1999
DOI: 10.1002/(sici)1098-2779(1999)5:4<305::aid-mrdd8>3.0.co;2-l
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Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome

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Cited by 25 publications
(17 citation statements)
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“…The exact mechanisms leading to neuronal damage by alcohol during fetal life have not been fully elucidated, and many proposed mechanisms have been suggested based on experimental models [2]. It is well understood that alcohol commonly impairs the development of the dopaminergic, noradrenergic, serotonergic, cholinergic, glutamatergic, and histaminergic systems [6]. The dopamine D1 receptors of the meso-cortical system is the most impaired of the dopaminergic receptors [9].…”
Section: Discussionmentioning
confidence: 99%
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“…The exact mechanisms leading to neuronal damage by alcohol during fetal life have not been fully elucidated, and many proposed mechanisms have been suggested based on experimental models [2]. It is well understood that alcohol commonly impairs the development of the dopaminergic, noradrenergic, serotonergic, cholinergic, glutamatergic, and histaminergic systems [6]. The dopamine D1 receptors of the meso-cortical system is the most impaired of the dopaminergic receptors [9].…”
Section: Discussionmentioning
confidence: 99%
“…Secondgeneration antipsychotics, which for the most part are serotonin-dopamine receptor antagonists, also possess anti-adrenergic and anti-histaminergic properties. These agents were used in the treatment of complications of seizure disorders associated with FASD [34], as adjunct therapy for Conduct Disorder [36], for disruptive behaviour in children with low IQ [5], and for secondary disabilities associated with FASD [6,18]. The most common antipsychotic drug used in children with FASD is Risperidone, which in some research has demonstrated strong benefits in the treatment of short-term aggressiveness [18].…”
Section: Discussionmentioning
confidence: 99%
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