A comprehensive review is shedding new light on Fabry disease, a rare inherited disorder that can progressively damage multiple organs and significantly affect quality of life.

Unusual behavior in the cells of mothers and babies with preeclampsia may provide new therapeutic targets for the condition, finds a new UCL-led study.

Unusual behavior in the cells of mothers and babies with preeclampsia may provide new therapeutic targets for the condition, a new UCL-led study finds.