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Mitochondrial neurogastrointestinal encephalomyopathy Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE), an autosomal recessive disorder first identified in 1978, 486 is characterized by a range of clinical symptoms including cachexia, gastrointestinal dysmotility, peripheral neuropathy, ophthalmoparesis, and leukoencephalopathy
لصقات للبقع الداكنة تحت العين
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Redefining noradrenergic neuromodulation of behavior: impacts of a modular locus coeruleus architecture
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