l-carnitine metabolic disorders Carnitine and novel clinical approaches: Mechanistic insights from deficiency management to liver and kidney disease treatment Role of carnitine in disease

DCM often runs in specific families within the breed

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Power calculation for the associations of genetically predicted l-carnitine and acetyl-carnitine with cardiovascular disease and its risk factors

Effects of doxorubicin-containing chemotherapy and a combination with L-carnitine on oxidative metabolism in patients with non-Hodgkin lymphoma

The following mechanisms may be proposed based on the findings of these diverse studies

Genetic variants in the genes encoding either of these enzymes can lead to creatine deficiency syndrome (CDS), which is neurologically manifested as cerebral creatine deficiency syndrome (CCDS), with genetic variants in the genes encoding the enzymes leading to the syndromes known as CCDS2 and CCDS3, respectively