Corticoreticulospinal tract neurophysiology in an arm and hand muscle in healthy and stroke subjects
Key points The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals. In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury...
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Published in | The Journal of physiology Vol. 599; no. 16; pp. 3955 - 3971 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.08.2021
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Subjects | |
Online Access | Get full text |
ISSN | 0022-3751 1469-7793 1469-7793 |
DOI | 10.1113/JP281681 |
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Abstract | Key points
The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals.
In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury.
In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation.
We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects.
These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans.
The corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and distal upper extremity muscles in humans. The contralesional CReST furthermore reorganizes after corticospinal tract (CST) injury in animals, but it is less clear whether CReST innervation changes after stroke in humans. We thus examined CReST functional connectivity, connection strength, and modulation in an arm and hand muscle of healthy (n = 15) and chronic stroke (n = 16) subjects. We delivered transcranial magnetic stimulation to the contralesional hemisphere (assigned in healthy subjects) to elicit ipsilateral motor evoked potentials (iMEPs) from the paretic biceps (BIC) and first dorsal interosseous (FDI) muscle. We operationalized CReST functional connectivity as iMEP presence/absence, CReST projection strength as iMEP size and CReST modulation as change in iMEP size by head rotation. We found comparable CReST functional connectivity to the BICs and FDIs in both subject groups. However, the pattern of CReST connection strength to the muscles diverged between groups, with stronger connections to FDIs than BICs in healthy subjects and stronger connections to BICs than FDIs in stroke subjects. Head rotation modulated only FDI iMEPs of healthy subjects. Our findings indicate that the healthy CReST does not have a proximal innervation bias, and its strong FDI connections may have functional relevance to finger individuation. The reversed CReST innervation pattern in stroke subjects confirms its reorganization after CST injury, and its strong BIC connections may indicate upregulation for particular upper extremity muscles or their functional actions.
Key points
The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals.
In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury.
In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation.
We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects.
These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans. |
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AbstractList | Key points
The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals.
In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury.
In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation.
We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects.
These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans.
The corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and distal upper extremity muscles in humans. The contralesional CReST furthermore reorganizes after corticospinal tract (CST) injury in animals, but it is less clear whether CReST innervation changes after stroke in humans. We thus examined CReST functional connectivity, connection strength, and modulation in an arm and hand muscle of healthy (n = 15) and chronic stroke (n = 16) subjects. We delivered transcranial magnetic stimulation to the contralesional hemisphere (assigned in healthy subjects) to elicit ipsilateral motor evoked potentials (iMEPs) from the paretic biceps (BIC) and first dorsal interosseous (FDI) muscle. We operationalized CReST functional connectivity as iMEP presence/absence, CReST projection strength as iMEP size and CReST modulation as change in iMEP size by head rotation. We found comparable CReST functional connectivity to the BICs and FDIs in both subject groups. However, the pattern of CReST connection strength to the muscles diverged between groups, with stronger connections to FDIs than BICs in healthy subjects and stronger connections to BICs than FDIs in stroke subjects. Head rotation modulated only FDI iMEPs of healthy subjects. Our findings indicate that the healthy CReST does not have a proximal innervation bias, and its strong FDI connections may have functional relevance to finger individuation. The reversed CReST innervation pattern in stroke subjects confirms its reorganization after CST injury, and its strong BIC connections may indicate upregulation for particular upper extremity muscles or their functional actions.
Key points
The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals.
In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury.
In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation.
We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects.
These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans. The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals. In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury. In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation. We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects. These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans.KEY POINTSThe corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals. In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury. In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation. We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects. These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans.The corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and distal upper extremity muscles in humans. The contralesional CReST furthermore reorganizes after corticospinal tract (CST) injury in animals, but it is less clear whether CReST innervation changes after stroke in humans. We thus examined CReST functional connectivity, connection strength, and modulation in an arm and hand muscle of healthy (n = 15) and chronic stroke (n = 16) subjects. We delivered transcranial magnetic stimulation to the contralesional hemisphere (assigned in healthy subjects) to elicit ipsilateral motor evoked potentials (iMEPs) from the paretic biceps (BIC) and first dorsal interosseous (FDI) muscle. We operationalized CReST functional connectivity as iMEP presence/absence, CReST projection strength as iMEP size and CReST modulation as change in iMEP size by head rotation. We found comparable CReST functional connectivity to the BICs and FDIs in both subject groups. However, the pattern of CReST connection strength to the muscles diverged between groups, with stronger connections to FDIs than BICs in healthy subjects and stronger connections to BICs than FDIs in stroke subjects. Head rotation modulated only FDI iMEPs of healthy subjects. Our findings indicate that the healthy CReST does not have a proximal innervation bias, and its strong FDI connections may have functional relevance to finger individuation. The reversed CReST innervation pattern in stroke subjects confirms its reorganization after CST injury, and its strong BIC connections may indicate upregulation for particular upper extremity muscles or their functional actions.ABSTRACTThe corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and distal upper extremity muscles in humans. The contralesional CReST furthermore reorganizes after corticospinal tract (CST) injury in animals, but it is less clear whether CReST innervation changes after stroke in humans. We thus examined CReST functional connectivity, connection strength, and modulation in an arm and hand muscle of healthy (n = 15) and chronic stroke (n = 16) subjects. We delivered transcranial magnetic stimulation to the contralesional hemisphere (assigned in healthy subjects) to elicit ipsilateral motor evoked potentials (iMEPs) from the paretic biceps (BIC) and first dorsal interosseous (FDI) muscle. We operationalized CReST functional connectivity as iMEP presence/absence, CReST projection strength as iMEP size and CReST modulation as change in iMEP size by head rotation. We found comparable CReST functional connectivity to the BICs and FDIs in both subject groups. However, the pattern of CReST connection strength to the muscles diverged between groups, with stronger connections to FDIs than BICs in healthy subjects and stronger connections to BICs than FDIs in stroke subjects. Head rotation modulated only FDI iMEPs of healthy subjects. Our findings indicate that the healthy CReST does not have a proximal innervation bias, and its strong FDI connections may have functional relevance to finger individuation. The reversed CReST innervation pattern in stroke subjects confirms its reorganization after CST injury, and its strong BIC connections may indicate upregulation for particular upper extremity muscles or their functional actions. The corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and distal upper extremity muscles in humans. The contralesional CReST furthermore reorganizes after corticospinal tract (CST) injury in animals, but it is less clear whether CReST innervation changes after stroke in humans. We thus examined CReST functional connectivity, connection strength, and modulation in an arm and hand muscle of healthy (n = 15) and chronic stroke (n = 16) subjects. We delivered transcranial magnetic stimulation to the contralesional hemisphere (assigned in healthy subjects) to elicit ipsilateral motor evoked potentials (iMEPs) from the paretic biceps (BIC) and first dorsal interosseous (FDI) muscle. We operationalized CReST functional connectivity as iMEP presence/absence, CReST projection strength as iMEP size and CReST modulation as change in iMEP size by head rotation. We found comparable CReST functional connectivity to the BICs and FDIs in both subject groups. However, the pattern of CReST connection strength to the muscles diverged between groups, with stronger connections to FDIs than BICs in healthy subjects and stronger connections to BICs than FDIs in stroke subjects. Head rotation modulated only FDI iMEPs of healthy subjects. Our findings indicate that the healthy CReST does not have a proximal innervation bias, and its strong FDI connections may have functional relevance to finger individuation. The reversed CReST innervation pattern in stroke subjects confirms its reorganization after CST injury, and its strong BIC connections may indicate upregulation for particular upper extremity muscles or their functional actions. The corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and distal upper extremity (UE) muscles in humans. The contralesional CReST furthermore reorganizes after corticospinal tract (CST) injury in animals, but it is less clear whether CReST innervation changes after stroke in humans. We thus examined CReST functional connectivity, connection strength, and modulation in an arm and hand muscle of healthy (n=15) and chronic stroke (n=16) subjects. We delivered transcranial magnetic stimulation to the contralesional hemisphere (assigned in healthy subjects) to elicit ipsilateral motor evoked potentials (iMEPs) from the paretic biceps (BIC) and first dorsal interosseous (FDI) muscle. We operationalized CReST functional connectivity as iMEP presence/absence, CReST projection strength as iMEP size, and CReST modulation as change in iMEP size by head rotation. We found comparable CReST functional connectivity to the BICs and FDIs in both subject groups. However, the pattern of CReST connection strength to the muscles diverged between groups, with stronger connections to FDIs than BICs in healthy subjects and stronger connections to BICs than FDIs in stroke subjects. Head rotation modulated only FDI iMEPs of healthy subjects. Our findings indicate that the healthy CReST does not have a proximal innervation bias, and its strong FDI connections may have functional relevance to finger individuation. The reversed CReST innervation pattern in stroke subjects confirms its reorganization after CST injury, and its strong BIC connections may indicate upregulation for particular UE muscles or their functional actions. The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals. In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury. In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation. We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects. These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans. The corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and distal upper extremity muscles in humans. The contralesional CReST furthermore reorganizes after corticospinal tract (CST) injury in animals, but it is less clear whether CReST innervation changes after stroke in humans. We thus examined CReST functional connectivity, connection strength, and modulation in an arm and hand muscle of healthy (n = 15) and chronic stroke (n = 16) subjects. We delivered transcranial magnetic stimulation to the contralesional hemisphere (assigned in healthy subjects) to elicit ipsilateral motor evoked potentials (iMEPs) from the paretic biceps (BIC) and first dorsal interosseous (FDI) muscle. We operationalized CReST functional connectivity as iMEP presence/absence, CReST projection strength as iMEP size and CReST modulation as change in iMEP size by head rotation. We found comparable CReST functional connectivity to the BICs and FDIs in both subject groups. However, the pattern of CReST connection strength to the muscles diverged between groups, with stronger connections to FDIs than BICs in healthy subjects and stronger connections to BICs than FDIs in stroke subjects. Head rotation modulated only FDI iMEPs of healthy subjects. Our findings indicate that the healthy CReST does not have a proximal innervation bias, and its strong FDI connections may have functional relevance to finger individuation. The reversed CReST innervation pattern in stroke subjects confirms its reorganization after CST injury, and its strong BIC connections may indicate upregulation for particular upper extremity muscles or their functional actions. The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals. In humans, the pattern of CReST innervation to upper limb muscles has not been carefully examined in healthy individuals or individuals with CST injury. In the present study, we assessed CReST projections to an arm and hand muscle on the same side of the body in healthy and chronic stoke subjects using transcranial magnetic stimulation. We show that CReST connection strength to the muscles differs between healthy and stroke subjects, with stronger connections to the hand than arm in healthy subjects, and stronger connections to the arm than hand in stroke subjects. These results help us better understand CReST innervation patterns in the upper limb, and may point to its role in normal motor function and motor recovery in humans. |
Author | Taga, Myriam Schambra, Heidi M. Stern, Elisa Lin, Jing Charalambous, Charalambos C. Zhang, Yian Raju, Sharmila |
AuthorAffiliation | 3 Center for Neuroscience and Integrative Brain Research (CENIBRE), Medical School, University of Nicosia, Nicosia, Cyprus 2 Department of Basic and Clinical Sciences, Medical School, University of Nicosia, Nicosia, Cyprus 4 Division of Biostatistics, Department of Population Health, School of Medicine, New York University, New York, United States 1 Department of Neurology, NYU Langone, School of Medicine, New York, United States |
AuthorAffiliation_xml | – name: 1 Department of Neurology, NYU Langone, School of Medicine, New York, United States – name: 4 Division of Biostatistics, Department of Population Health, School of Medicine, New York University, New York, United States – name: 3 Center for Neuroscience and Integrative Brain Research (CENIBRE), Medical School, University of Nicosia, Nicosia, Cyprus – name: 2 Department of Basic and Clinical Sciences, Medical School, University of Nicosia, Nicosia, Cyprus |
Author_xml | – sequence: 1 givenname: Myriam surname: Taga fullname: Taga, Myriam organization: School of Medicine, NYU Langone – sequence: 2 givenname: Charalambos C. surname: Charalambous fullname: Charalambous, Charalambos C. organization: University of Nicosia Medical School – sequence: 3 givenname: Sharmila surname: Raju fullname: Raju, Sharmila organization: School of Medicine, NYU Langone – sequence: 4 givenname: Jing orcidid: 0000-0003-3653-2597 surname: Lin fullname: Lin, Jing organization: School of Medicine, NYU Langone – sequence: 5 givenname: Yian surname: Zhang fullname: Zhang, Yian organization: New York University – sequence: 6 givenname: Elisa surname: Stern fullname: Stern, Elisa organization: School of Medicine, NYU Langone – sequence: 7 givenname: Heidi M. orcidid: 0000-0002-1886-2288 surname: Schambra fullname: Schambra, Heidi M. email: Heidi.Schambra@nyulangone.org organization: School of Medicine, NYU Langone |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34229359$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.neucli.2006.08.005 10.1007/s00221-003-1807-8 10.2340/1650197771331 10.1523/JNEUROSCI.3371-17.2018 10.1016/j.clinph.2007.10.021 10.1152/jn.00866.2012 10.1523/JNEUROSCI.1107-20.2020 10.1523/JNEUROSCI.1648-14.2014 10.1007/s00221-007-1169-8 10.1007/s002210050926 10.1007/BF00238464 10.1152/jn.01030.2011 10.1152/physrev.2001.81.4.1725 10.1523/JNEUROSCI.0649-19.2019 10.1007/s00221-004-2031-x 10.1093/brain/122.7.1327 10.1523/JNEUROSCI.4055-15.2016 10.1097/00001756-199607290-00012 10.1002/(SICI)1096-9861(19970113)377:2<234::AID-CNE6>3.0.CO;2-4 10.1152/jn.00852.2014 10.1002/(SICI)1096-9861(19971229)389:4<617::AID-CNE6>3.0.CO;2-3 10.1152/jn.00365.2010 10.1002/cphy.cp010214 10.1093/brain/60.4.389 10.1177/1545968319850138 10.1152/jn.1990.64.3.782 10.1007/BF00227284 10.1093/brain/aws115 10.1113/jphysiol.2006.126276 10.1523/JNEUROSCI.3368-16.2017 10.1523/JNEUROSCI.4384-13.2014 10.1523/JNEUROSCI.0040-07.2007 10.1002/ana.10686 10.1016/0306-4522(84)90038-1 10.1162/jocn.2007.19.7.1081 10.1146/annurev.neuro.31.060407.125547 10.1007/s00221-013-3639-5 10.1093/brain/120.9.1579 10.1212/WNL.41.11.1795 10.1152/jn.00950.2002 10.1016/0306-4522(84)90142-8 10.1113/jphysiol.2011.225169 10.1016/j.brs.2010.01.001 10.1523/JNEUROSCI.3720-08.2009 10.1152/jn.01139.2015 10.1007/s10548-005-6033-1 10.1093/brain/91.1.1 10.1152/jn.00878.2007 10.1016/j.clinph.2007.06.010 10.1016/S1388-2457(00)00430-2 10.1093/brain/91.1.15 10.1007/BF00248864 10.1002/mus.20817 10.1002/cne.901180109 10.1113/jphysiol.2011.215160 10.1113/jphysiol.2011.226209 10.1002/cphy.cp010213 10.1007/s00221-006-0374-1 10.1093/brain/119.6.1809 10.1152/jn.2001.86.5.2125 10.1111/j.1469-7793.1999.0895p.x 10.1212/01.WNL.0000101711.48946.35 10.1093/brain/74.4.443 10.1093/cercor/7.1.18 10.1111/j.2517-6161.1995.tb02031.x 10.1111/ejn.13576 10.1002/ar.1091280110 10.1093/cercor/4.2.166 10.1523/JNEUROSCI.11-03-00667.1991 10.1113/JP274968 10.1152/jn.00491.2009 10.1111/j.1468-1331.2008.02168.x 10.1523/JNEUROSCI.1379-20.2020 10.1016/j.clinph.2019.02.018 10.1016/0006-8993(67)90004-2 10.1073/pnas.0808362106 10.1161/01.STR.32.6.1304 10.1152/jn.00083.2003 10.1016/j.neuroimage.2006.02.004 10.3389/fneur.2017.00627 10.1113/JP280156 |
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Issue | 16 |
Keywords | corticoreticulospinal tract transcranial magnetic stimulation chronic stroke ipsilateral motor evoked potential corticospinal tract upper extremity |
Language | English |
License | 2021 The Authors. The Journal of Physiology © 2021 The Physiological Society. |
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Notes | These authors contributed equally to this work. The peer review history is available in the Supporting Information section of this article https://doi.org/10.1113/JP281681#support‐information‐section . Edited by: Richard Carson & Charlotte Stagg ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Sharmila Raju, MS, Chicago Medical School, Rosalind Franklin University, 3333 Green Bay Rd, North Chicago, IL 60064 Elisa Stern, MRes, Department of Psychiatry, Yale University School of Medicine, 333 Cedar Street, New Haven, CT, 06510 Yian Zhang, PhD, Division of Biostatistics, Department of Population Health, School of Medicine, New York University, New York, United States, 180 Madison Avenue, 2nd Floor, Cubicle 2-35C, NY 10016 Charalambos C. Charalambous, PhD, Department of Basic and Clinical Sciences, and Center for Neuroscience and Integrative Brain Research (CENIBRE), Medical School, University of Nicosia, Nicosia, Cyprus. 1 28th October Ave, Block D, Room 309, CY-2414, Nicosia, Cyprus Jing Lin, MD, NYU Grossman School of Medicine, Physical Medicine & Rehabilitation Residency Program, 240 east 38th street, NY, NY 10016 Shared authorship Myriam Taga, PhD, Department of Neurology, NYU Langone, School of Medicine, New York, United States. NYU Langone Health, 222 E 41st Street, 10th Floor, New York, NY 10017 Author’s contribution: HMS provided the funding and resources for the data acquisition and analysis and supervised the study. HMS, CCC, and SR led project administration. HMS and CCC developed the methodology of the study. CCC, SR, JL, ES performed the experiment. HMS, CCC, and MT were responsible for the conception and experimental design of the study. HMS, CCC, MT, SR, JL, and ES were responsible for data curation. CCC and MT developed codes for data acquisition and analysis. HMS, CCC, MT, and YZ analyzed the data. HMS, CCC, and MT validated the results. HMS, CCC, MT, and SR visualized the data. HMS and MT drafted the article. All authors revised the article critically for important intellectual content. All authors have approved the final version of the manuscript and greed to be accountable for all aspects of the work. All persons designated authors qualify for authorship, and all those who qualify for authorship are listed. |
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References | 2017; 8 2004; 62 2006; 31 1979; 36 2007; 580 1968b; 91 1991; 11 2010; 103 2010; 104 2006; 36 2017; 45 2006; 173 1999; 122 2008; 31 1999; 129 1968a; 91 2008; 185 2016; 36 2007; 36 2003; 54 2001; 86 1997; 7 1989; 74 1997; 389 1962; 118 1994; 100 2012; 135 2017; 37 1991; 41 1984; 11 1984; 12 2008; 119 2013; 110 2016; 115 1981 2013; 230 2010; 3 1975; 7 2021; 41 1951; 74 1996; 7 2003; 89 2007; 27 1997; 377 2007; 19 1957; 128 2011 2020; 40 2019; 33 1995; 57 1937; 60 2019; 39 2008 2008; 15 2000; 111 2012; 108 2009; 29 2011; 589 2004; 156 2012; 590 2001; 81 1990; 64 2007; 118 2004; 158 2004; 92 2015; 113 2020 1997; 120 2018; 596 1967; 4 2009; 101 2018 2020; 598 2019; 130 2005; 17 2014; 34 1996; 119 1994; 4 1999; 518 2001; 32 2009; 106 e_1_2_6_51_1 e_1_2_6_74_1 e_1_2_6_53_1 e_1_2_6_76_1 e_1_2_6_32_1 e_1_2_6_70_1 e_1_2_6_30_1 e_1_2_6_72_1 e_1_2_6_19_1 e_1_2_6_13_1 e_1_2_6_36_1 e_1_2_6_59_1 e_1_2_6_11_1 e_1_2_6_34_1 e_1_2_6_17_1 e_1_2_6_55_1 e_1_2_6_78_1 e_1_2_6_15_1 e_1_2_6_38_1 e_1_2_6_57_1 e_1_2_6_62_1 e_1_2_6_85_1 e_1_2_6_64_1 e_1_2_6_43_1 e_1_2_6_81_1 e_1_2_6_20_1 e_1_2_6_41_1 e_1_2_6_60_1 e_1_2_6_83_1 Perotto AO (e_1_2_6_58_1) 2011 e_1_2_6_9_1 e_1_2_6_5_1 e_1_2_6_7_1 e_1_2_6_24_1 e_1_2_6_49_1 e_1_2_6_3_1 e_1_2_6_22_1 e_1_2_6_66_1 e_1_2_6_28_1 e_1_2_6_45_1 e_1_2_6_26_1 e_1_2_6_47_1 e_1_2_6_68_1 e_1_2_6_52_1 e_1_2_6_73_1 e_1_2_6_54_1 e_1_2_6_75_1 e_1_2_6_10_1 e_1_2_6_31_1 e_1_2_6_50_1 e_1_2_6_71_1 e_1_2_6_14_1 e_1_2_6_35_1 e_1_2_6_12_1 e_1_2_6_33_1 e_1_2_6_18_1 e_1_2_6_39_1 e_1_2_6_56_1 e_1_2_6_77_1 e_1_2_6_16_1 e_1_2_6_37_1 e_1_2_6_79_1 e_1_2_6_63_1 e_1_2_6_84_1 e_1_2_6_42_1 e_1_2_6_65_1 e_1_2_6_21_1 e_1_2_6_80_1 e_1_2_6_40_1 e_1_2_6_61_1 e_1_2_6_82_1 e_1_2_6_8_1 e_1_2_6_4_1 e_1_2_6_6_1 e_1_2_6_25_1 e_1_2_6_48_1 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_29_1 e_1_2_6_44_1 e_1_2_6_67_1 e_1_2_6_27_1 e_1_2_6_46_1 e_1_2_6_69_1 |
References_xml | – year: 2011 – volume: 173 start-page: 25 year: 2006 end-page: 39 article-title: Bilateral actions of the reticulospinal tract on arm and shoulder muscles in the monkey: stimulus triggered averaging publication-title: Exp Brain Res – volume: 156 start-page: 458 year: 2004 end-page: 470 article-title: Target‐dependent differences between free and constrained arm movements in chronic hemiparesis publication-title: Exp Brain Res – volume: 103 start-page: 2821 year: 2010 end-page: 2832 article-title: Convergence of pyramidal and medial brain stem descending pathways onto macaque cervical spinal interneurons publication-title: J Neurophysiol – volume: 4 start-page: 151 year: 1967 end-page: 188 article-title: Cortical projections to the red nucleus and the brain stem in the Rhesus monkey publication-title: Brain Res – volume: 40 start-page: 8831 year: 2020 end-page: 8841 article-title: Distinct corticospinal and reticulospinal contributions to voluntary control of elbow flexor and extensor muscles in humans with tetraplegia publication-title: J Neurosci – volume: 130 start-page: 781 year: 2019 end-page: 788 article-title: The unsolved role of heightened connectivity from the unaffected hemisphere to paretic arm muscles in chronic stroke publication-title: Clin Neurophysiol – year: 2018 article-title: Classification of neurons in the primate reticular formation and changes after recovery from pyramidal tract lesion publication-title: J Neurosci – volume: 81 start-page: 1725 year: 2001 end-page: 1789 article-title: Spinal and supraspinal factors in human muscle fatigue publication-title: Physiol Rev – volume: 110 start-page: 1476 year: 2013 end-page: 1483 article-title: Evidence for reticulospinal contributions to coordinated finger movements in humans publication-title: J Neurophysiol – volume: 57 start-page: 289 year: 1995 end-page: 300 article-title: Controlling the false discovery rate – a practical and powerful approach to multiple testing publication-title: J Royal Statist Soc, Series B – volume: 4 start-page: 166 year: 1994 end-page: 194 article-title: Multiple corticospinal neuron populations in the macaque monkey are specified by their unique cortical origins, spinal terminations, and connections publication-title: Cereb Cortex – volume: 7 start-page: 18 year: 1997 end-page: 30 article-title: Structure of the human sensorimotor system. I: Morphology and cytoarchitecture of the central sulcus publication-title: Cereb Cortex – volume: 377 start-page: 234 year: 1997 end-page: 250 article-title: Multi‐segmental innervation of single pontine reticulospinal axons in the cervico‐thoracic region of the cat: anterograde PHA‐L tracing study publication-title: J Comp Neurol – volume: 37 start-page: 9778 year: 2017 end-page: 9784 article-title: Reticulospinal contributions to gross hand function after human spinal cord injury publication-title: J Neurosci – volume: 31 start-page: 1453 year: 2006 end-page: 1474 article-title: Three‐dimensional locations and boundaries of motor and premotor cortices as defined by functional brain imaging: a meta‐analysis publication-title: Neuroimage – start-page: 667 year: 1981 end-page: 702 – volume: 122 start-page: 1327 year: 1999 end-page: 1340 article-title: Corticomotoneuronal synaptic connections in normal man: An electrophysiological study publication-title: Brain – volume: 8 start-page: 627 year: 2017 article-title: The reticulospinal pathway does not increase its contribution to the strength of contralesional muscles in stroke survivors as compared to ipsilesional side or healthy controls publication-title: Front Neurol – volume: 598 start-page: 5487 year: 2020 end-page: 5504 article-title: Functional architecture of the motor homunculus detected by electrostimulation publication-title: J Physiol – volume: 12 start-page: 111 year: 1984 end-page: 128 article-title: Convergence and interaction of neck and macular vestibular inputs on reticulospinal neurons publication-title: Neuroscience – volume: 17 start-page: 253 year: 2005 end-page: 259 article-title: Accuracy of stereotaxic positioning of transcranial magnetic stimulation publication-title: Brain Topogr – volume: 41 start-page: 1005 year: 2021 end-page: 1018 article-title: Extensive cortical convergence to primate reticulospinal pathways publication-title: J Neurosci – volume: 113 start-page: 2592 year: 2015 end-page: 2604 article-title: Bilateral force transients in the upper limbs evoked by single‐pulse microstimulation in the pontomedullary reticular formation publication-title: J Neurophysiol – volume: 230 start-page: 153 year: 2013 end-page: 164 article-title: Recruitment of ipsilateral and contralateral upper limb muscles following stimulation of the cortical motor areas in the monkey publication-title: Exp Brain Res – volume: 32 start-page: 1304 year: 2001 end-page: 1309 article-title: Ipsilateral motor responses to focal transcranial magnetic stimulation in healthy subjects and acute‐stroke patients publication-title: Stroke – volume: 86 start-page: 2125 year: 2001 end-page: 2143 article-title: Constraints on somatotopic organization in the primary motor cortex publication-title: J Neurophysiol – volume: 33 start-page: 568 year: 2019 end-page: 580 article-title: Differential poststroke motor recovery in an arm versus hand muscle in the absence of motor evoked potentials publication-title: Neurorehabil Neural Repair – volume: 3 start-page: 119 year: 2010 end-page: 123 article-title: Optically tracked neuronavigation increases the stability of hand‐held focal coil positioning: evidence from “transcranial” magnetic stimulation‐induced electrical field measurements publication-title: Brain Stimul – volume: 589 start-page: 5603 year: 2011 end-page: 5612 article-title: The primate reticulospinal tract, hand function and functional recovery publication-title: J Physiol – year: 2008 – volume: 91 start-page: 15 year: 1968b end-page: 36 article-title: The functional organization of the motor system in the monkey. II. The effects of lesions of the descending brain‐stem pathways publication-title: Brain – volume: 118 start-page: 107 year: 1962 end-page: 137 article-title: Subcorticospinal projections in the Rhesus monkey publication-title: J Comp Neurol – volume: 31 start-page: 195 year: 2008 end-page: 218 article-title: Descending pathways in motor control publication-title: Annu Rev Neurosci – volume: 100 start-page: 121 year: 1994 end-page: 132 article-title: Cortical motor representation of the ipsilateral hand and arm publication-title: Exp Brain Res – volume: 596 start-page: 1211 year: 2018 end-page: 1225 article-title: Progressive recruitment of contralesional cortico‐reticulospinal pathways drives motor impairment post stroke publication-title: J Physiol – volume: 185 start-page: 509 year: 2008 end-page: 519 article-title: Ipsilateral versus contralateral cortical motor projections to a shoulder adductor in chronic hemiparetic stroke: implications for the expression of arm synergies publication-title: Exp Brain Res – volume: 15 start-page: 706 year: 2008 end-page: 711 article-title: The ipsilateral cortico‐spinal tract is activated after hemiparetic stroke publication-title: Eur J Neurol – volume: 590 start-page: 4011 year: 2012 end-page: 4027 article-title: Cells in the monkey ponto‐medullary reticular formation modulate their activity with slow finger movements publication-title: J Physiol – volume: 74 start-page: 443 year: 1951 end-page: 480 article-title: The restoration of motor function following hemiplegia in man publication-title: Brain – volume: 34 start-page: 3378 year: 2014 end-page: 3389 article-title: Sprouting of brainstem‐spinal tracts in response to unilateral motor cortex stroke in mice publication-title: J Neurosci – volume: 115 start-page: 1735 year: 2016 end-page: 1739 article-title: Are ipsilateral motor evoked potentials subject to intracortical inhibition? publication-title: J Neurophysiol – volume: 119 start-page: 667 year: 2008 end-page: 674 article-title: Acute and chronic effects of ethanol on cortical excitability publication-title: Clin Neurophysiol – volume: 54 start-page: 464 year: 2003 end-page: 472 article-title: Contribution of the ipsilateral motor cortex to recovery after chronic stroke publication-title: Ann Neurol – volume: 104 start-page: 2594 year: 2010 end-page: 2602 article-title: Theta burst stimulation of human primary motor cortex degrades selective muscle activation in the ipsilateral arm publication-title: J Neurophysiol – volume: 128 start-page: 113 year: 1957 end-page: 137 article-title: The origin of reticulospinal fibers in the cat; an experimental study publication-title: Anat Rec – volume: 36 start-page: 242 year: 2007 end-page: 250 article-title: Impact of gravity loading on post‐stroke reaching and its relationship to weakness publication-title: Muscle Nerve – volume: 590 start-page: 4045 year: 2012 end-page: 4060 article-title: Reticular formation responses to magnetic brain stimulation of primary motor cortex publication-title: J Physiol – volume: 389 start-page: 617 year: 1997 end-page: 641 article-title: Organization of the projections from the pericruciate cortex to the pontomedullary brainstem of the cat: a study using the anterograde tracer Phaseolus vulgaris‐leucoagglutinin publication-title: J Comp Neurol – volume: 106 start-page: 918 year: 2009 end-page: 923 article-title: Subdivisions of primary motor cortex based on cortico‐motoneuronal cells publication-title: Proc Natl Acad Sci U S A – volume: 91 start-page: 1 year: 1968a end-page: 14 article-title: The functional organization of the motor system in the monkey. I. The effects of bilateral pyramidal lesions publication-title: Brain – volume: 29 start-page: 4993 year: 2009 end-page: 4999 article-title: Direct and indirect connections with upper limb motoneurons from the primate reticulospinal tract publication-title: J Neurosci – volume: 11 start-page: 667 year: 1991 end-page: 689 article-title: The origin of corticospinal projections from the premotor areas in the frontal lobe publication-title: J Neurosci – volume: 129 start-page: 559 year: 1999 end-page: 572 article-title: The contribution of fast corticospinal input to the voluntary activation of proximal muscles in normal subjects and in stroke patients publication-title: Exp Brain Res – volume: 19 start-page: 1081 year: 2007 end-page: 1088 article-title: Improving lesion‐symptom mapping publication-title: J Cogn Neurosci – volume: 7 start-page: 1756 year: 1996 end-page: 1760 article-title: Cerebral plasticity after stroke as revealed by ipsilateral responses to magnetic stimulation publication-title: Neuroreport – volume: 7 start-page: 13 year: 1975 end-page: 31 article-title: The post‐stroke hemiplegic patient. 1. a method for evaluation of physical performance publication-title: Scand J Rehabil Med – volume: 36 start-page: 1 year: 1979 end-page: 20 article-title: Reticulospinal connections with limb and axial motoneurons publication-title: Exp Brain Res – volume: 119 start-page: 1809 year: 1996 end-page: 1833 article-title: Vestibulospinal, reticulospinal and descending propriospinal nerve fibres in man publication-title: Brain – volume: 41 start-page: 1795 year: 1991 end-page: 1799 article-title: Effects of transcranial magnetic stimulation on ipsilateral muscles publication-title: Neurology – volume: 60 start-page: 389 year: 1937 end-page: 443 article-title: Somatic motor and sensory representation in the cerebral cortex of man as studied by electrical stimulation publication-title: Brain – volume: 62 start-page: 114 year: 2004 end-page: 116 article-title: The acoustic startle reflex in ischemic stroke publication-title: Neurology – volume: 518 start-page: 895 year: 1999 end-page: 906 article-title: Dissociation of the pathways mediating ipsilateral and contralateral motor‐evoked potentials in human hand and arm muscles publication-title: J Physiol – volume: 39 start-page: 7306 year: 2019 end-page: 7320 article-title: Dynamic interaction between cortico‐brainstem pathways during training‐induced recovery in stroke model rats publication-title: J Neurosci – volume: 45 start-page: 1379 year: 2017 end-page: 1395 article-title: Corticobulbar projections from distinct motor cortical areas to the reticular formation in macaque monkeys publication-title: Eur J Neurosci – volume: 74 start-page: 311 year: 1989 end-page: 318 article-title: Distribution of corticospinal neurons with collaterals to the lower brain stem reticular formation in monkey (Macaca fascicularis) publication-title: Exp Brain Res – volume: 36 start-page: 219 year: 2006 end-page: 226 article-title: Does caffeine modify corticomotor excitability? publication-title: Neurophysiol Clin – volume: 120 start-page: 1579 year: 1997 end-page: 1586 article-title: Reorganization of motor output in the non‐affected hemisphere after stroke publication-title: Brain – volume: 64 start-page: 782 year: 1990 end-page: 795 article-title: Functional organization within the medullary reticular formation of intact unanesthetized cat. II. Electromyographic activity evoked by microstimulation publication-title: J Neurophysiol – volume: 34 start-page: 13924 year: 2014 end-page: 13934 article-title: Selective activation of ipsilateral motor pathways in intact humans publication-title: J Neurosci – volume: 108 start-page: 3096 year: 2012 end-page: 3104 article-title: Neck rotation modulates flexion synergy torques, indicating an ipsilateral reticulospinal source for impairment in stroke publication-title: J Neurophysiol – volume: 11 start-page: 473 year: 1984 end-page: 486 article-title: Responses of medullary reticulospinal neurons to sinusoidal rotation of neck in the decerebrate cat publication-title: Neuroscience – volume: 89 start-page: 1256 year: 2003 end-page: 1264 article-title: Organization of ipsilateral excitatory and inhibitory pathways in the human motor cortex publication-title: J Neurophysiol – year: 2020 – volume: 118 start-page: 2050 year: 2007 end-page: 2062 article-title: Side of lesion influences bilateral activation in chronic, post‐stroke hemiparesis publication-title: Clin Neurophysiol – volume: 101 start-page: 306 year: 2009 end-page: 314 article-title: Differential effects of startle on reaction time for finger and arm movements publication-title: J Neurophysiol – volume: 135 start-page: 2277 year: 2012 end-page: 2289 article-title: Changes in descending motor pathway connectivity after corticospinal tract lesion in macaque monkey publication-title: Brain – volume: 158 start-page: 385 year: 2004 end-page: 390 article-title: Bilateral responses of upper limb muscles to transcranial magnetic stimulation in human subjects publication-title: Exp Brain Res – start-page: 597 year: 2011 end-page: 666 – volume: 580 start-page: 777 year: 2007 end-page: 786 article-title: Differential control of the scapulothoracic muscles in humans publication-title: J Physiol – volume: 111 start-page: 1990 year: 2000 end-page: 1996 article-title: Ipsilateral activation of the unaffected motor cortex in patients with hemiparetic stroke publication-title: Clin Neurophysiol – volume: 36 start-page: 2605 year: 2016 end-page: 2616 article-title: Corticospinal inputs to primate motoneurons innervating the forelimb from two divisions of primary motor cortex and area 3a publication-title: J Neurosci – volume: 92 start-page: 83 year: 2004 end-page: 95 article-title: Motor outputs from the primate reticular formation to shoulder muscles as revealed by stimulus‐triggered averaging publication-title: J Neurophysiol – volume: 27 start-page: 8053 year: 2007 end-page: 8058 article-title: Bilateral spike‐triggered average effects in arm and shoulder muscles from the monkey pontomedullary reticular formation publication-title: J Neurosci – ident: e_1_2_6_15_1 doi: 10.1016/j.neucli.2006.08.005 – ident: e_1_2_6_8_1 doi: 10.1007/s00221-003-1807-8 – ident: e_1_2_6_31_1 doi: 10.2340/1650197771331 – ident: e_1_2_6_84_1 doi: 10.1523/JNEUROSCI.3371-17.2018 – ident: e_1_2_6_18_1 doi: 10.1016/j.clinph.2007.10.021 – ident: e_1_2_6_36_1 doi: 10.1152/jn.00866.2012 – ident: e_1_2_6_66_1 doi: 10.1523/JNEUROSCI.1107-20.2020 – ident: e_1_2_6_73_1 doi: 10.1523/JNEUROSCI.1648-14.2014 – ident: e_1_2_6_70_1 doi: 10.1007/s00221-007-1169-8 – ident: e_1_2_6_75_1 doi: 10.1007/s002210050926 – ident: e_1_2_6_59_1 doi: 10.1007/BF00238464 – ident: e_1_2_6_26_1 doi: 10.1152/jn.01030.2011 – ident: e_1_2_6_33_1 doi: 10.1152/physrev.2001.81.4.1725 – ident: e_1_2_6_37_1 doi: 10.1523/JNEUROSCI.0649-19.2019 – ident: e_1_2_6_7_1 doi: 10.1007/s00221-004-2031-x – ident: e_1_2_6_22_1 doi: 10.1093/brain/122.7.1327 – ident: e_1_2_6_82_1 doi: 10.1523/JNEUROSCI.4055-15.2016 – ident: e_1_2_6_12_1 doi: 10.1097/00001756-199607290-00012 – ident: e_1_2_6_49_1 doi: 10.1002/(SICI)1096-9861(19970113)377:2<234::AID-CNE6>3.0.CO;2-4 – ident: e_1_2_6_35_1 doi: 10.1152/jn.00852.2014 – ident: e_1_2_6_48_1 doi: 10.1002/(SICI)1096-9861(19971229)389:4<617::AID-CNE6>3.0.CO;2-3 – ident: e_1_2_6_11_1 doi: 10.1152/jn.00365.2010 – ident: e_1_2_6_81_1 doi: 10.1002/cphy.cp010214 – ident: e_1_2_6_57_1 doi: 10.1093/brain/60.4.389 – ident: e_1_2_6_67_1 doi: 10.1177/1545968319850138 – ident: e_1_2_6_23_1 doi: 10.1152/jn.1990.64.3.782 – ident: e_1_2_6_78_1 doi: 10.1007/BF00227284 – ident: e_1_2_6_83_1 doi: 10.1093/brain/aws115 – ident: e_1_2_6_3_1 doi: 10.1113/jphysiol.2006.126276 – ident: e_1_2_6_6_1 doi: 10.1523/JNEUROSCI.3368-16.2017 – ident: e_1_2_6_4_1 doi: 10.1523/JNEUROSCI.4384-13.2014 – ident: e_1_2_6_21_1 doi: 10.1523/JNEUROSCI.0040-07.2007 – ident: e_1_2_6_79_1 doi: 10.1002/ana.10686 – ident: e_1_2_6_72_1 doi: 10.1016/0306-4522(84)90038-1 – ident: e_1_2_6_64_1 doi: 10.1162/jocn.2007.19.7.1081 – ident: e_1_2_6_45_1 doi: 10.1146/annurev.neuro.31.060407.125547 – ident: e_1_2_6_54_1 doi: 10.1007/s00221-013-3639-5 – ident: e_1_2_6_56_1 doi: 10.1093/brain/120.9.1579 – ident: e_1_2_6_77_1 doi: 10.1212/WNL.41.11.1795 – ident: e_1_2_6_16_1 doi: 10.1152/jn.00950.2002 – volume-title: Anatomical guide for the electromyographer: The Limbs and Trunk year: 2011 ident: e_1_2_6_58_1 – ident: e_1_2_6_60_1 doi: 10.1016/0306-4522(84)90142-8 – ident: e_1_2_6_71_1 doi: 10.1113/jphysiol.2011.225169 – ident: e_1_2_6_17_1 doi: 10.1016/j.brs.2010.01.001 – ident: e_1_2_6_63_1 doi: 10.1523/JNEUROSCI.3720-08.2009 – ident: e_1_2_6_51_1 doi: 10.1152/jn.01139.2015 – ident: e_1_2_6_69_1 doi: 10.1007/s10548-005-6033-1 – ident: e_1_2_6_43_1 doi: 10.1093/brain/91.1.1 – ident: e_1_2_6_14_1 doi: 10.1152/jn.00878.2007 – ident: e_1_2_6_46_1 doi: 10.1016/j.clinph.2007.06.010 – ident: e_1_2_6_13_1 doi: 10.1016/S1388-2457(00)00430-2 – ident: e_1_2_6_44_1 doi: 10.1093/brain/91.1.15 – ident: e_1_2_6_39_1 doi: 10.1007/BF00248864 – ident: e_1_2_6_9_1 doi: 10.1002/mus.20817 – ident: e_1_2_6_41_1 doi: 10.1002/cne.901180109 – ident: e_1_2_6_5_1 doi: 10.1113/jphysiol.2011.215160 – ident: e_1_2_6_25_1 – ident: e_1_2_6_28_1 doi: 10.1113/jphysiol.2011.226209 – ident: e_1_2_6_42_1 doi: 10.1002/cphy.cp010213 – ident: e_1_2_6_20_1 doi: 10.1007/s00221-006-0374-1 – ident: e_1_2_6_55_1 doi: 10.1093/brain/119.6.1809 – ident: e_1_2_6_68_1 doi: 10.1152/jn.2001.86.5.2125 – ident: e_1_2_6_85_1 doi: 10.1111/j.1469-7793.1999.0895p.x – ident: e_1_2_6_38_1 doi: 10.1212/01.WNL.0000101711.48946.35 – ident: e_1_2_6_27_1 – ident: e_1_2_6_76_1 doi: 10.1093/brain/74.4.443 – ident: e_1_2_6_80_1 doi: 10.1093/cercor/7.1.18 – ident: e_1_2_6_10_1 doi: 10.1111/j.2517-6161.1995.tb02031.x – ident: e_1_2_6_30_1 doi: 10.1111/ejn.13576 – ident: e_1_2_6_74_1 doi: 10.1002/ar.1091280110 – ident: e_1_2_6_32_1 doi: 10.1093/cercor/4.2.166 – ident: e_1_2_6_24_1 doi: 10.1523/JNEUROSCI.11-03-00667.1991 – ident: e_1_2_6_52_1 doi: 10.1113/JP274968 – ident: e_1_2_6_62_1 doi: 10.1152/jn.00491.2009 – ident: e_1_2_6_53_1 doi: 10.1111/j.1468-1331.2008.02168.x – ident: e_1_2_6_29_1 doi: 10.1523/JNEUROSCI.1379-20.2020 – ident: e_1_2_6_34_1 doi: 10.1016/j.clinph.2019.02.018 – ident: e_1_2_6_40_1 doi: 10.1016/0006-8993(67)90004-2 – ident: e_1_2_6_61_1 doi: 10.1073/pnas.0808362106 – ident: e_1_2_6_2_1 doi: 10.1161/01.STR.32.6.1304 – ident: e_1_2_6_19_1 doi: 10.1152/jn.00083.2003 – ident: e_1_2_6_50_1 doi: 10.1016/j.neuroimage.2006.02.004 – ident: e_1_2_6_47_1 doi: 10.3389/fneur.2017.00627 – ident: e_1_2_6_65_1 doi: 10.1113/JP280156 |
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The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals.
In humans,... The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals. In humans, the... The corticoreticulospinal tract (CReST) is a descending motor pathway that reorganizes after corticospinal tract (CST) injury in animals. In humans, the... The corticoreticulospinal tract (CReST) is a major descending motor pathway in many animals, but little is known about its innervation patterns in proximal and... |
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SubjectTerms | Arm chronic stroke corticoreticulospinal tract corticospinal tract Evoked Potentials, Motor Hand Humans Innervation ipsilateral motor evoked potential Magnetic fields Motor Cortex Motor evoked potentials Muscle, Skeletal Muscles Neural networks Pyramidal tracts Stroke Transcranial Magnetic Stimulation upper extremity |
Title | Corticoreticulospinal tract neurophysiology in an arm and hand muscle in healthy and stroke subjects |
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