Cohort trends in the age of initiation of drug use in Australia.
Aust N Z J Public Health 2000;24:421–426.
De Graaf, R,
Van Os, J,
First cannabis use: does onset shift to younger ages? Findings from 1988 to 2003 from the Dutch National School Survey on Substance Use.
Age at first alcohol use: a risk factor for the development of alcohol disorders.
Am J Psychiatry 2000;157:745–750.
Cannabis use and the mental health of young people.
Aust N Z J Psychiatry 2006;40:105–113.
The relationships between substance use and mental health problems: evidence from longitudinal studies. In: Stockwell, T,
Loxley, W, eds. Preventing harmful substance use: the evidence base for policy and practice. John Wiley and Sons, Chichester, England. 2005:43–51.
6.De Bellis, MD,
Beers, SRet al. Hippocampal volume in adolescent-onset alcohol use disorders.
Am J Psychiatry 2000;157:737–744.
7.De Bellis, MD,
Prefrontal cortex, thalamus, and cerebellar volumes in adolescents and young adults with adolescent-onset alcohol use disorders and comorbid mental disorders.
Alcohol Clin Exp Res 2005;29:1590–1600.
Szulc, KUet al. A preliminary DTI study showing no brain structural change associated with adolescent cannabis use.
Harm Reduct J 2006;3:17.
Alcohol consumption and cognitive functioning in social drinkers.
J Stud Alcohol 1977;38:1224–1232.
Sexual dimorphism of the developing human brain.
Prog Neuropsychopharmacol Biol Psychiatry 1997;21:1185–1201.
Stuart, GWet al. An optimized method for estimating intracranial volume from magnetic resonance images.
Magn Reson Med 2000;44:973–977.
McGorry, PDet al. Hippocampal volume in first-episode psychoses and chronic schizophrenia: a high-resolution magnetic resonance imaging study.
Arch Gen Psychiatry 1999;56:133–141.
The neurobiological basis of temperament: towards a better understanding of psychopathology.
Neurosci Biobehav Rev 2006;30:511–525.
Cannabis and the brain.
Brain 2003;126(Pt 6):1252–1270.
Cannabis use and mental health in young people: cohort study.
Grieder, Tet al. An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia.
Biol Psychiatry 2000;48:147–162.
Martin, Aet al. Amygdala and hippocampal volumes in adolescents and adults with bipolar disorder.
Arch Gen Psychiatry 2003;60:1201–1208.
Zetzsche, Tet al. Enlargement of the amygdala in patients with a first episode of major depression.
Biol Psychiatry 2002;51:708–714.
Zetzsche, Tet al. Larger amygdala volumes in first depressive episode as compared to recurrent major depression and healthy control subjects.
Biol Psychiatry 2003;53:338–344.
The epidemiology of substance misuse and comorbid psychiatric disorders.
Acta Neuropsychiatrica 2004;16:3–8.
Functional neuroimaging studies in mood disorders.
Acta Neuropsychiatrica 2006;18:88–99.
Magnetic resonance imaging (MRI) measurement of hippocampal volume in posttraumatic stress disorder: a meta-analysis.
J Affect Disord 2005;88:79–86.
Age and dose-dependent effects of ethanol on the induction of hippocampal long-term potentiation.
Deficient social and play behavior in juvenile and adult rats after neonatal cortical lesion: effects of chronic pubertal cannabinoid treatment.
Adolescent exposure to cannabinoids induces long-lasting changes in the response to drugs of abuse of rat midbrain dopamine neurons.
Biol Psychiatry 2004;56:86–94.
Age-dependent inhibition of long-term potentiation by ethanol in immature versus mature hippocampus.
Alcohol Clin Exp Res 1995;19:1480–1485.