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Primary carnitine deficiency is a genetic disorder of the cellular carnitine-transporter system that typically appears by the age of five with symptoms of cardiomyopathy, skeletal-muscle weakness, and hypoglycemia
van de Ven, TG
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doi: 10.1002/14651858.CD007280.pub2
gingivalis , a keystone pathogen in periodontal disease, has emerged as a critical mechanistic link between oral dysbiosis and systemic TMAO regulation
The methods for evaluating sleepwake behavior in these patients is diverse and can be categorized into subjective and objective/semi-quantitative approaches
