An independent components and functional connectivity analysis of resting state fMRI data points to neural network dysregulation in adult ADHD

Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task‐positive counterpart, the DMN predominantly signals during a state of rest...

Full description

Saved in:
Bibliographic Details
Published inHuman brain mapping Vol. 35; no. 4; pp. 1261 - 1272
Main Authors Hoekzema, Elseline, Carmona, Susana, Ramos-Quiroga, J. Antoni, Richarte Fernández, Vanesa, Bosch, Rosa, Soliva, Juan Carlos, Rovira, Mariana, Bulbena, Antonio, Tobeña, Adolf, Casas, Miguel, Vilarroya, Oscar
Format Journal Article
LanguageEnglish
Published New York, NY Blackwell Publishing Ltd 01.04.2014
Wiley-Liss
John Wiley & Sons, Inc
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN1065-9471
1097-0193
1097-0193
DOI10.1002/hbm.22250

Cover

Abstract Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task‐positive counterpart, the DMN predominantly signals during a state of rest, and inappropriate regulation of this network has been associated with inattention, a core characteristic of attention‐deficit/hyperactivity disorder (ADHD). To examine whether abnormalities can be identified in the DMN component of patients with ADHD, we applied an independent components analysis to resting state functional magnetic resonance imaging data acquired from 22 male medication‐naïve adults with ADHD and 23 neurotypical individuals. We observed a stronger coherence of the left dorsolateral prefrontal cortex (dlPFC) with the DMN component in patients with ADHD which correlated with measures of selective attention. The increased left dlPFC‐DMN coherence also surfaced in a whole‐brain replication analysis involving an independent sample of 9 medication‐naïve adult patients and 9 controls. In addition, a post hoc seed‐to‐voxel functional connectivity analysis using the dlPFC as a seed region to further examine this region's suggested connectivity differences uncovered a higher temporal coherence with various other neural networks and confirmed a reduced anticorrelation with the DMN. These results point to a more diffuse connectivity between functional networks in patients with ADHD. Moreover, our findings suggest that state‐inappropriate neural activity in ADHD is not confined to DMN intrusion during attention‐demanding contexts, but also surfaces as an insufficient suppression of dlPFC signaling in relation to DMN activity during rest. Together with previous findings, these results point to a general dysfunction in the orthogonality of functional networks. Hum Brain Mapp 35:1261–1272, 2014. © 2013 Wiley Periodicals, Inc.
AbstractList Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task-positive counterpart, the DMN predominantly signals during a state of rest, and inappropriate regulation of this network has been associated with inattention, a core characteristic of attention-deficit/hyperactivity disorder (ADHD). To examine whether abnormalities can be identified in the DMN component of patients with ADHD, we applied an independent components analysis to resting state functional magnetic resonance imaging data acquired from 22 male medication-naïve adults with ADHD and 23 neurotypical individuals. We observed a stronger coherence of the left dorsolateral prefrontal cortex (dlPFC) with the DMN component in patients with ADHD which correlated with measures of selective attention. The increased left dlPFC-DMN coherence also surfaced in a whole-brain replication analysis involving an independent sample of 9 medication-naïve adult patients and 9 controls. In addition, a post hoc seed-to-voxel functional connectivity analysis using the dlPFC as a seed region to further examine this region's suggested connectivity differences uncovered a higher temporal coherence with various other neural networks and confirmed a reduced anticorrelation with the DMN. These results point to a more diffuse connectivity between functional networks in patients with ADHD. Moreover, our findings suggest that state-inappropriate neural activity in ADHD is not confined to DMN intrusion during attention-demanding contexts, but also surfaces as an insufficient suppression of dlPFC signaling in relation to DMN activity during rest. Together with previous findings, these results point to a general dysfunction in the orthogonality of functional networks. Hum Brain Mapp 35:1261-1272, 2014. © 2013 Wiley Periodicals, Inc. [PUBLICATION ABSTRACT]
Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task‐positive counterpart, the DMN predominantly signals during a state of rest, and inappropriate regulation of this network has been associated with inattention, a core characteristic of attention‐deficit/hyperactivity disorder (ADHD). To examine whether abnormalities can be identified in the DMN component of patients with ADHD, we applied an independent components analysis to resting state functional magnetic resonance imaging data acquired from 22 male medication‐naïve adults with ADHD and 23 neurotypical individuals. We observed a stronger coherence of the left dorsolateral prefrontal cortex (dlPFC) with the DMN component in patients with ADHD which correlated with measures of selective attention. The increased left dlPFC‐DMN coherence also surfaced in a whole‐brain replication analysis involving an independent sample of 9 medication‐naïve adult patients and 9 controls. In addition, a post hoc seed‐to‐voxel functional connectivity analysis using the dlPFC as a seed region to further examine this region's suggested connectivity differences uncovered a higher temporal coherence with various other neural networks and confirmed a reduced anticorrelation with the DMN. These results point to a more diffuse connectivity between functional networks in patients with ADHD. Moreover, our findings suggest that state‐inappropriate neural activity in ADHD is not confined to DMN intrusion during attention‐demanding contexts, but also surfaces as an insufficient suppression of dlPFC signaling in relation to DMN activity during rest. Together with previous findings, these results point to a general dysfunction in the orthogonality of functional networks. Hum Brain Mapp 35:1261–1272, 2014. © 2013 Wiley Periodicals, Inc.
Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task-positive counterpart, the DMN predominantly signals during a state of rest, and inappropriate regulation of this network has been associated with inattention, a core characteristic of attention-deficit/hyperactivity disorder (ADHD). To examine whether abnormalities can be identified in the DMN component of patients with ADHD, we applied an independent components analysis to resting state functional magnetic resonance imaging data acquired from 22 male medication-naïve adults with ADHD and 23 neurotypical individuals. We observed a stronger coherence of the left dorsolateral prefrontal cortex (dlPFC) with the DMN component in patients with ADHD which correlated with measures of selective attention. The increased left dlPFC-DMN coherence also surfaced in a whole-brain replication analysis involving an independent sample of 9 medication-naïve adult patients and 9 controls. In addition, a post hoc seed-to-voxel functional connectivity analysis using the dlPFC as a seed region to further examine this region's suggested connectivity differences uncovered a higher temporal coherence with various other neural networks and confirmed a reduced anticorrelation with the DMN. These results point to a more diffuse connectivity between functional networks in patients with ADHD. Moreover, our findings suggest that state-inappropriate neural activity in ADHD is not confined to DMN intrusion during attention-demanding contexts, but also surfaces as an insufficient suppression of dlPFC signaling in relation to DMN activity during rest. Together with previous findings, these results point to a general dysfunction in the orthogonality of functional networks.Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task-positive counterpart, the DMN predominantly signals during a state of rest, and inappropriate regulation of this network has been associated with inattention, a core characteristic of attention-deficit/hyperactivity disorder (ADHD). To examine whether abnormalities can be identified in the DMN component of patients with ADHD, we applied an independent components analysis to resting state functional magnetic resonance imaging data acquired from 22 male medication-naïve adults with ADHD and 23 neurotypical individuals. We observed a stronger coherence of the left dorsolateral prefrontal cortex (dlPFC) with the DMN component in patients with ADHD which correlated with measures of selective attention. The increased left dlPFC-DMN coherence also surfaced in a whole-brain replication analysis involving an independent sample of 9 medication-naïve adult patients and 9 controls. In addition, a post hoc seed-to-voxel functional connectivity analysis using the dlPFC as a seed region to further examine this region's suggested connectivity differences uncovered a higher temporal coherence with various other neural networks and confirmed a reduced anticorrelation with the DMN. These results point to a more diffuse connectivity between functional networks in patients with ADHD. Moreover, our findings suggest that state-inappropriate neural activity in ADHD is not confined to DMN intrusion during attention-demanding contexts, but also surfaces as an insufficient suppression of dlPFC signaling in relation to DMN activity during rest. Together with previous findings, these results point to a general dysfunction in the orthogonality of functional networks.
Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task‐positive counterpart, the DMN predominantly signals during a state of rest, and inappropriate regulation of this network has been associated with inattention, a core characteristic of attention‐deficit/hyperactivity disorder (ADHD). To examine whether abnormalities can be identified in the DMN component of patients with ADHD, we applied an independent components analysis to resting state functional magnetic resonance imaging data acquired from 22 male medication‐naïve adults with ADHD and 23 neurotypical individuals. We observed a stronger coherence of the left dorsolateral prefrontal cortex (dlPFC) with the DMN component in patients with ADHD which correlated with measures of selective attention. The increased left dlPFC‐DMN coherence also surfaced in a whole‐brain replication analysis involving an independent sample of 9 medication‐naïve adult patients and 9 controls. In addition, a post hoc seed‐to‐voxel functional connectivity analysis using the dlPFC as a seed region to further examine this region's suggested connectivity differences uncovered a higher temporal coherence with various other neural networks and confirmed a reduced anticorrelation with the DMN. These results point to a more diffuse connectivity between functional networks in patients with ADHD. Moreover, our findings suggest that state‐inappropriate neural activity in ADHD is not confined to DMN intrusion during attention‐demanding contexts, but also surfaces as an insufficient suppression of dlPFC signaling in relation to DMN activity during rest. Together with previous findings, these results point to a general dysfunction in the orthogonality of functional networks. Hum Brain Mapp 35:1261–1272, 2014 . © 2013 Wiley Periodicals, Inc.
Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default mode network (DMN). In contrast to its diametrically opposed task-positive counterpart, the DMN predominantly signals during a state of rest, and inappropriate regulation of this network has been associated with inattention, a core characteristic of attention-deficit/hyperactivity disorder (ADHD). To examine whether abnormalities can be identified in the DMN component of patients with ADHD, we applied an independent components analysis to resting state functional magnetic resonance imaging data acquired from 22 male medication-naïve adults with ADHD and 23 neurotypical individuals. We observed a stronger coherence of the left dorsolateral prefrontal cortex (dlPFC) with the DMN component in patients with ADHD which correlated with measures of selective attention. The increased left dlPFC-DMN coherence also surfaced in a whole-brain replication analysis involving an independent sample of 9 medication-naïve adult patients and 9 controls. In addition, a post hoc seed-to-voxel functional connectivity analysis using the dlPFC as a seed region to further examine this region's suggested connectivity differences uncovered a higher temporal coherence with various other neural networks and confirmed a reduced anticorrelation with the DMN. These results point to a more diffuse connectivity between functional networks in patients with ADHD. Moreover, our findings suggest that state-inappropriate neural activity in ADHD is not confined to DMN intrusion during attention-demanding contexts, but also surfaces as an insufficient suppression of dlPFC signaling in relation to DMN activity during rest. Together with previous findings, these results point to a general dysfunction in the orthogonality of functional networks.
Author Rovira, Mariana
Richarte Fernández, Vanesa
Hoekzema, Elseline
Ramos-Quiroga, J. Antoni
Soliva, Juan Carlos
Vilarroya, Oscar
Carmona, Susana
Casas, Miguel
Bosch, Rosa
Bulbena, Antonio
Tobeña, Adolf
AuthorAffiliation 3 Harvard Social Cognition and Affective Neuroscience Lab, Harvard University, Cambridge, Massachusetts
2 Grup de Recerca en Neuroimatge, Fundació IMIM, Barcelona, Spain
4 Department of Psychiatry, Hospital Universitari Vall d'Hebron, CIBERSAM, Barcelona, Spain
6 CRC Corporació Sanitaria, Barcelona, Spain
7 Institut de Neuropsiquiatria i Adiccions, Hospital del Mar, Barcelona, Spain
1 Unitat de Recerca en Neurociència Cognitiva, Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
5 Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
AuthorAffiliation_xml – name: 1 Unitat de Recerca en Neurociència Cognitiva, Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
– name: 2 Grup de Recerca en Neuroimatge, Fundació IMIM, Barcelona, Spain
– name: 7 Institut de Neuropsiquiatria i Adiccions, Hospital del Mar, Barcelona, Spain
– name: 3 Harvard Social Cognition and Affective Neuroscience Lab, Harvard University, Cambridge, Massachusetts
– name: 4 Department of Psychiatry, Hospital Universitari Vall d'Hebron, CIBERSAM, Barcelona, Spain
– name: 6 CRC Corporació Sanitaria, Barcelona, Spain
– name: 5 Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
Author_xml – sequence: 1
  givenname: Elseline
  surname: Hoekzema
  fullname: Hoekzema, Elseline
  email: hoekzema@gmail.com
  organization: Unitat de Recerca en Neurociència Cognitiva, Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
– sequence: 2
  givenname: Susana
  surname: Carmona
  fullname: Carmona, Susana
  organization: Unitat de Recerca en Neurociència Cognitiva, Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
– sequence: 3
  givenname: J. Antoni
  surname: Ramos-Quiroga
  fullname: Ramos-Quiroga, J. Antoni
  organization: Department of Psychiatry, Hospital Universitari Vall d'Hebron, CIBERSAM, Barcelona, Spain
– sequence: 4
  givenname: Vanesa
  surname: Richarte Fernández
  fullname: Richarte Fernández, Vanesa
  organization: Department of Psychiatry, Hospital Universitari Vall d'Hebron, CIBERSAM, Barcelona, Spain
– sequence: 5
  givenname: Rosa
  surname: Bosch
  fullname: Bosch, Rosa
  organization: Department of Psychiatry, Hospital Universitari Vall d'Hebron, CIBERSAM, Barcelona, Spain
– sequence: 6
  givenname: Juan Carlos
  surname: Soliva
  fullname: Soliva, Juan Carlos
  organization: Unitat de Recerca en Neurociència Cognitiva, Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
– sequence: 7
  givenname: Mariana
  surname: Rovira
  fullname: Rovira, Mariana
  organization: CRC Corporació Sanitaria, Barcelona, Spain
– sequence: 8
  givenname: Antonio
  surname: Bulbena
  fullname: Bulbena, Antonio
  organization: Institut de Neuropsiquiatria i Adiccions, Hospital del Mar, Barcelona, Spain
– sequence: 9
  givenname: Adolf
  surname: Tobeña
  fullname: Tobeña, Adolf
  organization: Unitat de Recerca en Neurociència Cognitiva, Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
– sequence: 10
  givenname: Miguel
  surname: Casas
  fullname: Casas, Miguel
  organization: Department of Psychiatry, Hospital Universitari Vall d'Hebron, CIBERSAM, Barcelona, Spain
– sequence: 11
  givenname: Oscar
  surname: Vilarroya
  fullname: Vilarroya, Oscar
  organization: Unitat de Recerca en Neurociència Cognitiva, Departament de Psiquiatria i Medicina Legal, Universitat Autònoma de Barcelona, Barcelona, Spain
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28293546$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/23417778$$D View this record in MEDLINE/PubMed
BookMark eNp1kstu1DAUhiNURC-w4AWQJYQEi7R2bMfJBmlooVOYgoS47SyP40zdZuzBdlryEjwzZ24FKtjEsc73_z7-ffazHeedybLHBB8SjIuji-n8sCgKju9lewTXIsekpjvL_5LnNRNkN9uP8RJjQjgmD7LdgjIihKj2sp8jh6xrzMLAxyWk_XwB5i5FpFyD2t7pZL1THVScM7C5tmmAmuqGaCPyLQomJutmKCaVDGrPP56hRiWFFt4ubZJHzvQBHJxJNz5coWaIwcz6Ti2d4XSkmr5LaHQyPnmY3W9VF82jzXqQfX7z-tPxOJ98OD07Hk1yzYXAeYkVntKynbK2Zg2FHcFM1FoZ1dSkKJuKTw3mbcUo41xhIbiuWW0MZ4oq0tCD7OXad9FP56bRcGHoUC6CnaswSK-s_Lvi7IWc-WtZVmVd0QoMnm8Mgv_eQwJybqM2Xaec8X2UEHTNSMF5CejTO-il7wMEuKKqCnNoEqgnf3Z028r2qQB4tgFU1Kprg3Laxt9cVdSUs-VxR2tOBx8h6FZqm1ZRw0VsJwmWy6GRMDRyNTSgeHFHsTX9F7txv7GdGf4PyvGr860iXytsTObHrUKFK1kKKrj8-v5UivHbd984ncgv9Bd1HeGZ
CitedBy_id crossref_primary_10_1016_j_bbr_2017_06_026
crossref_primary_10_1002_hbm_24187
crossref_primary_10_1111_jcpp_13330
crossref_primary_10_1371_journal_pone_0265300
crossref_primary_10_1007_s10548_019_00719_7
crossref_primary_10_1186_s11689_020_09311_8
crossref_primary_10_1177_0883073816685652
crossref_primary_10_1016_j_nicl_2017_03_008
crossref_primary_10_3389_fnhum_2018_00279
crossref_primary_10_1016_j_cobme_2017_03_003
crossref_primary_10_1007_s11042_023_17962_7
crossref_primary_10_1016_j_dcn_2022_101101
crossref_primary_10_1098_rstb_2019_0691
crossref_primary_10_1177_10870547231155436
crossref_primary_10_3389_fpsyt_2015_00063
crossref_primary_10_1089_brain_2017_0486
crossref_primary_10_1002_hbm_22790
crossref_primary_10_1515_tnsci_2022_0299
crossref_primary_10_1016_j_clinph_2015_02_060
crossref_primary_10_1016_j_bpsgos_2021_06_003
crossref_primary_10_1162_netn_a_00034
crossref_primary_10_1111_acps_12573
crossref_primary_10_3758_s13415_024_01156_1
crossref_primary_10_1093_cercor_bhac506
crossref_primary_10_1186_s12868_020_00589_x
crossref_primary_10_1016_j_psychres_2019_06_040
crossref_primary_10_1176_appi_neuropsych_15060142
crossref_primary_10_1111_psyp_13539
crossref_primary_10_3389_fnhum_2020_594830
crossref_primary_10_1109_ACCESS_2020_2982401
crossref_primary_10_1016_j_pnpbp_2017_02_005
crossref_primary_10_1007_s10548_015_0463_1
crossref_primary_10_1016_j_psychres_2020_112785
crossref_primary_10_3389_fnsys_2021_629488
crossref_primary_10_1126_sciadv_abm9898
crossref_primary_10_1016_j_bbr_2021_113312
crossref_primary_10_1038_s41598_024_74282_y
crossref_primary_10_1038_srep21697
crossref_primary_10_1371_journal_pone_0139819
crossref_primary_10_1002_hbm_22850
crossref_primary_10_1586_14737175_2014_907526
crossref_primary_10_3389_fpsyg_2014_00183
crossref_primary_10_1016_j_neuroimage_2018_12_006
crossref_primary_10_1016_j_bpsc_2017_10_005
crossref_primary_10_1162_jocn_a_01396
crossref_primary_10_1007_s11633_020_1252_1
crossref_primary_10_1007_s10566_019_09542_4
crossref_primary_10_1016_j_ejrad_2015_02_018
crossref_primary_10_1002_aur_1971
crossref_primary_10_1002_hbm_23933
crossref_primary_10_1016_j_media_2014_06_006
crossref_primary_10_1002_hbm_25197
crossref_primary_10_1177_1087054715611492
crossref_primary_10_1016_j_neuroimage_2022_119045
crossref_primary_10_1155_2019_9027803
crossref_primary_10_1371_journal_pone_0306538
crossref_primary_10_1016_j_ijcard_2016_09_067
crossref_primary_10_2174_0929867326666190805153610
crossref_primary_10_1007_s11065_014_9251_z
crossref_primary_10_1002_cad_20331
crossref_primary_10_1177_1087054719837749
crossref_primary_10_1093_ijnp_pyv094
crossref_primary_10_1016_j_sleep_2020_05_038
crossref_primary_10_1371_journal_pone_0048286
crossref_primary_10_1186_s12888_016_1047_7
crossref_primary_10_1016_S2215_0366_16_00096_1
crossref_primary_10_1371_journal_pone_0215095
crossref_primary_10_1002_hbm_24013
crossref_primary_10_1016_j_nicl_2019_101653
crossref_primary_10_1192_bjp_2018_248
crossref_primary_10_1017_S003329171900237X
crossref_primary_10_3389_fnhum_2016_00565
crossref_primary_10_1016_j_pnpbp_2021_110340
crossref_primary_10_1523_JNEUROSCI_1043_23_2023
crossref_primary_10_1007_s00426_019_01245_8
crossref_primary_10_1016_j_neuroimage_2020_116688
crossref_primary_10_1016_j_pnpbp_2016_01_011
crossref_primary_10_3389_fnins_2017_00056
crossref_primary_10_3389_fpsyt_2014_00062
crossref_primary_10_1016_j_ijpsycho_2015_05_012
crossref_primary_10_3389_fgene_2021_728913
crossref_primary_10_1093_cercor_bhaa242
crossref_primary_10_1523_ENEURO_0543_19_2020
crossref_primary_10_2139_ssrn_3986944
crossref_primary_10_1007_s12402_015_0171_4
crossref_primary_10_3390_biom11081093
crossref_primary_10_1007_s00406_024_01872_2
crossref_primary_10_1038_s41398_019_0469_7
crossref_primary_10_1016_j_bpsc_2016_03_004
crossref_primary_10_1016_j_jaac_2020_08_014
crossref_primary_10_1016_j_artmed_2021_102209
crossref_primary_10_3389_fpsyt_2023_1208120
crossref_primary_10_1016_j_neuroimage_2019_01_076
crossref_primary_10_1038_s41598_023_47034_7
crossref_primary_10_1093_braincomms_fcae001
crossref_primary_10_3389_fnins_2023_1170090
crossref_primary_10_1016_j_eurpsy_2014_03_005
crossref_primary_10_1192_j_eurpsy_2022_2325
crossref_primary_10_1016_j_jpsychires_2022_02_032
crossref_primary_10_1038_s41380_021_01022_3
crossref_primary_10_1016_j_nicl_2015_08_015
crossref_primary_10_1016_j_biopsych_2015_10_017
crossref_primary_10_1017_S135561771500020X
crossref_primary_10_1007_s00429_015_1161_1
crossref_primary_10_3390_brainsci11060708
crossref_primary_10_1016_j_jaac_2016_04_020
crossref_primary_10_1038_s41398_021_01335_5
crossref_primary_10_1371_journal_pone_0173289
crossref_primary_10_1093_cercor_bhw209
crossref_primary_10_1016_j_dcn_2021_100980
crossref_primary_10_1177_10870547241233207
crossref_primary_10_1038_s41598_017_04579_8
crossref_primary_10_1016_j_bspc_2018_02_018
Cites_doi 10.1016/j.neuroimage.2007.07.021
10.2466/pr0.1995.77.3.751
10.1016/j.neulet.2006.02.022
10.1002/hbm.1048
10.1073/pnas.0704380104
10.1016/j.biopsych.2005.01.034
10.1073/pnas.0708965105
10.1097/00004583-199707000-00021
10.1126/science.281.5380.1188
10.1093/cercor/bhn117
10.1111/j.1471-4159.2007.04927.x
10.1111/j.1749-6632.2001.tb05772.x
10.1016/j.neubiorev.2007.02.005
10.1073/pnas.0601417103
10.1093/cercor/bhq104
10.1038/sj.npp.1300110
10.1016/S0006-3223(02)01412-9
10.1016/j.rpsm.2012.05.004
10.1111/j.1460-9568.2008.06254.x
10.1016/S0896-6273(02)00817-6
10.1016/j.jneumeth.2007.11.031
10.1038/nrn2201
10.1016/j.neuroimage.2010.10.060
10.1016/S0149-7634(99)00055-X
10.1016/j.biopsych.2007.06.025
10.1016/j.eurpsy.2010.12.010
10.1016/j.tics.2006.01.011
10.1093/cercor/bhq268
10.1016/S0140-6736(05)66915-2
10.1002/hbm.20581
10.1016/j.neuroimage.2008.05.008
10.1159/000285781
10.1371/journal.pone.0002017
10.1002/hbm.20530
10.1002/hbm.21368
10.1007/s00115-002-1447-4
10.1002/hbm.21170
10.1038/nn1727
10.1073/pnas.0504136102
10.1016/j.neuroimage.2011.10.010
10.3389/fnsys.2010.00021
10.1016/j.biopsych.2010.07.003
10.1093/cercor/bhq071
10.1073/pnas.0710329105
10.1016/j.biopsych.2006.04.031
10.1176/ajp.2007.164.3.450
10.1038/35094500
10.1016/j.neuroimage.2008.01.051
10.1371/journal.pone.0001794
10.1002/mpr.241
10.1002/hbm.20988
10.1016/j.braindev.2007.10.005
10.1080/02643291003665688
10.1093/cercor/bhn059
10.1016/j.brainres.2009.02.070
10.1177/070674370905401003
10.1080/09297040802646991
10.1126/science.1194144
10.1371/journal.pone.0048286
10.1176/appi.ajp.2009.08050724
10.1016/j.neuroimage.2010.02.010
10.1016/S0006-3223(98)00240-6
10.1001/archgenpsychiatry.2010.139
10.1016/j.neuroimage.2007.01.037
10.1073/pnas.98.2.676
10.1176/appi.ajp.2010.10030385
10.1038/nn1616
ContentType Journal Article
Copyright Copyright © 2013 Wiley Periodicals, Inc.
2015 INIST-CNRS
Copyright_xml – notice: Copyright © 2013 Wiley Periodicals, Inc.
– notice: 2015 INIST-CNRS
DBID BSCLL
AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7QR
7TK
7U7
8FD
C1K
FR3
K9.
P64
7X8
5PM
DOI 10.1002/hbm.22250
DatabaseName Istex
CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Chemoreception Abstracts
Neurosciences Abstracts
Toxicology Abstracts
Technology Research Database
Environmental Sciences and Pollution Management
Engineering Research Database
ProQuest Health & Medical Complete (Alumni)
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Technology Research Database
Toxicology Abstracts
ProQuest Health & Medical Complete (Alumni)
Chemoreception Abstracts
Engineering Research Database
Neurosciences Abstracts
Biotechnology and BioEngineering Abstracts
Environmental Sciences and Pollution Management
MEDLINE - Academic
DatabaseTitleList Technology Research Database

MEDLINE - Academic

CrossRef
MEDLINE
Database_xml – sequence: 1
  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: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Anatomy & Physiology
DocumentTitleAlternate Neural Network Dysregulation in Adult ADHD
EISSN 1097-0193
EndPage 1272
ExternalDocumentID PMC6869838
3251401561
23417778
28293546
10_1002_hbm_22250
HBM22250
ark_67375_WNG_7HJKX53L_V
Genre article
Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: Ministerio de Ciencia e Innovación research grant from the Centro para el Desarrollo Tecnológico Industrial
  funderid: SAF2009‐10901
– fundername: Ministerio de Educación y Ciencia (Spanish Government), Ph.D. Post Doctoral
– fundername: Ministerio de Ciencia e Innovación research grant from the Centro para el Desarrollo Tecnológico Industrial
  grantid: SAF2009‐10901
GroupedDBID ---
.3N
.GA
.Y3
05W
0R~
10A
1L6
1OB
1OC
1ZS
24P
31~
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5VS
66C
702
7PT
7X7
8-0
8-1
8-3
8-4
8-5
8FI
8FJ
8UM
930
A03
AAESR
AAEVG
AAFWJ
AAMMB
AANHP
AAONW
AAYCA
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABIVO
ABJNI
ABPVW
ABUWG
ACBWZ
ACCMX
ACGFS
ACIWK
ACPOU
ACPRK
ACRPL
ACSCC
ACXQS
ACYXJ
ADBBV
ADEOM
ADIZJ
ADMGS
ADNMO
ADPDF
ADXAS
AEFGJ
AEIMD
AENEX
AFBPY
AFGKR
AFKRA
AFPKN
AFRAH
AFZJQ
AGQPQ
AGXDD
AHMBA
AIDQK
AIDYY
AIQQE
AIURR
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
ASPBG
ATUGU
AUFTA
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BENPR
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BSCLL
BY8
CCPQU
CS3
D-E
D-F
DCZOG
DPXWK
DR1
DR2
DU5
EBD
EBS
EJD
EMOBN
F00
F01
F04
F5P
FEDTE
FYUFA
G-S
G.N
GAKWD
GNP
GODZA
GROUPED_DOAJ
H.T
H.X
HBH
HF~
HHY
HHZ
HMCUK
HVGLF
HZ~
IAO
IHR
ITC
IX1
J0M
JPC
KQQ
L7B
LAW
LC2
LC3
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
M6M
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
OK1
OVD
OVEED
P2P
P2W
P2X
P4D
PALCI
PHGZM
PHGZT
PIMPY
PQQKQ
PUEGO
Q.N
Q11
QB0
QRW
R.K
RIWAO
RJQFR
ROL
RPM
RX1
RYL
SAMSI
SUPJJ
SV3
TEORI
UB1
UKHRP
V2E
W8V
W99
WBKPD
WIB
WIH
WIK
WIN
WJL
WNSPC
WOHZO
WQJ
WXSBR
WYISQ
XG1
XSW
XV2
ZZTAW
~IA
~WT
33P
AAHHS
ACCFJ
ADZOD
AEEZP
AEQDE
AEUQT
AFPWT
AIWBW
AJBDE
ALIPV
C45
RWD
RWI
WRC
WUP
AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7QR
7TK
7U7
8FD
C1K
FR3
K9.
P64
7X8
5PM
ID FETCH-LOGICAL-c5770-60a0b36fb4f94d30a010479caead9126d85be05f843455a0775c949ee54a3a1d3
IEDL.DBID DR2
ISSN 1065-9471
1097-0193
IngestDate Thu Aug 21 14:10:53 EDT 2025
Sat Sep 27 23:27:05 EDT 2025
Sat Jul 26 02:26:28 EDT 2025
Mon Jul 21 05:48:52 EDT 2025
Wed Apr 02 07:37:51 EDT 2025
Thu Apr 24 23:07:57 EDT 2025
Tue Jul 01 04:26:01 EDT 2025
Wed Jan 22 16:31:00 EST 2025
Sun Sep 21 06:30:35 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Nervous system diseases
Radiodiagnosis
Hyperactivity
Central nervous system
Functional analysis
attention-deficit/hyperactivity disorder
Prefrontal cortex
Neural network
Nuclear magnetic resonance imaging
dorsolateral prefrontal cortex
Encephalon
Rest
independent components analysis
default mode network
functional magnetic resonance imaging
Functional imaging
rest
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
CC BY 4.0
Copyright © 2013 Wiley Periodicals, Inc.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c5770-60a0b36fb4f94d30a010479caead9126d85be05f843455a0775c949ee54a3a1d3
Notes ark:/67375/WNG-7HJKX53L-V
Ministerio de Educación y Ciencia (Spanish Government), Ph.D. Post Doctoral
ArticleID:HBM22250
istex:CA429A91A4ACB2D4606F188E03963C83B43BA608
Ministerio de Ciencia e Innovación research grant from the Centro para el Desarrollo Tecnológico Industrial - No. SAF2009-10901
These authors contributed equally to this work.
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
ObjectType-Article-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/6869838
PMID 23417778
PQID 1508805345
PQPubID 996345
PageCount 12
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_6869838
proquest_miscellaneous_1509412556
proquest_journals_1508805345
pubmed_primary_23417778
pascalfrancis_primary_28293546
crossref_citationtrail_10_1002_hbm_22250
crossref_primary_10_1002_hbm_22250
wiley_primary_10_1002_hbm_22250_HBM22250
istex_primary_ark_67375_WNG_7HJKX53L_V
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate April 2014
PublicationDateYYYYMMDD 2014-04-01
PublicationDate_xml – month: 04
  year: 2014
  text: April 2014
PublicationDecade 2010
PublicationPlace New York, NY
PublicationPlace_xml – name: New York, NY
– name: United States
– name: San Antonio
– name: Hoboken
PublicationTitle Human brain mapping
PublicationTitleAlternate Hum. Brain Mapp
PublicationYear 2014
Publisher Blackwell Publishing Ltd
Wiley-Liss
John Wiley & Sons, Inc
John Wiley and Sons Inc
Publisher_xml – name: Blackwell Publishing Ltd
– name: Wiley-Liss
– name: John Wiley & Sons, Inc
– name: John Wiley and Sons Inc
References Fox MD, Snyder AZ, Vincent JL, Corbetta M, Van Essen DC, Raichle ME (2005): The human brain is intrinsically organized into dynamic, anticorrelated functional networks. Proc Natl Acad Sci USA 102:9673-9678.
Wagner AD, Schacter DL, Rotte M, Koutstaal W, Maril A, Dale AM, Rosen BR, Buckner RL (1998): Building memories: remembering and forgetting of verbal experiences as predicted by brain activity. Science 281:1188-1191.
Yeh CB, Gau SS, Kessler RC, Wu YY (2008): Psychometric properties of the Chinese version of the adult ADHD Self-report Scale. Int J Methods Psychiatr Res 17:45-54.
Castellanos FX, Sonuga-Barke EJ, Milham MP, Tannock R (2006): Characterizing cognition in ADHD: Beyond executive dysfunction. Trends Cogn Sci 10:117-123.
Carmona S, Hoekzema E, Ramos-Quiroga JA, Richarte V, Canals C, Bosch R, Rovira M, Carlos SJ, Bulbena A, Tobena A, Casas M, Vilarroya O (2011): Response inhibition and reward anticipation in medication-naive adults with attention-deficit/hyperactivity disorder: A within-subject case-control neuroimaging study. Hum Brain Mapp 33:2350-2361.
Harrison BJ, Pujol J, Ortiz H, Fornito A, Pantelis C, Yucel M (2008): Modulation of brain resting-state networks by sad mood induction. PLoS One 3:e1794.
Buzy WM, Medoff DR, Schweitzer JB (2009): Intra-individual variability among children with ADHD on a working memory task: An ex-Gaussian approach. Child Neuropsychol 15:441-459.
Fox MD, Raichle ME (2007): Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging. Nat Rev Neurosci 8:700-711.
American Psychiatric Association. Task Force on DSM-IV (2000):Diagnostic and Statistical Manual of Mental Disorders: DSM IV-TR. Washington, DC:American Psychiatric Association.
Retz-Junginger P, Retz W, Blocher D, Stieglitz RD, Georg T, Supprian T, Wender PH, Rosler M (2003): Reliability and validity of the Wender-Utah-Rating-Scale short form. Retrospective assessment of symptoms for attention deficit/hyperactivity disorder. Nervenarzt 74:987-993.
Fransson P, Aden U, Blennow M, Lagercrantz H (2011): The functional architecture of the infant brain as revealed by resting-state FMRI. Cereb Cortex 21:145-154.
Hamilton AC, Martin RC, Burton PC (2010): Converging functional magnetic resonance imaging evidence for a role of the left inferior frontal lobe in semantic retention during language comprehension. Cogn Neuropsychol 26:685-704.
Mostofsky SH, Cooper KL, Kates WR, Denckla MB, Kaufmann WE (2002): Smaller prefrontal and premotor volumes in boys with attention-deficit/hyperactivity disorder. Biol Psychiatry 52:785-794.
Peterson BS, Potenza MN, Wang Z, Zhu H, Martin A, Marsh R, Plessen KJ, Yu S (2009): An FMRI study of the effects of psychostimulants on default-mode processing during Stroop task performance in youths with ADHD. Am J Psychiatry 166:1286-1294.
Sonuga-Barke EJ, Castellanos FX (2007): Spontaneous attentional fluctuations in impaired states and pathological conditions: a neurobiological hypothesis. Neurosci Biobehav Rev 31:977-986.
Fox MD, Snyder AZ, Zacks JM, Raichle ME (2006): Coherent spontaneous activity accounts for trial-to-trial variability in human evoked brain responses. Nat Neurosci 9:23-25.
Kelly AM, Di MA, Uddin LQ, Shehzad Z, Gee DG, Reiss PT, Margulies DS, Castellanos FX, Milham MP (2009): Development of anterior cingulate functional connectivity from late childhood to early adulthood. Cereb Cortex 19:640-657.
First M, Gibbon M, Spitzer R, William BW, Benjamin LS (1997):Interview for DSM-IV Axis II Personality Disorders SCID-II. Washington, DC:American Psychiatric Press.
Seidman LJ, Valera EM, Makris N, Monuteaux MC, Boriel DL, Kelkar K, Kennedy DN, Caviness VS, Bush G, Aleardi M, Faraone SV, Biederman J (2006): Dorsolateral prefrontal and anterior cingulate cortex volumetric abnormalities in adults with attention-deficit/hyperactivity disorder identified by magnetic resonance imaging. Biol Psychiatry 60:1071-1080.
Tomasi D, Volkow ND (2011): Association between functional connectivity hubs and brain networks. Cereb Cortex 21:2003-2013.
Singh KD, Fawcett IP (2008): Transient and linearly graded deactivation of the human default-mode network by a visual detection task. Neuroimage 41:100-112.
Volkow ND, Fowler JS, Wang GJ, Telang F, Logan J, Wong C, Ma J, Pradhan K, Benveniste H, Swanson JM (2008): Methylphenidate decreased the amount of glucose needed by the brain to perform a cognitive task. PLoS One 3:e2017.
Jezierski G, Zehle S, Bock J, Braun K, Gruss M (2007): Early stress and chronic methylphenidate cross-sensitize dopaminergic responses in the adolescent medial prefrontal cortex and nucleus accumbens. J Neurochem 103:2234-2244.
Dosenbach NU, Nardos B, Cohen AL, Fair DA, Power JD, Church JA, Nelson SM, Wig GS, Vogel AC, Lessov-Schlaggar CN, Barnes KA, Dubis JW, Feczko E, Coalson RS, Pruett JR Jr, Barch DM, Petersen SE, Schlaggar BL (2010): Prediction of individual brain maturity using fMRI. Science 329:1358-1361.
Rodriguez-Jimenez R, Ponce G, Monasor R, Jimenez-Gimenez M, Perez-Rojo JA, Rubio G, Jimenez A, Palomo T (2001): Validation in the adult Spanish population of the Wender Utah Rating Scale for the retrospective evaluation in adults of attention deficit/hyperactivity disorder in childhood. Rev Neurol 33:138-144.
Rossini ED, O'Connor MA (1995): Retrospective self-reported symptoms of attention-deficit hyperactivity disorder: Reliability of the Wender Utah Rating Scale. Psychol Rep 77:751-754.
Schweitzer JB, Lee DO, Hanford RB, Tagamets MA, Hoffman JM, Grafton ST, Kilts CD (2003): A positron emission tomography study of methylphenidate in adults with ADHD: alterations in resting blood flow and predicting treatment response. Neuropsychopharmacology 28:967-973.
Jolles DD, van Buchem MA, Crone EA, Rombouts SA (2011): A comprehensive study of whole-brain functional connectivity in children and young adults. Cereb Cortex 21:385-391.
Bush G, Valera EM, Seidman LJ (2005): Functional neuroimaging of attention-deficit/hyperactivity disorder: A review and suggested future directions. Biol Psychiatry 57:1273-1284.
Fair DA, Posner J, Nagel BJ, Bathula D, Dias TG, Mills KL, Blythe MS, Giwa A, Schmitt CF, Nigg JT (2010): Atypical default network connectivity in youth with attention-deficit/hyperactivity disorder. Biol Psychiatry 68:1084-1091.
Tian L, Jiang T, Liang M, Zang Y, He Y, Sui M, Wang Y (2008): Enhanced resting-state brain activities in ADHD patients: A fMRI study. Brain Dev 30:342-348.
DuPaul GJ, Power TJ, Anastopoulos AD, Reid R (1998):The ADHD rating scale-IV: Checklist, norms, and clinical interpretation. New York:Guilford Press.
Fassbender C, Zhang H, Buzy WM, Cortes CR, Mizuiri D, Beckett L, Schweitzer JB (2009): A lack of default network suppression is linked to increased distractibility in ADHD. Brain Res 1273:114-128.
Allen EA, Erhardt EB, Wei Y, Eichele T, Calhoun VD (2012): Capturing inter-subject variability with group independent component analysis of fMRI data: A simulation study. Neuroimage 59:4141-4159.
First M, Spitzer R, Gibbon M, Williams JBW (2002):Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Patient Edition. New York:Biometrics Research, New York State Psychiatric Institute.
Uddin LQ, Kelly AM, Biswal BB, Margulies DS, Shehzad Z, Shaw D, Ghaffari M, Rotrosen J, Adler LA, Castellanos FX, Milham MP (2008): Network homogeneity reveals decreased integrity of default-mode network in ADHD. J Neurosci Methods 169:249-254.
Uddin LQ, Supekar K, Menon V (2010): Typical and atypical development of functional human brain networks: Insights from resting-state FMRI. Front Syst Neurosci 4:21.
Garrity AG, Pearlson GD, McKiernan K, Lloyd D, Kiehl KA, Calhoun VD (2007): Aberrant "default mode" functional connectivity in schizophrenia. Am J Psychiatry 164:450-457.
Andersen SL, Napierata L, Brenhouse HC, Sonntag KC (2008): Juvenile methylphenidate modulates reward-related behaviors and cerebral blood flow by decreasing cortical D3 receptors. Eur J Neurosci 27:2962-2972.
Varoquaux G, Sadaghiani S, Pinel P, Kleinschmidt A, Poline JB, Thirion B (2010): A group model for stable multi-subject ICA on fMRI datasets. Neuroimage 51:288-299.
Tian L, Jiang T, Wang Y, Zang Y, He Y, Liang M, Sui M, Cao Q, Hu S, Peng M, Zhuo Y (2006): Altered resting-state functional connectivity patterns of anterior cingulate cortex in adolescents with attention deficit hyperactivity disorder. Neurosci Lett 400:39-43.
Stein MA, Sandoval R, Szumowski E, Roizen N, Reinecke MA, Blondis TA, Klein Z (1995): Psychometric characteristics of the Wender Utah Rating Scale (WURS): reliability and factor structure for men and women. Psychopharmacol Bull 31:425-433.
Wechsler D (1997):Wechsler Adult Intelligence Scale-III. San Antonio, TX: The Psychological Corporation.
Biederman J, Faraone SV (2005): Attention-deficit hyperactivity disorder. Lancet 366:237-248.
Hoekzema E, Carmona S, Ramos-Quiroga JA, Canals C, Moreno A, Richarte Fernández V, Picado M, Bosch R, Duno L, Soliva JC, Rovira M, Bulbena A, Tobena A, Casas M, Vilarroya O (2012a): Stimulant drugs trigger transient volumetric changes in the human ventral striatum. Brain Struct Funct. Epub ahead of print.
Greicius MD, Supekar K, Menon V, Dougherty RF (2009): Resting-state functional connectivity reflects structural connectivity in the default mode network. Cereb Cortex 19:72-78.
Guo Y, Pagnoni G (2008): A unified framework for group independent component analysis for multi-subject fMRI data. Neuroimage 42:1078-1093.
van 't Ent D, Lehn H, Derks EM, Hudziak JJ, Van Strien NM, Veltman DJ, De Geus EJ, Todd RD, Boomsma DI (2007): A structural MRI study in monozygotic twins concordant or discordant for attention/hyperactivity problems: Evidence for genetic and environmental heterogeneity in the developing brain. Neuroimage 35:1004-1020.
Hoekzema E, Carmona S, Ramos-Quiroga JA, Richarte Fernández V, Picado M, Bosch R, Soliva JC, Rovira M, Vives Y, Bulbena A, Tobena A, Casas M, Vilarroya O (2012b): Laminar thickness alterations in the fronto-parietal cortic
2007; 103
1995; 31
2007; 104
1998; 281
2002; 52
1995; 77
2011; 54
2008; 105
2008; 3
2008; 30
2012; 59
2007; 31
2007; 35
1998; 44
2010; 61
2007; 38
2010; 67
2006; 60
2011; 168
2010; 26
2009; 54
2010; 68
2000
2005; 102
2008; 29
2008; 27
2007; 8
2009; 166
2011; 21
2012a
2008; 63
2012; 27
2009; 1273
2009; 19
2001; 14
2010; 4
2009; 15
2001; 931
2006; 400
2001; 98
2010; 31
2010; 329
2006; 10
2000; 24
2002; 35
2006; 9
2007; 164
2008; 17
1998
1997
2011; 33
2011; 32
2008; 169
2002
2003; 74
2009; 30
2005; 366
1997; 36
1993; 150
2003; 28
2001; 2
2008; 41
2008; 42
2001; 33
2005; 16
2012; 5
2010; 51
2005; 57
2006; 103
2012b; 7
e_1_2_6_51_1
e_1_2_6_74_1
e_1_2_6_32_1
e_1_2_6_70_1
e_1_2_6_30_1
e_1_2_6_72_1
e_1_2_6_19_1
e_1_2_6_13_1
e_1_2_6_36_1
e_1_2_6_59_1
e_1_2_6_11_1
e_1_2_6_34_1
Stein MA (e_1_2_6_62_1) 1995; 31
Oncu B (e_1_2_6_47_1) 2005; 16
e_1_2_6_55_1
e_1_2_6_78_1
e_1_2_6_15_1
e_1_2_6_38_1
e_1_2_6_57_1
First M (e_1_2_6_23_1) 1997
e_1_2_6_64_1
e_1_2_6_43_1
e_1_2_6_20_1
e_1_2_6_41_1
e_1_2_6_60_1
Hoekzema E (e_1_2_6_37_1) 2012
e_1_2_6_9_1
e_1_2_6_5_1
e_1_2_6_7_1
e_1_2_6_49_1
e_1_2_6_22_1
e_1_2_6_66_1
e_1_2_6_28_1
e_1_2_6_45_1
Ward MF (e_1_2_6_75_1) 1993; 150
e_1_2_6_26_1
e_1_2_6_68_1
e_1_2_6_52_1
e_1_2_6_73_1
e_1_2_6_54_1
e_1_2_6_10_1
e_1_2_6_31_1
e_1_2_6_50_1
e_1_2_6_71_1
Rodriguez‐Jimenez R (e_1_2_6_53_1) 2001; 33
Wechsler D (e_1_2_6_76_1) 1997
e_1_2_6_14_1
e_1_2_6_35_1
e_1_2_6_12_1
e_1_2_6_33_1
e_1_2_6_18_1
e_1_2_6_39_1
e_1_2_6_56_1
e_1_2_6_77_1
e_1_2_6_16_1
e_1_2_6_58_1
e_1_2_6_63_1
e_1_2_6_42_1
e_1_2_6_65_1
e_1_2_6_21_1
e_1_2_6_40_1
e_1_2_6_61_1
e_1_2_6_8_1
American Psychiatric Association. Task Force on DSM‐IV (e_1_2_6_3_1) 2000
e_1_2_6_4_1
DuPaul GJ (e_1_2_6_17_1) 1998
First M (e_1_2_6_24_1) 2002
e_1_2_6_6_1
e_1_2_6_25_1
e_1_2_6_48_1
e_1_2_6_2_1
e_1_2_6_29_1
e_1_2_6_44_1
e_1_2_6_67_1
e_1_2_6_27_1
e_1_2_6_46_1
e_1_2_6_69_1
References_xml – reference: Peterson BS, Potenza MN, Wang Z, Zhu H, Martin A, Marsh R, Plessen KJ, Yu S (2009): An FMRI study of the effects of psychostimulants on default-mode processing during Stroop task performance in youths with ADHD. Am J Psychiatry 166:1286-1294.
– reference: Allen EA, Erhardt EB, Wei Y, Eichele T, Calhoun VD (2012): Capturing inter-subject variability with group independent component analysis of fMRI data: A simulation study. Neuroimage 59:4141-4159.
– reference: Uddin LQ, Supekar K, Menon V (2010): Typical and atypical development of functional human brain networks: Insights from resting-state FMRI. Front Syst Neurosci 4:21.
– reference: Volkow ND, Fowler JS, Wang GJ, Telang F, Logan J, Wong C, Ma J, Pradhan K, Benveniste H, Swanson JM (2008): Methylphenidate decreased the amount of glucose needed by the brain to perform a cognitive task. PLoS One 3:e2017.
– reference: Harrison BJ, Pujol J, Ortiz H, Fornito A, Pantelis C, Yucel M (2008): Modulation of brain resting-state networks by sad mood induction. PLoS One 3:e1794.
– reference: Calhoun VD, Kiehl KA, Pearlson GD (2008): Modulation of temporally coherent brain networks estimated using ICA at rest and during cognitive tasks. Hum Brain Mapp 29:828-838.
– reference: Erhardt EB, Rachakonda S, Bedrick EJ, Allen EA, Adali T, Calhoun VD (2011): Comparison of multi-subject ICA methods for analysis of fMRI data. Hum Brain Mapp 32:2075-2095.
– reference: Retz-Junginger P, Retz W, Blocher D, Stieglitz RD, Georg T, Supprian T, Wender PH, Rosler M (2003): Reliability and validity of the Wender-Utah-Rating-Scale short form. Retrospective assessment of symptoms for attention deficit/hyperactivity disorder. Nervenarzt 74:987-993.
– reference: Christiansen H, Kis B, Hirsch O, Matthies S, Hebebrand J, Uekermann J, bdel-Hamid M, Kraemer M, Wiltfang J, Graf E, Colla M, Sobanski E, Alm B, Rosler M, Jacob C, Jans T, Huss M, Schimmelmann BG, Philipsen A (2012): German validation of the conners adult ADHD rating scales (CAARS) II: reliability, validity, diagnostic sensitivity and specificity. Eur Psychiatry 27:321-328.
– reference: Kelly AM, Di MA, Uddin LQ, Shehzad Z, Gee DG, Reiss PT, Margulies DS, Castellanos FX, Milham MP (2009): Development of anterior cingulate functional connectivity from late childhood to early adulthood. Cereb Cortex 19:640-657.
– reference: Rubia K (2007): Neuro-anatomic evidence for the maturational delay hypothesis of ADHD. Proc Natl Acad Sci USA 104:19663-19664.
– reference: Tian L, Jiang T, Wang Y, Zang Y, He Y, Liang M, Sui M, Cao Q, Hu S, Peng M, Zhuo Y (2006): Altered resting-state functional connectivity patterns of anterior cingulate cortex in adolescents with attention deficit hyperactivity disorder. Neurosci Lett 400:39-43.
– reference: Wang L, Zhu C, He Y, Zang Y, Cao Q, Zhang H, Zhong Q, Wang Y (2009): Altered small-world brain functional networks in children with attention-deficit/hyperactivity disorder. Hum Brain Mapp 30:638-649.
– reference: Wechsler D (1997):Wechsler Adult Intelligence Scale-III. San Antonio, TX: The Psychological Corporation.
– reference: Jezierski G, Zehle S, Bock J, Braun K, Gruss M (2007): Early stress and chronic methylphenidate cross-sensitize dopaminergic responses in the adolescent medial prefrontal cortex and nucleus accumbens. J Neurochem 103:2234-2244.
– reference: Ward MF, Wender PH, Reimherr FW (1993): The Wender Utah Rating Scale: An aid in the retrospective diagnosis of childhood attention deficit hyperactivity disorder. Am J Psychiatry 150:885-890.
– reference: Giedd JN, Blumenthal J, Molloy E, Castellanos FX (2001): Brain imaging of attention deficit/hyperactivity disorder. Ann N Y Acad Sci 931:33-49.
– reference: Oncu B, Olmez S, Senturk V (2005): Validity and reliability of the Turkish version of the Wender Utah Rating Scale for attention-deficit/hyperactivity disorder in adults. Turk Psikiyatri Derg 16:252-259.
– reference: Rubia K, Overmeyer S, Taylor E, Brammer M, Williams SC, Simmons A, Andrew C, Bullmore ET (2000): Functional frontalisation with age: Mapping neurodevelopmental trajectories with fMRI. Neurosci Biobehav Rev 24:13-19.
– reference: Yeh CB, Gau SS, Kessler RC, Wu YY (2008): Psychometric properties of the Chinese version of the adult ADHD Self-report Scale. Int J Methods Psychiatr Res 17:45-54.
– reference: Rossini ED, O'Connor MA (1995): Retrospective self-reported symptoms of attention-deficit hyperactivity disorder: Reliability of the Wender Utah Rating Scale. Psychol Rep 77:751-754.
– reference: Biederman J, Faraone SV (2005): Attention-deficit hyperactivity disorder. Lancet 366:237-248.
– reference: Fox MD, Snyder AZ, Zacks JM, Raichle ME (2006): Coherent spontaneous activity accounts for trial-to-trial variability in human evoked brain responses. Nat Neurosci 9:23-25.
– reference: Varoquaux G, Sadaghiani S, Pinel P, Kleinschmidt A, Poline JB, Thirion B (2010): A group model for stable multi-subject ICA on fMRI datasets. Neuroimage 51:288-299.
– reference: Castellanos FX, Margulies DS, Kelly C, Uddin LQ, Ghaffari M, Kirsch A, Shaw D, Shehzad Z, Di MA, Biswal B, Sonuga-Barke EJ, Rotrosen J, Adler LA, Milham MP (2008): Cingulate-precuneus interactions: A new locus of dysfunction in adult attention-deficit/hyperactivity disorder. Biol Psychiatry 63:332-337.
– reference: Shaw P, Gilliam M, Liverpool M, Weddle C, Malek M, Sharp W, Greenstein D, Evans A, Rapoport J, Giedd J (2011): Cortical development in typically developing children with symptoms of hyperactivity and impulsivity: support for a dimensional view of attention deficit hyperactivity disorder. Am J Psychiatry 168:143-151.
– reference: Dosenbach NU, Nardos B, Cohen AL, Fair DA, Power JD, Church JA, Nelson SM, Wig GS, Vogel AC, Lessov-Schlaggar CN, Barnes KA, Dubis JW, Feczko E, Coalson RS, Pruett JR Jr, Barch DM, Petersen SE, Schlaggar BL (2010): Prediction of individual brain maturity using fMRI. Science 329:1358-1361.
– reference: Fox MD, Snyder AZ, Vincent JL, Corbetta M, Van Essen DC, Raichle ME (2005): The human brain is intrinsically organized into dynamic, anticorrelated functional networks. Proc Natl Acad Sci USA 102:9673-9678.
– reference: Andersen SL, Napierata L, Brenhouse HC, Sonntag KC (2008): Juvenile methylphenidate modulates reward-related behaviors and cerebral blood flow by decreasing cortical D3 receptors. Eur J Neurosci 27:2962-2972.
– reference: Tian L, Jiang T, Liang M, Zang Y, He Y, Sui M, Wang Y (2008): Enhanced resting-state brain activities in ADHD patients: A fMRI study. Brain Dev 30:342-348.
– reference: Mostofsky SH, Cooper KL, Kates WR, Denckla MB, Kaufmann WE (2002): Smaller prefrontal and premotor volumes in boys with attention-deficit/hyperactivity disorder. Biol Psychiatry 52:785-794.
– reference: Kaufman J, Birmaher B, Brent D, Rao U, Flynn C, Moreci P, Williamson D, Ryan N (1997): Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): Initial reliability and validity data. J Am Acad Child Adolesc Psychiatry 36:980-988.
– reference: Damoiseaux JS, Rombouts SA, Barkhof F, Scheltens P, Stam CJ, Smith SM, Beckmann CF (2006): Consistent resting-state networks across healthy subjects. Proc Natl Acad Sci USA 103:13848-13853.
– reference: Tomasi D, Volkow ND (2011): Association between functional connectivity hubs and brain networks. Cereb Cortex 21:2003-2013.
– reference: Fassbender C, Zhang H, Buzy WM, Cortes CR, Mizuiri D, Beckett L, Schweitzer JB (2009): A lack of default network suppression is linked to increased distractibility in ADHD. Brain Res 1273:114-128.
– reference: Rodriguez-Jimenez R, Ponce G, Monasor R, Jimenez-Gimenez M, Perez-Rojo JA, Rubio G, Jimenez A, Palomo T (2001): Validation in the adult Spanish population of the Wender Utah Rating Scale for the retrospective evaluation in adults of attention deficit/hyperactivity disorder in childhood. Rev Neurol 33:138-144.
– reference: Vanderhasselt MA, De RR, Leyman L, Baeken C (2010): Role of the left DLPFC in endogenous task preparation: Experimental repetitive transcranial magnetic stimulation study. Neuropsychobiology 61:162-168.
– reference: Castellanos FX, Kelly C, Milham MP (2009): The restless brain: Attention-deficit hyperactivity disorder, resting-state functional connectivity, and intrasubject variability. Can J Psychiatry 54:665-672.
– reference: Singh KD, Fawcett IP (2008): Transient and linearly graded deactivation of the human default-mode network by a visual detection task. Neuroimage 41:100-112.
– reference: Seidman LJ, Valera EM, Makris N, Monuteaux MC, Boriel DL, Kelkar K, Kennedy DN, Caviness VS, Bush G, Aleardi M, Faraone SV, Biederman J (2006): Dorsolateral prefrontal and anterior cingulate cortex volumetric abnormalities in adults with attention-deficit/hyperactivity disorder identified by magnetic resonance imaging. Biol Psychiatry 60:1071-1080.
– reference: Uddin LQ, Kelly AM, Biswal BB, Margulies DS, Shehzad Z, Shaw D, Ghaffari M, Rotrosen J, Adler LA, Castellanos FX, Milham MP (2008): Network homogeneity reveals decreased integrity of default-mode network in ADHD. J Neurosci Methods 169:249-254.
– reference: Gusnard DA, Raichle ME, Raichle ME (2001): Searching for a baseline: functional imaging and the resting human brain. Nat Rev Neurosci 2:685-694.
– reference: Fair DA, Posner J, Nagel BJ, Bathula D, Dias TG, Mills KL, Blythe MS, Giwa A, Schmitt CF, Nigg JT (2010): Atypical default network connectivity in youth with attention-deficit/hyperactivity disorder. Biol Psychiatry 68:1084-1091.
– reference: Bush G, Valera EM, Seidman LJ (2005): Functional neuroimaging of attention-deficit/hyperactivity disorder: A review and suggested future directions. Biol Psychiatry 57:1273-1284.
– reference: Eichele T, Debener S, Calhoun VD, Specht K, Engel AK, Hugdahl K, von Cramon DY, Ullsperger M (2008): Prediction of human errors by maladaptive changes in event-related brain networks. Proc Natl Acad Sci USA 105:6173-6178.
– reference: Calhoun VD, Adali T, Pearlson GD, Pekar JJ (2001): A method for making group inferences from functional MRI data using independent component analysis. Hum Brain Mapp 14:140-151.
– reference: Tomasi D, Volkow ND, Wang GJ, Wang R, Telang F, Caparelli EC, Wong C, Jayne M, Fowler JS (2011): Methylphenidate enhances brain activation and deactivation responses to visual attention and working memory tasks in healthy controls. Neuroimage 54:3101-3110.
– reference: American Psychiatric Association. Task Force on DSM-IV (2000):Diagnostic and Statistical Manual of Mental Disorders: DSM IV-TR. Washington, DC:American Psychiatric Association.
– reference: Ramos-Quiroga JA, Bosch R, Richarte Fernández V, Valero S, Gómez-Barros N, Nogueira M, Palomar G, Corrales M, Sáez-Francàs N, Corominas M, Real A, Vidal R, Chalita PJ, Casas M (2012): Validez de criterio y concurrente de la versión española de la Conners Adult ADHD Diagnostic Interview for DSM-IV. Rev Psiquiatr Salud Ment (Barc) 5:229-235.
– reference: Fox MD, Raichle ME (2007): Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging. Nat Rev Neurosci 8:700-711.
– reference: van 't Ent D, Lehn H, Derks EM, Hudziak JJ, Van Strien NM, Veltman DJ, De Geus EJ, Todd RD, Boomsma DI (2007): A structural MRI study in monozygotic twins concordant or discordant for attention/hyperactivity problems: Evidence for genetic and environmental heterogeneity in the developing brain. Neuroimage 35:1004-1020.
– reference: Hoekzema E, Carmona S, Ramos-Quiroga JA, Canals C, Moreno A, Richarte Fernández V, Picado M, Bosch R, Duno L, Soliva JC, Rovira M, Bulbena A, Tobena A, Casas M, Vilarroya O (2012a): Stimulant drugs trigger transient volumetric changes in the human ventral striatum. Brain Struct Funct. Epub ahead of print.
– reference: First M, Spitzer R, Gibbon M, Williams JBW (2002):Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Patient Edition. New York:Biometrics Research, New York State Psychiatric Institute.
– reference: Jolles DD, van Buchem MA, Crone EA, Rombouts SA (2011): A comprehensive study of whole-brain functional connectivity in children and young adults. Cereb Cortex 21:385-391.
– reference: Sonuga-Barke EJ, Castellanos FX (2007): Spontaneous attentional fluctuations in impaired states and pathological conditions: a neurobiological hypothesis. Neurosci Biobehav Rev 31:977-986.
– reference: Fransson P, Aden U, Blennow M, Lagercrantz H (2011): The functional architecture of the infant brain as revealed by resting-state FMRI. Cereb Cortex 21:145-154.
– reference: Raichle ME, MacLeod AM, Snyder AZ, Powers WJ, Gusnard DA, Shulman GL (2001): A default mode of brain function. Proc Natl Acad Sci USA 98:676-682.
– reference: Schweitzer JB, Lee DO, Hanford RB, Tagamets MA, Hoffman JM, Grafton ST, Kilts CD (2003): A positron emission tomography study of methylphenidate in adults with ADHD: alterations in resting blood flow and predicting treatment response. Neuropsychopharmacology 28:967-973.
– reference: Hoekzema E, Carmona S, Tremols V, Gispert JD, Guitart M, Fauquet J, Rovira M, Bielsa A, Soliva JC, Tomas X, Bulbena A, Ramos-Quiroga A, Casas M, Tobena A, Vilarroya O (2010): Enhanced neural activity in frontal and cerebellar circuits after cognitive training in children with attention-deficit/hyperactivity disorder. Hum Brain Mapp 31:1942-1950.
– reference: Li CS, Yan P, Bergquist KL, Sinha R (2007): Greater activation of the "default" brain regions predicts stop signal errors. Neuroimage 38:640-648.
– reference: Greicius MD, Supekar K, Menon V, Dougherty RF (2009): Resting-state functional connectivity reflects structural connectivity in the default mode network. Cereb Cortex 19:72-78.
– reference: Hoekzema E, Carmona S, Ramos-Quiroga JA, Richarte Fernández V, Picado M, Bosch R, Soliva JC, Rovira M, Vives Y, Bulbena A, Tobena A, Casas M, Vilarroya O (2012b): Laminar thickness alterations in the fronto-parietal cortical mantle of patients with attention-deficit/hyperactivity disorder. PLoS One 7:e48286.
– reference: Weissman DH, Roberts KC, Visscher KM, Woldorff MG (2006): The neural bases of momentary lapses in attention. Nat Neurosci 9:971-978.
– reference: Pessoa L, Gutierrez E, Bandettini P, Ungerleider L (2002): Neural correlates of visual working memory: fMRI amplitude predicts task performance. Neuron 35:975-987.
– reference: Guo Y, Pagnoni G (2008): A unified framework for group independent component analysis for multi-subject fMRI data. Neuroimage 42:1078-1093.
– reference: DuPaul GJ, Power TJ, Anastopoulos AD, Reid R (1998):The ADHD rating scale-IV: Checklist, norms, and clinical interpretation. New York:Guilford Press.
– reference: Faraone SV, Biederman J (1998): Neurobiology of attention-deficit hyperactivity disorder. Biol Psychiatry 44:951-958.
– reference: First M, Gibbon M, Spitzer R, William BW, Benjamin LS (1997):Interview for DSM-IV Axis II Personality Disorders SCID-II. Washington, DC:American Psychiatric Press.
– reference: Carmona S, Hoekzema E, Ramos-Quiroga JA, Richarte V, Canals C, Bosch R, Rovira M, Carlos SJ, Bulbena A, Tobena A, Casas M, Vilarroya O (2011): Response inhibition and reward anticipation in medication-naive adults with attention-deficit/hyperactivity disorder: A within-subject case-control neuroimaging study. Hum Brain Mapp 33:2350-2361.
– reference: Castellanos FX, Sonuga-Barke EJ, Milham MP, Tannock R (2006): Characterizing cognition in ADHD: Beyond executive dysfunction. Trends Cogn Sci 10:117-123.
– reference: Fransson P, Skiold B, Horsch S, Nordell A, Blennow M, Lagercrantz H, Aden U (2007): Resting-state networks in the infant brain. Proc Natl Acad Sci USA 104:15531-15536.
– reference: Wagner AD, Schacter DL, Rotte M, Koutstaal W, Maril A, Dale AM, Rosen BR, Buckner RL (1998): Building memories: remembering and forgetting of verbal experiences as predicted by brain activity. Science 281:1188-1191.
– reference: Buzy WM, Medoff DR, Schweitzer JB (2009): Intra-individual variability among children with ADHD on a working memory task: An ex-Gaussian approach. Child Neuropsychol 15:441-459.
– reference: Hamilton AC, Martin RC, Burton PC (2010): Converging functional magnetic resonance imaging evidence for a role of the left inferior frontal lobe in semantic retention during language comprehension. Cogn Neuropsychol 26:685-704.
– reference: Garrity AG, Pearlson GD, McKiernan K, Lloyd D, Kiehl KA, Calhoun VD (2007): Aberrant "default mode" functional connectivity in schizophrenia. Am J Psychiatry 164:450-457.
– reference: Kuntsi J, Wood AC, Rijsdijk F, Johnson KA, Andreou P, Albrecht B, rias-Vasquez A, Buitelaar JK, McLoughlin G, Rommelse NN, Sergeant JA, Sonuga-Barke EJ, Uebel H, van der Meere JJ, Banaschewski T, Gill M, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Steinhausen HC, Faraone SV, Asherson P (2010): Separation of cognitive impairments in attention-deficit/hyperactivity disorder into 2 familial factors. Arch Gen Psychiatry 67:1159-1167.
– reference: Stein MA, Sandoval R, Szumowski E, Roizen N, Reinecke MA, Blondis TA, Klein Z (1995): Psychometric characteristics of the Wender Utah Rating Scale (WURS): reliability and factor structure for men and women. Psychopharmacol Bull 31:425-433.
– volume: 169
  start-page: 249
  year: 2008
  end-page: 254
  article-title: Network homogeneity reveals decreased integrity of default‐mode network in ADHD
  publication-title: J Neurosci Methods
– volume: 77
  start-page: 751
  year: 1995
  end-page: 754
  article-title: Retrospective self‐reported symptoms of attention‐deficit hyperactivity disorder: Reliability of the Wender Utah Rating Scale
  publication-title: Psychol Rep
– volume: 931
  start-page: 33
  year: 2001
  end-page: 49
  article-title: Brain imaging of attention deficit/hyperactivity disorder
  publication-title: Ann N Y Acad Sci
– volume: 28
  start-page: 967
  year: 2003
  end-page: 973
  article-title: A positron emission tomography study of methylphenidate in adults with ADHD: alterations in resting blood flow and predicting treatment response
  publication-title: Neuropsychopharmacology
– volume: 150
  start-page: 885
  year: 1993
  end-page: 890
  article-title: The Wender Utah Rating Scale: An aid in the retrospective diagnosis of childhood attention deficit hyperactivity disorder
  publication-title: Am J Psychiatry
– volume: 103
  start-page: 13848
  year: 2006
  end-page: 13853
  article-title: Consistent resting‐state networks across healthy subjects
  publication-title: Proc Natl Acad Sci USA
– volume: 19
  start-page: 72
  year: 2009
  end-page: 78
  article-title: Resting‐state functional connectivity reflects structural connectivity in the default mode network
  publication-title: Cereb Cortex
– volume: 15
  start-page: 441
  year: 2009
  end-page: 459
  article-title: Intra‐individual variability among children with ADHD on a working memory task: An ex‐Gaussian approach
  publication-title: Child Neuropsychol
– volume: 42
  start-page: 1078
  year: 2008
  end-page: 1093
  article-title: A unified framework for group independent component analysis for multi‐subject fMRI data
  publication-title: Neuroimage
– volume: 3
  start-page: e2017
  year: 2008
  article-title: Methylphenidate decreased the amount of glucose needed by the brain to perform a cognitive task
  publication-title: PLoS One
– volume: 31
  start-page: 977
  year: 2007
  end-page: 986
  article-title: Spontaneous attentional fluctuations in impaired states and pathological conditions: a neurobiological hypothesis
  publication-title: Neurosci Biobehav Rev
– volume: 8
  start-page: 700
  year: 2007
  end-page: 711
  article-title: Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
  publication-title: Nat Rev Neurosci
– volume: 2
  start-page: 685
  year: 2001
  end-page: 694
  article-title: Searching for a baseline: functional imaging and the resting human brain
  publication-title: Nat Rev Neurosci
– volume: 102
  start-page: 9673
  year: 2005
  end-page: 9678
  article-title: The human brain is intrinsically organized into dynamic, anticorrelated functional networks
  publication-title: Proc Natl Acad Sci USA
– year: 2012a
  article-title: Stimulant drugs trigger transient volumetric changes in the human ventral striatum
  publication-title: Brain Struct Funct.
– volume: 400
  start-page: 39
  year: 2006
  end-page: 43
  article-title: Altered resting‐state functional connectivity patterns of anterior cingulate cortex in adolescents with attention deficit hyperactivity disorder
  publication-title: Neurosci Lett
– year: 1998
– volume: 329
  start-page: 1358
  year: 2010
  end-page: 1361
  article-title: Prediction of individual brain maturity using fMRI
  publication-title: Science
– volume: 63
  start-page: 332
  year: 2008
  end-page: 337
  article-title: Cingulate–precuneus interactions: A new locus of dysfunction in adult attention‐deficit/hyperactivity disorder
  publication-title: Biol Psychiatry
– volume: 166
  start-page: 1286
  year: 2009
  end-page: 1294
  article-title: An FMRI study of the effects of psychostimulants on default‐mode processing during Stroop task performance in youths with ADHD
  publication-title: Am J Psychiatry
– volume: 38
  start-page: 640
  year: 2007
  end-page: 648
  article-title: Greater activation of the “default” brain regions predicts stop signal errors
  publication-title: Neuroimage
– volume: 51
  start-page: 288
  year: 2010
  end-page: 299
  article-title: A group model for stable multi‐subject ICA on fMRI datasets
  publication-title: Neuroimage
– volume: 52
  start-page: 785
  year: 2002
  end-page: 794
  article-title: Smaller prefrontal and premotor volumes in boys with attention‐deficit/hyperactivity disorder
  publication-title: Biol Psychiatry
– volume: 36
  start-page: 980
  year: 1997
  end-page: 988
  article-title: Schedule for Affective Disorders and Schizophrenia for School‐Age Children‐Present and Lifetime Version (K‐SADS‐PL): Initial reliability and validity data
  publication-title: J Am Acad Child Adolesc Psychiatry
– volume: 16
  start-page: 252
  year: 2005
  end-page: 259
  article-title: Validity and reliability of the Turkish version of the Wender Utah Rating Scale for attention‐deficit/hyperactivity disorder in adults
  publication-title: Turk Psikiyatri Derg
– volume: 168
  start-page: 143
  year: 2011
  end-page: 151
  article-title: Cortical development in typically developing children with symptoms of hyperactivity and impulsivity: support for a dimensional view of attention deficit hyperactivity disorder
  publication-title: Am J Psychiatry
– year: 1997
– volume: 33
  start-page: 138
  year: 2001
  end-page: 144
  article-title: Validation in the adult Spanish population of the Wender Utah Rating Scale for the retrospective evaluation in adults of attention deficit/hyperactivity disorder in childhood
  publication-title: Rev Neurol
– volume: 30
  start-page: 342
  year: 2008
  end-page: 348
  article-title: Enhanced resting‐state brain activities in ADHD patients: A fMRI study
  publication-title: Brain Dev
– volume: 30
  start-page: 638
  year: 2009
  end-page: 649
  article-title: Altered small‐world brain functional networks in children with attention‐deficit/hyperactivity disorder
  publication-title: Hum Brain Mapp
– volume: 21
  start-page: 2003
  year: 2011
  end-page: 2013
  article-title: Association between functional connectivity hubs and brain networks
  publication-title: Cereb Cortex
– volume: 5
  start-page: 229
  year: 2012
  end-page: 235
  article-title: Validez de criterio y concurrente de la versión española de la Conners Adult ADHD Diagnostic Interview for DSM‐IV
  publication-title: Rev Psiquiatr Salud Ment (Barc)
– volume: 24
  start-page: 13
  year: 2000
  end-page: 19
  article-title: Functional frontalisation with age: Mapping neurodevelopmental trajectories with fMRI
  publication-title: Neurosci Biobehav Rev
– volume: 54
  start-page: 3101
  year: 2011
  end-page: 3110
  article-title: Methylphenidate enhances brain activation and deactivation responses to visual attention and working memory tasks in healthy controls
  publication-title: Neuroimage
– volume: 164
  start-page: 450
  year: 2007
  end-page: 457
  article-title: Aberrant “default mode” functional connectivity in schizophrenia
  publication-title: Am J Psychiatry
– volume: 59
  start-page: 4141
  year: 2012
  end-page: 4159
  article-title: Capturing inter‐subject variability with group independent component analysis of fMRI data: A simulation study
  publication-title: Neuroimage
– volume: 35
  start-page: 1004
  year: 2007
  end-page: 1020
  article-title: A structural MRI study in monozygotic twins concordant or discordant for attention/hyperactivity problems: Evidence for genetic and environmental heterogeneity in the developing brain
  publication-title: Neuroimage
– volume: 67
  start-page: 1159
  year: 2010
  end-page: 1167
  article-title: Separation of cognitive impairments in attention‐deficit/hyperactivity disorder into 2 familial factors
  publication-title: Arch Gen Psychiatry
– year: 2000
– volume: 366
  start-page: 237
  year: 2005
  end-page: 248
  article-title: Attention‐deficit hyperactivity disorder
  publication-title: Lancet
– volume: 14
  start-page: 140
  year: 2001
  end-page: 151
  article-title: A method for making group inferences from functional MRI data using independent component analysis
  publication-title: Hum Brain Mapp
– volume: 98
  start-page: 676
  year: 2001
  end-page: 682
  article-title: A default mode of brain function
  publication-title: Proc Natl Acad Sci USA
– volume: 74
  start-page: 987
  year: 2003
  end-page: 993
  article-title: Reliability and validity of the Wender‐Utah‐Rating‐Scale short form. Retrospective assessment of symptoms for attention deficit/hyperactivity disorder
  publication-title: Nervenarzt
– volume: 27
  start-page: 2962
  year: 2008
  end-page: 2972
  article-title: Juvenile methylphenidate modulates reward‐related behaviors and cerebral blood flow by decreasing cortical D3 receptors
  publication-title: Eur J Neurosci
– volume: 26
  start-page: 685
  year: 2010
  end-page: 704
  article-title: Converging functional magnetic resonance imaging evidence for a role of the left inferior frontal lobe in semantic retention during language comprehension
  publication-title: Cogn Neuropsychol
– volume: 29
  start-page: 828
  year: 2008
  end-page: 838
  article-title: Modulation of temporally coherent brain networks estimated using ICA at rest and during cognitive tasks
  publication-title: Hum Brain Mapp
– volume: 60
  start-page: 1071
  year: 2006
  end-page: 1080
  article-title: Dorsolateral prefrontal and anterior cingulate cortex volumetric abnormalities in adults with attention‐deficit/hyperactivity disorder identified by magnetic resonance imaging
  publication-title: Biol Psychiatry
– volume: 61
  start-page: 162
  year: 2010
  end-page: 168
  article-title: Role of the left DLPFC in endogenous task preparation: Experimental repetitive transcranial magnetic stimulation study
  publication-title: Neuropsychobiology
– volume: 10
  start-page: 117
  year: 2006
  end-page: 123
  article-title: Characterizing cognition in ADHD: Beyond executive dysfunction
  publication-title: Trends Cogn Sci
– volume: 44
  start-page: 951
  year: 1998
  end-page: 958
  article-title: Neurobiology of attention‐deficit hyperactivity disorder
  publication-title: Biol Psychiatry
– volume: 104
  start-page: 15531
  year: 2007
  end-page: 15536
  article-title: Resting‐state networks in the infant brain
  publication-title: Proc Natl Acad Sci USA
– volume: 57
  start-page: 1273
  year: 2005
  end-page: 1284
  article-title: Functional neuroimaging of attention‐deficit/hyperactivity disorder: A review and suggested future directions
  publication-title: Biol Psychiatry
– volume: 281
  start-page: 1188
  year: 1998
  end-page: 1191
  article-title: Building memories: remembering and forgetting of verbal experiences as predicted by brain activity
  publication-title: Science
– volume: 41
  start-page: 100
  year: 2008
  end-page: 112
  article-title: Transient and linearly graded deactivation of the human default‐mode network by a visual detection task
  publication-title: Neuroimage
– volume: 21
  start-page: 145
  year: 2011
  end-page: 154
  article-title: The functional architecture of the infant brain as revealed by resting‐state FMRI
  publication-title: Cereb Cortex
– volume: 35
  start-page: 975
  year: 2002
  end-page: 987
  article-title: Neural correlates of visual working memory: fMRI amplitude predicts task performance
  publication-title: Neuron
– volume: 9
  start-page: 23
  year: 2006
  end-page: 25
  article-title: Coherent spontaneous activity accounts for trial‐to‐trial variability in human evoked brain responses
  publication-title: Nat Neurosci
– volume: 19
  start-page: 640
  year: 2009
  end-page: 657
  article-title: Development of anterior cingulate functional connectivity from late childhood to early adulthood
  publication-title: Cereb Cortex
– volume: 9
  start-page: 971
  year: 2006
  end-page: 978
  article-title: The neural bases of momentary lapses in attention
  publication-title: Nat Neurosci
– volume: 68
  start-page: 1084
  year: 2010
  end-page: 1091
  article-title: Atypical default network connectivity in youth with attention‐deficit/hyperactivity disorder
  publication-title: Biol Psychiatry
– volume: 31
  start-page: 425
  year: 1995
  end-page: 433
  article-title: Psychometric characteristics of the Wender Utah Rating Scale (WURS): reliability and factor structure for men and women
  publication-title: Psychopharmacol Bull
– year: 2002
– volume: 104
  start-page: 19663
  year: 2007
  end-page: 19664
  article-title: Neuro‐anatomic evidence for the maturational delay hypothesis of ADHD
  publication-title: Proc Natl Acad Sci USA
– volume: 3
  start-page: e1794
  year: 2008
  article-title: Modulation of brain resting‐state networks by sad mood induction
  publication-title: PLoS One
– volume: 21
  start-page: 385
  year: 2011
  end-page: 391
  article-title: A comprehensive study of whole‐brain functional connectivity in children and young adults
  publication-title: Cereb Cortex
– volume: 4
  start-page: 21
  year: 2010
  article-title: Typical and atypical development of functional human brain networks: Insights from resting‐state FMRI
  publication-title: Front Syst Neurosci
– volume: 33
  start-page: 2350
  year: 2011
  end-page: 2361
  article-title: Response inhibition and reward anticipation in medication‐naive adults with attention‐deficit/hyperactivity disorder: A within‐subject case–control neuroimaging study
  publication-title: Hum Brain Mapp
– volume: 54
  start-page: 665
  year: 2009
  end-page: 672
  article-title: The restless brain: Attention‐deficit hyperactivity disorder, resting‐state functional connectivity, and intrasubject variability
  publication-title: Can J Psychiatry
– volume: 32
  start-page: 2075
  year: 2011
  end-page: 2095
  article-title: Comparison of multi‐subject ICA methods for analysis of fMRI data
  publication-title: Hum Brain Mapp
– volume: 7
  start-page: e48286
  year: 2012b
  article-title: Laminar thickness alterations in the fronto‐parietal cortical mantle of patients with attention‐deficit/hyperactivity disorder
  publication-title: PLoS One
– volume: 1273
  start-page: 114
  year: 2009
  end-page: 128
  article-title: A lack of default network suppression is linked to increased distractibility in ADHD
  publication-title: Brain Res
– volume: 17
  start-page: 45
  year: 2008
  end-page: 54
  article-title: Psychometric properties of the Chinese version of the adult ADHD Self‐report Scale
  publication-title: Int J Methods Psychiatr Res
– volume: 27
  start-page: 321
  year: 2012
  end-page: 328
  article-title: German validation of the conners adult ADHD rating scales (CAARS) II: reliability, validity, diagnostic sensitivity and specificity
  publication-title: Eur Psychiatry
– volume: 103
  start-page: 2234
  year: 2007
  end-page: 2244
  article-title: Early stress and chronic methylphenidate cross‐sensitize dopaminergic responses in the adolescent medial prefrontal cortex and nucleus accumbens
  publication-title: J Neurochem
– volume: 105
  start-page: 6173
  year: 2008
  end-page: 6178
  article-title: Prediction of human errors by maladaptive changes in event‐related brain networks
  publication-title: Proc Natl Acad Sci USA
– volume: 31
  start-page: 1942
  year: 2010
  end-page: 1950
  article-title: Enhanced neural activity in frontal and cerebellar circuits after cognitive training in children with attention‐deficit/hyperactivity disorder
  publication-title: Hum Brain Mapp
– ident: e_1_2_6_45_1
  doi: 10.1016/j.neuroimage.2007.07.021
– ident: e_1_2_6_54_1
  doi: 10.2466/pr0.1995.77.3.751
– ident: e_1_2_6_64_1
  doi: 10.1016/j.neulet.2006.02.022
– volume-title: The ADHD rating scale‐IV: Checklist, norms, and clinical interpretation
  year: 1998
  ident: e_1_2_6_17_1
– ident: e_1_2_6_8_1
  doi: 10.1002/hbm.1048
– ident: e_1_2_6_29_1
  doi: 10.1073/pnas.0704380104
– ident: e_1_2_6_6_1
  doi: 10.1016/j.biopsych.2005.01.034
– ident: e_1_2_6_18_1
  doi: 10.1073/pnas.0708965105
– ident: e_1_2_6_42_1
  doi: 10.1097/00004583-199707000-00021
– ident: e_1_2_6_73_1
  doi: 10.1126/science.281.5380.1188
– ident: e_1_2_6_43_1
  doi: 10.1093/cercor/bhn117
– ident: e_1_2_6_40_1
  doi: 10.1111/j.1471-4159.2007.04927.x
– volume-title: Diagnostic and Statistical Manual of Mental Disorders: DSM IV‐TR
  year: 2000
  ident: e_1_2_6_3_1
– ident: e_1_2_6_31_1
  doi: 10.1111/j.1749-6632.2001.tb05772.x
– volume: 16
  start-page: 252
  year: 2005
  ident: e_1_2_6_47_1
  article-title: Validity and reliability of the Turkish version of the Wender Utah Rating Scale for attention‐deficit/hyperactivity disorder in adults
  publication-title: Turk Psikiyatri Derg
– ident: e_1_2_6_61_1
  doi: 10.1016/j.neubiorev.2007.02.005
– ident: e_1_2_6_15_1
  doi: 10.1073/pnas.0601417103
– ident: e_1_2_6_41_1
  doi: 10.1093/cercor/bhq104
– volume: 150
  start-page: 885
  year: 1993
  ident: e_1_2_6_75_1
  article-title: The Wender Utah Rating Scale: An aid in the retrospective diagnosis of childhood attention deficit hyperactivity disorder
  publication-title: Am J Psychiatry
– volume-title: Structured Clinical Interview for DSM‐IV‐TR Axis I Disorders, Research Version, Patient Edition
  year: 2002
  ident: e_1_2_6_24_1
– ident: e_1_2_6_57_1
  doi: 10.1038/sj.npp.1300110
– volume-title: Interview for DSM‐IV Axis II Personality Disorders SCID‐II
  year: 1997
  ident: e_1_2_6_23_1
– ident: e_1_2_6_46_1
  doi: 10.1016/S0006-3223(02)01412-9
– ident: e_1_2_6_51_1
  doi: 10.1016/j.rpsm.2012.05.004
– ident: e_1_2_6_4_1
  doi: 10.1111/j.1460-9568.2008.06254.x
– ident: e_1_2_6_48_1
  doi: 10.1016/S0896-6273(02)00817-6
– ident: e_1_2_6_67_1
  doi: 10.1016/j.jneumeth.2007.11.031
– ident: e_1_2_6_25_1
  doi: 10.1038/nrn2201
– ident: e_1_2_6_66_1
  doi: 10.1016/j.neuroimage.2010.10.060
– ident: e_1_2_6_56_1
  doi: 10.1016/S0149-7634(99)00055-X
– ident: e_1_2_6_12_1
  doi: 10.1016/j.biopsych.2007.06.025
– ident: e_1_2_6_14_1
  doi: 10.1016/j.eurpsy.2010.12.010
– ident: e_1_2_6_13_1
  doi: 10.1016/j.tics.2006.01.011
– ident: e_1_2_6_65_1
  doi: 10.1093/cercor/bhq268
– ident: e_1_2_6_5_1
  doi: 10.1016/S0140-6736(05)66915-2
– ident: e_1_2_6_9_1
  doi: 10.1002/hbm.20581
– ident: e_1_2_6_33_1
  doi: 10.1016/j.neuroimage.2008.05.008
– volume: 31
  start-page: 425
  year: 1995
  ident: e_1_2_6_62_1
  article-title: Psychometric characteristics of the Wender Utah Rating Scale (WURS): reliability and factor structure for men and women
  publication-title: Psychopharmacol Bull
– ident: e_1_2_6_70_1
  doi: 10.1159/000285781
– ident: e_1_2_6_72_1
  doi: 10.1371/journal.pone.0002017
– ident: e_1_2_6_74_1
  doi: 10.1002/hbm.20530
– ident: e_1_2_6_10_1
  doi: 10.1002/hbm.21368
– year: 2012
  ident: e_1_2_6_37_1
  article-title: Stimulant drugs trigger transient volumetric changes in the human ventral striatum
  publication-title: Brain Struct Funct.
– ident: e_1_2_6_52_1
  doi: 10.1007/s00115-002-1447-4
– ident: e_1_2_6_19_1
  doi: 10.1002/hbm.21170
– ident: e_1_2_6_77_1
  doi: 10.1038/nn1727
– ident: e_1_2_6_26_1
  doi: 10.1073/pnas.0504136102
– ident: e_1_2_6_2_1
  doi: 10.1016/j.neuroimage.2011.10.010
– ident: e_1_2_6_68_1
  doi: 10.3389/fnsys.2010.00021
– ident: e_1_2_6_20_1
  doi: 10.1016/j.biopsych.2010.07.003
– ident: e_1_2_6_28_1
  doi: 10.1093/cercor/bhq071
– ident: e_1_2_6_55_1
  doi: 10.1073/pnas.0710329105
– ident: e_1_2_6_58_1
  doi: 10.1016/j.biopsych.2006.04.031
– ident: e_1_2_6_30_1
  doi: 10.1176/ajp.2007.164.3.450
– ident: e_1_2_6_34_1
  doi: 10.1038/35094500
– ident: e_1_2_6_60_1
  doi: 10.1016/j.neuroimage.2008.01.051
– ident: e_1_2_6_36_1
  doi: 10.1371/journal.pone.0001794
– ident: e_1_2_6_78_1
  doi: 10.1002/mpr.241
– ident: e_1_2_6_39_1
  doi: 10.1002/hbm.20988
– ident: e_1_2_6_63_1
  doi: 10.1016/j.braindev.2007.10.005
– ident: e_1_2_6_35_1
  doi: 10.1080/02643291003665688
– ident: e_1_2_6_32_1
  doi: 10.1093/cercor/bhn059
– volume-title: Wechsler Adult Intelligence Scale‐III
  year: 1997
  ident: e_1_2_6_76_1
– ident: e_1_2_6_22_1
  doi: 10.1016/j.brainres.2009.02.070
– ident: e_1_2_6_11_1
  doi: 10.1177/070674370905401003
– ident: e_1_2_6_7_1
  doi: 10.1080/09297040802646991
– ident: e_1_2_6_16_1
  doi: 10.1126/science.1194144
– ident: e_1_2_6_38_1
  doi: 10.1371/journal.pone.0048286
– ident: e_1_2_6_49_1
  doi: 10.1176/appi.ajp.2009.08050724
– volume: 33
  start-page: 138
  year: 2001
  ident: e_1_2_6_53_1
  article-title: Validation in the adult Spanish population of the Wender Utah Rating Scale for the retrospective evaluation in adults of attention deficit/hyperactivity disorder in childhood
  publication-title: Rev Neurol
– ident: e_1_2_6_71_1
  doi: 10.1016/j.neuroimage.2010.02.010
– ident: e_1_2_6_21_1
  doi: 10.1016/S0006-3223(98)00240-6
– ident: e_1_2_6_44_1
  doi: 10.1001/archgenpsychiatry.2010.139
– ident: e_1_2_6_69_1
  doi: 10.1016/j.neuroimage.2007.01.037
– ident: e_1_2_6_50_1
  doi: 10.1073/pnas.98.2.676
– ident: e_1_2_6_59_1
  doi: 10.1176/appi.ajp.2010.10030385
– ident: e_1_2_6_27_1
  doi: 10.1038/nn1616
SSID ssj0011501
Score 2.4777446
Snippet Spontaneous fluctuations can be measured in the brain that reflect dissociable functional networks oscillating at synchronized frequencies, such as the default...
SourceID pubmedcentral
proquest
pubmed
pascalfrancis
crossref
wiley
istex
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1261
SubjectTerms Adult
Attention Deficit Disorder with Hyperactivity - physiopathology
attention-deficit/hyperactivity disorder
Biological and medical sciences
Brain - physiopathology
Brain Mapping - methods
default mode network
dorsolateral prefrontal cortex
Electrodiagnosis. Electric activity recording
Functional Laterality
functional magnetic resonance imaging
Humans
independent components analysis
Investigative techniques, diagnostic techniques (general aspects)
Magnetic Resonance Imaging - methods
Male
Medical sciences
Nervous system
Neural Pathways - physiopathology
Prefrontal Cortex - physiopathology
Radiodiagnosis. Nmr imagery. Nmr spectrometry
rest
Rest - physiology
Signal Processing, Computer-Assisted
Title An independent components and functional connectivity analysis of resting state fMRI data points to neural network dysregulation in adult ADHD
URI https://api.istex.fr/ark:/67375/WNG-7HJKX53L-V/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.22250
https://www.ncbi.nlm.nih.gov/pubmed/23417778
https://www.proquest.com/docview/1508805345
https://www.proquest.com/docview/1509412556
https://pubmed.ncbi.nlm.nih.gov/PMC6869838
Volume 35
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fb9MwED5NQ0K8wNiAhY3JIDTtJV1S20ksngplhEH3MDHoA1Lk_GLVWDKtqcT4I_ibubOTjMKQEG-NfHbl0-e7s33-DuB5oTxPh1Hu8jxTLoIic1VEdHd-xkupeRmV9FB4chTEJ-JwKqcr8KJ7C2P5IfoDN1oZxl7TAtfpfP-aNPQ0PR_QZoX26z4PiDd_fNxTR1GgYzZb6GJdhRa4YxXyhvt9zyVfdIvU-o1yI_Uc1VPauhY3BZ5_5k_-Gtcax3RwDz53U7L5KGeDRZMOsu-_sT3-55zX4G4bsLKRRdh9WCmqddgYVbhZP79iu8ykkJqz-XW4PWlv6jfgx6his77EbsModb2uKGuD6Spn5E7tKSS2oKnPbBELbLMcKawuGVUNQcfKzJsnVk6O3zLKZ2UX9YyGaWpGZJw4QmVT2Vl-hTr-0tYjw39nhlyEjcbx-AGcHLz-8Cp229oPbibDEHe0nvZSHpSpKJXIOX4Rp4TKNCJf-cMgj2RaeLKMBBdSaiLyy5RQRSGF5trP-UNYrXBam8DQA6PckKtCcZF5hVJ5Tix2aHwQmqF2YK9DQZK1xOhUn-NrYimdhwmqPTFqd-BZL3ph2UBuEto1UOol9OUZpc-FMvl09CYJ48N3U8nfJx8d2FnCWt-Bbre5FIED2x34kta0zBMi8I_QdArpwNO-GY0C3fToqqgXRkYJn9jlHHhksXo9OM49DMPIgXAJxb0AEY4vt1SzU0M8HkSBijj23DMg_bsKkvjlxPx4_O-iW3AHg9E2K2obVpvLRfEEA74m3TEr-yeF_FLB
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxEB5VrQRceLQ8FkoxCFW9bLqJ7d21xCVQyrZNcqhayAVZ3heNSnerNpEoP4LfzIy92RIoEuKWlceOPPo8M7bH3wC8LlQQmCjOfZ5nykdQZL6Kie6um_FSGl7GJT0UHo7C5Fjsj-V4Cd7M38I4foj2wI1WhrXXtMDpQHr7mjX0JD3r0G4FN-wr9n6OQqLDljyKQh273UIn6yu0wXNeoaC33XZd8EYrpNhvlB1pLlFBpatscVPo-WcG5a-RrXVNu_fg83xSLiPltDObpp3s-298j_876_twt4lZWd-B7AEsFdUqrPUr3K-fXbFNZrNI7fH8KtwaNpf1a_CjX7FJW2V3yih7va4ocYOZKmfkUd1BJLagtc9cHQtsczQprC4ZFQ5B38rssydWDg_3GKW0svN6QsNMa0Z8nDhC5bLZWX6FSv7SlCTDf2eWX4T1d5Kdh3C8-_7oXeI35R_8TEYRbmoDE6Q8LFNRKpFz_CJaCZUZBL_q9sI8lmkRyDIWXEhpiMsvU0IVhRSGm27OH8FyhdN6AgydMMr1uCoUF1lQKJXnRGSH9gfRGRkPtuYw0FnDjU4lOr5qx-rc06h2bdXuwatW9NwRgtwktGmx1EqYi1PKoIuk_jT6oKNk_2As-UB_9GBjAWxtB7rg5lKEHqzP0acb63KpicM_RusppAcv22a0C3TZY6qinlkZJbpEMOfBYwfW68Fx7lEUxR5ECzBuBYhzfLGlmpxY7vEwDlXMseeWRenfVaCTt0P74-m_i76A28nRcKAHe6ODZ3AHY9MmSWodlqcXs-I5xn_TdMMu85-DbFbf
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxEB5VrVRx4dHyWCjFIFT1sukmtnfX4hQIIX0kQhWFHJAs74tGpbtRm0iUH8FvZsbebAkUCXHLymNHHn2eGdvjbwBe5ioITBRnPs9S5SMoUl_FRHfXTnkhDS_igh4KD0fh4EQcjOV4BV4t3sI4fojmwI1WhrXXtMCnWbF3TRp6mpy3aLOC-_U1EaKbpIjouOGOokjH7rbQx_oKTfCCVijo7DVdl5zRGun1GyVHmkvUT-EKW9wUef6ZQPlrYGs9U_8OfF7MySWknLXms6SVfv-N7vE_J30XbtcRK-s6iN2DlbzcgM1uibv18yu2w2wOqT2c34D1YX1Vvwk_uiWbNDV2Z4xy16uS0jaYKTNG_tQdQ2IL2vrUVbHANkeSwqqCUdkQ9KzMPnpixfB4n1FCK5tWExpmVjFi48QRSpfLzrIr1PGXuiAZ_juz7CKs2xv07sNJ_-2HNwO_Lv7gpzKKcEsbmCDhYZGIQomM4xeRSqjUIPRVuxNmsUzyQBax4EJKQ0x-qRIqz6Uw3LQz_gBWS5zWI2DoglGuw1WuuEiDXKksIxo7tD6Izch4sLtAgU5rZnQq0PFVO07njka1a6t2D140olNHB3KT0I6FUiNhLs4ofy6S-tPonY4GB4djyY_0Rw-2l7DWdKDrbS5F6MHWAny6ti2Xmhj8Y7SdQnrwvGlGq0BXPabMq7mVUaJN9HIePHRYvR4c5x5FUexBtITiRoAYx5dbysmpZR4P41DFHHvuWpD-XQV68Hpofzz-d9FnsP6-19dH-6PDJ3ALA9M6Q2oLVmcX8_wpBn-zZNsu8p9DYVWO
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=An+independent+components+and+functional+connectivity+analysis+of+resting+state+fMRI+data+points+to+neural+network+dysregulation+in+adult+ADHD&rft.jtitle=Human+brain+mapping&rft.au=Hoekzema%2C+Elseline&rft.au=Carmona%2C+Susana&rft.au=Ramos-Quiroga%2C+J+Antoni&rft.au=Richarte+Fern%C3%A1ndez%2C+Vanesa&rft.date=2014-04-01&rft.eissn=1097-0193&rft.volume=35&rft.issue=4&rft.spage=1261&rft_id=info:doi/10.1002%2Fhbm.22250&rft_id=info%3Apmid%2F23417778&rft.externalDocID=23417778
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1065-9471&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1065-9471&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1065-9471&client=summon