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Showing 1 to 4 of 4 for “"mitochondrial disorder"”.

  1. Novel time resolved optical and machine learning methods for label free biomedical imaging

    … methods for cell and tissue diagnosis. Mitochondrial disorder is a type of disorder that affects the cell's mitochondria and impacts the cell's functionality as a whole. Roughly, these mitochondrial disorders affect between 1 in 6000 and 1 in 8000 live births. These disorders are hard to …

    colostate Repository record for Novel time resolved optical and machine learning methods for label free biomedical imaging (opens in a new tab)

  2. Molekulare Ursachen des Mohr-Tranebjaerg-Syndromes

    … DDP1 and Tim13 Mohr-Tranebjaerg syndrome is a mitochondrial disorder caused by a defects in the biogenesis of the human TIM23 translocase Tim8 and Tim13 of yeast belong to a family of evolutionary conserved zinc finger proteins that are organised in hetero-oligomeric complexes in the …

    lmu-germany Repository record for Molekulare Ursachen des Mohr-Tranebjaerg-Syndromes (opens in a new tab)

  3. Hypoglycemia In Mitochondrial Disorders

    … of adenosine triphosphate (ATP). Defects in the mitochondrial or nuclear DNA that codes for components of the ETC lead to mitochondrial disorders (MTDs). MTDs are multi-system conditions affecting the heart, muscles, and especially brain. The endocrine system is commonly affected in MTDs, and …

    uthsc Repository record for Hypoglycemia In Mitochondrial Disorders (opens in a new tab)

  4. Distinct Neuropsychological Profile and Associated Neurochemical Changes in Individuals with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS)

    <p>Background: Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) is a maternally inherited progressive multisystemic disorder. Occurrence of seizure and/or stroke-like episode, as well as classic biomarkers (i.e., cerebral lactic acidosis, depleted N-acetylaspartate …

    cuny-grad Repository record for Distinct Neuropsychological Profile and Associated Neurochemical Changes in Individuals with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) (opens in a new tab)