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Defining the molecular mechanism in hereditary cytoplasmic body myopathy with early respiratory failure: implications for understanding ventilatory failure in muscular dystrophies

Defining the molecular mechanism in hereditary cytoplasmic body myopathy with early respiratory failure: implications for understanding ventilatory failure in muscular dystrophies
定义遗传性细胞质体肌病伴早期呼吸衰竭的分子机制：对理解肌营养不良症通气衰竭的意义
批准号：
208695
负责人：
Pfeffer Gerald
金额：
$1.46万
依托单位：
University of Newcastle upon Tyne (UK)
依托单位国家：
加拿大
项目类别：
Fellowship Programs
财政年份：
2010
资助国家：
加拿大
项目状态：
已结题
起止时间：
2010-02-01 至 2014-02-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=208695&lang=en
关键词：
Genetics Hereditary Cytoplasmic Body Myopathy Muscular Dystrophy Neuromuscular Disease Respiratory Failure

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中文摘要
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英文摘要
Hereditary cytoplasmic body myopathy with early respiratory failure (HCBM) is a hereditary muscle disease which selectively affects muscles required for breathing, early in its disease course (among other select muscles). Respiratory dysfunction also occu
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The oral and gut microbiome and their derived metabolites in sex differences in amyotrophic lateral sclerosis
  • 批准号：
    464091
  • 项目类别：
    Operating Grants
  • 资助金额：
    $0.0万
  • 财政年份：
    2022
  • 负责人：
    Pfeffer Gerald
  • 依托单位：
    University of Calgary
Defining the molecular mechanism in hereditary cytoplasmic body myopathy with early respiratory failure: implications for understanding ventilatory failure in muscular dystrophies
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