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The International Journal of Neuropsychopharmacology|October 24, 2007
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DSElena Michaelovsky, Doron Gothelf, Michael Korostishevsky, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|June 22, 2016
Pharmacogenetics of citalopram-related side effects in children with depression and/or anxiety disordersMaya Amitai, Sefi Kronenberg, Miri Carmel, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|May 6, 2003
DRD4 exon III polymorphism and response to risperidone in Israeli adolescents with schizophrenia: a pilot pharmacogenetic studyGil Zalsman, Amos Frisch, Shaul Lev-Ran, et al.Journal of Psychiatric Research|August 6, 2013
Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypesOmer Zarchi, Miri Carmel, Chen Avni, et al.Journal of Child and Adolescent Psychopharmacology|January 16, 2016
The Relationship Between Plasma Cytokine Levels and Response to Selective Serotonin Reuptake Inhibitor Treatment in Children and Adolescents with Depression and/or Anxiety DisordersMaya Amitai, Michal Taler, Miri Carmel, et al.Archives of Women'S Mental Health|June 19, 2013
Association between a common CYP17A1 haplotype and anxiety in female anorexia nervosaEfrat Czerniak, Michael Korostishevsky, Amos Frisch, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 25, 2005
Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family triosElena Michaelovsky, Amos Frisch, Shani Leor, et al.Biological Psychiatry|September 3, 2013
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndromeDoron Gothelf, Amanda J Law, Amos Frisch, et al.The International Journal of Neuropsychopharmacology|June 1, 2006
Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndromeDoron Gothelf, Elena Michaelovsky, Amos Frisch, et al.Pediatric Research|January 13, 2015
Thymic and bone marrow output in individuals with 22q11.2 deletion syndromeNina Dar, Doron Gothelf, David Korn, et al.Pageof 3