Functional magnetic resonance imaging exploration of combined hand and speech movements in Parkinson's disease

Among the repertoire of motor functions, although hand movement and speech production tasks have been investigated widely by functional neuroimaging, paradigms combining both movements have been studied less so. Such paradigms are of particular interest in Parkinson's disease, in which patients...

Full description

Saved in:
Bibliographic Details
Published in:Movement disorders Vol. 26; no. 12; pp. 2212 - 2219
Main Authors: Pinto, Serge, Mancini, Laura, Jahanshahi, Marjan, Thornton, John S., Tripoliti, Elina, Yousry, Tarek A., Limousin, Patricia
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.10.2011
Wiley
Subjects:
ISSN:0885-3185, 1531-8257, 1531-8257
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Among the repertoire of motor functions, although hand movement and speech production tasks have been investigated widely by functional neuroimaging, paradigms combining both movements have been studied less so. Such paradigms are of particular interest in Parkinson's disease, in which patients have specific difficulties performing two movements simultaneously. In 9 unmedicated patients with Parkinson's disease and 15 healthy control subjects, externally cued tasks (i.e., hand movement, speech production, and combined hand movement and speech production) were performed twice in a random order and functional magnetic resonance imaging detected cerebral activations, compared to the rest. F‐statistics tested within‐group (significant activations at P values < 0.05, familywise error corrected), between‐group, and between‐task comparisons (regional activations significant at P values < 0.001, uncorrected, with cluster size > 10 voxels). For control subjects, the combined task activations comprised the sum of those obtained during hand movement and speech production performed separately, reflecting the neural correlates of performing movements sharing similar programming modalities. In patients with Parkinson's disease, only activations underlying hand movement were observed during the combined task. We interpreted this phenomenon as patients' potential inability to recruit facilitatory activations while performing two movements simultaneously. This lost capacity could be related to a functional prioritization of one movement (i.e., hand movement), in comparison with the other (i.e., speech production). Our observation could also reflect the inability of patients with Parkinson's disease to intrinsically engage the motor coordination necessary to perform a combined task. © 2011 Movement Disorder Society
AbstractList Among the repertoire of motor functions, although hand movement and speech production tasks have been investigated widely by functional neuroimaging, paradigms combining both movements have been studied less so. Such paradigms are of particular interest in Parkinson's disease, in which patients have specific difficulties performing two movements simultaneously. In 9 unmedicated patients with Parkinson's disease and 15 healthy control subjects, externally cued tasks (i.e., hand movement, speech production, and combined hand movement and speech production) were performed twice in a random order and functional magnetic resonance imaging detected cerebral activations, compared to the rest. F‐statistics tested within‐group (significant activations at P values < 0.05, familywise error corrected), between‐group, and between‐task comparisons (regional activations significant at P values < 0.001, uncorrected, with cluster size > 10 voxels). For control subjects, the combined task activations comprised the sum of those obtained during hand movement and speech production performed separately, reflecting the neural correlates of performing movements sharing similar programming modalities. In patients with Parkinson's disease, only activations underlying hand movement were observed during the combined task. We interpreted this phenomenon as patients' potential inability to recruit facilitatory activations while performing two movements simultaneously. This lost capacity could be related to a functional prioritization of one movement (i.e., hand movement), in comparison with the other (i.e., speech production). Our observation could also reflect the inability of patients with Parkinson's disease to intrinsically engage the motor coordination necessary to perform a combined task. © 2011 Movement Disorder Society
Among the repertoire of motor functions, although hand movement and speech production tasks have been investigated widely by functional neuroimaging, paradigms combining both movements have been studied less so. Such paradigms are of particular interest in Parkinson's disease, in which patients have specific difficulties performing two movements simultaneously. In 9 unmedicated patients with Parkinson's disease and 15 healthy control subjects, externally cued tasks (i.e., hand movement, speech production, and combined hand movement and speech production) were performed twice in a random order and functional magnetic resonance imaging detected cerebral activations, compared to the rest. F-statistics tested within-group (significant activations at P values < 0.05, familywise error corrected), between-group, and between-task comparisons (regional activations significant at P values < 0.001, uncorrected, with cluster size > 10 voxels). For control subjects, the combined task activations comprised the sum of those obtained during hand movement and speech production performed separately, reflecting the neural correlates of performing movements sharing similar programming modalities. In patients with Parkinson's disease, only activations underlying hand movement were observed during the combined task. We interpreted this phenomenon as patients' potential inability to recruit facilitatory activations while performing two movements simultaneously. This lost capacity could be related to a functional prioritization of one movement (i.e., hand movement), in comparison with the other (i.e., speech production). Our observation could also reflect the inability of patients with Parkinson's disease to intrinsically engage the motor coordination necessary to perform a combined task.Among the repertoire of motor functions, although hand movement and speech production tasks have been investigated widely by functional neuroimaging, paradigms combining both movements have been studied less so. Such paradigms are of particular interest in Parkinson's disease, in which patients have specific difficulties performing two movements simultaneously. In 9 unmedicated patients with Parkinson's disease and 15 healthy control subjects, externally cued tasks (i.e., hand movement, speech production, and combined hand movement and speech production) were performed twice in a random order and functional magnetic resonance imaging detected cerebral activations, compared to the rest. F-statistics tested within-group (significant activations at P values < 0.05, familywise error corrected), between-group, and between-task comparisons (regional activations significant at P values < 0.001, uncorrected, with cluster size > 10 voxels). For control subjects, the combined task activations comprised the sum of those obtained during hand movement and speech production performed separately, reflecting the neural correlates of performing movements sharing similar programming modalities. In patients with Parkinson's disease, only activations underlying hand movement were observed during the combined task. We interpreted this phenomenon as patients' potential inability to recruit facilitatory activations while performing two movements simultaneously. This lost capacity could be related to a functional prioritization of one movement (i.e., hand movement), in comparison with the other (i.e., speech production). Our observation could also reflect the inability of patients with Parkinson's disease to intrinsically engage the motor coordination necessary to perform a combined task.
Among the repertoire of motor functions, although hand movement and speech production tasks have been investigated widely by functional neuroimaging, paradigms combining both movements have been studied less so. Such paradigms are of particular interest in Parkinson's disease, in which patients have specific difficulties performing two movements simultaneously. In 9 unmedicated patients with Parkinson's disease and 15 healthy control subjects, externally cued tasks (i.e., hand movement, speech production, and combined hand movement and speech production) were performed twice in a random order and functional magnetic resonance imaging detected cerebral activations, compared to the rest. F-statistics tested within-group (significant activations at P values < 0.05, familywise error corrected), between-group, and between-task comparisons (regional activations significant at P values < 0.001, uncorrected, with cluster size > 10 voxels). For control subjects, the combined task activations comprised the sum of those obtained during hand movement and speech production performed separately, reflecting the neural correlates of performing movements sharing similar programming modalities. In patients with Parkinson's disease, only activations underlying hand movement were observed during the combined task. We interpreted this phenomenon as patients' potential inability to recruit facilitatory activations while performing two movements simultaneously. This lost capacity could be related to a functional prioritization of one movement (i.e., hand movement), in comparison with the other (i.e., speech production). Our observation could also reflect the inability of patients with Parkinson's disease to intrinsically engage the motor coordination necessary to perform a combined task.
Author Jahanshahi, Marjan
Limousin, Patricia
Thornton, John S.
Pinto, Serge
Yousry, Tarek A.
Mancini, Laura
Tripoliti, Elina
Author_xml – sequence: 1
  givenname: Serge
  surname: Pinto
  fullname: Pinto, Serge
  email: serge.pinto@lpl-aix.fr
  organization: Laboratoire Parole et Langage, Aix-en-Provence, France
– sequence: 2
  givenname: Laura
  surname: Mancini
  fullname: Mancini, Laura
  organization: Queen Square Imaging Center, London, United Kingdom
– sequence: 3
  givenname: Marjan
  surname: Jahanshahi
  fullname: Jahanshahi, Marjan
  organization: Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London, United Kingdom
– sequence: 4
  givenname: John S.
  surname: Thornton
  fullname: Thornton, John S.
  organization: Lysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, UCLH NHS Trust, London, United Kingdom
– sequence: 5
  givenname: Elina
  surname: Tripoliti
  fullname: Tripoliti, Elina
  organization: Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London, United Kingdom
– sequence: 6
  givenname: Tarek A.
  surname: Yousry
  fullname: Yousry, Tarek A.
  organization: Queen Square Imaging Center, London, United Kingdom
– sequence: 7
  givenname: Patricia
  surname: Limousin
  fullname: Limousin, Patricia
  organization: Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London, United Kingdom
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24704436$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/21714000$$D View this record in MEDLINE/PubMed
BookMark eNp9kU9v1DAQxS3Uim4LB74A8gVVHNKOY8d2jqiw_aO2IAGCm-U4k9aQOFs7C-23x9vdFgmJHkYjjX7vSfPeLtkKY0BCXjE4YADl4dCmg5Krun5GZqzirNBlpbbIDLSuCs50tUN2U_oBwFjF5HOyUzLFBADMSJgvg5v8GGxPB3sVcPKORkz5EBxSn28-XFG8XfRjtCuQjh1149D4gC29tqGlq0kLRHdNh_EXDhimRH2gn2z86UO22k-09Qltwhdku7N9wpebvUe-zj98OTopzj8enx69Oy-cqHldcIDaMdSixLYCQMld07TQQIdaN6xEZJ1qtZaVRN6VWjagWNPKWiiHiiu-R_bXvos43iwxTWbwyWHf24DjMpkaQHLNVZXJ1xty2QzYmkXMP8c78xBRBt5sAJuc7buYg_HpLycUCMFl5t6uORfHlCJ2jwgDs6rJ5JrMfU2ZPfyHdX66T3eK1vdPKX77Hu_-b20u3n9-UBRrhU8T3j4qcidG5ogq8-3y2JxpNT8Rojbf-R-wj7MH
CitedBy_id crossref_primary_10_3389_fnhum_2023_1250114
crossref_primary_10_1016_j_parkreldis_2021_04_025
crossref_primary_10_3389_fneur_2020_00127
crossref_primary_10_2217_nmt_15_16
crossref_primary_10_1038_s41531_022_00286_y
crossref_primary_10_1212_WNL_0000000000012878
crossref_primary_10_3389_fnhum_2024_1383714
crossref_primary_10_1038_s41531_023_00495_z
crossref_primary_10_1371_journal_pone_0049056
crossref_primary_10_1038_s41531_019_0092_6
crossref_primary_10_1002_hbm_22397
crossref_primary_10_1016_j_neures_2014_10_004
crossref_primary_10_1111_cns_13304
crossref_primary_10_1038_s41598_021_01386_0
crossref_primary_10_1002_hbm_22748
crossref_primary_10_1016_j_nicl_2023_103399
crossref_primary_10_1016_j_jcomdis_2021_106149
crossref_primary_10_1016_j_nicl_2020_102285
crossref_primary_10_1371_journal_pone_0056133
crossref_primary_10_1007_s11682_016_9588_4
crossref_primary_10_1002_mds_27791
crossref_primary_10_1016_j_wocn_2017_01_009
crossref_primary_10_3917_rfla_172_0019
crossref_primary_10_1002_mds_28468
crossref_primary_10_1016_j_bspc_2014_04_009
Cites_doi 10.1016/j.neuroimage.2006.11.047
10.1016/S1471-1931(00)00028-8
10.1002/mds.20958
10.1093/brain/awh569
10.1016/0306-4522(94)90536-3
10.1093/brain/123.2.394
10.1159/000314357
10.1136/jnnp.2007.126599
10.1016/0166-2236(90)90107-L
10.1093/brain/118.4.913
10.1093/brain/awh074
10.1093/brain/awl162
10.1002/hbm.20859
10.1037/0033-2909.116.2.220
10.1136/jnnp.51.6.745
10.1111/j.1600-0404.2007.00818.x
10.1016/j.tins.2008.02.011
10.1002/mds.21548
10.1016/S0093-934X(02)00002-0
10.1093/brain/awf036
10.1111/j.1468-1331.2009.02612.x
10.1002/mds.22296
10.1523/JNEUROSCI.5441-06.2007
10.1016/j.neuroimage.2005.12.024
10.1002/mds.22219
10.1044/1058-0360(2008/08-0004)
10.1212/WNL.60.3.432
10.1002/1531-8249(200008)48:2<268::AID-ANA21>3.0.CO;2-4
10.1016/j.jns.2008.06.024
10.1002/hbm.460020402
10.1016/S1053-8119(03)00059-4
ContentType Journal Article
Copyright Copyright © 2011 Movement Disorder Society
2015 INIST-CNRS
Copyright © 2011 Movement Disorder Society.
Copyright_xml – notice: Copyright © 2011 Movement Disorder Society
– notice: 2015 INIST-CNRS
– notice: Copyright © 2011 Movement Disorder Society.
DBID BSCLL
AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1002/mds.23799
DatabaseName Istex
CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList CrossRef

MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1531-8257
EndPage 2219
ExternalDocumentID 21714000
24704436
10_1002_mds_23799
MDS23799
ark_67375_WNG_J87FH449_X
Genre article
Research Support, Non-U.S. Gov't
Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NINDS NIH HHS
  grantid: R01-NS40856-02
– fundername: Department of Health
– fundername: Wellcome Trust
– fundername: NINDS NIH HHS
  grantid: R01-NS40902
– fundername: NINDS NIH HHS
  grantid: R01 NS040865
– fundername: NINDS NIH HHS
  grantid: R01 NS040902
GroupedDBID ---
.3N
.GA
.GJ
.Y3
05W
0R~
10A
123
1CY
1L6
1OB
1OC
1ZS
31~
33P
3PY
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5VS
66C
6PF
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
AAESR
AAEVG
AAHQN
AAIPD
AAMMB
AAMNL
AANHP
AANLZ
AAONW
AASGY
AAWTL
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABJNI
ABLJU
ABPVW
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCZN
ACGFS
ACGOF
ACMXC
ACPOU
ACPRK
ACRPL
ACSCC
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
AEFGJ
AEIGN
AEIMD
AENEX
AEUYR
AEYWJ
AFBPY
AFFPM
AFGKR
AFWVQ
AFZJQ
AGHNM
AGQPQ
AGXDD
AGYGG
AHBTC
AHMBA
AIACR
AIDQK
AIDYY
AIQQE
AITYG
AIURR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BSCLL
BY8
C45
CS3
D-6
D-7
D-E
D-F
DCZOG
DPXWK
DR1
DR2
DRFUL
DRMAN
DRSTM
DU5
EBD
EBS
EJD
EMOBN
F00
F01
F04
F5P
FEDTE
FUBAC
FYBCS
G-S
G.N
GNP
GODZA
H.X
HBH
HF~
HGLYW
HHY
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KBYEO
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
M6M
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
PQQKQ
Q.N
Q11
QB0
QRW
R.K
RIWAO
RJQFR
ROL
RX1
RYL
SAMSI
SUPJJ
SV3
TEORI
TWZ
UB1
V2E
V9Y
W8V
W99
WBKPD
WHWMO
WIB
WIH
WIJ
WIK
WJL
WOHZO
WQJ
WVDHM
WXI
WXSBR
XG1
XV2
ZGI
ZZTAW
~IA
~WT
AAYXX
CITATION
O8X
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7X8
ID FETCH-LOGICAL-c4939-3009c1e842ed500e63cbbd0b0fe88b12ee1f7d88656e3f286b071bd6947ce7373
IEDL.DBID DRFUL
ISICitedReferencesCount 34
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000296610900015&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 0885-3185
1531-8257
IngestDate Fri Jul 11 08:09:49 EDT 2025
Mon Jul 21 05:50:49 EDT 2025
Mon Jul 21 09:12:10 EDT 2025
Tue Nov 18 21:01:51 EST 2025
Sat Nov 29 07:04:53 EST 2025
Sun Sep 21 06:19:21 EDT 2025
Sun Sep 21 06:19:07 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 12
Keywords Nervous system diseases
Parkinson's disease
Parkinson disease
Exploration
dual task
speech production
Nuclear magnetic resonance imaging
Hand
Cerebral disorder
Central nervous system disease
Speech
Degenerative disease
functional magnetic resonance imaging
Extrapyramidal syndrome
Functional imaging
hand movement
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
CC BY 4.0
Copyright © 2011 Movement Disorder Society.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4939-3009c1e842ed500e63cbbd0b0fe88b12ee1f7d88656e3f286b071bd6947ce7373
Notes Full financial disclosures and author roles may be found in the online version of this article.
Relevant conflicts of interest/financial disclosures: Nothing to report.
ArticleID:MDS23799
ark:/67375/WNG-J87FH449-X
Funding agencies: Fondation Simone et Cino Del Duca, The Wellcome Trust, Medtronic, National Institutes of Health (Bethesda, MD) contracts RO1-NS40902 (PI: Daniel Corcos) and RO1-NS40856-02 (PI: M.J.), the Parkinson's Disease Society UK, and the Parkinson's Appeal. This work was undertaken at UCLH/UCL, which received a proportion of funding from the Department of Health's NIHR Biomedical Research Centers funding scheme.
istex:7E42461455C59B1B37A4EF0EECE281E61FA5FABB
Nothing to report.
Relevant conflicts of interest/financial disclosures
Funding agencies
Fondation Simone et Cino Del Duca, The Wellcome Trust, Medtronic, National Institutes of Health (Bethesda, MD) contracts RO1‐NS40902 (PI: Daniel Corcos) and RO1‐NS40856‐02 (PI: M.J.), the Parkinson's Disease Society UK, and the Parkinson's Appeal. This work was undertaken at UCLH/UCL, which received a proportion of funding from the Department of Health's NIHR Biomedical Research Centers funding scheme.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/3184369
PMID 21714000
PQID 900638375
PQPubID 23479
PageCount 8
ParticipantIDs proquest_miscellaneous_900638375
pubmed_primary_21714000
pascalfrancis_primary_24704436
crossref_primary_10_1002_mds_23799
crossref_citationtrail_10_1002_mds_23799
wiley_primary_10_1002_mds_23799_MDS23799
istex_primary_ark_67375_WNG_J87FH449_X
PublicationCentury 2000
PublicationDate October 2011
PublicationDateYYYYMMDD 2011-10-01
PublicationDate_xml – month: 10
  year: 2011
  text: October 2011
PublicationDecade 2010
PublicationPlace Hoboken
PublicationPlace_xml – name: Hoboken
– name: Hoboken, NJ
– name: United States
PublicationTitle Movement disorders
PublicationTitleAlternate Mov. Disord
PublicationYear 2011
Publisher Wiley Subscription Services, Inc., A Wiley Company
Wiley
Publisher_xml – name: Wiley Subscription Services, Inc., A Wiley Company
– name: Wiley
References Jahanshahi M, Jenkins HI, Brown RG, Marsden CD, Pasingham RE, Brooks D. Self-initiated versus externally triggered movements. I. An investigation using measurement of regional cerebral blood flow with PET and movement-related potentials in normal and Parkinson's disease subjects. Brain 1995; 118: 913-933.
Gibb WR, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1988; 51: 745-752.
World Medical Association General Assembly. Declaration of Helsinki, Amendment. Tokyo: 2004.
Talairach J, Tournoux P. Co-planar Stereotaxic Atlas of the Human Brain. New York: Thième Medical; 1988.
Wu T, Hallett M. Neural correlates of dual task performance in patients with Parkinson's disease. J Neurol Neurosurg Psychiatry 2008; 79: 760-766.
Pashler H. Dual-task interference in simple tasks: data and theory. Psychol Bull 1994; 116: 101-132.
Graber S, Hertrich I, Daum I, Spieker S, Ackermann H. Speech perception deficits in Parkinson's disease: underestimation of time intervals compromises identification of durational phonetic contrasts. Brain Lang 2002; 82: 65-74.
Rochester L, Nieuwboer A, Baker K, et al. Walking speed during single and dual tasks in Parkinson's disease: which characteristics are important? Mov Disord 2008; 23: 2312-2318.
Wu T, Hallett M. A functional MRI study of automatic movements in patients with Parkinson's disease. Brain 2005; 28: 2250-2259.
Yu H, Sternad D, Corcos DM, Vaillancourt DE. Role of hyperactive cerebellum and motor cortex in Parkinson's disease. Neuroimage 2007; 35: 222-233.
Bloem BR, Grimbergen YA, Cramer M, Valkenburg VV. "Stops walking when talking" does not predict falls in Parkinson's disease. Ann Neurol 2000; 48: 268.
Sachin S, Senthil Kumaran S, Singh S, Goyal V, Shukla G, Mahajan H, Behari M. Functional mapping in PD and PSP for sustained phonation and phoneme tasks. J Neurol Sci 2008; 273: 51-56.
Rektorova I, Barrett J, Mikl M, Rektor I, Paus T. Functional abnormalities in the primary orofacial sensorimotor cortex during speech in Parkinson's disease. Mov Disord 2007; 22: 2043-2051.
Asanuma K, Tang C, Ma Y, et al. Network modulation in the treatment of Parkinson's disease. Brain 2006; 129: 2667-2678.
Trost M, Su S, Su P, et al. Network modulation by the subthalamic nucleus in the treatment of Parkinson's disease. Neuroimage 2006; 31: 301-307.
Aström M, Tripoliti E, Hariz MI, Zrinzo LU, Martinez-Torres I, Limousin P, Wårdell K. Patient-specific model-based investigation of speech intelligibility and movement during deep brain stimulation. Stereotact Funct Neurosurg 2010; 88: 224-233.
Turner RS, Grafton ST, McIntosh AR, DeLong MR, Hoffman JM. The functional anatomy of parkinsonian bradykinesia. Neuroimage 2003; 19: 163-179.
Rowe J, Stephan KE, Friston K, Frackowiak R, Lees A, Passingham R. Attention to action in Parkinson's disease. Impaired effective connectivity among frontal cortical regions. Brain 2002; 125: 276-289.
Ackermann H. Cerebellar contributions to speech production and speech perception: psycholinguistic and neurobiological perspectives. Trends Neurosci 2008; 31: 265-272.
Narayana S, Fox PT, Zhang W, Franklin C, Robin DA, Vogel D, Ramig LO. Neural correlates of efficacy of voice therapy in Parkinson's disease identified by performance-correlation analysis. Hum Brain Map 2010; 31: 222-236.
Purzner J, Paradiso GO, Cunic D, et al. Involvement of the basal ganglia and cerebellar motor pathways in the preparation of self-initiated and externally triggered movements in humans. J Neurosci 2007; 27: 6029-6036.
Sabatini U, Boulanouar K, Fabre N, et al. Cortical motor reorganization in akinetic patients with Parkinson's disease: a functional MRI study. Brain 2000; 23: 394-403.
Pinto S, Thobois S, Costes N, et al. Subthalamic nucleus stimulation and dysarthria in Parkinson's disease: a PET study. Brain 2004; 127: 602-615.
Alexander GE, Crutcher MD. Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci 1990; 13: 266-271.
Tripoliti E, Zrinzo L, Martinez-Torres I, et al. Effects of contact location and voltage amplitude on speech and movement in bilateral subthalamic nucleus deep brain stimulation. Mov Disord 2008; 23: 2377-2383.
Obeso JA, Rodriguez-Oroz MC, Rodriguez M, Lanciego JL, Artieda J, Gonzalo N, Olanow CW. Pathophysiology of the basal ganglia in Parkinson's disease. Trends Neurosci 2000; 23: S8-S19.
Joel D, Weiner I. The organization of the basal ganglia-thalamocortical circuits: open interconnected rather than closed segregated. Neuroscience 1994; 63: 363-379.
Narayana S, Jacks A, Robin DA, et al. A noninvasive imaging approach to understanding speech changes following deep brain stimulation in Parkinson's disease. Am J Speech Lang Pathol 2009; 18: 146-161.
Kopell BH, Rezai AR, Chang JW, Vitek JL. Anatomy and physiology of the basal ganglia: implications for deep brain stimulation for Parkinson's disease. Mov Disord 2006; 21: S238-S246.
Liotti M, Ramig LO, Vogel D, et al. Hypophonia in Parkinson's disease: neural correlates of voice treatment revealed by PET. Neurology 2003; 60: 432-440.
Friston K, Holmes A, Worsley K, Poline J, Frith C, Frackowiak R. Statistical parametric maps in functional imaging: a general linear approach. Hum Brain Map 1995; 2: 189-210.
Beauchet O, Annweiler C, Dubost V, et al. Stops walking when talking: a predictor of falls in older adults? Eur J Neurol 2009; 16: 786-795.
2010; 31
2004; 127
1994; 116
2006; 31
1990; 13
2000; 48
2000; 23
1995; 118
2008; 79
1988; 51
2004
2002; 82
2003; 19
2008; 31
1995; 2
2005; 28
2007; 35
1994; 63
2010; 88
2006; 21
2002; 125
1987
2008; 23
2003; 60
2007; 22
2006; 129
2008; 273
2009; 16
2009; 18
1988
2007; 27
e_1_2_8_27_2
e_1_2_8_28_2
e_1_2_8_29_2
e_1_2_8_23_2
(e_1_2_8_16_2) 2004
e_1_2_8_24_2
e_1_2_8_25_2
e_1_2_8_26_2
e_1_2_8_9_2
Pashler H (e_1_2_8_34_2) 1994; 116
Talairach J (e_1_2_8_18_2) 1988
e_1_2_8_2_2
e_1_2_8_4_2
e_1_2_8_3_2
e_1_2_8_6_2
e_1_2_8_5_2
e_1_2_8_8_2
e_1_2_8_7_2
e_1_2_8_20_2
e_1_2_8_21_2
e_1_2_8_22_2
e_1_2_8_17_2
e_1_2_8_19_2
e_1_2_8_12_2
e_1_2_8_13_2
e_1_2_8_14_2
e_1_2_8_15_2
e_1_2_8_31_2
e_1_2_8_30_2
e_1_2_8_10_2
e_1_2_8_33_2
e_1_2_8_11_2
e_1_2_8_32_2
References_xml – reference: Kopell BH, Rezai AR, Chang JW, Vitek JL. Anatomy and physiology of the basal ganglia: implications for deep brain stimulation for Parkinson's disease. Mov Disord 2006; 21: S238-S246.
– reference: Alexander GE, Crutcher MD. Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci 1990; 13: 266-271.
– reference: Sabatini U, Boulanouar K, Fabre N, et al. Cortical motor reorganization in akinetic patients with Parkinson's disease: a functional MRI study. Brain 2000; 23: 394-403.
– reference: Asanuma K, Tang C, Ma Y, et al. Network modulation in the treatment of Parkinson's disease. Brain 2006; 129: 2667-2678.
– reference: Rektorova I, Barrett J, Mikl M, Rektor I, Paus T. Functional abnormalities in the primary orofacial sensorimotor cortex during speech in Parkinson's disease. Mov Disord 2007; 22: 2043-2051.
– reference: Sachin S, Senthil Kumaran S, Singh S, Goyal V, Shukla G, Mahajan H, Behari M. Functional mapping in PD and PSP for sustained phonation and phoneme tasks. J Neurol Sci 2008; 273: 51-56.
– reference: Rochester L, Nieuwboer A, Baker K, et al. Walking speed during single and dual tasks in Parkinson's disease: which characteristics are important? Mov Disord 2008; 23: 2312-2318.
– reference: Ackermann H. Cerebellar contributions to speech production and speech perception: psycholinguistic and neurobiological perspectives. Trends Neurosci 2008; 31: 265-272.
– reference: Friston K, Holmes A, Worsley K, Poline J, Frith C, Frackowiak R. Statistical parametric maps in functional imaging: a general linear approach. Hum Brain Map 1995; 2: 189-210.
– reference: Purzner J, Paradiso GO, Cunic D, et al. Involvement of the basal ganglia and cerebellar motor pathways in the preparation of self-initiated and externally triggered movements in humans. J Neurosci 2007; 27: 6029-6036.
– reference: Liotti M, Ramig LO, Vogel D, et al. Hypophonia in Parkinson's disease: neural correlates of voice treatment revealed by PET. Neurology 2003; 60: 432-440.
– reference: Pashler H. Dual-task interference in simple tasks: data and theory. Psychol Bull 1994; 116: 101-132.
– reference: Turner RS, Grafton ST, McIntosh AR, DeLong MR, Hoffman JM. The functional anatomy of parkinsonian bradykinesia. Neuroimage 2003; 19: 163-179.
– reference: Rowe J, Stephan KE, Friston K, Frackowiak R, Lees A, Passingham R. Attention to action in Parkinson's disease. Impaired effective connectivity among frontal cortical regions. Brain 2002; 125: 276-289.
– reference: Beauchet O, Annweiler C, Dubost V, et al. Stops walking when talking: a predictor of falls in older adults? Eur J Neurol 2009; 16: 786-795.
– reference: Yu H, Sternad D, Corcos DM, Vaillancourt DE. Role of hyperactive cerebellum and motor cortex in Parkinson's disease. Neuroimage 2007; 35: 222-233.
– reference: Talairach J, Tournoux P. Co-planar Stereotaxic Atlas of the Human Brain. New York: Thième Medical; 1988.
– reference: Obeso JA, Rodriguez-Oroz MC, Rodriguez M, Lanciego JL, Artieda J, Gonzalo N, Olanow CW. Pathophysiology of the basal ganglia in Parkinson's disease. Trends Neurosci 2000; 23: S8-S19.
– reference: Narayana S, Jacks A, Robin DA, et al. A noninvasive imaging approach to understanding speech changes following deep brain stimulation in Parkinson's disease. Am J Speech Lang Pathol 2009; 18: 146-161.
– reference: Aström M, Tripoliti E, Hariz MI, Zrinzo LU, Martinez-Torres I, Limousin P, Wårdell K. Patient-specific model-based investigation of speech intelligibility and movement during deep brain stimulation. Stereotact Funct Neurosurg 2010; 88: 224-233.
– reference: Trost M, Su S, Su P, et al. Network modulation by the subthalamic nucleus in the treatment of Parkinson's disease. Neuroimage 2006; 31: 301-307.
– reference: Jahanshahi M, Jenkins HI, Brown RG, Marsden CD, Pasingham RE, Brooks D. Self-initiated versus externally triggered movements. I. An investigation using measurement of regional cerebral blood flow with PET and movement-related potentials in normal and Parkinson's disease subjects. Brain 1995; 118: 913-933.
– reference: Tripoliti E, Zrinzo L, Martinez-Torres I, et al. Effects of contact location and voltage amplitude on speech and movement in bilateral subthalamic nucleus deep brain stimulation. Mov Disord 2008; 23: 2377-2383.
– reference: Bloem BR, Grimbergen YA, Cramer M, Valkenburg VV. "Stops walking when talking" does not predict falls in Parkinson's disease. Ann Neurol 2000; 48: 268.
– reference: Pinto S, Thobois S, Costes N, et al. Subthalamic nucleus stimulation and dysarthria in Parkinson's disease: a PET study. Brain 2004; 127: 602-615.
– reference: Gibb WR, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1988; 51: 745-752.
– reference: Wu T, Hallett M. A functional MRI study of automatic movements in patients with Parkinson's disease. Brain 2005; 28: 2250-2259.
– reference: Joel D, Weiner I. The organization of the basal ganglia-thalamocortical circuits: open interconnected rather than closed segregated. Neuroscience 1994; 63: 363-379.
– reference: Wu T, Hallett M. Neural correlates of dual task performance in patients with Parkinson's disease. J Neurol Neurosurg Psychiatry 2008; 79: 760-766.
– reference: Narayana S, Fox PT, Zhang W, Franklin C, Robin DA, Vogel D, Ramig LO. Neural correlates of efficacy of voice therapy in Parkinson's disease identified by performance-correlation analysis. Hum Brain Map 2010; 31: 222-236.
– reference: World Medical Association General Assembly. Declaration of Helsinki, Amendment. Tokyo: 2004.
– reference: Graber S, Hertrich I, Daum I, Spieker S, Ackermann H. Speech perception deficits in Parkinson's disease: underestimation of time intervals compromises identification of durational phonetic contrasts. Brain Lang 2002; 82: 65-74.
– volume: 16
  start-page: 786
  year: 2009
  end-page: 795
  article-title: Stops walking when talking: a predictor of falls in older adults?
  publication-title: Eur J Neurol
– volume: 13
  start-page: 266
  year: 1990
  end-page: 271
  article-title: Functional architecture of basal ganglia circuits: neural substrates of parallel processing
  publication-title: Trends Neurosci
– volume: 27
  start-page: 6029
  year: 2007
  end-page: 6036
  article-title: Involvement of the basal ganglia and cerebellar motor pathways in the preparation of self‐initiated and externally triggered movements in humans
  publication-title: J Neurosci
– volume: 273
  start-page: 51
  year: 2008
  end-page: 56
  article-title: Functional mapping in PD and PSP for sustained phonation and phoneme tasks
  publication-title: J Neurol Sci
– volume: 23
  start-page: 394
  year: 2000
  end-page: 403
  article-title: Cortical motor reorganization in akinetic patients with Parkinson's disease: a functional MRI study
  publication-title: Brain
– volume: 48
  start-page: 268
  year: 2000
  article-title: “Stops walking when talking” does not predict falls in Parkinson's disease
  publication-title: Ann Neurol
– volume: 118
  start-page: 913
  year: 1995
  end-page: 933
  article-title: Self‐initiated versus externally triggered movements. I. An investigation using measurement of regional cerebral blood flow with PET and movement‐related potentials in normal and Parkinson's disease subjects
  publication-title: Brain
– volume: 23
  start-page: 2377
  year: 2008
  end-page: 2383
  article-title: Effects of contact location and voltage amplitude on speech and movement in bilateral subthalamic nucleus deep brain stimulation
  publication-title: Mov Disord
– volume: 19
  start-page: 163
  year: 2003
  end-page: 179
  article-title: The functional anatomy of parkinsonian bradykinesia
  publication-title: Neuroimage
– volume: 51
  start-page: 745
  year: 1988
  end-page: 752
  article-title: The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
  publication-title: J Neurol Neurosurg Psychiatry
– volume: 63
  start-page: 363
  year: 1994
  end-page: 379
  article-title: The organization of the basal ganglia‐thalamocortical circuits: open interconnected rather than closed segregated
  publication-title: Neuroscience
– volume: 18
  start-page: 146
  year: 2009
  end-page: 161
  article-title: A noninvasive imaging approach to understanding speech changes following deep brain stimulation in Parkinson's disease
  publication-title: Am J Speech Lang Pathol
– volume: 21
  start-page: S238
  year: 2006
  end-page: S246
  article-title: Anatomy and physiology of the basal ganglia: implications for deep brain stimulation for Parkinson's disease
  publication-title: Mov Disord
– volume: 116
  start-page: 101
  year: 1994
  end-page: 132
  article-title: Dual‐task interference in simple tasks: data and theory
  publication-title: Psychol Bull
– volume: 31
  start-page: 222
  year: 2010
  end-page: 236
  article-title: Neural correlates of efficacy of voice therapy in Parkinson's disease identified by performance‐correlation analysis
  publication-title: Hum Brain Map
– volume: 125
  start-page: 276
  year: 2002
  end-page: 289
  article-title: Attention to action in Parkinson's disease. Impaired effective connectivity among frontal cortical regions
  publication-title: Brain
– volume: 35
  start-page: 222
  year: 2007
  end-page: 233
  article-title: Role of hyperactive cerebellum and motor cortex in Parkinson's disease
  publication-title: Neuroimage
– year: 1988
– year: 2004
– volume: 23
  start-page: S8
  year: 2000
  end-page: S19
  article-title: Pathophysiology of the basal ganglia in Parkinson's disease
  publication-title: Trends Neurosci
– volume: 28
  start-page: 2250
  year: 2005
  end-page: 2259
  article-title: A functional MRI study of automatic movements in patients with Parkinson's disease
  publication-title: Brain
– volume: 129
  start-page: 2667
  year: 2006
  end-page: 2678
  article-title: Network modulation in the treatment of Parkinson's disease
  publication-title: Brain
– volume: 31
  start-page: 301
  year: 2006
  end-page: 307
  article-title: Network modulation by the subthalamic nucleus in the treatment of Parkinson's disease
  publication-title: Neuroimage
– volume: 22
  start-page: 2043
  year: 2007
  end-page: 2051
  article-title: Functional abnormalities in the primary orofacial sensorimotor cortex during speech in Parkinson's disease
  publication-title: Mov Disord
– start-page: 153
  year: 1987
  end-page: 164
– volume: 79
  start-page: 760
  year: 2008
  end-page: 766
  article-title: Neural correlates of dual task performance in patients with Parkinson's disease
  publication-title: J Neurol Neurosurg Psychiatry
– volume: 23
  start-page: 2312
  year: 2008
  end-page: 2318
  article-title: Walking speed during single and dual tasks in Parkinson's disease: which characteristics are important?
  publication-title: Mov Disord
– volume: 31
  start-page: 265
  year: 2008
  end-page: 272
  article-title: Cerebellar contributions to speech production and speech perception: psycholinguistic and neurobiological perspectives
  publication-title: Trends Neurosci
– volume: 82
  start-page: 65
  year: 2002
  end-page: 74
  article-title: Speech perception deficits in Parkinson's disease: underestimation of time intervals compromises identification of durational phonetic contrasts
  publication-title: Brain Lang
– volume: 60
  start-page: 432
  year: 2003
  end-page: 440
  article-title: Hypophonia in Parkinson's disease: neural correlates of voice treatment revealed by PET
  publication-title: Neurology
– volume: 127
  start-page: 602
  year: 2004
  end-page: 615
  article-title: Subthalamic nucleus stimulation and dysarthria in Parkinson's disease: a PET study
  publication-title: Brain
– volume: 2
  start-page: 189
  year: 1995
  end-page: 210
  article-title: Statistical parametric maps in functional imaging: a general linear approach
  publication-title: Hum Brain Map
– volume: 88
  start-page: 224
  year: 2010
  end-page: 233
  article-title: Patient‐specific model‐based investigation of speech intelligibility and movement during deep brain stimulation
  publication-title: Stereotact Funct Neurosurg
– ident: e_1_2_8_7_2
  doi: 10.1016/j.neuroimage.2006.11.047
– ident: e_1_2_8_25_2
  doi: 10.1016/S1471-1931(00)00028-8
– ident: e_1_2_8_26_2
  doi: 10.1002/mds.20958
– ident: e_1_2_8_6_2
  doi: 10.1093/brain/awh569
– ident: e_1_2_8_27_2
  doi: 10.1016/0306-4522(94)90536-3
– ident: e_1_2_8_3_2
  doi: 10.1093/brain/123.2.394
– ident: e_1_2_8_23_2
  doi: 10.1159/000314357
– ident: e_1_2_8_32_2
  doi: 10.1136/jnnp.2007.126599
– ident: e_1_2_8_24_2
  doi: 10.1016/0166-2236(90)90107-L
– ident: e_1_2_8_2_2
  doi: 10.1093/brain/118.4.913
– ident: e_1_2_8_10_2
  doi: 10.1093/brain/awh074
– volume-title: World Medical Association General Assembly. Declaration of Helsinki, Amendment
  year: 2004
  ident: e_1_2_8_16_2
– ident: e_1_2_8_19_2
  doi: 10.1093/brain/awl162
– ident: e_1_2_8_9_2
  doi: 10.1002/hbm.20859
– volume: 116
  start-page: 101
  year: 1994
  ident: e_1_2_8_34_2
  article-title: Dual‐task interference in simple tasks: data and theory
  publication-title: Psychol Bull
  doi: 10.1037/0033-2909.116.2.220
– ident: e_1_2_8_14_2
  doi: 10.1136/jnnp.51.6.745
– ident: e_1_2_8_15_2
  doi: 10.1111/j.1600-0404.2007.00818.x
– ident: e_1_2_8_21_2
  doi: 10.1016/j.tins.2008.02.011
– ident: e_1_2_8_13_2
  doi: 10.1002/mds.21548
– ident: e_1_2_8_28_2
  doi: 10.1016/S0093-934X(02)00002-0
– ident: e_1_2_8_5_2
  doi: 10.1093/brain/awf036
– ident: e_1_2_8_30_2
  doi: 10.1111/j.1468-1331.2009.02612.x
– ident: e_1_2_8_22_2
  doi: 10.1002/mds.22296
– ident: e_1_2_8_29_2
  doi: 10.1523/JNEUROSCI.5441-06.2007
– ident: e_1_2_8_20_2
  doi: 10.1016/j.neuroimage.2005.12.024
– ident: e_1_2_8_33_2
  doi: 10.1002/mds.22219
– ident: e_1_2_8_11_2
  doi: 10.1044/1058-0360(2008/08-0004)
– ident: e_1_2_8_8_2
  doi: 10.1212/WNL.60.3.432
– ident: e_1_2_8_31_2
  doi: 10.1002/1531-8249(200008)48:2<268::AID-ANA21>3.0.CO;2-4
– ident: e_1_2_8_12_2
  doi: 10.1016/j.jns.2008.06.024
– ident: e_1_2_8_17_2
  doi: 10.1002/hbm.460020402
– ident: e_1_2_8_4_2
  doi: 10.1016/S1053-8119(03)00059-4
– volume-title: Co‐planar Stereotaxic Atlas of the Human Brain
  year: 1988
  ident: e_1_2_8_18_2
SSID ssj0011516
Score 2.1885536
Snippet Among the repertoire of motor functions, although hand movement and speech production tasks have been investigated widely by functional neuroimaging, paradigms...
SourceID proquest
pubmed
pascalfrancis
crossref
wiley
istex
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 2212
SubjectTerms Acoustic Stimulation
Adult
Aged
Biological and medical sciences
Brain - blood supply
Brain - pathology
Brain - physiopathology
Brain Mapping
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
dual task
Female
Functional Laterality
functional magnetic resonance imaging
Hand - physiopathology
hand movement
Humans
Image Processing, Computer-Assisted
Magnetic Resonance Imaging - methods
Male
Medical sciences
Middle Aged
Movement - physiology
Neurology
Neuropsychological Tests
Oxygen - blood
Parkinson Disease - pathology
Parkinson Disease - physiopathology
Parkinson's disease
Photic Stimulation
Psychomotor Performance - physiology
Speech
speech production
Title Functional magnetic resonance imaging exploration of combined hand and speech movements in Parkinson's disease
URI https://api.istex.fr/ark:/67375/WNG-J87FH449-X/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmds.23799
https://www.ncbi.nlm.nih.gov/pubmed/21714000
https://www.proquest.com/docview/900638375
Volume 26
WOSCitedRecordID wos000296610900015&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVWIB
  databaseName: Wiley Online Library Full Collection 2020
  customDbUrl:
  eissn: 1531-8257
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0011516
  issn: 0885-3185
  databaseCode: DRFUL
  dateStart: 19990101
  isFulltext: true
  titleUrlDefault: https://onlinelibrary.wiley.com
  providerName: Wiley-Blackwell
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB61uwhxobwJj5WFEHAJTWxvbKsnRAkVoisEVOzNih2nXYlNqmaL-PmMnUe1UpGQOETKwU7i8Uzmsz3zDcBLYQ2nhRJxZksW8yyzseGqiguO6L9QlhllQrEJsVjI5VJ92YGDIRem44cYN9y8ZYT_tTfwwrT7V6Sh67J9S5lQahemFPWWT2B6-DU_-TweIqAzyzoQOQ9JwgOxUEL3x85b7mjqJfvbh0cWLUqo6kpbXIc9t6Fs8EX53n-N4g7c7iEoedfpzF3YcfU9uHncH7LfhzpHX9dtEZJ1cVr7NEeCq_LGc3M4slqHwkbEhei9MLGkqQi-GBfZriR-K574qz13zp6RdRMoyTctWdXEJ1mHfLPXLenPhh7ASf7h-_ujuC_LEFuumI-USJRNneTUlfMkcRmzxpSJSSonpUmpc2klSikRKTpWUZkZhDGmzBQX1gkm2EOY1E3tHgORwiBgEmXlecVSi1jVL7dUxV1iDK50IngzzI62PWe5L53xU3dsy1Sj_HSQXwQvxqbnHVHHdY1ehSkeW-CgfWSbmOsfi4_6kxT5EedKLyOYbenA2IFykXDOsgjIoBQaDdKfshS1ay5brQIKxEdG8KhTlqvOvto8-iAcVtCJv3-oPj78Fm6e_HvTp3CLDgGK6TOYbC4u3XO4YX9tVu3FDHbFUs56E_kD82QS6g
linkProvider Wiley-Blackwell
linkToHtml http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB6VXUS58H6ER7EQAi6hieONbYkLooQFdlcIWnVvVuw4ZSU2qZot4uczdh7VSkVC4hApBzuJ7ZnM5_HMNwAvuNGM5pKHqSmSkKWpCTWTZZgzRP-5NImW2heb4IuFWC7l1x142-fCtPwQg8PNaYb_XzsFdw7p_QvW0HXRvKEJl_IKjBmK0WQE44Nv2dFsOEVAa5a2KHLis4R7ZqGI7g-dt-zR2E3tbxcfmTc4RWVb2-Iy8LmNZb0xym7-3zBuwY0OhJJ3rdTchh1b3YFr8-6Y_S5UGVq71klI1vlJ5RIdCe7La8fOYclq7UsbEevj9_zSkrok-GbcZtuCOGc8cVdzaq35Qda1JyXfNGRVEZdm7TPOXjWkOx26B0fZh8P307ArzBAaJhMXKxFJE1vBqC0mUWTTxGhdRDoqrRA6ptbGJS-EQKxok5KKVCOQ0UUqGTeWJzy5D6OqruxDIIJrhEy8KB2zWGwQrboNlyyZjbTGvU4Ar_vlUaZjLXfFM36qlm-ZKpw_5ecvgOdD09OWquOyRi_9Gg8tcNAuto1P1PHio_oseDZlTKplAHtbQjB0oIxHjCVpAKSXCoUq6c5Z8srW542SHgfiIwN40ErLRWdXbx6tEA7LC8XfP1TND777m0f_3vQZ7E4P5zM1-7T48hiu0z5cMX4Co83ZuX0KV82vzao52-s05Q_jzRXy
linkToPdf http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB6VLqq4lDekQLEQAi6heXjjWOKCWEKBdlUBVfdmxc6kXYlNVs226s9n7DyqlYqExCFSDnYS2zOZb-yZbwBeC6N5lEvhJ6aIfZ4kxtdcln7OCf3n0sRaaldsQkyn6WwmjzbgQ58L0_JDDBtuVjPc_9oqOC6Lcu-aNXRRNO-jWEh5C0Z8LBNSy9HkR3Z8MJwikDVLWhQ5dlnCPbNQEO0Nndfs0chO7ZWNj8wbmqKyrW1xE_hcx7LOGGV3_28Y92C7A6HsYys192EDqwewddgdsz-EKiNr124SskV-WtlER0Z-eW3ZOZDNF660EUMXv-eWltUlozeTm40Fs5vxzF7NEtGcsUXtSMlXDZtXzKZZu4yztw3rTocewXH2-denfb8rzOAbLmMbKxFIE2LKIyzGQYBJbLQuAh2UmKY6jBDDUhRpSlgR4zJKE01ARheJ5MKgiEX8GDarusKnwFKhCTKJorTMYqEhtGodLllyDLQmX8eDd_3yKNOxltviGb9Vy7ccKZo_5ebPg1dD02VL1XFTozdujYcWNGgb2ybG6mT6RX1LRbbPuVQzD3bXhGDoEHERcB4nHrBeKhSppD1nySusLxolHQ6kR3rwpJWW68623jxZIRqWE4q_f6g6nPx0Nzv_3vQlbB1NMnXwdfr9GdyJ-mjF8Dlsrs4v8AXcNpereXO-2ynKH1CHFW0
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Functional+magnetic+resonance+imaging+exploration+of+combined+hand+and+speech+movements+in+Parkinson%27s+disease&rft.jtitle=Movement+disorders&rft.au=Pinto%2C+Serge&rft.au=Mancini%2C+Laura&rft.au=Jahanshahi%2C+Marjan&rft.au=Thornton%2C+John+S&rft.date=2011-10-01&rft.issn=1531-8257&rft.eissn=1531-8257&rft.volume=26&rft.issue=12&rft.spage=2212&rft_id=info:doi/10.1002%2Fmds.23799&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0885-3185&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0885-3185&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0885-3185&client=summon