Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks
Aim Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene. Methods Ten SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological examination. A beamformer algorithm reconstructed the acti...
Saved in:
Published in | Neurological sciences Vol. 40; no. 5; pp. 979 - 984 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
01.05.2019
Springer Nature B.V Springer Verlag |
Subjects | |
Online Access | Get full text |
ISSN | 1590-1874 1590-3478 1590-3478 |
DOI | 10.1007/s10072-019-3725-y |
Cover
Abstract | Aim
Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.
Methods
Ten SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological examination. A beamformer algorithm reconstructed the activity of 90 brain areas. The phase lag index was used to estimate synchrony between brain areas. The minimum spanning tree was used to estimate topological metrics such as the leaf fraction (a measure of network integration) and the degree divergence (a measure of the resilience of the network against pathological events). The betweenness centrality (a measure to estimate the centrality of the brain areas) was used to estimate the centrality of each brain area.
Results
Our results showed topological rearrangements in the beta band. Specifically, the degree divergence was lower in patients as compared to controls and this parameter related to clinical disability. No differences appeared in leaf fraction nor in betweenness centrality.
Conclusion
Mutations in the SPAST gene are related to a reorganization of the brain topology. |
---|---|
AbstractList | AimOur aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.MethodsTen SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological examination. A beamformer algorithm reconstructed the activity of 90 brain areas. The phase lag index was used to estimate synchrony between brain areas. The minimum spanning tree was used to estimate topological metrics such as the leaf fraction (a measure of network integration) and the degree divergence (a measure of the resilience of the network against pathological events). The betweenness centrality (a measure to estimate the centrality of the brain areas) was used to estimate the centrality of each brain area.ResultsOur results showed topological rearrangements in the beta band. Specifically, the degree divergence was lower in patients as compared to controls and this parameter related to clinical disability. No differences appeared in leaf fraction nor in betweenness centrality.ConclusionMutations in the SPAST gene are related to a reorganization of the brain topology. Aim Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene. Methods Ten SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological examination. A beamformer algorithm reconstructed the activity of 90 brain areas. The phase lag index was used to estimate synchrony between brain areas. The minimum spanning tree was used to estimate topological metrics such as the leaf fraction (a measure of network integration) and the degree divergence (a measure of the resilience of the network against pathological events). The betweenness centrality (a measure to estimate the centrality of the brain areas) was used to estimate the centrality of each brain area. Results Our results showed topological rearrangements in the beta band. Specifically, the degree divergence was lower in patients as compared to controls and this parameter related to clinical disability. No differences appeared in leaf fraction nor in betweenness centrality. Conclusion Mutations in the SPAST gene are related to a reorganization of the brain topology. Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.AIMOur aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.Ten SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological examination. A beamformer algorithm reconstructed the activity of 90 brain areas. The phase lag index was used to estimate synchrony between brain areas. The minimum spanning tree was used to estimate topological metrics such as the leaf fraction (a measure of network integration) and the degree divergence (a measure of the resilience of the network against pathological events). The betweenness centrality (a measure to estimate the centrality of the brain areas) was used to estimate the centrality of each brain area.METHODSTen SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological examination. A beamformer algorithm reconstructed the activity of 90 brain areas. The phase lag index was used to estimate synchrony between brain areas. The minimum spanning tree was used to estimate topological metrics such as the leaf fraction (a measure of network integration) and the degree divergence (a measure of the resilience of the network against pathological events). The betweenness centrality (a measure to estimate the centrality of the brain areas) was used to estimate the centrality of each brain area.Our results showed topological rearrangements in the beta band. Specifically, the degree divergence was lower in patients as compared to controls and this parameter related to clinical disability. No differences appeared in leaf fraction nor in betweenness centrality.RESULTSOur results showed topological rearrangements in the beta band. Specifically, the degree divergence was lower in patients as compared to controls and this parameter related to clinical disability. No differences appeared in leaf fraction nor in betweenness centrality.Mutations in the SPAST gene are related to a reorganization of the brain topology.CONCLUSIONMutations in the SPAST gene are related to a reorganization of the brain topology. Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene. Ten SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological examination. A beamformer algorithm reconstructed the activity of 90 brain areas. The phase lag index was used to estimate synchrony between brain areas. The minimum spanning tree was used to estimate topological metrics such as the leaf fraction (a measure of network integration) and the degree divergence (a measure of the resilience of the network against pathological events). The betweenness centrality (a measure to estimate the centrality of the brain areas) was used to estimate the centrality of each brain area. Our results showed topological rearrangements in the beta band. Specifically, the degree divergence was lower in patients as compared to controls and this parameter related to clinical disability. No differences appeared in leaf fraction nor in betweenness centrality. Mutations in the SPAST gene are related to a reorganization of the brain topology. |
Author | Sorrentino, Giuseppe Jacini, Francesca Vettoliere, Antonio Rucco, Rosaria Baselice, Fabio Criscuolo, Chiara Antenora, Antonella Mandolesi, Laura De Michele, Giuseppe Liparoti, Marianna Sorrentino, Pierpaolo |
Author_xml | – sequence: 1 givenname: Rosaria surname: Rucco fullname: Rucco, Rosaria organization: Department of Science and Technology, University of Naples Parthenope, Institute of Applied Sciences and Intelligent Systems, CNR – sequence: 2 givenname: Marianna surname: Liparoti fullname: Liparoti, Marianna organization: Department of Motor Sciences and Wellness, University of Naples Parthenope – sequence: 3 givenname: Francesca surname: Jacini fullname: Jacini, Francesca organization: Department of Motor Sciences and Wellness, University of Naples Parthenope, Hermitage-Capodimonte Hospital – sequence: 4 givenname: Fabio surname: Baselice fullname: Baselice, Fabio organization: Department of Engineering, University of Naples Parthenope – sequence: 5 givenname: Antonella surname: Antenora fullname: Antenora, Antonella organization: Department of Neurosciences, Reproductive, and Odontostomatological Sciences, University of Naples Federico II – sequence: 6 givenname: Giuseppe surname: De Michele fullname: De Michele, Giuseppe organization: Department of Neurosciences, Reproductive, and Odontostomatological Sciences, University of Naples Federico II – sequence: 7 givenname: Chiara surname: Criscuolo fullname: Criscuolo, Chiara email: sky569@hotmail.com organization: Department of Neurosciences, Reproductive, and Odontostomatological Sciences, University of Naples Federico II – sequence: 8 givenname: Antonio surname: Vettoliere fullname: Vettoliere, Antonio organization: Institute of Applied Sciences and Intelligent Systems, CNR – sequence: 9 givenname: Laura surname: Mandolesi fullname: Mandolesi, Laura organization: Department of Humanistic Studies, University of Naples Federico II – sequence: 10 givenname: Giuseppe surname: Sorrentino fullname: Sorrentino, Giuseppe email: giuseppe.sorrentino@uniparthenope.it organization: Department of Motor Sciences and Wellness, University of Naples Parthenope, Hermitage-Capodimonte Hospital – sequence: 11 givenname: Pierpaolo surname: Sorrentino fullname: Sorrentino, Pierpaolo organization: Institute of Applied Sciences and Intelligent Systems, CNR, Department of Engineering, University of Naples Parthenope |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30737580$$D View this record in MEDLINE/PubMed https://hal.science/hal-03599058$$DView record in HAL |
BookMark | eNp9Uk1v1DAQjVAR_YAfwAVZ4lIOAdux4-SCtKqAIi0CqeVseZ1J1sW1g-0U7X_gR-MoWworwWU8mnnvzYfntDhy3kFRPCf4NcFYvImzpSUmbVkJysvdo-KE8BaXFRPN0d4njWDHxWmMNxhjwkj1pDiusKgEb_BJ8fPTlFQy3kVkHEpbQFdfVlfXaAAHSKspGjegLQToTFJhh-KoYjIajSqo0cJgFFIBUACrEnQoeTRYv1E2e6O3fjA6-8omCA9VNkFl209Oz6Gcd5B--PAtPi0e98pGeLZ_z4qv799dX1yW688fPl6s1qXmmKWSd5QzranaaNxzrhmrsWY1EOh72rBNW1cdbftOVFwLjQlpWiwaLnrVKEp7VZ0VbxfdcdrcQqfBpaCsHIO5zTNKr4z8O-PMVg7-TtZ5rzVjWeDVIrA9oF2u1nKO4Yq3LebNHcnY832x4L9PEJO8NVGDtcqBn6KklFQtpS2boS8PoDd-CnlDGUWEYKytCc2oF392_7v-_admgFgAOvgYA_RSm-WT8zDGSoLlfDhyOR-Zz0fO5yN3mUkOmPfi_-PQhRMz1g0QHpr-N-kXTS3Z-A |
CitedBy_id | crossref_primary_10_1007_s00415_020_10387_4 crossref_primary_10_1089_brain_2019_0705 crossref_primary_10_1007_s10072_021_05437_2 crossref_primary_10_1145_3464423 crossref_primary_10_1038_s41598_023_49588_y crossref_primary_10_1002_jnr_24898 crossref_primary_10_1111_ejn_16442 crossref_primary_10_1007_s10072_020_04287_8 crossref_primary_10_3923_ijp_2022_1296_1308 crossref_primary_10_3389_fneur_2019_00967 crossref_primary_10_1089_brain_2020_0741 crossref_primary_10_3390_s24072301 crossref_primary_10_1016_j_neurobiolaging_2023_08_003 crossref_primary_10_1089_brain_2020_0985 crossref_primary_10_3389_fpsyg_2020_550749 crossref_primary_10_1016_j_neuroimage_2021_118253 crossref_primary_10_1016_j_clinph_2024_04_003 crossref_primary_10_1038_s41598_021_83425_4 crossref_primary_10_1212_WNL_0000000000201200 |
Cites_doi | 10.1038/nrn3801 10.1212/01.wnl.0000344303.72193.d5 10.1006/nimg.2001.0978 10.1016/j.neuroimage.2014.10.015 10.1093/hmg/9.4.637 10.1088/0031-9155/48/22/002 10.1038/sj.ejhg.5200528 10.1016/j.neuroimage.2012.10.001 10.1002/humu.9340 10.1002/hbm.1058 10.3233/RNN-2012-120227 10.1016/j.nicl.2018.08.001 10.1088/1741-2560/13/3/036015 10.2307/2346101 10.1093/brain/awv178 10.1371/journal.pone.0117666 10.1371/journal.pone.0036505 10.1016/j.jns.2012.03.025 10.1111/j.1468-1331.2004.00888.x 10.1002/hbm.21424 10.1093/cercor/bhn102 10.1002/mds.23211 10.1136/jnnp.44.10.871 10.1090/S0002-9939-1956-0078686-7 10.1002/hbm.20346 10.1016/j.neurol.2017.03.034 10.1155/2011/156869 10.1212/WNL.55.1.89 10.1016/j.neuroimage.2018.02.032 10.1016/j.jns.2017.10.048 10.1016/j.ijpsycho.2014.04.001 10.1016/S0140-6736(83)92879-9 10.1007/s00401-013-1115-8 10.1007/s00439-015-1536-7 10.1089/brain.2016.0469 10.1148/radiol.14141715 10.1038/ejhg.2008.147 10.1089/brain.2012.0106 10.1016/j.tics.2012.02.004 10.1001/archneur.61.6.849 10.1016/j.expneurol.2014.06.011 10.1109/10.623056 |
ContentType | Journal Article |
Copyright | The Author(s) 2019 Neurological Sciences is a copyright of Springer, (2019). All Rights Reserved. © 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Distributed under a Creative Commons Attribution 4.0 International License |
Copyright_xml | – notice: The Author(s) 2019 – notice: Neurological Sciences is a copyright of Springer, (2019). All Rights Reserved. © 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: Distributed under a Creative Commons Attribution 4.0 International License |
DBID | C6C AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7TK 7X7 7XB 88E 88G 8AO 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH GNUQQ K9- K9. M0R M0S M1P M2M PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQQKQ PQUKI PSYQQ Q9U 7X8 1XC 5PM |
DOI | 10.1007/s10072-019-3725-y |
DatabaseName | Springer Nature OA Free Journals CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Neurosciences Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Psychology Database (Alumni) ProQuest Pharma Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials ProQuest Central ProQuest One Community College ProQuest Central Korea Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student Consumer Health Database ProQuest Health & Medical Complete (Alumni) Consumer Health Database ProQuest Health & Medical Collection Medical Database Psychology Database Proquest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest One Psychology ProQuest Central Basic MEDLINE - Academic Hyper Article en Ligne (HAL) PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest One Psychology ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing ProQuest Pharma Collection ProQuest Family Health (Alumni Edition) ProQuest Central ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Health & Medical Research Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Central Basic ProQuest Family Health ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Psychology Journals (Alumni) Neurosciences Abstracts ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest Psychology Journals ProQuest One Academic UKI Edition ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | ProQuest One Psychology MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: C6C name: Springer Nature OA Free Journals url: http://www.springeropen.com/ sourceTypes: Publisher – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 4 dbid: BENPR name: ProQuest Central url: http://www.proquest.com/pqcentral?accountid=15518 sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1590-3478 |
EndPage | 984 |
ExternalDocumentID | PMC6478644 oai_HAL_hal_03599058v1 30737580 10_1007_s10072_019_3725_y |
Genre | Journal Article |
GrantInformation_xml | – fundername: Regione Campania (Sportello Innovazione) and University of Naples Parthenope “Ricerca locale” – fundername: ; |
GroupedDBID | --- -53 -5E -5G -BR -EM -~C .86 .VR 06C 06D 0R~ 0VY 123 199 1N0 203 29N 29~ 2J2 2JN 2JY 2KG 2KM 2LR 2~H 30V 36B 4.4 406 408 409 40D 40E 53G 5VS 67Z 6NX 78A 7X7 88E 8AO 8FI 8FJ 8TC 8UJ 95- 95. 95~ 96X AAAVM AABHQ AACDK AAHNG AAIAL AAJBT AAJKR AANZL AARTL AASML AATNV AATVU AAUYE AAWCG AAWTL AAYIU AAYQN AAYZH ABAKF ABBBX ABBXA ABDBF ABDZT ABECU ABFTV ABHLI ABHQN ABIPD ABIVO ABJNI ABJOX ABKCH ABKTR ABMNI ABMQK ABNWP ABPLI ABQBU ABSXP ABTEG ABTKH ABTMW ABUWG ABWNU ABXPI ACAOD ACDTI ACGFS ACHSB ACHXU ACKNC ACMDZ ACMLO ACOKC ACOMO ACPIV ACPRK ACSNA ACUHS ACZOJ ADBBV ADHIR ADIMF ADINQ ADJJI ADKNI ADKPE ADRFC ADTPH ADURQ ADYFF ADZKW AEFQL AEGAL AEGNC AEJHL AEJRE AEMSY AENEX AEOHA AEPYU AESKC AETLH AEVLU AEXYK AFBBN AFKRA AFLOW AFQWF AFWTZ AFZKB AGAYW AGDGC AGJBK AGMZJ AGQEE AGQMX AGRTI AGWIL AGWZB AGYKE AHAVH AHBYD AHIZS AHMBA AHSBF AHYZX AIAKS AIGIU AIIXL AILAN AITGF AJRNO AJZVZ AKMHD ALIPV ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AOCGG ARMRJ AXYYD AZFZN AZQEC B-. B0M BA0 BDATZ BENPR BGNMA BKNYI BPHCQ BSONS BVXVI C6C CCPQU CS3 CSCUP DDRTE DL5 DNIVK DPUIP DU5 DWQXO EAD EAP EAS EBC EBD EBLON EBS EBX ECV EHN EIOEI EJD EMB EMK EMOBN ENC ENX EPAXT EPL EPS EPT ESBYG ESX F5P FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRRFC FSGXE FWDCC FYUFA G-Y G-Z GGCAI GGRSB GJIRD GNUQQ GNWQR GQ6 GQ7 GQ8 GXS HF~ HG5 HG6 HMCUK HMJXF HQYDN HRMNR HVGLF HZ~ I09 IJ- IKXTQ IMOTQ IWAJR IXC IXD IXE IZIGR IZQ I~X I~Z J-C J0Z JBSCW JCJTX JZLTJ K9- KDC KOV KPH LAS LLZTM M0R M1P M2M M4Y MA- N9A NB0 NPVJJ NQJWS NU0 O93 O9G O9I O9J OAM P19 P2P P9S PF0 PQQKQ PROAC PSQYO PSYQQ PT4 PT5 Q2X QOR QOS Q~Q R89 R9I ROL RPX RRX RSV S16 S27 S37 S3B SAP SDH SDM SHX SISQX SJYHP SMD SNE SNPRN SNX SOHCF SOJ SPISZ SRMVM SSLCW SSXJD STPWE SV3 SZ9 SZN T13 TSG TSK TSV TT1 TUC TUS U2A U9L UG4 UKHRP UOJIU UTJUX VC2 W23 W48 WJK WK8 YLTOR Z45 Z7U Z82 Z83 Z87 Z8O Z8V Z91 ZMTXR ZOVNA ~8M ~A9 -Y2 2.D 2P1 2VQ AANXM AAPKM AARHV AAYTO AAYXX ABBRH ABDBE ABFSG ABQSL ABULA ACBXY ACSTC ACUDM ADHKG ADPHR AEBTG AEKMD AEZWR AFDZB AFEXP AFHIU AFOHR AGQPQ AHPBZ AHWEU AIXLP AJBLW ATHPR AYFIA CAG CITATION COF EN4 GRRUI H13 IHE N2Q NDZJH OVD PHGZM PHGZT RIG S1Z S26 S28 SCLPG SDE T16 TEORI UZXMN VFIZW CGR CUY CVF ECM EIF NPM 3V. 7TK 7XB 8FK ABRTQ K9. PJZUB PKEHL PPXIY PQEST PQUKI Q9U 7X8 PUEGO 1XC 5PM |
ID | FETCH-LOGICAL-c504t-5d254cc2abc0f55c4460c46e1eff284b963d29fd735c7c0118907857fa8a22fa3 |
IEDL.DBID | 7X7 |
ISSN | 1590-1874 1590-3478 |
IngestDate | Thu Aug 21 18:29:36 EDT 2025 Fri Sep 12 12:54:54 EDT 2025 Fri Sep 05 11:00:59 EDT 2025 Sat Aug 23 14:20:05 EDT 2025 Thu Apr 03 06:59:19 EDT 2025 Thu Apr 24 23:03:14 EDT 2025 Tue Jul 01 00:41:40 EDT 2025 Fri Feb 21 02:36:55 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 5 |
Keywords | Hereditary spastic paraplegia Motoneuron disease Magnetic source imaging Neural synchronization Magnetoencephalography Brain network |
Language | English |
License | Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c504t-5d254cc2abc0f55c4460c46e1eff284b963d29fd735c7c0118907857fa8a22fa3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 PMCID: PMC6478644 |
ORCID | 0000-0002-3685-7554 0000-0003-0943-131X 0000-0002-5623-9657 0000-0002-5964-8667 0000-0003-0800-2433 0000-0003-2192-6841 0000-0002-9556-9800 |
OpenAccessLink | https://doi.org/10.1007/s10072-019-3725-y |
PMID | 30737580 |
PQID | 2177449612 |
PQPubID | 27321 |
PageCount | 6 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_6478644 hal_primary_oai_HAL_hal_03599058v1 proquest_miscellaneous_2213922941 proquest_journals_2177449612 pubmed_primary_30737580 crossref_citationtrail_10_1007_s10072_019_3725_y crossref_primary_10_1007_s10072_019_3725_y springer_journals_10_1007_s10072_019_3725_y |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-05-01 |
PublicationDateYYYYMMDD | 2019-05-01 |
PublicationDate_xml | – month: 05 year: 2019 text: 2019-05-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | Cham |
PublicationPlace_xml | – name: Cham – name: Italy – name: Milano |
PublicationTitle | Neurological sciences |
PublicationTitleAbbrev | Neurol Sci |
PublicationTitleAlternate | Neurol Sci |
PublicationYear | 2019 |
Publisher | Springer International Publishing Springer Nature B.V Springer Verlag |
Publisher_xml | – name: Springer International Publishing – name: Springer Nature B.V – name: Springer Verlag |
References | Benjamini, Hochberg (CR35) 1995; 57 Palva, Palva (CR42) 2012; 16 Henson, Zhu, Hardaway, Wetzel, Stefan, Albers, Nicholls (CR8) 2012; 7 White, Ince, Lusher, Lindsey, Cookson, Bashir, Shaw, Bushby (CR36) 2000; 55 Sorrentino, Nieboer, Twisk, Stam, Douw, Hillebrand (CR39) 2017; 7 Kruskal (CR31) 1956; 7 Stam, Tewarie, Van Dellen (CR32) 2014; 92 Harding (CR1) 1981; 44 Shoukier, Neesen, Sauter, Argyriou, Doerwald, Pantakani, Mannan (CR13) 2009; 17 Gross, Baillet, Barnes, Henson, Hillebrand, Jensen, Jerbi, Litvak, Maess, Oostenveld, Parkkonen, Taylor, van Wassenhove, Wibral, Schoffelen (CR23) 2013; 65 Fonknechten, Mavel, Byrne, Davoine, Cruaud, Bönsch, Samson, Coutinho, Hutchinson, McMonagle, Burgunder, Tartaglione, Heinzlef, Feki, Deufel, Parfrey, Brice, Fontaine, Prud'homme, Weissenbach, Dürr, Hazan (CR9) 2000; 9 Nichols, Holmes (CR34) 2002; 15 Nolte (CR25) 2003; 48 Schoonheim, Geurts, Landi, Douw, van der Meer, Vrenken, Polman, Barkhof, Stam (CR37) 2013; 34 Tewarie, van Dellen, Hillebrand, Stam (CR20) 2015; 104 Nielsen, Johnsen, Koefoed, Scheuer, Gronbech-Jensen, Law, Krabbe, Norremolle, Eiberg, Sondergard, Dam, Rehfeld, Krarup, Paulson, Hasholt, Sorensen (CR14) 2004; 11 Duning, Warnecke, Schirmacher, Schiffbauer, Lohmann, Mohammadi, Young, Deppe (CR40) 2010; 25 Pellegrino, Tomasevic, Tombini, Assenza, Bravi, Sterzi, Giacobbe, Zollo, Guglielmelli, Cavallo, Vernieri, Tecchio (CR38) 2012; 30 Palva, Wang, Palva, Zhigalov, Monto, Brookes, Schoffelen, Jerbi (CR30) 2018; 173 Sorrentino, Rucco, Jacini, Trojsi, Lardone, Baselice, Femiano, Santangelo, Granata, Vettoliere, Monsurrò, Tedeschi, Sorrentino (CR18) 2018; 20 Boersma, Smit, Boomsma, de Geus, Delemarre-van de Waal, Stam (CR33) 2013; 3 Liao, Huang, Xing, Wu, Liao, Wang, Tang, Shen (CR17) 2018; 384 Bürger, Fonknechten, Hoeltzenbein, Neumann, Bratanoff, Hazan, Reis (CR11) 2000; 8 Orlacchio, Kawarai, Totaro, Errico, St George-Hyslop, Rugarli, Bernardi (CR12) 2004; 61 Stam (CR19) 2014; 15 Patrono, Scarano, Cricchi, Melone, Chiriaco, Napolitano, Malandrini, de Michele, Petrozzi, Giraldi, Santoro, Servidei, Casali, Filla, Santorelli (CR21) 2005; 25 Fink (CR4) 2013; 126 Harding (CR3) 1983; 321 Tesson, Koht, Stevanin (CR6) 2015; 134 Oostenveld, Fries, Maris, Schoffelen (CR22) 2011; 2011 CR26 Solowska, Baas (CR7) 2015; 138 Finsterer, Löscher, Quasthoff, Wanschitz, Auer-Grumbach, Stevanin (CR10) 2012; 318 Rezende, de Albuquerque, Lamas, Martinez, Campos, Casseb, Silva, Branco, D'Abreu, Lopes-Cendes, Cendes, França (CR16) 2015; 10 Lo, Lombardi, Santorelli (CR5) 2014; 261 Fraschini, Demuru, Crobe, Marrosu, Stam, Hillebrand (CR24) 2016; 13 Gong, He, Concha, Lebel, Gross, Evans, Beaulieu (CR27) 2009; 19 Tzourio-Mazoyer, Landeau, Papathanassiou, Crivello, Etard, Delcroix, Mazoyer, Joliot (CR28) 2002; 15 Agosta, Scarlato, Spinelli, Canu, Benedetti, Bassi, Casali, Sessa, Copetti, Pagani, Comi, Ferrari, Falini, Filippi (CR41) 2015; 276 Stam, Nolte, Daffertshofer (CR29) 2007; 28 Parodi, Fenu, Stevanin, Durr (CR2) 2017; 173 McDermott (CR15) 2009; 72 JM Palva (3725_CR30) 2018; 173 JK Fink (3725_CR4) 2013; 126 BJ Henson (3725_CR8) 2012; 7 Y Benjamini (3725_CR35) 1995; 57 P Tewarie (3725_CR20) 2015; 104 AE Harding (3725_CR3) 1983; 321 MM Schoonheim (3725_CR37) 2013; 34 AE Harding (3725_CR1) 1981; 44 J Finsterer (3725_CR10) 2012; 318 J Gross (3725_CR23) 2013; 65 G Pellegrino (3725_CR38) 2012; 30 3725_CR26 P Sorrentino (3725_CR39) 2017; 7 L Parodi (3725_CR2) 2017; 173 A Orlacchio (3725_CR12) 2004; 61 M Boersma (3725_CR33) 2013; 3 GT Lo (3725_CR5) 2014; 261 J Bürger (3725_CR11) 2000; 8 CJ McDermott (3725_CR15) 2009; 72 F Agosta (3725_CR41) 2015; 276 TJR Rezende (3725_CR16) 2015; 10 JB Kruskal (3725_CR31) 1956; 7 N Fonknechten (3725_CR9) 2000; 9 C Tesson (3725_CR6) 2015; 134 G Gong (3725_CR27) 2009; 19 CJ Stam (3725_CR19) 2014; 15 JM Solowska (3725_CR7) 2015; 138 N Tzourio-Mazoyer (3725_CR28) 2002; 15 JE Nielsen (3725_CR14) 2004; 11 T Duning (3725_CR40) 2010; 25 S Palva (3725_CR42) 2012; 16 X Liao (3725_CR17) 2018; 384 CJ Stam (3725_CR32) 2014; 92 P Sorrentino (3725_CR18) 2018; 20 CJ Stam (3725_CR29) 2007; 28 M Shoukier (3725_CR13) 2009; 17 KD White (3725_CR36) 2000; 55 C Patrono (3725_CR21) 2005; 25 M Fraschini (3725_CR24) 2016; 13 R Oostenveld (3725_CR22) 2011; 2011 TE Nichols (3725_CR34) 2002; 15 G Nolte (3725_CR25) 2003; 48 |
References_xml | – volume: 15 start-page: 683 year: 2014 end-page: 695 ident: CR19 article-title: Modern network science of neurological disorders publication-title: Nat Rev Neurosci doi: 10.1038/nrn3801 – volume: 72 start-page: 1534 year: 2009 ident: CR15 article-title: Clinical features of hereditary spastic paraplegia due to spastin mutation publication-title: Neurology doi: 10.1212/01.wnl.0000344303.72193.d5 – volume: 15 start-page: 273 year: 2002 end-page: 289 ident: CR28 article-title: Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain publication-title: Neuroimage doi: 10.1006/nimg.2001.0978 – volume: 104 start-page: 177 year: 2015 end-page: 188 ident: CR20 article-title: The minimum spanning tree: an unbiased method for brain network analysis publication-title: Neuroimage doi: 10.1016/j.neuroimage.2014.10.015 – volume: 9 start-page: 637 year: 2000 end-page: 644 ident: CR9 article-title: Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia publication-title: Hum Mol Genet doi: 10.1093/hmg/9.4.637 – volume: 48 start-page: 3637 year: 2003 end-page: 3652 ident: CR25 article-title: The magnetic lead field theorem in the quasi-static approximation and its use for magnetoencephalography forward calculation in realistic volume conductors publication-title: Phys Med Biol doi: 10.1088/0031-9155/48/22/002 – volume: 8 start-page: 771 year: 2000 end-page: 776 ident: CR11 article-title: Hereditary spastic paraplegia caused by mutations in the SPG4 gene publication-title: Eur J Hum Genet doi: 10.1038/sj.ejhg.5200528 – volume: 65 start-page: 349 year: 2013 end-page: 363 ident: CR23 article-title: Good practice for conducting and reporting MEG research publication-title: Neuroimage doi: 10.1016/j.neuroimage.2012.10.001 – volume: 25 start-page: 506 year: 2005 ident: CR21 article-title: Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations publication-title: Hum Mutat doi: 10.1002/humu.9340 – volume: 15 start-page: 1 year: 2002 end-page: 25 ident: CR34 article-title: Nonparametric permutation tests for functional neuroimaging: a primer with examples publication-title: Hum Brain Mapp doi: 10.1002/hbm.1058 – volume: 30 start-page: 497 year: 2012 end-page: 510 ident: CR38 article-title: Inter-hemispheric coupling changes associate with motor improvements after robotic stroke rehabilitation publication-title: Restor Neurol Neurosci doi: 10.3233/RNN-2012-120227 – volume: 20 start-page: 564 year: 2018 end-page: 571 ident: CR18 article-title: Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study publication-title: Neuroimage Clin doi: 10.1016/j.nicl.2018.08.001 – volume: 13 year: 2016 ident: CR24 article-title: The effect of epoch length on estimated EEG functional connectivity and brain network organisation publication-title: J Neural Eng doi: 10.1088/1741-2560/13/3/036015 – volume: 57 start-page: 289 year: 1995 end-page: 300 ident: CR35 article-title: Controlling the false discovery rate: a practical and powerful approach to multiple testing publication-title: J R Stat Soc Ser B doi: 10.2307/2346101 – volume: 138 start-page: 2471 year: 2015 end-page: 2484 ident: CR7 article-title: Hereditary spastic paraplegia SPG4: what is known and not known about the disease publication-title: Brain doi: 10.1093/brain/awv178 – volume: 261 start-page: 518 year: 2014 end-page: 539 ident: CR5 article-title: Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms publication-title: Exp Neurol – volume: 10 start-page: e0117666 year: 2015 ident: CR16 article-title: Multimodal MRI-based study in patients with SPG4 mutations publication-title: PLoS One doi: 10.1371/journal.pone.0117666 – volume: 7 start-page: e36505 year: 2012 ident: CR8 article-title: Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia publication-title: PLoS One doi: 10.1371/journal.pone.0036505 – volume: 318 start-page: 1 year: 2012 end-page: 18 ident: CR10 article-title: Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance publication-title: J Neurol Sci doi: 10.1016/j.jns.2012.03.025 – volume: 11 start-page: 817 year: 2004 end-page: 824 ident: CR14 article-title: Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation publication-title: Eur J Neurol doi: 10.1111/j.1468-1331.2004.00888.x – volume: 34 start-page: 52 year: 2013 end-page: 61 ident: CR37 article-title: Functional connectivity changes in multiple sclerosis patients: a graph analytical study of MEG resting state data publication-title: Hum Brain Mapp doi: 10.1002/hbm.21424 – volume: 19 start-page: 524 year: 2009 end-page: 536 ident: CR27 article-title: Mapping anatomical connectivity patterns of human cerebral cortex using in vivo diffusion tensor imaging tractography publication-title: Cereb Cortex doi: 10.1093/cercor/bhn102 – volume: 25 start-page: 1986 year: 2010 end-page: 1992 ident: CR40 article-title: Specific pattern of early white-matter changes in pure hereditary spastic paraplegia publication-title: Mov Disord doi: 10.1002/mds.23211 – volume: 44 start-page: 871 year: 1981 end-page: 883 ident: CR1 article-title: Hereditary “pure” spastic paraplegia: a clinical and genetic study of 22 families publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.44.10.871 – volume: 7 start-page: 48 year: 1956 ident: CR31 article-title: On the shortest spanning subtree of a graph and the traveling salesman problem publication-title: Proc Am Math Soc doi: 10.1090/S0002-9939-1956-0078686-7 – volume: 28 start-page: 1178 year: 2007 end-page: 1193 ident: CR29 article-title: Phase lag index: assessment of functional connectivity from multi channel EEG and MEG with diminished bias from common sources publication-title: Hum Brain Mapp doi: 10.1002/hbm.20346 – volume: 173 start-page: 352 year: 2017 end-page: 360 ident: CR2 article-title: Hereditary spastic paraplegia: more than an upper motor neuron disease publication-title: Rev Neurol (Paris) doi: 10.1016/j.neurol.2017.03.034 – volume: 2011 start-page: 1 year: 2011 end-page: 9 ident: CR22 article-title: FieldTrip: open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data publication-title: Comput Intell Neurosci doi: 10.1155/2011/156869 – volume: 55 start-page: 89 year: 2000 end-page: 94 ident: CR36 article-title: Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation publication-title: Neurology doi: 10.1212/WNL.55.1.89 – volume: 173 start-page: 632 year: 2018 end-page: 643 ident: CR30 article-title: Ghost interactions in MEG/EEG source space: a note of caution on inter-areal coupling measures publication-title: Neuroimage doi: 10.1016/j.neuroimage.2018.02.032 – volume: 384 start-page: 1 year: 2018 end-page: 6 ident: CR17 article-title: Resting state fMRI studies in SPG4-linked hereditary spastic paraplegia publication-title: J Neurol Sci doi: 10.1016/j.jns.2017.10.048 – volume: 92 start-page: 129 year: 2014 end-page: 138 ident: CR32 article-title: The trees and the forest: characterization of complex brain networks with minimum spanning trees publication-title: Int J Psychophysiol doi: 10.1016/j.ijpsycho.2014.04.001 – volume: 321 start-page: 1151 year: 1983 end-page: 1155 ident: CR3 article-title: Classification of the hereditary ataxias and paraplegias publication-title: Lancet doi: 10.1016/S0140-6736(83)92879-9 – volume: 126 start-page: 307 year: 2013 end-page: 328 ident: CR4 article-title: Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms publication-title: Acta Neuropathol doi: 10.1007/s00401-013-1115-8 – volume: 134 start-page: 511 year: 2015 end-page: 538 ident: CR6 article-title: Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology publication-title: Hum Genet doi: 10.1007/s00439-015-1536-7 – volume: 7 start-page: 321 year: 2017 end-page: 330 ident: CR39 article-title: The hierarchy of brain networks is related to insulin growth factor-1 in a large, middle-aged, healthy cohort: an exploratory magnetoencephalography study publication-title: Brain Connect doi: 10.1089/brain.2016.0469 – volume: 276 start-page: 207 year: 2015 end-page: 218 ident: CR41 article-title: Hereditary spastic paraplegia: beyond clinical phenotypes toward a unified pattern of central nervous system damage publication-title: Radiology doi: 10.1148/radiol.14141715 – volume: 17 start-page: 187 year: 2009 end-page: 194 ident: CR13 article-title: Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia publication-title: Eur J Hum Genet doi: 10.1038/ejhg.2008.147 – volume: 3 start-page: 50 year: 2013 end-page: 60 ident: CR33 article-title: Growing trees in child brains: graph theoretical analysis of electroencephalography-derived minimum spanning tree in 5- and 7-year-old children reflects brain maturation publication-title: Brain Connect doi: 10.1089/brain.2012.0106 – volume: 16 start-page: 219 year: 2012 end-page: 230 ident: CR42 article-title: Discovering oscillatory interaction networks with M/EEG: challenges and breakthroughs publication-title: Trends Cogn Sci doi: 10.1016/j.tics.2012.02.004 – volume: 61 start-page: 849 year: 2004 end-page: 855 ident: CR12 article-title: Hereditary spastic paraplegia: clinical genetic study of 15 families publication-title: Arch Neurol doi: 10.1001/archneur.61.6.849 – ident: CR26 – volume: 173 start-page: 352 year: 2017 ident: 3725_CR2 publication-title: Rev Neurol (Paris) doi: 10.1016/j.neurol.2017.03.034 – volume: 55 start-page: 89 year: 2000 ident: 3725_CR36 publication-title: Neurology doi: 10.1212/WNL.55.1.89 – volume: 7 start-page: e36505 year: 2012 ident: 3725_CR8 publication-title: PLoS One doi: 10.1371/journal.pone.0036505 – volume: 65 start-page: 349 year: 2013 ident: 3725_CR23 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2012.10.001 – volume: 15 start-page: 1 year: 2002 ident: 3725_CR34 publication-title: Hum Brain Mapp doi: 10.1002/hbm.1058 – volume: 7 start-page: 48 year: 1956 ident: 3725_CR31 publication-title: Proc Am Math Soc doi: 10.1090/S0002-9939-1956-0078686-7 – volume: 61 start-page: 849 year: 2004 ident: 3725_CR12 publication-title: Arch Neurol doi: 10.1001/archneur.61.6.849 – volume: 19 start-page: 524 year: 2009 ident: 3725_CR27 publication-title: Cereb Cortex doi: 10.1093/cercor/bhn102 – volume: 11 start-page: 817 year: 2004 ident: 3725_CR14 publication-title: Eur J Neurol doi: 10.1111/j.1468-1331.2004.00888.x – volume: 3 start-page: 50 year: 2013 ident: 3725_CR33 publication-title: Brain Connect doi: 10.1089/brain.2012.0106 – volume: 318 start-page: 1 year: 2012 ident: 3725_CR10 publication-title: J Neurol Sci doi: 10.1016/j.jns.2012.03.025 – volume: 30 start-page: 497 year: 2012 ident: 3725_CR38 publication-title: Restor Neurol Neurosci doi: 10.3233/RNN-2012-120227 – volume: 28 start-page: 1178 year: 2007 ident: 3725_CR29 publication-title: Hum Brain Mapp doi: 10.1002/hbm.20346 – volume: 7 start-page: 321 year: 2017 ident: 3725_CR39 publication-title: Brain Connect doi: 10.1089/brain.2016.0469 – volume: 9 start-page: 637 year: 2000 ident: 3725_CR9 publication-title: Hum Mol Genet doi: 10.1093/hmg/9.4.637 – volume: 44 start-page: 871 year: 1981 ident: 3725_CR1 publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.44.10.871 – volume: 10 start-page: e0117666 year: 2015 ident: 3725_CR16 publication-title: PLoS One doi: 10.1371/journal.pone.0117666 – volume: 57 start-page: 289 year: 1995 ident: 3725_CR35 publication-title: J R Stat Soc Ser B doi: 10.2307/2346101 – volume: 261 start-page: 518 year: 2014 ident: 3725_CR5 publication-title: Exp Neurol doi: 10.1016/j.expneurol.2014.06.011 – volume: 13 year: 2016 ident: 3725_CR24 publication-title: J Neural Eng doi: 10.1088/1741-2560/13/3/036015 – volume: 2011 start-page: 1 year: 2011 ident: 3725_CR22 publication-title: Comput Intell Neurosci doi: 10.1155/2011/156869 – volume: 384 start-page: 1 year: 2018 ident: 3725_CR17 publication-title: J Neurol Sci doi: 10.1016/j.jns.2017.10.048 – volume: 8 start-page: 771 year: 2000 ident: 3725_CR11 publication-title: Eur J Hum Genet doi: 10.1038/sj.ejhg.5200528 – volume: 104 start-page: 177 year: 2015 ident: 3725_CR20 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2014.10.015 – volume: 15 start-page: 683 year: 2014 ident: 3725_CR19 publication-title: Nat Rev Neurosci doi: 10.1038/nrn3801 – volume: 134 start-page: 511 year: 2015 ident: 3725_CR6 publication-title: Hum Genet doi: 10.1007/s00439-015-1536-7 – volume: 276 start-page: 207 year: 2015 ident: 3725_CR41 publication-title: Radiology doi: 10.1148/radiol.14141715 – ident: 3725_CR26 doi: 10.1109/10.623056 – volume: 92 start-page: 129 year: 2014 ident: 3725_CR32 publication-title: Int J Psychophysiol doi: 10.1016/j.ijpsycho.2014.04.001 – volume: 48 start-page: 3637 year: 2003 ident: 3725_CR25 publication-title: Phys Med Biol doi: 10.1088/0031-9155/48/22/002 – volume: 16 start-page: 219 year: 2012 ident: 3725_CR42 publication-title: Trends Cogn Sci doi: 10.1016/j.tics.2012.02.004 – volume: 25 start-page: 506 year: 2005 ident: 3725_CR21 publication-title: Hum Mutat doi: 10.1002/humu.9340 – volume: 34 start-page: 52 year: 2013 ident: 3725_CR37 publication-title: Hum Brain Mapp doi: 10.1002/hbm.21424 – volume: 72 start-page: 1534 year: 2009 ident: 3725_CR15 publication-title: Neurology doi: 10.1212/01.wnl.0000344303.72193.d5 – volume: 321 start-page: 1151 year: 1983 ident: 3725_CR3 publication-title: Lancet doi: 10.1016/S0140-6736(83)92879-9 – volume: 126 start-page: 307 year: 2013 ident: 3725_CR4 publication-title: Acta Neuropathol doi: 10.1007/s00401-013-1115-8 – volume: 138 start-page: 2471 year: 2015 ident: 3725_CR7 publication-title: Brain doi: 10.1093/brain/awv178 – volume: 20 start-page: 564 year: 2018 ident: 3725_CR18 publication-title: Neuroimage Clin doi: 10.1016/j.nicl.2018.08.001 – volume: 173 start-page: 632 year: 2018 ident: 3725_CR30 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2018.02.032 – volume: 25 start-page: 1986 year: 2010 ident: 3725_CR40 publication-title: Mov Disord doi: 10.1002/mds.23211 – volume: 17 start-page: 187 year: 2009 ident: 3725_CR13 publication-title: Eur J Hum Genet doi: 10.1038/ejhg.2008.147 – volume: 15 start-page: 273 year: 2002 ident: 3725_CR28 publication-title: Neuroimage doi: 10.1006/nimg.2001.0978 |
SSID | ssj0001413 |
Score | 2.3262386 |
Snippet | Aim
Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.
Methods
Ten SPG4 patients and ten controls... Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene. Ten SPG4 patients and ten controls underwent a... AimOur aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.MethodsTen SPG4 patients and ten controls... Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene.AIMOur aim was to describe the rearrangements... |
SourceID | pubmedcentral hal proquest pubmed crossref springer |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 979 |
SubjectTerms | Adult Aged Beta Rhythm Brain - physiopathology Cognitive science Cohort Studies Cortical Synchronization Female Hereditary spastic paraplegia Humans Leaves Magnetoencephalography Male Medicine Medicine & Public Health Middle Aged Mutation Neurology Neuroradiology Neuroscience Neurosciences Neurosurgery Original Original Article Paralysis Psychiatry Rest Spastic Paraplegia, Hereditary - genetics Spastic Paraplegia, Hereditary - physiopathology Spasticity Spastin - genetics |
SummonAdditionalLinks | – databaseName: Springer Nature OA Free Journals dbid: C6C link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3di9NAEB-8E8QX8dvoKav4pAS2m93u5rEUjyKeCHcH9xZ2N7vXwpGWNhX6P_hHO5Ov0jsVfAkl2WbTzndm5jcAH60KKH9-nAbuCVTbxNREPGjllY6ZIQR0qrb4Pp5dyq9X6qoDi6ZemFv5e2px45qKB3IUBaHS3RHcV6h3iZmn4-mgdEeymYSMxplSlVr2Ccw_3eLABB3NqQDyrnd5t0jyVqa0MUCnj-FR5zmySUvqJ3AvVE_hwVmXG38Gv862bVp9wxYVQ7-Onf-YnF8w5JDAvKUC92s2p9Gci9qudwxVCWE0MwL_Xt2E64Vldh1Y09wSSlYvWQsWgp9WvYZkTXJ9v4ujAROMbGP7SpFVbVX55jlcnn65mM7SbtZC6hWXdapKjBS9F9Z5HpXyGCVyL8dhFGJEC-ZQTkuRx1JnymtP7aoYVRskpzVWiGizF3BcLavwCpg0LsjcZFbyTEYX8ywvTbBOo3fiYukS4P3fX_gOiJzmYdwUewhloliBFCuIYsUugU_DV1YtCse_Fn9Amg7rCD97NvlW0DnCK8y5Mj9HCZz0JC86qd0UGJ5pKXN0-hJ4P1xGeaMkiq3CcotrBPrMQuQSb_Gy5ZBhK9KXGH_xBPQB7xw8y-GVajFvML2p5Rdd0wQ-91y2f6y__tLX_7X6DTwUJARNteYJHNfrbXiLHlXt3jWy9Bs6yhn6 priority: 102 providerName: Springer Nature |
Title | Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks |
URI | https://link.springer.com/article/10.1007/s10072-019-3725-y https://www.ncbi.nlm.nih.gov/pubmed/30737580 https://www.proquest.com/docview/2177449612 https://www.proquest.com/docview/2213922941 https://hal.science/hal-03599058 https://pubmed.ncbi.nlm.nih.gov/PMC6478644 |
Volume | 40 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1bb9MwFD5im4R4QdwJjMkgnkARqWPXyRNKq5YKWDWxVSpPkePYa6UpLW2K1P_Aj-acXFqVib0kVe3m0nP3Of4OwHstLcqf6fo2MASqHTk_cnhQ0kjlwogQ0KnaYtwdTcTXqZw2C27rpqyy1YmVos4XhtbIP6HrrISI0SB_Xv7yqWsUZVebFhpHcNJBT4RaN6jpLuCiGsaqwF7GlL9Uos1q1lvnAkVFCTGKGJf-9sAuHc2oKvK2y3m7cvKf9GlllYaP4GHjTrKkpv9juGeLJ3D_vEmYP4U_55s6175m84Khs8cuL5LLK4ZsY5nRVPV-zWbUr3Ne6tWWoX4h4GZGiODLG3s910yvLKt2vNiclQtWI4jgp2WrNlmVcd_fJaOuE4wMZr3OyIq61Hz9DCbDwVV_5DcNGHwjA1H6Msfw0RiuMxM4KQ2GjoERXduxzqFZy1B4cx67XIXSKEN7WDHUjpDGOtKcOx0-h-NiUdiXwESUWRFHoRZBKFzm4jDOI6szhS5L5vLMg6D9-1PToJNTk4ybdI-rTBRLkWIpUSzdevBh95NlDc1x1-R3SNPdPALVHiXfU_qOQAzjQEa_Ox6ctiRPG1Fep3vG8-DtbhiFkDIrurCLDc7h6EhzHgu8xIuaQ3a3IiWKQVnggTrgnYNnORwp5rMK6Jv2AaO_6sHHlsv2j_XfN31190u8hgecuL6q2TyF43K1sW_Qryqzs0p4zuAkGfZ6Yzp_-fltgOfeYHzxA0f73T4eJzz5C7oEJ38 |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB61qQRcEG8MBRYEF5CFs96N7UOFArRKaRJVNJV6c9fr3SZS5YTEAeU_8Jv4bcz4FYWK3nqJrHj9WM_sPHZmvgF4q6TB9ac7rvE0gWqH1g0t_gRSy8D6ISGgU7bFsNM7Fd_O5NkW_KlrYSitspaJhaBOp5r2yD-i6RwIEaFC_jT74VLXKIqu1i00VNVaId0rIMaqwo4js_qFLtxi7_Ar0vsd5wf7oy89t-oy4GrpidyVKfpIWnOVaM9KqdE_8rTomLaxFmV3ghya8simgS91oKlQE_3JECeiQsW5VT7edxt2BG2gtGDn8_7w-HujC9qiaNCMNgNFUANRx1XL4j0voLSICBc5l-5qQzNujykv86rRezV3858AbqEXD-7B3cqgZd2SA-_DlskewK1BFbJ_CL8HyzLav2CTjKG5yU6OuycjhoxrmFaUd3_BxtQxdJKr-YqhhCPoaEaY5LNLczFRTM0NK2puTMryKSsxTPBoVgtuVsT8109JqO8FI5Vd7nSyrEx2XzyC0xshzmNoZdPMPAUmwsSIKPSV8HxhExv5URoalQRoNCU2TRzw6s8f6wofndp0XMZrZGeiWIwUi4li8cqB980lsxIc5LrBb5CmzTiC9e51-zH9RzCKkSfDn20HdmuSx5UwWcRr1nfgdXMaxQDFdlRmpkscw9GU5zwSeIsnJYc0jyIxjm6h50CwwTsb77J5JpuMC6hxqkRGi9mBDzWXrV_rvzN9dv0kXsHt3mjQj_uHw6PncIfTCigySHehlc-X5gVaeXnyslpKDM5vevX-BQoxZE8 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB71IVVcUHmbFlgQXEBWnfVubB8qFGijlLZRRFupN3e93m0iVU5IHFD-A7-MX8WMX1Go6K2XKIo3ttfz9sx8A_BeSYPyp9uu8TSBaofWDS1-BFLLwPohIaBTtUW_3bsQ3y7l5Rr8qXthqKyy1omFok7Hmt6R76HrHAgRoUHes1VZxOCg-3nyw6UJUpRprcdpqGrMQrpfwI1VTR7HZvELw7nZ_tEB0v4D593D8689t5o44GrpidyVKcZLWnOVaM9KqTFW8rRom5axFvV4gtya8simgS91oKlpE2PLEDelQsW5VT6edx02A7T6GAhufjnsD743dqElimHN6D9QNjUQdY61bOTzAiqRiFDguXQXK1ZyfUg1mrcd4Nt1nP8kcwsb2d2Gh5VzyzolNz6CNZM9hq3TKn3_BH6fzsvM_4yNMoauJzsbdM7OGTKxYVpRDf41G9L00FGupguG2o5gpBnhk09uzPVIMTU1rOi_MSnLx6zEM8Fvk1qJsyL_v7xKQjMwGJnv8q0ny8rC99lTuLgX4jyDjWycmRfARJgYEYW-Ep4vbGIjP0pDo5IAHajEpokDXv34Y11hpdPIjpt4ifJMFIuRYjFRLF448LH5y6QECrlr8TukabOOIL57nZOYfiNIxciT4c-WA7s1yeNKsczipRg48LY5jCqB8jwqM-M5ruHo1nMeCTzF85JDmkuRSscQ0XMgWOGdlXtZPZKNhgXsOHUlo_fswKeay5a39d-dvrx7E29gC6U4PjnqH-_AA04CUBST7sJGPp2bV-jw5cnrSpIYXN238P4F6b9okw |
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=Mutations+in+the+SPAST+gene+causing+hereditary+spastic+paraplegia+are+related+to+global+topological+alterations+in+brain+functional+networks&rft.jtitle=Neurological+sciences&rft.au=Rucco%2C+Rosaria&rft.au=Liparoti%2C+Marianna&rft.au=Jacini%2C+Francesca&rft.au=Baselice%2C+Fabio&rft.date=2019-05-01&rft.pub=Springer+Nature+B.V&rft.issn=1590-1874&rft.eissn=1590-3478&rft.volume=40&rft.issue=5&rft.spage=979&rft.epage=984&rft_id=info:doi/10.1007%2Fs10072-019-3725-y&rft.externalDBID=HAS_PDF_LINK |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1590-1874&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1590-1874&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1590-1874&client=summon |