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[19] [21] Dosage adjustments may be necessary in patients with renal impairment, G6PD deficiency, or other comorbidities
Am J Prev Med 42:563570
SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) ( Beyond genetic determinants, OCTN2 expression and function undergo significant physiological and pharmacological regulation
Respuesta paradjica de empeoramiento neuroptico en contexto oncolgico
Redox proteomic identification of carbonylated proteins in autism plasma: insight into oxidative stress and its related biomarkers in autism
