Publications by authors named "A S Tiganov"

In the International Classification of Diseases, 10th Revision (ICD-10) two opposing principles are combined and mixed: atheoreticity that is necessary for the natural classification and commitment to nosology. Implementation of these principles requires a two-stage qualification. The first stage should be narrative detailed syndromological qualifications with identification of psychotic level of disorders.

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Background: Bipolar disorder (BD) is a common and highly heritable disorder of mood. Genome-wide association studies (GWAS) have identified several independent susceptibility loci. In order to extract more biological information from GWAS data, multi-locus approaches represent powerful tools since they utilize knowledge about biological processes to integrate functional sets of genes at strongly to moderately associated loci.

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Aim: To assess the efficacy and safety of pantogam active (PA) in prevention and correction of neurological side-effects during the course neuroleptic treatment of acute endogenous psychoses.

Material And Methods: Eighty schizophrenic patients (mean age 33 years) with acute psychosis were examined. All patients received 28-day course treatment with typical and atypical neuroleptics.

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Article Synopsis
  • Bipolar disorder (BD) is a highly hereditary mental illness marked by alternating episodes of mania and depression, sharing significant genetic and clinical traits with schizophrenia (SCZ).
  • A study involving a large dataset of BD patients and controls found that 22 out of 107 genetic variants (SNPs) identified in SCZ research showed a link to BD, indicating shared genetic risk factors.
  • Notably, one significant SNP was near the TRANK1 gene, known to be associated with BD; this study also highlighted potential disease pathways involving calcium and glutamate signaling, which could lead to new treatment strategies for both disorders.
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Bipolar disorder (BD) is a severe and highly heritable neuropsychiatric disorder with a lifetime prevalence of 1%. Molecular genetic studies have identified the first BD susceptibility genes. However, the disease pathways remain largely unknown.

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