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PROJECT SUMMARY/ABSTRACT We are requesting support for a study of brain sensorimotor abnormalities in childhood onset psychotic illnesses. Motor deficits are consistently found in psychotic patient populations and have also been identified as among a few promising early childhood risk factors for psychosis. We will employ a combination of neurobehavioral methods with non-invasive neuroimaging using magnetoencephalography (MEG) and structural magnetic resonance imaging (MRI). Eighty young participants with either childhood onset psychotic bipolar disorder (N=40) or schizophrenia (N=40) will be compared to age and gender matched comparison subjects (N=40) without personal or family history of psychotic and/or bipolar mood disorders. Our general perspective on motor coordination deficits is two-fold. First, we propose that a failure in inter-hemispheric motor inhibition results in failures to properly coordinate timing signals in bimanual coordination. Second, we believe that a failure in feed-forward efferent copy mechanisms from motor to somatosensory cortex results in improper perceptual feedback during patient's own movements. Our long term goals for this research are to refine the neurobiology of motor deficits in psychotic disorders, develop biomarkers for future family-based studies of genetic risk and evaluate neurobiological differences between schizophreniform and mood-related psychotic illnesses. Some of these biomarkers should be associated with psychosis per se and others with more disorder specific clinical manifestations. Such knowledge could a) contribute to earlier and more accurate diagnosis, b) lead to improved treatment planning at onset of illness, c) assist with more accurate estimate of illness trajectory and prognosis, d) aid in the development of possible new endophenotypic markers for psychosis, and e) form the basis for future family studies relating to genetic vs. developmental contributions to these disorders.
期刊论文(2)
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DOI: 10.1371/journal.pone.0085748
发表时间: 2014
期刊: PloS one
影响因子: 3.7
作者: [McFadden KL, Steinmetz SE, Carroll AM, Simon ST, Wallace A, Rojas DC]
通讯作者: Rojas DC
DOI: 10.1212/01.con.0000466662.89908.e7
发表时间: 2015-06-01
期刊: Continuum (Minneapolis, Minn.)
影响因子: --
作者: [Arciniegas, David B]
通讯作者: Arciniegas, David B
Neural synchronydysfunction of gamma oscillations in autism
  • 批准号:
    7781001
  • 项目类别:
  • 资助金额:
    $26.56万
  • 财政年份:
    2009
  • 负责人:
    DONALD C. ROJAS
  • 依托单位:
Neural synchronydysfunction of gamma oscillations in autism
  • 批准号:
    8197005
  • 项目类别:
  • 资助金额:
    $26.51万
  • 财政年份:
    2009
  • 负责人:
    DONALD C. ROJAS
  • 依托单位:
Neural synchronydysfunction of gamma oscillations in autism
  • 批准号:
    8372405
  • 项目类别:
  • 资助金额:
    $25.45万
  • 财政年份:
    2009
  • 负责人:
    DONALD C. ROJAS
  • 依托单位:
Neural synchronydysfunction of gamma oscillations in autism
  • 批准号:
    7991379
  • 项目类别:
  • 资助金额:
    $26.51万
  • 财政年份:
    2009
  • 负责人:
    DONALD C. ROJAS
  • 依托单位:
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海外基金
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  • 项目类别:
    省市级项目
  • 资助金额:
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  • 批准年份:
    2025
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    2025JJ70209
  • 项目类别:
    省市级项目
  • 资助金额:
    --
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    2025
  • 负责人:
    雷芬芳
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AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
    --
  • 项目类别:
    面上项目
  • 资助金额:
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  • 批准年份:
    2024
  • 负责人:
    万荣
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