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2 ut not control, mice of both sexes developed periorbital allodynia following inhalational umbellulone
6 han two weeks was observed, characterized by periorbital and cutaneous mechanical allodynia/hyperalge
7 of mechanical and thermal pain thresholds of periorbital and forearm skin areas in the absence of, an
12 ivity (4/5, 80% for whole face; 3/5, 60% for periorbital and perinasal regions) and specificity (45/5
13 ofibromas (PNs) involving the eyelid, orbit, periorbital, and facial structures (orbital-periorbital
14 restricted to the head, often affecting the periorbital area and the eye, and intensifies when intra
15 ds (ie, overall, forehead, glabella, lateral periorbital area, lips, and marionette lines), with scor
18 8 (2.81) g, Day 7: 3.34 (2.22) g, P < 0.001; periorbital baseline: 6.13 (2.07) g, Day 7: 2.35 (1.91)
26 y with presence of telangiectasias), and (3) periorbital (e.g., superior sulcus hollowing, proptosis,
28 e most frequent adverse events observed were periorbital edema (69%), anemia (55%), diarrhea (45%), t
29 most common ocular manifestation, comprising periorbital edema (n = 83, 40.7%), orbital myositis (n =
30 rlier resolution of inflammation in terms of periorbital edema (P = .002 at day 7), conjunctival chem
32 ed as persons presenting with myalgia and/or periorbital edema and Trichinella-specific immunoglobuli
35 decontamination, but 5 patients developed a periorbital edema, 2 experienced radiating neuropathic p
37 ated with elevated intraocular pressure from periorbital edema, direct compression on the eye, and in
39 hyperthyroidism, resulting in exophthalmos, periorbital edema, pain, double vision, optic neuropathy
44 change in hair color, nausea, dysgeusia, and periorbital edema; adverse events rarely led to disconti
45 tensities and 3 durations of airpuff (AP) or periorbital electrical stimulation (ES) were monitored b
48 activated levator motoneurons revealed that periorbital electrical stimulation produced bilateral, l
49 unpaired (control) presentations of tone and periorbital electrical stimulation, were used to assess
51 r erythema (n = 18), lip hyperemia (n = 17), periorbital erythema and edema (n = 7), strawberry tongu
53 ing cosmetically significant alopecia (30%), periorbital hyperpigmentation (30%), deep rhytides on th
54 flammatory hyperpigmentation (7126 [14.8%]), periorbital hyperpigmentation (7076 [14.7%]), vitiligo (
56 Neutralizing PN attenuated stress-induced periorbital hypersensitivity and priming to SNP, with no
58 A febrile 2-year-old male presented with periorbital inflammation and exudative retinal detachmen
66 dently generated orofacial and headache-like periorbital mechanical hypersensitivity after administra
70 presentation and management of patients with periorbital necrotizing fasciitis (PONF) through an obse
71 ynamic and sensory responses to percutaneous periorbital noxious stimuli recorded in S1 and insular o
74 kull base and continued through extracranial periorbital, olfactory, nasopharyngeal and hard palate l
75 ion diminished the neuronal firing evoked by periorbital or meningeal electrical stimulation; this in
76 (WDR) cells sensitive to stimulation of the periorbital or meningeal region were performed in male W
78 -year old man presented with blepharoptosis, periorbital pain, decreased vision and limbal ischemia.
80 eptive and nonreceptive tissues, we compared periorbital pathway and target tissue phenotypes prior t
81 lities of localized facial features, such as periorbital, perinasal, and perioral patches, and the co
82 periorbital, and facial structures (orbital-periorbital plexiform neurofibroma [OPPN]) can result in
83 ggest that systemic adiposity extends to the periorbital region and highlight the relevance of consid
84 ministration induced mechanical allodynia in periorbital region and paw as well as impaired social be
94 upper blepharoplasty provides comprehensive periorbital rejuvenation, addressing lateral brow ptosis
101 paired trials of a tone coterminating with a periorbital shock (conditioning) or trials in which thes
103 eyeblink (EB) conditioning, using tones and periorbital shock as the conditioned and unconditioned s
105 e experiments were performed in which either periorbital shock or a corneal airpuff served as the unc
107 tone conditioned stimulus (CS) paired with a periorbital shock unconditioned stimulus (US; presented
110 y be high (i.e., during exposure to aversive periorbital shock), other structures (such as amygdala)
111 ctrum of ocular pathologies including eyelid/periorbital skin lesions, blepharoconjunctivitis, and ke
115 both, leading to collapse of the lip, cheek, periorbital soft tissues, and palatal competence present
117 tone conditioned stimulus was paired with a periorbital stimulation unconditioned stimulus (750-ms d
118 tone conditioned stimulus was paired with a periorbital stimulation unconditioned stimulus (750-ms d
119 one conditioned stimulus (CS), light CS, and periorbital stimulation unconditioned stimulus (US), rat
120 npaired presentations of the auditory CS and periorbital stimulation unconditioned stimulus (US).
121 th a reinforcing unconditioned stimulus like periorbital stimulation, the unconditioned stimulus prom
124 s 24 months, with nasal symptoms, proptosis, periorbital swelling, and pain being the most common pre
126 Exposure keratopathy occurred after severe periorbital thermal injuries and followed a predictable
127 the ocular surface for patients with severe periorbital thermal injuries and resultant exposure kera
128 tive patients (16 eyes) who sustained severe periorbital thermal injuries during combat missions in I