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1 ntral nervous system (CNS) damage, promoting functional recovery.
2  compensation in perilesion cortex, enabling functional recovery.
3 trol of corticospinal connections to promote functional recovery.
4  prolonged hemorrhage, and impaired forelimb functional recovery.
5 ons that regulates motor behavior capable of functional recovery.
6 ings were noted in analyses of survival with functional recovery.
7 l repair cell, neuronal death and failure of functional recovery.
8 tive neurogenesis and accelerates vestibular functional recovery.
9 e to their distal counterparts contribute to functional recovery.
10 ition following spinal cord injury and limit functional recovery.
11 formation of new synaptic contacts to enable functional recovery.
12  and synaptic connections that drive greater functional recovery.
13 ction and an improved in vitro post-ischemic functional recovery.
14 ently accompanied by a degree of spontaneous functional recovery.
15 roke-induced signal for axonal sprouting and functional recovery.
16 tive program to enable axon regeneration and functional recovery.
17 ure myocytes may have contributed to delayed functional recovery.
18 tiated into GFAP+ astrocytes, and diminished functional recovery.
19 rategies that improve nerve regeneration and functional recovery.
20 -macular traction was associated with a full functional recovery.
21 l cord injury (SCI) is a major impediment to functional recovery.
22 onal program to enable axon regeneration and functional recovery.
23 brain tissue damage, and improves the animal functional recovery.
24  drugs) receptor hM4di abrogated spontaneous functional recovery.
25  and bipolar disorder (BD) impedes patients' functional recovery.
26 h acute ischemic stroke to improve patients' functional recovery.
27 n regaining tissue homeostasis and promoting functional recovery.
28 y neuromuscular junctions and enhanced motor functional recovery.
29 e failed to demonstrate long-term benefit on functional recovery.
30 g cells that surround hair cells, leading to functional recovery.
31 n regeneration, cutaneous reinnervation, and functional recovery.
32 ng mechanisms that promote kidney repair and functional recovery.
33 ional primary motor cortex (iM1) can promote functional recovery.
34 ndrocytes from progenitor cells and promotes functional recovery.
35 esis, thereby accelerating muscle repair and functional recovery.
36 stem (CNS) to regenerate causes very limited functional recovery.
37 eneration, circuit formation, and eventually functional recovery.
38 st-like cells did not reveal histological or functional recovery.
39 hemicord is one mechanism thought to mediate functional recovery.
40 esion site is pivotal for axon re-growth and functional recovery.
41 ession alters the pain threshold and impairs functional recovery.
42 lted in a concomitant increase in postinjury functional recovery.
43 rct size, attenuated apoptosis, and improved functional recovery.
44 t poststroke cortical plasticity and thereby functional recovery.
45 ptoms that are linked to poorer physical and functional recovery.
46 esulting in cumulative brain injury and poor functional recovery.
47 trimental and resulted in delayed repair and functional recovery.
48  SVZ manipulation is associated with DAergic functional recovery.
49 ation of the eCSC abolishes regeneration and functional recovery.
50 atment, which may contribute to the observed functional recovery.
51 e energy predicts late viability, defined by functional recovery.
52 rganization after SCI that may contribute to functional recovery.
53  score (mNSS) test was performed to evaluate functional recovery.
54 ors and other inflammatory responses prevent functional recovery.
55 which aim to enhance tissue regeneration and functional recovery.
56 uggesting a limited role for this pathway in functional recovery.
57 yelin synthesis to enhance myelin repair and functional recovery.
58 anges when considering therapies targeted at functional recovery.
59 s have suggested that amantadine may promote functional recovery.
60 on of BDNF signaling pathways may facilitate functional recovery.
61 rinsic power of myelin plasticity to promote functional recovery.
62 ing altered astrocyte responses and impaired functional recovery.
63  treatment can produce persistent effects on functional recovery.
64  that cell-based interventions may influence functional recovery.
65 ion of individual MAPKs allowed only partial functional recovery.
66 ssessments of muscle tissue regeneration and functional recovery.
67 obal I/R ex vivo and showed improved cardiac functional recovery.
68  but little is known about those who achieve functional recovery.
69 y lacks effective therapy enabling long-term functional recovery.
70 vomarkedly accelerated axon regeneration and functional recovery.
71 5%) were observed for up to 1 year to assess functional recovery.
72 L and OL progenitor replacement, and chronic functional recovery.
73 s of survival to discharge and survival with functional recovery.
74 vived to discharge, and 7176 (7.4%) achieved functional recovery.
75 dendritic plasticity and to induce long-term functional recovery.
76 s, promotes circuit restoration and improves functional recovery.
77 ly distinct subsets of neurons, resulting in functional recovery.
78 n functional connectivity is associated with functional recovery 1 year after cardiac arrest (CA).
79 rodent spinal cord, yet they support delayed functional recovery, a finding of great importance in pl
80                                              Functional recovery after a peripheral nerve injury (PNI
81 c syndrome that diminishes the potential for functional recovery after a transcatheter aortic valve r
82 ncy enhances cardiomyocyte regeneration with functional recovery after adult myocardial infarction as
83                           A major hurdle for functional recovery after both spinal cord injury and co
84                                              Functional recovery after brain injury in animals is imp
85  the enhancement of both axonal regrowth and functional recovery after central nervous system injury
86 uced the risk of death and increased cardiac functional recovery after chronic myocardial ischemia.
87  an important therapeutic goal for achieving functional recovery after CNS injuries.
88        Cardiomyocyte proliferation and heart functional recovery after coronary artery ligation both
89 , epinephrine reduces long-term survival and functional recovery after CPR.
90 tributor to oligodendrocyte regeneration and functional recovery after DWMI.
91                                  To describe functional recovery after elective surgery and to determ
92 hether delirium influences the trajectory of functional recovery after elective surgery.
93 at aggravates secondary injury and restrains functional recovery after experimental spinal cord injur
94 e ABC treatment promotes neuroanatomical and functional recovery after focal ischaemic stroke in an e
95 asticity in damaged spinal cord and promotes functional recovery after HX SCI.
96 rated from skin or nerve promotes repair and functional recovery after incomplete cervical crush inju
97  little capacity to regrow, thereby impeding functional recovery after injury.
98 gonists is an attractive approach to improve functional recovery after ischaemic brain injury.
99 p normally, but show enhanced anatomical and functional recovery after mid-thoracic dorsal hemisectio
100 ed the role of MDMs in long-term spontaneous functional recovery after middle cerebral artery occlusi
101 bl-deficient mice demonstrated a more robust functional recovery after myocardial ischemia/reperfusio
102                                However, full functional recovery after nerve injuries remains poor.
103 t 24-month-old mice exhibit an impairment of functional recovery after nerve injury compared to 2-mon
104 ications for promoting axon regeneration and functional recovery after nerve injury.
105 harmacological approach for the promotion of functional recovery after nerve injury.In vitroandin viv
106 ience research toward the goal of maximizing functional recovery after neurological injury.
107 oned mouse optic nerves (MONs) showed better functional recovery after OGD than the non-preconditione
108 lular changes associated to regeneration and functional recovery after peripheral nerve injury.
109 ty of signal on T2-weighted images relate to functional recovery after reperfused AMI.
110  apoptosis after free radicals induction and functional recovery after ROS damage.
111 vel function of HDAC3 inhibitor in promoting functional recovery after SCI by dampening inflammatory
112 ects both mechanisms and improves repair and functional recovery after SCI.
113 cing intact circuit rearrangement to promote functional recovery after SCI.
114 precedented speed, level, and persistence of functional recovery after SCI.
115 impaired with age corresponding with reduced functional recovery after SCI.
116 gulated lesional inflammation and to restore functional recovery after SCI.
117 imental roles of the innate immunity may aid functional recovery after SCI.
118 4 signaling impairs white matter sparing and functional recovery after SCI.
119 ow that aged mice (18-19 months) had reduced functional recovery after spinal cord injury (SCI) assoc
120                       Robot therapy promotes functional recovery after spinal cord injury (SCI) in an
121  for rebuilding neuronal circuits to improve functional recovery after spinal cord injury (SCI).
122 1R axis enhances axonal sprouting as well as functional recovery after spinal cord injury.
123 onal growth and neuronal rewiring facilitate functional recovery after spinal cord injury.
124 of late gadolinium-enhancement in predicting functional recovery after ST-segment-elevation myocardia
125 d research efforts have focused on promoting functional recovery after stroke.
126 rly after the insult contribute to long-term functional recovery after stroke.
127 GDF10 produced axonal sprouting and enhanced functional recovery after stroke; knocking down GDF10 bl
128 ir families with appropriate expectations of functional recovery after TAVR.
129 jured motor circuit plasticity in supporting functional recovery after trauma, and support a focus of
130 e of propofol on endogenous neurogenesis and functional recovery after traumatic brain injury, rats w
131 r neurogenesis and significantly accelerates functional recovery after unilateral vestibular injury.
132 ss and to identify independent predictors of functional recovery among older ICU survivors.
133 e than nonhemorrhagic infarcts, with lack of functional recovery and adverse LV left ventricular remo
134  (plasma troponin I, myocardial lactate) and functional recovery and between myocardial tissue and pl
135 al symptoms after minor injury and long-term functional recovery and disability.
136           Intranasal 9cRA can facilitate the functional recovery and endogenous repair in the ischemi
137 otic polyneuropathy is characterized by poor functional recovery and impaired nerve regenerative resp
138 ted efficacy from targeting this pathway for functional recovery and neural repair after spinal cord
139 enous Nogo receptor antagonist, in promoting functional recovery and neural repair after spinal cord
140 rophic factor (BDNF) can modulate vestibular functional recovery and neurogenesis in mammals, in this
141             TLR4-deficient mice showed worse functional recovery and reduced OL numbers compared with
142 mediates S129 phosphorylation) showed better functional recovery and smaller infarcts when subjected
143 vo resulted in an improvement in ventricular functional recovery and the prevention of myocardial rem
144                Also, 23% had achieved a good functional recovery, and 70% had returned to work/study
145 of sudden cardiac death and likelihood of LV functional recovery, and has significant potential to gu
146 hemia time are important for long-term renal functional recovery, and hypothermia should be considere
147 urviving networks appears to be critical for functional recovery, and this may be promoted with speci
148 al pathways to reduce spasticity and improve functional recovery are poorly understood.
149  although specific sensory reinnervation and functional recovery are usually worse for large myelinat
150 ly involved in structural reorganization and functional recovery, are poorly understood.
151 mate the dynamic probability of survival and functional recovery as a function of resuscitation effor
152 oliposomal treatment for 3 consecutive days, functional recovery as indicated by improved neurologic
153 e promoted axonal regeneration, which led to functional recovery as measured by sustained gait improv
154  epithelia, was coupled with a corresponding functional recovery, as seen in the suprathreshold ampli
155 Moreover, iM1 neuronal stimulations promoted functional recovery, as stimulated stroke mice showed fa
156 injury were associated with neurological and functional recovery at 1-year follow-up.
157 air regulating the rate of remyelination and functional recovery at early phases following injury.
158                                     Notably, functional recovery began more than 1 year after graftin
159 ssociated with decreased mortality or better functional recovery but being underweight predicted unfa
160 ervention, persisting hyperglycemia prevents functional recovery but promotes beta-cell mass increase
161 I had similar predictive accuracy to SEE for functional recovery but was not assessable in 25% of pat
162 te, which accompanies significantly enhanced functional recovery by 32 d after lesion.
163 nnections, and RhoA-ROCK inhibition enhances functional recovery by blocking this detrimental effect.
164 ty-modifying molecular agents may facilitate functional recovery by selectively enhancing existing ne
165 ence that maximal circuit reorganization and functional recovery can be achieved by combining molecul
166                    Studies show that limited functional recovery can be achieved by plasticity and ad
167                                      Limited functional recovery can be achieved through rehabilitati
168 smaller than 10 mm in rodents, nearly normal functional recovery can be achieved; for longer gaps, ho
169 have resulted in promising, yet insufficient functional recovery compared to the clinical standard of
170 eived SCs from either source showed improved functional recovery compared with media- or fibroblast-t
171 ersed these structural defects, suggesting a functional recovery confirmed by electrophysiological re
172          However, despite this protection no functional recovery could be detected in rats, which was
173 ion at acute imaging and odds ratio (OR) for functional recovery decreased with increasing SEE, altho
174 ation in rates of survival and survival with functional recovery (defined as Cerebral Performance Cat
175 nsplants in vivo, we show that the extent of functional recovery depends on the age of the nerve graf
176  impairs excitation-contraction coupling and functional recovery during chronic LVAD unloading.
177  percutaneous revascularization, with serial functional recovery evaluated for 1 month (n = 12).
178 greatly reduced and there was no significant functional recovery even in Ryk conditional knockout mic
179 se of optical coherence tomography (SD-OCT), functional recovery evidenced by multifocal-electroretin
180 M residuals, we constructed the FRESH score (Functional Recovery Expected after Subarachnoid Hemorrha
181 ous circulation, and the probability of good functional recovery fell to 1%.
182 ivated microglia contribute deleteriously to functional recovery following a neuronal lesion.
183 ity, since it undergoes near full growth and functional recovery following acute depletion of granule
184 to achieve significant anatomical repair and functional recovery following CNS injury by manipulating
185 e mice, IL-4-deficient animals had decreased functional recovery following CNS injury; however, trans
186  quality of the home environment may promote functional recovery following early TBI.
187  on potential mechanisms that may facilitate functional recovery following focal brain injury.
188 ivity, and CatK-deficient mice show impaired functional recovery following hindlimb ischaemia.
189     Similarly, sEH(-/-) mice showed impaired functional recovery following hindlimb ischemia, which w
190 NS) pose barriers to axonal regeneration and functional recovery following injury.
191                                    Augmented functional recovery following MSC transplantation was bl
192 flammation-resolving cells, and promotion of functional recovery following SCI.
193  the degree of spontaneous remyelination and functional recovery following spinal cord injury.
194 t mammalian heart is incapable of meaningful functional recovery following substantial cardiomyocyte
195                                              Functional recovery for older adults following injury ma
196 es were labeled by the biosensor, suggesting functional recovery from apoptotic caspase activation.
197                           Motor learning and functional recovery from brain damage involve changes in
198 ter ICH, confirming the role of TGF-beta1 in functional recovery from ICH.
199           This plasticity allows for partial functional recovery from stroke induced sensorimotor imp
200                                              Functional recovery (GOS-E = 8) [odds ratio (OR) 3.1, 95
201                        The time required for functional recovery, however, increases with advancing a
202  efficacy of daidzein on neuroprotection and functional recovery in a clinically relevant mouse model
203 nd PPARgamma agonist administration improved functional recovery in a clinically relevant mouse strok
204     These connections support proprioceptive functional recovery in a conditioning lesion paradigm, a
205 y prostacyclin triggers axonal sprouting and functional recovery in a mouse model of inflammatory spi
206 lays their molecular maturation, and impedes functional recovery in a mouse model of spinal cord inju
207 ce cardiac regeneration and left ventricular functional recovery in a swine model of chronic ischemic
208 oproteinase inhibitor, on cardiac injury and functional recovery in a swine model of neonatal hypoxia
209 stered intravenously induced morphologic and functional recovery in AKI, the Drosha-knockdown counter
210 fter stroke plays a crucial role in limiting functional recovery in an experimental model of diabetes
211 ngiogenesis, arteriogenesis, blood flow, and functional recovery in an ischemic hindlimb.
212 uman heart failure, and restoration produces functional recovery in animal models and in failing huma
213 ministration is neuroprotective and promotes functional recovery in animal models of adult spinal cor
214 hile early mobilization is safe and enhances functional recovery in critically ill adults, rehabilita
215 n of the injured brain and provided a better functional recovery in female, but not male, mice.
216                             Among survivors, functional recovery in global longitudinal strain (>15%
217 istration promotes beta-cell replication and functional recovery in human islets following implantati
218 al to replace deficient cells and to improve functional recovery in injury or disease settings.
219 d the potential for molecular, cellular, and functional recovery in mice from the severe disruption o
220 ing the repair phase was reported to enhance functional recovery in mice suggesting that GABA plays a
221  cardiac energy production and post-ischemic functional recovery in neonatal rabbit hearts subjected
222 cline attenuates cardiac injury and improves functional recovery in newborn piglets with hypoxia-reox
223  injuries are often followed by considerable functional recovery in patients and animal models, large
224 s system (CNS) axons is a major obstacle for functional recovery in patients suffering neurological d
225 arginase significantly improved postischemic functional recovery in rat hearts if administered in who
226 ved precursors (SKP-SCs) promoted repair and functional recovery in rats with thoracic contusions.
227  and 18 months and to compare structural and functional recovery in regions that received MSC injecti
228 g in neuroprotective phenotypes and improved functional recovery in SCI model.
229 as a novel, translatable strategy to promote functional recovery in stroke patients without adverse a
230 in serves as a potential strategy to promote functional recovery in stroke patients.
231  in hibernating myocardium have an impact on functional recovery in the absence of infarction.
232 o be tested whether such methods can promote functional recovery in translatable settings.
233                   After sciatic nerve crush, functional recovery in vivo was retarded in SNS-gp130(-/
234 arable therapeutic capabilities in improving functional recovery in vivo.
235 to identify the pathways driving spontaneous functional recovery in wild-type and plasticity-sensitiz
236 fusion with carnosine promoted post-ischemic functional recovery in WT but not in AR-null mouse heart
237 motion more or less unchanged, but abolished functional recovery, indicating that dI3 interneurons ar
238 ted benefit of the BDNFVal66Met carriers for functional recovery, involving structural and molecular
239 on improves coordinated locomotion, and this functional recovery is accompanied by preservation of my
240                                              Functional recovery is an important outcome following in
241 nds on acute infarct size, whereas long-term functional recovery is an important outcome in patients.
242                                         This functional recovery is produced by training-induced alte
243 tance, directing circuit rewiring to promote functional recovery may be achieved.
244  TBI care, outcomes-based metrics, including functional recovery, may be more accurate than current p
245 th the early compensatory mechanisms and the functional recovery mechanisms, with reduced aromatic L-
246                                 The enhanced functional recovery observed following such a controlled
247 propriate rehabilitation, it brought about a functional recovery of abnormally wired neuronal network
248 rd below the level of injury and facilitated functional recovery of both locomotor and urinary system
249 o strongly influence the injury response and functional recovery of CNS tissues.
250 function, indicating that miR combo promotes functional recovery of damaged myocardium.
251 n of brain tissue was reflected in efficient functional recovery of inhibitor-injected animals.
252                                              Functional recovery of injured peripheral neurons often
253  of CD200L expression by CNS-resident cells, functional recovery of mice following SCI was impaired.
254  increases MBP, leading to remyelination and functional recovery of mice.
255                                              Functional recovery of mouse hippocampal networks after
256 r development for neuroprotection as well as functional recovery of patients with multiple sclerosis.
257                              To evaluate the functional recovery of patients with symptomatic vitreom
258 ed whether VEGF could promote anatomical and functional recovery of peripheral nerves after injury us
259 ct the circuit in breeding birds, leading to functional recovery of song behavior.
260  sufficiently restored to enable significant functional recovery of the deprived eye.
261 kidney-pancreas transplant by evaluating the functional recovery of the graft and biochemical markers
262 mation, allowing structural regeneration and functional recovery of the injured kidney.
263 ondrial uncoupling protein 3 (UCP3) improves functional recovery of the rodent heart during reperfusi
264 f contralesional hemispheric compensation to functional recovery of the upper extremity after a unila
265 This post-lesion treatment paradigm improved functional recovery on elevated plus maze and Morris wat
266 ociations with mortality, cardiac morbidity, functional recovery, or length of hospital stay.
267 electric electroencephalogram predicted good functional recovery (P=.01).
268 utcome, but there are little data on whether functional recovery post-stroke varies among hospitals.
269 dence interval, 1.32-1.46) and survival with functional recovery (range, 0.8%-21.0%; median odds rati
270 dependent or dead 3 months postacute stroke; functional recovery rates varied considerably among hosp
271 arge (rho=-0.22, P<0.0001) and survival with functional recovery (rho=-0.14, P=0.001).
272  brain after stroke underlies the incomplete functional recovery seen in patients and that boosting h
273 ntly acceleratedin vivoaxon regeneration and functional recovery similar to GSK3alpha(S/A)/beta(S/A)
274 ted neuroinflammation after ICH and promotes functional recovery, suggesting that TGF-beta1 may be a
275 rticipants with delirium demonstrated lesser functional recovery than their counterparts without deli
276 c stroke contribute to long-term spontaneous functional recovery through inflammation-resolving activ
277 tent and clinically meaningful impairment of functional recovery, to 18 months.
278                 Interestingly, the degree of functional recovery tracked directly with circuit restor
279  highest TCR affinity, correlating with full functional recovery upon PD-1 ligand 1 (PD-L1) blockade.
280                                    Likewise, functional recovery upon reoxygenation was much slower a
281 9%), and the risk-standardized survival with functional recovery was 7.4% (range, 0.9%-30.8%).
282         Xenon induced cell survival or graft functional recovery was abolished by HIF-1alpha siRNA.
283   This effect was ER-alpha mediated, because functional recovery was blocked with an ER-alpha antagon
284                                              Functional recovery was defined as returning to a disabi
285 g the Confusion Assessment Method, and their functional recovery was followed for 18 months thereafte
286                                         Such functional recovery was not seen if instead, the anterio
287                                              Functional recovery was observed for 114 (52.3%) of the
288 n an attempt to identify agents that promote functional recovery, we discovered that an FDA-approved
289 processes are coordinated over the course of functional recovery, we tracked receptive field reorgani
290  peri-infarct area, infarct size, and animal functional recovery were assessed at 1, 2, and 3 weeks a
291 s and LV dysfunction, mortality rates and LV functional recovery were comparable between valve replac
292 s sprouting of intact CST axons and promotes functional recovery when applied soon after injury.
293 pathway that could be manipulated to improve functional recovery when combined with rehabilitation pr
294 gen-glucose deprivation, they show a reduced functional recovery when returned to oxygen-glucose but
295 mpared to young rats, adult rats had delayed functional recovery, whereas the aged rats were deficien
296 reshold of 2.8 W m(-2) s(-2)x10(5) predicted functional recovery with sensitivity and specificity of
297 reexisting cardiomyocytes, resulting in full functional recovery within 21 d.
298 mpairment were strongly associated with poor functional recovery within 6 months, whereas higher body
299 d starting 4 h postinjury, LM11A-31 promotes functional recovery without causing any toxicity or incr
300  at high risk for death or severely impaired functional recovery without offering patients and their

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