l carnitine hyperammonemia Acute pediatric hyperammonemia: current diagnosis and management strategies Hyperammonemia - Wikipedia

1 2 "De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes"

Histological and biochemical similarities have been found on muscle biopsies from patients with mitochondrial encephalomyopathy or with migraine [22,23]

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Genome-wide analyses of circadian transcriptome in fly heads by microarray [8], [22][24], or RNA-seq [25] suggests that the expression of some genes comprising glutathione-synthesizing and conjugating systems may occur in a circadian manner

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