001     62197
005     20180211162250.0
024 7 _ |2 pmid
|a pmid:18356764
024 7 _ |2 DOI
|a 10.1097/CHI.0b013e3181676545
024 7 _ |2 WOS
|a WOS:000255261000010
037 _ _ |a PreJuSER-62197
041 _ _ |a eng
082 _ _ |a 150
084 _ _ |2 WoS
|a Psychology, Developmental
084 _ _ |2 WoS
|a Pediatrics
084 _ _ |2 WoS
|a Psychiatry
100 1 _ |a Huebner, T.
|b 0
|0 P:(DE-HGF)0
245 _ _ |a Morphometric brain abnormalities in boys with conduct disorder
260 _ _ |a Kidlington [u.a.]
|b Elsevier
|c 2008
300 _ _ |a 540 - 547
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Journal of the American Academy of Child and Adolescent Psychiatry
|x 0890-8567
|0 18041
|y 5
|v 47
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Children with the early-onset type of conduct disorder (CD) are at high risk for developing an antisocial personality disorder. Although there have been several neuroimaging studies on morphometric differences in adults with antisocial personality disorder, little is known about structural brain aberrations in boys with CD.Magnetic resonance imaging and voxel-based morphometry were used to assess abnormalities in gray matter volumes in 23 boys ages 12 to 17 years with CD (17 comorbid for attention-deficit/hyperactivity disorder) in comparison with age- and IQ-matched controls.Compared with healthy controls, mean gray matter volume was 6% smaller in the clinical group. Compared with controls, reduced gray matter volumes were found in the left orbitofrontal region and bilaterally in the temporal lobes, including the amygdala and hippocampus on the left side in the CD group. Regression analyses in the clinical group indicated an inverse association of hyperactive/impulsive symptoms and widespread gray matter abnormalities in the frontoparietal and temporal cortices. By contrast, CD symptoms correlated primarily with gray matter reductions in limbic brain structures.The data suggest that boys with CD and comorbid attention-deficit/hyperactivity disorder show brain abnormalities in frontolimbic areas that resemble structural brain deficits, which are typically observed in adults with antisocial behavior.
536 _ _ |a Funktion und Dysfunktion des Nervensystems
|c P33
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK409
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Adolescent
650 _ 2 |2 MeSH
|a Amygdala: pathology
650 _ 2 |2 MeSH
|a Antisocial Personality Disorder: diagnosis
650 _ 2 |2 MeSH
|a Antisocial Personality Disorder: physiopathology
650 _ 2 |2 MeSH
|a Attention Deficit Disorder with Hyperactivity: diagnosis
650 _ 2 |2 MeSH
|a Attention Deficit Disorder with Hyperactivity: physiopathology
650 _ 2 |2 MeSH
|a Brain: pathology
650 _ 2 |2 MeSH
|a Child
650 _ 2 |2 MeSH
|a Comorbidity
650 _ 2 |2 MeSH
|a Conduct Disorder: diagnosis
650 _ 2 |2 MeSH
|a Conduct Disorder: physiopathology
650 _ 2 |2 MeSH
|a Dominance, Cerebral: physiology
650 _ 2 |2 MeSH
|a Frontal Lobe: pathology
650 _ 2 |2 MeSH
|a Hippocampus: pathology
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Image Processing, Computer-Assisted
650 _ 2 |2 MeSH
|a Magnetic Resonance Imaging
650 _ 2 |2 MeSH
|a Male
650 _ 2 |2 MeSH
|a Parahippocampal Gyrus: pathology
650 _ 2 |2 MeSH
|a Parietal Lobe: pathology
650 _ 2 |2 MeSH
|a Prefrontal Cortex: pathology
650 _ 2 |2 MeSH
|a Risk Factors
650 _ 2 |2 MeSH
|a Temporal Lobe: pathology
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a conduct disorder
653 2 0 |2 Author
|a morphometry
653 2 0 |2 Author
|a magnetic resonance imaging
653 2 0 |2 Author
|a limbic system
700 1 _ |a Vloet, T. D.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Marx, I.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Konrad, K.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Fink, G. R.
|b 4
|u FZJ
|0 P:(DE-Juel1)131720
700 1 _ |a Herpertz, S.
|b 5
|0 P:(DE-HGF)0
700 1 _ |a Herpertz-Dahlmann, B.
|b 6
|0 P:(DE-HGF)0
773 _ _ |a 10.1097/CHI.0b013e3181676545
|g Vol. 47, p. 540 - 547
|p 540 - 547
|q 47<540 - 547
|0 PERI:(DE-600)2022051-0
|t Journal of the American Academy of Child and Adolescent Psychiatry
|v 47
|y 2008
|x 0890-8567
909 C O |o oai:juser.fz-juelich.de:62197
|p VDB
913 1 _ |k P33
|v Funktion und Dysfunktion des Nervensystems
|l Funktion und Dysfunktion des Nervensystems
|b Gesundheit
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914 1 _ |y 2008
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |d 31.12.2008
|g INB
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|l Medizin
|0 I:(DE-Juel1)INB-3-20090406
|x 0
920 1 _ |0 I:(DE-82)080010_20140620
|k JARA-BRAIN
|l Jülich-Aachen Research Alliance - Translational Brain Medicine
|g JARA
|x 1
970 _ _ |a VDB:(DE-Juel1)98217
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)INB-3-20090406
980 _ _ |a I:(DE-82)080010_20140620
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)VDB1046


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