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European Psychiatry : the Journal of the Association of European Psychiatrists|August 25, 2009
Family history and obstetric complications in deficit and non-deficit schizophrenia: preliminary resultsS Dollfus, S Germain-Robin, B Chabot, et al.
Psychiatric Genetics|January 1, 1994
No major role for the dopamine D2 receptor Ser-->Cys311 mutation in schizophreniaC Laurent, S Bodeau-Péan, D Campion, et al.
Psychiatry Research|November 29, 1995
No evidence for linkage or association between the dopamine transporter gene and schizophrenia in a French populationS Bodeau-Péan, C Laurent, D Campion, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|July 1, 1995
A rare allele of a microsatellite located in the tyrosine hydroxylase gene found in schizophrenic patientsR Meloni, C Laurent, D Campion, et al.
The American Journal of Psychiatry|March 30, 2000
Proton magnetic resonance spectroscopy of the medial prefrontal cortex in patients with deficit schizophrenia: preliminary reportP Delamillieure, J Fernandez, J M Constans, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|June 8, 2002
Cognitive patterns in subtypes of schizophreniaP Brazo, R M Marié, I Halbecq, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|November 26, 1999
Month of birth in deficit and non-deficit schizophrenic patientsS Dollfus, P Brazo, S Langlois, et al.
Psychiatry Research|June 1, 1996
Association study between schizophrenia and monoamine oxidase A and B DNA polymorphismsB Coron, D Campion, F Thibaut, et al.
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