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Here, we update and discuss current rationale, evidence, and dosing guidelines for mitochondrial medicine therapies in patients with PMD including practical considerations as to which therapies may be administered parenterally and which genetic etiologies and/or phenotypes might be particularly responsive to specific therapies[25]

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A dimostrazione della funzione della carnitina sul metabolismo lipidico sono alcune rare malattie genetiche in cui il soggetto non in grado di produrre carnitina endogena

Maintains the body's ability to metabolize nutrients

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