A recent joint investigation identified uncommon mutations in the YKT6 gene as the source of a novel neurological illness characterised by developmental delays, severe progressive liver disease, and a risk…
A Covid-19 diagnosis is no longer as frightening as it used to…
Scientists at the DZD partner German Institute of Human Nutrition Potsdam-Rehbrucke (DIfE)…
The waist-to-height ratio predicts the incidence of heart failure, according to data…
When obese children receive weight-loss treatment, the effects last throughout their lives,…
Muscle movement is enabled by signals conveyed from the brain…
The study confirms research completed in 2023, which revealed that…
A novel way of scanning lungs can demonstrate the impact…
For the first time, researchers have identified at least three…
Researchers at Penn Medicine's Abramson Cancer Centre and the University…
A remarkable development in breast cancer research has revealed a…
"Younger women generally have a higher risk of recurrence than…
Researchers at EPFL and Lausanne University Hospital (CHUV), led by…
A new study by The Hospital for Sick Children (SickKids)…
As we age, our cognitive and motor functions degrade, reducing…
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