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...

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Published inNeurological sciences Vol. 40; no. 5; pp. 979 - 984
Main Authors Rucco, Rosaria, Liparoti, Marianna, Jacini, Francesca, Baselice, Fabio, Antenora, Antonella, De Michele, Giuseppe, Criscuolo, Chiara, Vettoliere, Antonio, Mandolesi, Laura, Sorrentino, Giuseppe, Sorrentino, Pierpaolo
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.05.2019
Springer Nature B.V
Springer Verlag
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ISSN1590-1874
1590-3478
1590-3478
DOI10.1007/s10072-019-3725-y

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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
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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
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Issue 5
Keywords Hereditary spastic paraplegia
Motoneuron disease
Magnetic source imaging
Neural synchronization
Magnetoencephalography
Brain network
Language English
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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
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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...
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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
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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
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