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Clinical Takeaway: Personalised Nutritional and Lifestyle Support Understanding a patients MTHFR status allows for personalised interventions that address root biochemical dysfunctions rather than just symptoms

Bmp6 expression in murine liver non parenchymal cells: a mechanism to control their high iron exporter activity and protect hepatocytes from iron overload

After the discovery of the molecular basis of FRDA in 1996, over two decades of research have been dedicated to understanding the temporal manifestations of disease both at the whole body and molecular level

Hama Aziz et al., 2023)

These findings indicate that vitamin E administration may provide significant advantages in lowering the incidence of CAP among high-risk elderly male smokers [39]

This is an inherited genetic disease called pyroglutamic aciduria which manifests as hemolytic anemia and metabolic acidosis, causing neurological disorders and vulnerability to bacterial infections, and which can be classified as mild, moderate or severe depending on the severity of the symptoms