Cited by 1,938Stroke Rehabilitation and RecoveryAcute Ischemic Stroke ManagementNeurogenesis and neuroplasticity mechanisms

The DOI matches its Crossref record; 169 of the 169 references it cites were found in a registry or an index.

Plasticity during stroke recovery: from synapse to behaviour

Murphy, Timothy H., Corbett, Dale·2009·Nature Reviews Neuroscience

DOI 10.1038/nrn2735

Open this paper in CoChat — free account

Abstract

Reductions in blood flow to the brain of sufficient duration and extent lead to stroke, which results in damage to neuronal networks and the impairment of sensation, movement or cognition. Evidence from animal models suggests that a time-limited window of neuroplasticity opens following a stroke, during which the greatest gains in recovery occur. Plasticity mechanisms include activity-dependent rewiring and synapse strengthening. The challenge for improving stroke recovery is to understand how to optimally engage and modify surviving neuronal networks, to provide new response strategies that compensate for tissue lost to injury.

Integrity signals

Registry

Crossref · 10.1038/nrn2735

Cites

169 of 169 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Reversible middle cerebral artery occlusion without craniectomy in rats.
Longa, E. Z., Weinstein, P. R., Carlson, S., & Cummins, R. (1989) · Stroke · doi:10.1161/01.str.20.1.84 · Cited by 7,463
The Organization of Behavior; A Neuropsychological Theory.
Attneave, F., B., M., & Hebb, D. O. (1950) · The American Journal of Psychology · doi:10.2307/1418888 · Cited by 5,146
Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015
The Organization of Behavior: A Neuropsychological Theory
(1950) · JAMA · doi:10.1001/jama.1950.02910470083028 · Cited by 4,272
Pathobiology of ischaemic stroke: an integrated view
Dirnagl, U., Iadecola, C., & Moskowitz, M. A. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01401-0 · Cited by 3,943
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
The period of susceptibility to the physiological effects of unilateral eye closure in kittens
Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030
Competitive Hebbian learning through spike-timing-dependent synaptic plasticity
Song, S., Miller, K. D., & Abbott, L. F. (2000) · Nature Neuroscience · doi:10.1038/78829 · Cited by 2,794
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
Silent Brain Infarcts and the Risk of Dementia and Cognitive Decline
Vermeer, S. E., Prins, N. D., den Heijer, T., Hofman, A., Koudstaal, P. J., & Breteler, M. M. B. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa022066 · Cited by 2,313

Flagged first, then by citations

Show all 168 references

Research works printed but not linked: 1

Lashley, K. S. In search of the engram. Symp. Soc. Exp. Biol. 4, 454–482 (1950).

Sorted by citations

Items 501–600 of 1,000

Effects of coupling inhibitory and facilitatory repetitive transcranial magnetic stimulation on motor recovery in patients following acute cerebral infarction
Chen, Q., Shen, D., Sun, H., Ke, J., Wang, H., Pan, S., Liu, H., Wang, D., Su, M., & Fang, Q. (2020) · Neurorehabilitation · doi:10.3233/nre-201606 · Cited by 41
Repetitive Transcranial Magnetic Stimulation on the Affected Hemisphere Enhances Hand Functional Recovery in Subacute Adult Stroke Patients: A Randomized Trial
Yang, Y., Pan, H.-J., Pan, W., Liu, Y., Song, X., Niu, C., Feng, W., Wang, J.-X., & Xie, Q. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.636184 · Cited by 37
Auditory Comprehension Deficits in Post-stroke Aphasia: Neurologic and Demographic Correlates of Outcome and Recovery
Lwi, S. J., Herron, T. J., Curran, B. C., Ivanova, M. V., Schendel, K. L., Dronkers, N. F., & Baldo, J. V. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.680248 · Cited by 40
Extracellular matrix modulation is driven by experience-dependent plasticity during stroke recovery.
Quattromani, M. J., Pruvost, M., Guerreiro, C., Backlund, F., Englund, E., Aspberg, A., Jaworski, T., Hakon, J., Ruscher, K., Kaczmarek, L., et al. (2018) · Molecular Neurobiology · doi:10.1007/s12035-017-0461-2 · Cited by 39
Sensory Enculturation and Neuroanthropology
Downey, G. (2016) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780199357376.013.23 · Cited by 39
Homotopic contralesional excitation suppresses spontaneous circuit repair and global network reconnections following ischemic stroke
Bice, A. R., Xiao, Q., Kong, J., Yan, P., Rosenthal, Z. P., Kraft, A. W., Smith, K. P., Wieloch, T. W., Lee, J., Culver, J. P., et al. (2022) · eLife · doi:10.7554/elife.68852 · Cited by 36
Stroke Rehabilitation and Motor Recovery
O’Dell, M. W. (2023) · CONTINUUM Lifelong Learning in Neurology · doi:10.1212/con.0000000000001218 · Cited by 39
Optimal timing of speech and language therapy for aphasia after stroke: more evidence needed
Nouwens, F., Visch-Brink, E. G., van de Sandt-Koenderman, M. W. M. E., Dippel, D. W. J., Koudstaal, P. J., & de Lau, L. M. L. (2015) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.2015.1058161 · Cited by 42
Evaluation of spontaneous recovery of behavioral and brain injury profiles in zebrafish after hypoxia
Braga, M. M., Rico, E. P., Córdova, S. D., Pinto, C. B., Blaser, R. E., Dias, R. D., Rosemberg, D. B., de Oliveira, D. L., & Souza, D. O. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.019 · Cited by 41
A pilot study on transient ischemic stroke induced with endothelin-1 in the rhesus monkeys
Dai, P., Huang, H., Zhang, L., He, J., Zhao, X., Yang, F., Zhao, N., Yang, J., Ge, L., Lin, Y. H., et al. (2017) · Scientific Reports · doi:10.1038/srep45097 · Cited by 39
The Interval Between VNS-Tone Pairings Determines the Extent of Cortical Map Plasticity
Borland, M. S., Engineer, C. T., Vrana, W. A., Moreno, N. A., Engineer, N. D., Vanneste, S., Sharma, P., Pantalia, M., Lane, M. C., Rennaker, R. L., et al. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.11.004 · Cited by 39
SPARC and GluA1-Containing AMPA Receptors Promote Neuronal Health Following CNS Injury
Jones, E. V., Bernardinelli, Y., Zarruk, J. G., Chierzi, S., & Murai, K. K. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00022 · Cited by 39
Time spent lying, sitting, and upright during hospitalization after stroke: a prospective observation study
Norvang, O. P., Hokstad, A., Taraldsen, K., Tan, X., Lydersen, S., Indredavik, B., & Askim, T. (2018) · BMC Neurology · doi:10.1186/s12883-018-1134-0 · Cited by 40
Patterns of motor recovery and structural neuroplasticity after basal ganglia infarcts
Liu, H., Peng, X., Dahmani, L., Wang, H., Zhang, M., Shan, Y., Rong, D., Guo, Y., Li, J., Li, N., et al. (2020) · Neurology · doi:10.1212/wnl.0000000000010149 · Cited by 39
Neuronal Network Topology Indicates Distinct Recovery Processes after Stroke
Latifi, S., Mitchell, S. A., Habibey, R., Hosseini, F., Donzis, E. J., Estrada‐Sánchez, A. M., Nejad, H. R., Levine, M. S., Golshani, P., & Carmichael, S. T. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa191 · Cited by 40
Influence of Inflammation on Poststroke Plasticity
Liguz‐Lecznar, M., & Kossut, M. M. (2013) · Neural Plasticity · doi:10.1155/2013/258582 · Cited by 40
Lyophilized Powder of Catalpol and Puerarin Protects Neurovascular Unit from Stroke
Qiang, X. U. E., Liu, Y., He, R., Yang, S., Tong, J., Xu, L., Chen, Y., & Xu, X. (2016) · International Journal of Biological Sciences · doi:10.7150/ijbs.14059 · Cited by 39
The Neuropsychological Assessment of Unilateral Spatial Neglect Through Computerized and Virtual Reality Tools: A Scoping Review
Terruzzi, S., Albini, F., Massetti, G., Etzi, R., Gallace, A., & Vallar, G. (2023) · Neuropsychology Review · doi:10.1007/s11065-023-09586-3 · Cited by 38
Moderate intensity aerobic exercise may enhance neuroplasticity of the contralesional hemisphere after stroke: a randomised controlled study
Hill, G., Johnson, F., Uy, J., Serrada, I., Benyamin, B., van den Berg, M., & Hordacre, B. G. (2023) · Scientific Reports · doi:10.1038/s41598-023-40902-2 · Cited by 38
Vagus nerve stimulation in cerebral stroke: biological mechanisms, therapeutic modalities, clinical applications, and future directions
Du, L., He, X., Xiong, X., Zhang, X., Jian, Z., & Yang, Z. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.389365 · Cited by 40
Bilateral cortical hyperactivity detected by fMRI associates with improved motor function following intravenous infusion of mesenchymal stem cells in a rat stroke model
Suzuki, J., Sasaki, M., Harada, K., Bando, M., Kataoka, Y., Onodera, R., Mikami, T., Wanibuchi, M., Mikuni, N., Kocsis, J. D., et al. (2013) · Brain Research · doi:10.1016/j.brainres.2012.12.028 · Cited by 38
Cognitive Rehabilitation Reduces Cognitive Impairment and Normalizes Hippocampal CA1 Architecture in a Rat Model of Vascular Dementia
Langdon, K. D., Granter‐Button, S., Harley, C. W., Moody‐Corbett, F., Peeling, J., & Corbett, D. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.21 · Cited by 38
Self-citation
Does neuroimaging help to deliver better recovery of movement after stroke?
Ward, N. (2015) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000223 · Cited by 40
Brain–Computer Interface Training after Stroke Affects Patterns of Brain–Behavior Relationships in Corticospinal Motor Fibers
Young, B. M., Stamm, J. M., Song, J., Remsik, A. B., Nair, V. A., Tyler, M. E., Edwards, D. F., Caldera, K. E., Sattin, J. A., Williams, J. C., et al. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00457 · Cited by 39
Therapeutic Benefits of Mesenchymal Stromal Cells in a Rat Model of Hemoglobin-Induced Hypertensive Intracerebral Hemorrhage
Ding, R., Lin, C., Wei, S., Zhang, N., Tang, L., Lin, Y., Chen, Z., Xie, T., Chen, X., Feng, Y., et al. (2017) · Molecules and Cells · doi:10.14348/molcells.2017.2251 · Cited by 38
Developmental synaptic regulator, TWEAK/Fn14 signaling, is a determinant of synaptic function in models of stroke and neurodegeneration
Nagy, D., Ennis, K. A., Wei, R., Su, S. C., Hinckley, C. A., Gu, R.-F., Gao, B., Massol, R., Ehrenfels, C., Jandreski, L., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2001679118 · Cited by 38
The presence of a single-nucleotide polymorphism in the BDNF gene affects the rate of locomotor adaptation after stroke
Helm, E. E., Tyrell, C. M., Pohlig, R. T., Brady, L. D., & Reisman, D. S. (2015) · Experimental Brain Research · doi:10.1007/s00221-015-4465-8 · Cited by 39
Characterizing Spontaneous Motor Recovery Following Cortical and Subcortical Stroke in the Rat
Karthikeyan, S., Jeffers, M. S., Carter, A., & Corbett, D. (2018) · Neurorehabilitation and neural repair · doi:10.1177/1545968318817823 · Cited by 38
Self-citation
Stroke Recovery–Related Changes in Cortical Reactivity Based on Modulation of Intracortical Inhibition
Harquel, S., Cadic‐Melchior, A., Morishita, T., Fleury, L., Witon, A., Ceroni, M., Brügger, J., Meyer, N. H., Evangelista, G. G., Egger, P., et al. (2024) · Stroke · doi:10.1161/strokeaha.123.045174 · Cited by 42
Running exercise enhances motor functional recovery with inhibition of dendritic regression in the motor cortex after collagenase-induced intracerebral hemorrhage in rats
Takamatsu, Y., Tamakoshi, K., Waseda, Y., & Ishida, K. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.12.003 · Cited by 37
Efficacy and Safety of Very Early Mobilization in Patients with Acute Stroke: A Systematic Review and Meta-analysis
Xu, T., Yu, X., Ou, S., Liu, X., Yuan, J., & Chen, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-06871-z · Cited by 37
Pharmacotherapy and motor recovery after stroke
Viale, L., Catoira, N. P., Girolamo, G. D., & González, C. D. (2017) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2018.1400910 · Cited by 40
Microfluidics for electrophysiology, imaging, and behavioral analysis of Hydra
Badhiwala, K. N., Gonzales, D. L., Vercosa, D. G., Avants, B. W., & Robinson, J. T. (2018) · Lab on a Chip · doi:10.1039/c8lc00475g · Cited by 36
Brain ischemic insult induces cofilin rod formation leading to synaptic dysfunction in neurons
Shu, L., Chen, B., Chen, B., Xu, H., Wang, G., Huang, Y., Zhao, Y., Gong, H., Jiang, M., Chen, L., et al. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18785567 · Cited by 37
Microglia Enable Cross-Modal Plasticity by Removing Inhibitory Synapses
Hashimoto, A., Kawamura, N., Tarusawa, E., Takeda, I., Aoyama, Y., Ohno, N., Inoue, M., Kagamiuchi, M., Kato, D., Matsumoto, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2023.112383 · Cited by 37
Does the endogenous neurogenic response alter behavioral recovery following stroke?
Lagace, D. C. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.08.045 · Cited by 39
Axonal remodeling for motor recovery after traumatic brain injury requires downregulation of γ-aminobutyric acid signaling
Lee, S., Ueno, M., & Yamashita, T. (2011) · Cell Death and Disease · doi:10.1038/cddis.2011.16 · Cited by 35
How Can You Mend a Broken Brain? - Neurorestorative Approaches to Stroke Recovery
Corbett, D., Nguemeni, C., & Gomez-Smith, M. (2014) · Cerebrovascular Diseases · doi:10.1159/000368887 · Cited by 38
Self-citation
Characterization of the Ubiquitin-Modified Proteome Regulated by Transient Forebrain Ischemia
Iwabuchi, M., Sheng, H., Thompson, J., Wang, L., Dubois, L. G., Gooden, D. M., Moseley, M., Paschen, W., & Yang, W. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.210 · Cited by 35
Correlative two-photon and light sheet microscopy
Silvestri, L., Mascaro, A. L. A., Costantini, I., Sacconi, L., & Pavone, F. S. (2013) · Methods · doi:10.1016/j.ymeth.2013.06.013 · Cited by 36
Intravenous Administration of Human Umbilical Tissue-Derived Cells Improves Neurological Function in Aged Rats after Embolic Stroke
Zhang, L., Li, Y., Chopp, M., Kramer, B. C., Romanko, M. J., Gosiewska, A., & Hong, K. (2013) · Cell Transplantation · doi:10.3727/096368912x658674 · Cited by 36
Hydrogels-Assisted Cell Engraftment for Repairing the Stroke-Damaged Brain: Chimera or Reality
González‐Nieto, D., Fernández-García, L., Pérez‐Rigueiro, J., Guinea, G., & Panetsos, F. (2018) · Polymers · doi:10.3390/polym10020184 · Cited by 38
Growth Hormone Promotes Motor Function after Experimental Stroke and Enhances Recovery-Promoting Mechanisms within the Peri-Infarct Area
Sanchez‐Bezanilla, S., Åberg, N. D., Crock, P., Walker, F. R., Nilsson, M., Isgaard, J., & Ong, L. K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020606 · Cited by 36
The Cytoskeletal Elements MAP2 and NF-L Show Substantial Alterations in Different Stroke Models While Elevated Serum Levels Highlight Especially MAP2 as a Sensitive Biomarker in Stroke Patients
Mages, B., Fuhs, T., Aleithe, S., Blietz, A., Hobusch, C., Härtig, W., Schob, S., Krueger, M., & Michalski, D. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02372-3 · Cited by 38
The Role of DNA Methylation in Stroke Recovery
Choi, D., Choi, I.-A., & Lee, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810373 · Cited by 35
Reflections of experience‐expectant development in repair of the adult damaged brain
Jones, T. A., & Jefferson, S. C. (2011) · Developmental Psychobiology · doi:10.1002/dev.20557 · Cited by 37
Effects of treadmill exercise on the expression of netrin-1 and its receptors in rat brain after cerebral ischemia
Liu, N., Huang, H., Lin, F. Y., Chen, A., Zhang, Y., Chen, R., & Du, H. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.07.037 · Cited by 36
Disability in multiple sclerosis: When synaptic long-term potentiation fails
Weiss, S., Mori, F., Rossi, S., & Centonze, D. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.03.023 · Cited by 36
Rehabilitation Improves Behavioral Recovery and Lessens Cell Death Without Affecting Iron, Ferritin, Transferrin, or Inflammation After Intracerebral Hemorrhage in Rats
Caliaperumal, J., & Colbourne, F. (2013) · Neurorehabilitation and neural repair · doi:10.1177/1545968313517758 · Cited by 36
Rethinking aphasia therapy: A neuroscience perspective
Varley, R. A. (2011) · International Journal of Speech-Language Pathology · doi:10.3109/17549507.2010.497561 · Cited by 39
Excitatory-Inhibitory Homeostasis and Diaschisis: Tying the Local and Global Scales in the Post-stroke Cortex
dos Santos, F. P., & Verschure, P. F. M. J. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.806544 · Cited by 35
Efficacy and safety of very early rehabilitation for acute ischemic stroke: a systematic review and meta-analysis
Lou, Y., Liu, Z., Ji, Y., Cheng, J., Zhao, C., & Li, L. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1423517 · Cited by 36
Parvalbumin interneurons regulate rehabilitation-induced functional recovery after stroke and identify a rehabilitation drug
Okabe, N., Wei, X., Abumeri, F., Batac, J., Hovanesyan, M., Dai, W., Azarapetian, S., Campagna, J. J., Pilati, N., Marasco, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-57860-0 · Cited by 34
Melanocortins as potential therapeutic agents in severe hypoxic conditions
Giuliani, D., Minutoli, L., Ottani, A., Spaccapelo, L., Bitto, A., Galantucci, M., Altavilla, D., Squadrito, F., & Guarini, S. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2012.04.001 · Cited by 35
Reorganization of Motor Execution Networks During Sub-Acute Phase After Stroke
Cheng, L., Wu, Z., Sun, J., Fu, Y., Wang, X., Yang, G., Miao, F., & Tong, S. (2015) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2015.2401978 · Cited by 35
Mobilisation of Hematopoietic CD34+ Precursor Cells in Patients with Acute Stroke Is Safe - Results of an Open-Labeled Non Randomized Phase I/II Trial
Boy, S., Sauerbruch, S., Kraemer, M., Schormann, T., Schlachetzki, F., Schuierer, G. R., Luerding, R., Hennemann, B., Orsó, E., Dabringhaus, A., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023099 · Cited by 35
The Optimal Speed for Cortical Activation of Passive Wrist Movements Performed by a Rehabilitation Robot: A Functional NIRS Study
Bae, S., Jang, S. H., Seo, J. P., & Chang, P. H. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00194 · Cited by 35
Stroke triggers nigrostriatal plasticity and increases alcohol consumption in rats
Huang, C. C., Ma, T., Roltsch, E. A., Wang, X., Selvamani, A., Lu, J., Sohrabji, F., & Wang, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-02714-z · Cited by 31
Transcranial direct current stimulation over multiple days enhances motor performance of a grip task
Fan, J., Voisin, J. I. A., Milot, M.-H., Higgins, J., & Boudrias, M. (2017) · Annals of Physical and Rehabilitation Medicine · doi:10.1016/j.rehab.2017.07.001 · Cited by 35
Augmenting LTP-Like Plasticity in Human Motor Cortex by Spaced Paired Associative Stimulation
Müller‐Dahlhaus, F., Lücke, C., Lu, M., Arai, N., Fuhl, A., Herrmann, E. M., & Ziemann, U. (2015) · PLoS ONE · doi:10.1371/journal.pone.0131020 · Cited by 35
Magnetoencephalography in Stroke Recovery and Rehabilitation
Paggiaro, A., Birbaumer, N., Cavinato, M., Turco, C., Formaggio, E., Felice, A. D., Masiero, S., & Piccione, F. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00035 · Cited by 38
The Effects of Modified Constraint-Induced Movement Therapy in Acute Subcortical Cerebral Infarction
Yu, C., Wang, W., Zhang, Y., Wang, Y., Hou, W., Liu, S., Gao, C., Wang, C., Mo, L., & Wu, J. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00265 · Cited by 35
Inhibition of Tnf-α R1 signaling can rescue functional cortical plasticity impaired in early post-stroke period
Liguz‐Lecznar, M., Zakrzewska, R., & Kossut, M. M. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.06.015 · Cited by 34
Acute exercise induces cortical inhibition and reduces arousal in response to visual stimulation in young children
Mierau, A., Hülsdünker, T., Mierau, J., Hense, A., Hense, J., & Strüder, H. K. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2013.12.009 · Cited by 38
Effect of Inhibition of DNA Methylation Combined with Task-Specific Training on Chronic Stroke Recovery
Choi, I.-A., Lee, C.-S., Kim, H. Y., Choi, D., & Lee, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19072019 · Cited by 34
40-Hz optogenetic stimulation rescues functional synaptic plasticity after stroke
Wang, C., Lin, C., Zhao, Y., Samantzis, M., Sedlak, P. L., Sah, P., & Balbi, M. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113475 · Cited by 32
EEG patterns from acute to chronic stroke phases in focal cerebral ischemic rats: correlations with functional recovery
Zhang, S., Ke, Z., Li, L., Yip, S. P., & Tong, R. K. (2013) · Physiological Measurement · doi:10.1088/0967-3334/34/4/423 · Cited by 34
Kinematic analyses reveal impaired locomotion following injury of the motor cortex in mice
Ueno, M., & Yamashita, T. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.05.006 · Cited by 31
Enhanced detection threshold forin vivocortical stimulation produced by Hebbian conditioning
Rebesco, J. M., & Miller, L. E. (2011) · Journal of Neural Engineering · doi:10.1088/1741-2560/8/1/016011 · Cited by 36
BCI-FES With Multimodal Feedback for Motor Recovery Poststroke
Remsik, A. B., van Kan, P. L. E., Gloe, S., Gjini, K., Williams, L. M., Nair, V. A., Caldera, K. E., Williams, J. C., & Prabhakaran, V. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.725715 · Cited by 33
Mechanisms of Post-Stroke Fatigue: A Follow-Up From the Third Stroke Recovery and Rehabilitation Roundtable
Kuppuswamy, A., Billinger, S. A., Coupland, K., English, C., Kutlubaev, M. A., Moseley, G. L., Pittman, Q. J., Simpson, D. B., Sutherland, B. A., Wong, C. H. Y., et al. (2023) · Neurorehabilitation and neural repair · doi:10.1177/15459683231219266 · Cited by 33
Self-citation
Disentangling neuroplasticity mechanisms in post-stroke language recovery
Billot, A., & Kiran, S. (2024) · Brain and Language · doi:10.1016/j.bandl.2024.105381 · Cited by 37
Half a century legacy of long-term potentiation
Caya-Bissonnette, L., & Béïque, J.-C. (2024) · Current Biology · doi:10.1016/j.cub.2024.05.008 · Cited by 41
Hebbian plasticity induced by temporally coincident BCI enhances post-stroke motor recovery
Krueger, J., Krauth, R., Reichert, C., Perdikis, S., Vogt, S., Huchtemann, T., Dürschmid, S., Sickert, A., Lamprecht, J., Huremovic, A., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-69037-8 · Cited by 36
Mildronate treatment improves functional recovery following middle cerebral artery occlusion in rats
Švalbe, B., Zvejniece, L., Vavers, E., Pugovičs, O., Muceniece, R., Liepinsh, E., & Dambrova, M. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.03.027 · Cited by 33
Rehabilitation of the hemiparetic gait by nociceptive withdrawal reflex-based functional electrical therapy: a randomized, single-blinded study
Spaich, E. G., Svaneborg, N., Jørgensen, H. R. M., & Andersen, O. K. (2014) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/1743-0003-11-81 · Cited by 33
Optical inhibition of striatal neurons promotes focal neurogenesis and neurobehavioral recovery in mice after middle cerebral artery occlusion
He, X., Lu, Y., Lin, X., Jiang, L., Tang, Y., Tang, G., Chen, X., Zhang, Z., Wang, Y., & Yang, G. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x16642242 · Cited by 33
Effects of Transcranial Direct Current Stimulation With Sensory Modulation on Stroke Motor Rehabilitation: A Randomized Controlled Trial
Koh, C., Lin, J., Jeng, J., Huang, S., & Hsieh, C. (2017) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2017.05.025 · Cited by 33
Cortex-dependent recovery of unassisted hindlimb locomotion after complete spinal cord injury in adult rats
Manohar, A., Foffani, G., Ganzer, P. D., Bethea, J. R., & Moxon, K. A. (2017) · eLife · doi:10.7554/elife.23532 · Cited by 38
Dissociating nNOS (Neuronal NO Synthase)-CAPON (Carboxy-Terminal Postsynaptic Density-95/Discs Large/Zona Occludens-1 Ligand of nNOS) Interaction Promotes Functional Recovery After Stroke via Enhanced Structural Neuroplasticity
Ni, H., Song, Y., Lin, Y., Cao, B., Wang, D., Zhang, Y., Dong, J. P., Liang, H., Xu, K., Li, T., et al. (2019) · Stroke · doi:10.1161/strokeaha.118.022647 · Cited by 33
Physical activity after ischemic stroke and its association with adverse outcomes: A nationwide population-based cohort study
Kang, S.-M., Kim, S., Han, K.-D., Paik, N., & Kim, W. (2020) · Topics in Stroke Rehabilitation · doi:10.1080/10749357.2020.1799292 · Cited by 34
Effect of Diabetes on Post-stroke Recovery: A Systematic Narrative Review
Yang, S., Boudier‐Revéret, M., Kwon, S., Lee, M. Y., & Chang, M. C. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.747878 · Cited by 33
Stroke: Working toward a Prioritized World Agenda
Hachinski, V., Donnan, G. A., Gorelick, P. B., Hacke, W., Cramer, S. C., Kaste, M., Fisher, M., Brainin, M., Buchan, A. M., Lo, E. H., et al. (2010) · Cerebrovascular Diseases · doi:10.1159/000315099 · Cited by 35
Early constraint-induced movement therapy promotes functional recovery and neuronal plasticity in a subcortical hemorrhage model rat
Ishida, A., Misumi, S., Ueda, Y., Shimizu, Y., Jung, C., Tamakoshi, K., Ishida, K., & Hida, H. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.02.022 · Cited by 35
A randomized controlled trial of very early rehabilitation in speech after stroke
Godecke, E., Armstrong, E. A., Rai, T., Middleton, S., Ciccone, N., Whitworth, A., Rose, M., Holland, A., Ellery, F., Hankey, G. J., et al. (2016) · International Journal of Stroke · doi:10.1177/1747493016641116 · Cited by 32
Revisiting dose and intensity of training: Opportunities to enhance recovery following stroke
Donnellan-Fernandez, K., Ioakim, A., & Hordacre, B. G. (2022) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2022.106789 · Cited by 33
Intra-parenchymal ferrous iron infusion causes neuronal atrophy, cell death and progressive tissue loss: Implications for intracerebral hemorrhage
Caliaperumal, J., Ma, Y., & Colbourne, F. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.07.001 · Cited by 32
Prediction of post-stroke dementia using NINDS-CSN 5-minute neuropsychology protocol in acute stroke
Lim, J., Oh, M. S., Lee, J.-H., Jung, S., Kim, C., Jang, M. U., Lee, S., Kim, Y. J., Kim, Y., Park, J., et al. (2017) · International Psychogeriatrics · doi:10.1017/s1041610216002520 · Cited by 31
Abnormal EEG Responses to TMS During the Cortical Silent Period Are Associated With Hand Function in Chronic Stroke
Gray, W. A., Palmer, J. A., Wolf, S. L., & Borich, M. R. (2017) · Neurorehabilitation and neural repair · doi:10.1177/1545968317712470 · Cited by 32
Lesion location impact on functional recovery of the hemiparetic upper limb
Frenkel‐Toledo, S., Fridberg, G., Ofir, S., Bartur, G., Raz, J. L., Granot, O., Handelzalts, S., & Soroker, N. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219738 · Cited by 32
Neurogenesis promoted by the CD200/CD200R signaling pathway following treadmill exercise enhances post-stroke functional recovery in rats
Sun, H., Li, A., Hou, T., Tao, X., Chen, M., Wu, C., Chen, S., Zhu, L., & Liao, H. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.09.005 · Cited by 32
Gait-Synchronized Rhythmic Brain Stimulation Improves Poststroke Gait Disturbance
Koganemaru, S., Kitatani, R., Fukushima-Maeda, A., Mikami, Y., Okita, Y., Matsuhashi, M., Ohata, K., Kansaku, K., & Mima, T. (2019) · Stroke · doi:10.1161/strokeaha.119.025354 · Cited by 31
Limited capacity for ipsilateral secondary motor areas to support hand function post‐stroke
Wilkins, K. B., Yao, J., Owen, M., Karbasforoushan, H., Carmona, C., & Dewald, J. P. A. (2020) · The Journal of Physiology · doi:10.1113/jp279377 · Cited by 31
A Review on Treatment-Related Brain Changes in Aphasia
Schevenels, K., Price, C. J., Zink, I., Smedt, B. D., & Vandermosten, M. (2020) · Neurobiology of Language · doi:10.1162/nol_a_00019 · Cited by 32
Barrel cortex plasticity after photothrombotic stroke involves potentiating responses of pre-existing circuits but not functional remapping to new circuits
Zeiger, W., Marosi, M., Saggi, S. S., Noble, N., Samad, I., & Portera‐Cailliau, C. (2021) · Nature Communications · doi:10.1038/s41467-021-24211-8 · Cited by 32
Brain plasticity and vagus nerve stimulation
Keute, M., & Gharabaghi, A. (2021) · Autonomic Neuroscience · doi:10.1016/j.autneu.2021.102876 · Cited by 32
The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia
Aswendt, M., Green, C., Sadler, R., Llovera, G., Dzikowski, L., Heindl, S., de Agüero, M. G., Diedenhofen, M., Vogel, S. N., Wieters, F., et al. (2021) · iScience · doi:10.1016/j.isci.2021.103095 · Cited by 33
From competition to cooperation: Visual neglect across the hemispheres
Bartolomeo, P. (2021) · Revue Neurologique · doi:10.1016/j.neurol.2021.07.015 · Cited by 32
Aβand Aδbut not C-fibres are involved in stroke related pain and allodynia: an experimental study in mice
Takami, K., Fujita‐Hamabe, W., Harada, S., & Tokuyama, S. (2011) · Journal of Pharmacy and Pharmacology · doi:10.1111/j.2042-7158.2010.01231.x · Cited by 32
The effects of combined repetitive transcranial magnetic stimulation and transcranial direct current stimulation on motor function in patients with stroke
Kwon, T. G., Park, E., Kang, C., Chang, W. H., & Kim, Y. (2016) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-160654 · Cited by 32

Authors: Murphy, T. H., & Corbett, D.
Affiliations: University of British Columbia (CA)
Memorial University of Newfoundland (CA)
ORCID: Murphy, Timothy H.
Corbett, Dale
Venue: Nature Reviews Neuroscience
Publisher: Springer Science and Business Media LLC
Published: 2009-11-04
Volume: 10
Issue: 12
Pages: 861-872
ISSN: 1471-003X (ISSN-L)
1471-0048
DOI: 10.1038/nrn2735
OpenAlex: W2045421141
Cited by: 1,938
References: 168
Citations by year: 2026: 126 · 2025: 120 · 2024: 125 · 2023: 135 · 2022: 120 · 2021: 161 · 2020: 135 · 2019: 131 · 2018: 125 · 2017: 146 · 2016: 101 · 2015: 114 · 2014: 120 · 2013: 99 · 2012: 67
FWCI: 7.83
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
www.springer.com/tdm (vor)
Locations: Nature reviews. Neuroscience (publishedVersion)
PubMed (publishedVersion)
Funders: Heart and Stroke Foundation of British Columbia and Yukon
Canadian Institutes of Health Research
Topics: Health Sciences › Medicine › Rehabilitation › Stroke Rehabilitation and Recovery
Health Sciences › Medicine › Clinical Neurology › Acute Ischemic Stroke Management
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: stroke recovery, neuroplasticity, behavioral recovery, developmental plasticity, animal models of stroke
MeSH terms: Animals, Brain Ischemia, Disease Models, Animal, Humans, Learning, Neuronal Plasticity, Synapses, Recovery of Function, Stroke

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Plasticity during stroke recovery: from synapse to behaviour

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks