domain in developing and postnatal inte

228 egions were obtained: cornea, equatorial and posterior sclera, and posterior pole containing the opti

229 an expansion of activation into anterior and posterior sectors of the right insula, as well as bilate

230 l acuity, refractive error, and slitlamp and posterior segment eye examination findings) were assesse

231 nvaluable supplemental information about the posterior segment in eyes with corneal opacification.

232 The latter rapidly diffuse to the posterior segment, triggering retinal damage.

233 n adult cochlea via virus injection into the posterior semicircular canal.

234 n age-related decrease in the recruitment of posterior sensory regions coupled with an increased recr

235 e of insula, located in its mid-dorsal part (posterior short gyrus).

236 ups was observed towards the lateral and the posterior sides of prostate.

237 la hematopoietic organ, the lymph gland, the posterior signaling center (PSC) acts as a niche to regu

238 Interestingly, the cells of the posterior signaling center were preserved in these mutan

239 anin volume in PD was most pronounced in the posterior SNpc (median, -83%; P < .001), followed by the

240 was delivered over the face-selective right posterior STS (rpSTS) or over the vertex control site.

241 hyper-direct connectivity with anterior and posterior subregions of the subthalamic nucleus.

242 , the goal was to validate free water in the posterior substantia nigra as a progression marker in Pa

243 findings demonstrate that free water in the posterior substantia nigra is a valid, progression imagi

244 ear and 2-year increase in free water in the posterior substantia nigra predicts subsequent long-term

245 ior work demonstrated that free water in the posterior substantia nigra was elevated in Parkinson's d

246 f low-level acoustic features of speech from posterior superior temporal gyrus toward anterior superi

247 ft anterior temporal regions; language: left posterior superior temporal lobe and supramarginal gyrus

248 We applied MVPD to the posterior superior temporal sulcus (pSTS) and to the fus

249 The human posterior superior temporal sulcus (pSTS), a brain regio

250 aphasia; and (iv) bilateral precentral/left posterior superior-frontal regions and speech arrest.

251 The 3rd-order RMS of the posterior surface (AUC: 0.928) obtained the highest disc

252 OPL had two origins: one originated from the posterior surface of the posteromedial tibia condyle, me

253 te among beta-propeller enzymes cited on the posterior surface of the rhamnosidase.

254 metry and elevation of both the anterior and posterior surfaces were exported from the Pentacam HR so

255 a (HR = 2.87 [95% CI, 1.41-5.82], P = .004), posterior synechia at presentation (HR = 2.85 [95% CI, 1

256 IOP (75%), keratitis (59%), dry eyes (34%), posterior synechiae (34%), cataract (32%), and glaucoma

257 ) values (OR 1.74, P = .01), and presence of posterior synechiae (OR 3.28, P = .004).

258 the ventral striatum ('VS dopamine') and the posterior tail of the striatum ('TS dopamine').

259 n and erosion) and 2 locations (anterior and posterior teeth; n = 12 for each anterior group, n = 13

260 of alpha and beta frequency within the left posterior temporal and occipital cortices in patients wi

261 regions including insular, lateral frontal, posterior temporal and opercular cortex.

262 ing of the dorsomedial prefrontal cortex and posterior temporal cortex.

263 des left-hemispheric premotor, parietal, and posterior temporal cortices is activated even under subl

264 to a white matter network including the left posterior temporal region and its connections to the mid

265 e most frequent patterns were left and right posterior-temporal delta brushes which were associated i

266 Elevated posterior temporoparietal and occipital AV-1451 uptake i

267 obable DLB had greater AV-1451 uptake in the posterior temporoparietal and occipital cortex compared

268 allidus (n = 13), substantia nigra (n = 13), posterior thalamus (n = 12), red nucleus (n = 10), colli

269 he haemodynamic findings, which included the posterior thalamus (pulvinar) and the medio-dorsal thala

270 ate connectivity of the left amygdala to the posterior thalamus in male but not female patients.

271 prefrontal cortex, and greater GM volume in posterior thalamus, hypothalamus and midbrain.

272 kin within a large plaque of FDH on her left posterior thigh and calf.

273 er 23 (18.4%) anterior tibial and 13 (10.4%) posterior tibial arteries had >/=50% stenosis.

274 ndon is frequently used for the treatment of posterior tibial tendon insufficiency or chronic Achille

275 Percentages of uncut anterior and posterior tissue, midpoint depth, and degrees of side cu

276 growth are coordinated between the different posterior tissues (e.g. neural tube, axial and paraxial

277 its Eya-So activation of select target genes posterior to the furrow to ensure properly timed mitotic

278 ther an increased atrial adipose tissue mass posterior to the left atrium is related to AF independen

279 In addition, we found a posterior-to-anterior organization of the LOTC for concr

280 of oral cavity as compared to the palate and posterior tongue.

281 birth in the hypothalamus, dorsal thalamus, posterior tuberculum, and the preoptic region, and this

282 Posterior urethral valves are associated with considerab

283 es treated with episcleral brachytherapy for posterior uveal melanoma from January 2004 to December 2

284 nce following brachytherapy in patients with posterior uveal melanoma, given that an understanding of

285 Posterior uveitis is an ocular complication that can occ

286 Panuveitis and posterior uveitis were the most frequent findings.

287 sion loss in bilateral chronic noninfectious posterior uveitis, and is currently being treated using

288 ISUAL-2) noninfectious intermediate uveitis, posterior uveitis, and panuveitis was conducted in the U

289 tment of noninfectious intermediate uveitis, posterior uveitis, and panuveitis.

290 nts with noninfectious intermediate uveitis, posterior uveitis, and panuveitis.

291 patients with noninfectious intermediate or posterior uveitis.

292 ly reveal that axon initiation is delayed in posterior vagus motor neurons independent of neuron birt

293 (predators, conspecifics) in the lateral and posterior visual fields, respectively.

294 oroidal melanoma underwent complete 25-gauge posterior vitrectomy followed by transvitrector port fin

295 Retinal tears complicating the course of a posterior vitreous detachment (PVD) may be unique or mul

296 Despite posterior vitreous detachment being a common ocular even

297 Retinal break associated with induction of posterior vitreous detachment was the most common (8 eye

298 ip between the esophagus and the left atrial posterior wall is variable, and the esophagus is most su

299 r septum, 12+/-4 [7-23] mm; left ventricular posterior wall, 11+/-4 [7-21] mm; left ventricular mass,

300 isymmetric models show that the anterior and posterior zonules may have a greater impact on shape cha