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Effects of oral L-carnitine supplementation in low-birth-weight premature infants maintained on human milk

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Large-sample and well-designed studies have identified a deletion of exon 2 of the trimethyllysine hydroxylase epsilon (TMLHE) gene and linked this deletion with autism spectrum disorder (ASD)

Alterations in the transforming growth factor (TGF)-beta pathway as a potential factor in the pathogenesis of Peyronie's disease

10.1093/brain/awf167 111 MiquelE.CassinaA.Martinez-PalmaL.BolattoC.TrasE.GandelmanM.et al