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C Gillberg

Showing results (311-320 of 319) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2007
Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5-microsatellite repeat, but not with DRD4 or SLC6A3 VNTRsS Johansson, H Halleland, A Halmøy, et al.
Translational Psychiatry|November 12, 2014
The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disordersC Pagan, R Delorme, J Callebert, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|April 7, 2009
An exploratory study of the association between reactive attachment disorder and attachment narratives in early school-age childrenHelen Minnis, Jonathan Green, Thomas G O'Connor, et al.
Human Molecular Genetics|April 10, 1999
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair StudyA Philippe, M Martinez, M Guilloud-Bataille, et al.
Journal of Attention Disorders|April 11, 2003
Guidelines and algorithms for the use of methylphenidate in children with Attention-Deficit/ Hyperactivity DisorderL Greenhill, D H Beyer, J Finkleson, et al.
Molecular Psychiatry|August 10, 2005
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorderR Delorme, C Betancur, M Wagner, et al.
Translational Psychiatry|October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHEC Nava, F Lamari, D Héron, et al.
Molecular Psychiatry|September 16, 2015
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autismM Pilorge, C Fassier, H Le Corronc, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
Pageof 32

Showing results (311-320 of 319) with videos related to

Sort By:
Pageof 32
You have reached the last page of results.This site can display upto 319 results.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2007
Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5-microsatellite repeat, but not with DRD4 or SLC6A3 VNTRsS Johansson, H Halleland, A Halmøy, et al.
Translational Psychiatry|November 12, 2014
The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disordersC Pagan, R Delorme, J Callebert, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|April 7, 2009
An exploratory study of the association between reactive attachment disorder and attachment narratives in early school-age childrenHelen Minnis, Jonathan Green, Thomas G O'Connor, et al.
Human Molecular Genetics|April 10, 1999
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair StudyA Philippe, M Martinez, M Guilloud-Bataille, et al.
Journal of Attention Disorders|April 11, 2003
Guidelines and algorithms for the use of methylphenidate in children with Attention-Deficit/ Hyperactivity DisorderL Greenhill, D H Beyer, J Finkleson, et al.
Molecular Psychiatry|August 10, 2005
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorderR Delorme, C Betancur, M Wagner, et al.
Translational Psychiatry|October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHEC Nava, F Lamari, D Héron, et al.
Molecular Psychiatry|September 16, 2015
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autismM Pilorge, C Fassier, H Le Corronc, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
Pageof 32