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1 f recruited neurons and a surrounding 'ictal penumbra'.
2 mbral pattern (large core or small or absent penumbra).
3 f salvageable ischemic brain tissue (ie, the penumbra).
4 core seizure territory from the surrounding penumbra.
5 an10, Tspan14, Tspan15, Tspan17, and Tspan33/Penumbra.
6 el that included the volume of non-infarcted penumbra.
7 damage to the surrounding area known as the penumbra.
8 ked beta-catenin degradation in the ischemic penumbra.
9 ng and neuronal excitotoxicity in the injury penumbra.
10 a defect that is reversed by reexpression of Penumbra.
11 r in the delayed cell losses of the ischemic penumbra.
12 ion and apoptotic cell death in the ischemic penumbra.
13 rization and cell death, particularly in the penumbra.
14 ution of irreversible damage in the ischemic penumbra.
15 the temporal and spatial progression of the penumbra.
16 in diabetic rats in both ischemic focus and penumbra.
17 a 67.9% (p<0.05) increase in APP mRNA in the penumbra.
18 xia that mimics many features of an ischemic penumbra.
19 chemic region, and to a lesser extent in the penumbra.
20 ate and GABA observed in the focal ischaemic penumbra.
21 bition of glutamate release in the ischaemic penumbra.
22 rstanding the pathophysiology of an ischemic penumbra.
23 th potentially increased significance of the penumbra.
24 bility by maintaining blood flow to ischemic penumbra.
25 na; Hasten Biopharmaceutic; Genesis Medtech; Penumbra.
26 es and identifying patients with salvageable penumbra.
27 creases in extracellular potassium levels in penumbra.
28 osis), could better reproduce aspects of the penumbra.
29 abnormalities serves as an indicator of the penumbra.
30 n may represent resolution of the reversible penumbra.
31 and their continued accumulation within the penumbra.
32 proposed as a metabolic marker of ischaemic penumbra.
33 ard afforded due to sharp lateral and distal penumbras.
35 eas temperature was highest in the potential penumbra (37.7 versus 37.3 degrees C in lesion core, P <
36 igger spreading depolarizations in ischaemic penumbra (4-fold increase in spreading depolarization oc
37 vely) was much smaller than that of salvaged penumbra (59.3 and 93 ml, respectively), it was substant
38 k of a simple in vitro model of the ischemic penumbra, a clinically relevant region of stroke-afflict
39 ls) of reperfusion catheters manufactured by Penumbra, a US-based medical device company, illustrates
40 he ischemic core and diffuse to the ischemic penumbra, activating microglia and promoting proinflamma
41 astrocyte signalling through the 'mechanical penumbra' affects the activity of neural circuits distan
42 inistered during periods of the inflammatory penumbra after active lesion formation, and was shown to
43 Thus, increasing the energy imbalance in the penumbra after multiple SDs may hasten the deterioration
44 , California) (40%) and the Penumbra System (Penumbra, Alameda, California) (9%), represented a large
47 ng reduction of the GAG chains in the lesion penumbra and allowed axons to regenerate around the core
49 d reduced in-plane vessel length between the penumbra and contralateral gray matter (-16.7% vs. -20.5
50 whole-brain coverage to measure the ischemic penumbra and core and to compare its performance to that
55 volume at CT perfusion was compared with the penumbra and core reference values at magnetic resonance
56 in ischemic volume delineated by the optimal penumbra and core threshold was determined as the brain
59 btained were compared to the distribution of penumbra and core within the ischaemic area received fro
60 iently increased at 5 h in both the ischemic penumbra and core, and the total protein level of beta-c
66 of different perfusion CT thresholds for the penumbra and infarct core with each postprocessing metho
67 as shown that there is marked variability in penumbra and infarct prediction among various deconvolut
69 ith significant fewer apoptotic cells in the penumbra and less BBB disruption; PHD3-/- mice had impai
72 c rats enhanced angiogenesis in the ischemic penumbra and significantly improved neurological recover
73 induced by IS accurately mimics the in vivo penumbra and thus whether our model system is suitable f
74 mbining clinicoradiological information (ie, penumbra and vessel status), anticoagulant activity and
76 adiomic features of the primary tumor, tumor penumbra, and bone marrow identifies lung cancer disease
77 xture features from the primary tumor, tumor penumbra, and bone marrow predicts disease-free survival
78 target of acute stroke therapy, the ischemic penumbra, and clinically available imaging modalities su
79 is this boundary zone that comprises the new penumbra, and future investigations should dissect where
81 esonance imaging responses and non-infarcted penumbra, and tested the hypothesis that the former do t
82 f LRP in neurons within the area of ischemic penumbra, and this effect was attenuated in mice treated
83 identify a small ischemic core and ischemic penumbra, and this information will contribute increasin
84 idence of cortical ischemia with salvageable penumbra, and were ineligible for reperfusion therapies.
85 nge between these thresholds was termed the "penumbra," and restitution of flow above the functional
88 Taken together, our findings suggest that penumbras are pertinent for understanding variation in t
90 concentrations of reactive aldehydes in the penumbra area, we investigated if the hydrazine function
91 low voltage areas, unipolar low voltage and penumbra areas) and morphology characteristics (presence
93 motor and somatosensory areas of the injury penumbra as compared to the parietal association and vis
98 e than 2 seconds most accurately defined the penumbra (AUC = 0.86, P = .046, mean volume difference b
101 ed preferentially in neurons in the ischemic penumbra but not in the ischemic core or in brain region
102 the tissue putrescine level was found in the penumbra but there was no difference in the putrescine l
106 tion of erythropoiesis, we identified murine Penumbra cDNA from a multipotent hematopoietic cell line
107 wing image coregistration, the non-infarcted penumbra comprised all acutely ischaemic voxels (identif
109 rvation of these glial cells in the ischemic penumbra corresponded with a markedly reduced area of in
110 Selective neuronal loss (SNL) in the rescued penumbra could account for suboptimal clinical recovery
111 rombectomy (baseline mRS 0-1) and had viable penumbra (CT perfusion or Alberta Stroke Program Early C
114 netic resonance imaging (MRI) mismatch-based penumbra detection against full quantitative positron em
118 severe, cerebral blood flow in the ischemic penumbra during reperfusion was reduced, and NMDA neurot
119 ggest that stroke victims with a significant penumbra estimated by the diffusion/perfusion mismatch o
123 CT perfusion allowed differentiation of the penumbra from the ischemic core in patients with acute i
125 Tmax (AUC 0.9) was the best estimator of the penumbra (group A), CBF relative to the contralateral he
126 f 2.6 +/- 2.1 days, the estimation regarding penumbra (group A, ATI: r = 0.63/0.69, ATS: r = 0.64) an
128 therapeutic approaches aiming to rescue the penumbra have failed, likely due to unspecific targeting
129 in the scar, increased vessel density in the penumbra, higher tumor necrosis factor alpha plasma leve
130 ing depolarizations in an electrophysiologic penumbra (i.e. isoelectric cortex with no spontaneous ac
131 ntracerebally transplanted into the ischemic penumbra immediately (within 1 h) after stroke surgery.
133 f occludin serine 490 (S490) in the ischemic penumbra in a tPA-dependent manner, as tPA-/- mice were
134 ies that selectively target the inflammatory penumbra in experimental autoimmune encephalomyelitis le
135 stantial percentage of patients have notable penumbra in extended time windows; the findings of this
136 stigated genetic determinants of the size of penumbra in mice subjected to middle cerebral artery occ
140 l role of PGs, and particularly those in the penumbra, in causing regeneration failure in the adult s
141 aluated the Indigo CAT RX Aspiration System (Penumbra Inc, Alameda CA) for sustained mechanical aspir
143 osis/autophagy characteristic of the in vivo penumbra, including: (1) short-term elevation of [ATP] f
144 After an initial decrease, blood flow in the penumbra increased during the first 10 min after injury,
145 lude that our in vitro model of the ischemic penumbra induces autophagy and apoptosis in cultured neu
148 ause vasoconstriction and recruitment of the penumbra into the ischemic core in the critical first ho
149 levation in diffusion lesion core, potential penumbra, ipsilateral and contralateral normal brain and
153 er, we find evidence that entering a group's penumbra is associated with a change in attitude on grou
155 at 1-3 months after stroke the non-infarcted penumbra is capable of neuronal activation, consistent w
159 produce a square-shaped lesion surrounding a penumbra-like "area at risk" in middle cerebral artery t
160 uorescent protein-expressing neurons in this penumbra-like area at risk revealed that SDs were tempor
162 that increase in BVR expression in ischemic penumbra may present a cellular defense mechanism agains
163 latory history and clinical evidence for the Penumbra medical devices were analyzed through a qualita
165 ischaemic core volume (ICV>=110 mL) or core-penumbra mismatch ratio (MMR<=1.4) thresholds resulted i
167 Bland-Altman plots indicated that these penumbra-nulled IR images provided more accurate predict
168 btained from tp3 T2-weighted images and the "penumbra" obtained from the tp1 perfusion-weighted image
169 in significantly reduced CSPG levels in the penumbra of 49% at 14 and 40% at 28 days post-injury com
172 amples were harvested from ischemic core and penumbra of cortices at one hour and twenty-four hours f
173 accumulates within neuronal processes in the penumbra of hypoxic damage in adult brain, and within ne
175 e or male human iESCs were injected into the penumbra of ischemic myocardial tissue of female mice or
178 rmine whether new emphysema arises from this penumbra of mechanically affected lung (MAL) or from sma
179 in the form of neurofibrillary tangles or a penumbra of neurites surrounding amyloid cores also dist
181 xercise-induced angiogenesis in the ischemic penumbra of rat brains, and whether caveolin-1 changes c
182 nes were then transplanted into the striatal penumbra of rats, 1 h following middle cerebral artery o
183 ty have largely focused on activation in the penumbra of the lesion or in contralesional, homotopic r
186 polyubiquitinated proteins were increased in penumbra of WT mouse brains but not in KI mouse brains a
187 the largest effect size among patients with penumbras of 120 mL or more (adjusted common odds ratio
188 the smallest effect size among patients with penumbras of 72 mL or less (ACOR, 0.49 [95% CI, 0.22-1.0
189 us to learn about the characteristics of the penumbras of politically relevant groups such as gay peo
190 eals major and systematic differences in the penumbras of various social groups, even ones of similar
192 ute anterior circulation stroke, presence of penumbra on computed tomography perfusion performed with
194 ificantly reduced in the whole non-infarcted penumbra (P < 0.01) but not within the functional magnet
195 ct growth (P = .004) and had higher salvaged penumbra (P = .009) volumes than patients without reperf
197 lesion core (42 versus 26 units in potential penumbra, P < 0.05), whereas temperature was highest in
198 mic core, which gradually expands toward the penumbra, partly as the result of a neuroinflammatory re
199 fusion-weighted imaging lesion) and presumed penumbra (perfusion-diffusion mismatch [threshold = T(ma
201 The main therapeutic target is the ischemic penumbra, potentially salvageable brain tissue that dies
202 There were 156 bone marrow and 512 tumor and penumbra radiomic features computed from the PET series.
205 amine the effects of genetic variants on the penumbra ratio, defined as the ratio of the infarct volu
206 We have identified 6 candidate genes for penumbra ratio: Clint1, Nbea, Smtnl2, Rin3, Dclk1, and S
207 e present at elevated levels in the ischemic penumbra region after middle cerebral artery occlusion.
208 eath but not typical apoptosis occurs in the penumbra region and non-ischemic thalamus after cerebral
209 placed into the previously defined ischemic penumbra region and perfused with a salicylate/CSF solut
210 of free radical adduct formation within the penumbra region during cerebral ischemia/reperfusion may
212 lial activation state were visualized in the penumbra region of mice before and after ischemia induce
213 ositive cells in the thalamus and the cortex penumbra region represented a hybrid death, featured by
215 n that tissue putrescine is increased in the penumbra region, an area of incomplete ischemia that is
221 gulatory analysis indicated that each of the Penumbra reperfusion catheters was cleared under the 510
225 we found increased flow at the periphery, or penumbra (rostral, p < 0.05; caudal, p < 0.01), followin
231 ctal discharges in both the seizure core and penumbra (spatial seizure domains defined by multiunit a
236 rily associated with neurons in the ischemic penumbra, suggesting an important role for PPARgamma in
237 erfusion; however, recent examination of the penumbra suggests a central role for NADPH-oxidase (Nox)
238 newborn neurons are present in the ischemic penumbra surrounding cerebral cortical infarcts, where t
240 selected to null signal from the peripheral penumbra surrounding the ablation zone (r = 0.939, P < .
241 al, Mountain View, California) (40%) and the Penumbra System (Penumbra, Alameda, California) (9%), re
242 h the MERCI Retriever and 0% to 11% with the Penumbra System) or asymptomatic (13 studies; 28% to 43%
245 bone marrow texture features, one tumor with penumbra texture feature, and two penumbra texture featu
246 tumor with penumbra texture feature, and two penumbra texture features (concordance, 0.78; 95% confid
249 on and microvascular patency in the ischemic penumbra that is coordinated by S1P signaling and can be
251 Accurate identification of the ischemic penumbra, the therapeutic target in acute clinical strok
254 lectively dilates arterioles in the ischemic penumbra, thereby increasing collateral blood flow and s
256 an be repeatedly investigated to demonstrate penumbra tissue, which can benefit from therapeutic inte
257 ential in the transfer of the concept of the penumbra to clinical stroke and thereby had a great impa
258 e, we utilized a novel in vitro model of the penumbra to examine the free radical profile of ischemic
259 l and ischemic brain, but the ability of the penumbra to recover from the insult is compromised.
260 became upregulated in vessels of the stroke penumbra using a mouse model of reversible middle cerebr
261 e estimate of ischemic core volume (ICV) and penumbra volume (PV) is important in decision-making for
262 rial, there was a direct interaction between penumbra volume and treatment effect, and a trend toward
263 e of penumbra salvaged (CT perfusion-defined penumbra volume at baseline minus CT infarct volume at 2
265 t was analyzed in subgroups of core volumes, penumbra volume, and mismatch ratios using ordinal regre
267 d ischaemic core and potentially salvageable penumbra volumes were associated with functional outcome
272 maging activation clusters and non-infarcted penumbra was mapped, and binding potential values then c
274 Cell death in the thalamus and the cortex penumbra were attenuated by delayed administration of th
275 ted tissue, and the eventually non-infarcted penumbra, were determined by performing voxel-wise analy
276 ion size and neuronal damage in the ischemic penumbra when administered six hours post middle cerebra
277 o gives valuable information on the ischemic penumbra which are very important in early diagnosis and
278 RTD; and (iii) prolonged RTD representing a 'penumbra', which slowly succumbs to molecularly governed
280 t artery-targeted photothrombosis widens the penumbra while maintaining the ability to create localiz
281 central umbra is surrounded by a filamentary penumbra, whose complicated fine structure has only rece
282 ies demonstrate that imaging of the ischemic penumbra with diffusion/perfusion magnetic resonance ima
283 ollows the dynamics of the ischemic core and penumbra with submillimeter spatial and second-scale tem
284 nt of a more severe perfusion deficit in the penumbra within 4 h of MCAO supports the hypothesis that
285 rons surrounding the ischemic core (ischemic penumbra) within 6 hours of occlusion of the middle cere