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Fabry Disease Fabry disease is a genetic disorder caused by a deficiency in lysosomal -galactosidase A, of which neuropathic pain is the hallmark

A further 13 patients were enrolled under an expanded openlabel protocol with completion of treatment expected by February 2016, but Clinuvel is yet to publish these results

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View in: Pubmed A phase I clinical trial of continual alternating etoposide and topotecan in refractory solid tumours

This study explored the efficacy of MT-treated hiPSCs-derived DAPCs, which exhibited improved functionality and efficiency in regenerating PD midbrain nerves and highlights MTs potential to increase the neuroprotective effects of DAPCs in vivo, suggesting its clinical utility in combination with neural progenitor cells from hiPSCs for PD treatment

this serves to regulate intracellular trafficking of carbons between mitochondria and cytosol [55]