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,…
Hormone modulating therapy (HMT) used for the treatment of breast…
Early exposure to antibiotics might increase long-term vulnerability to asthma.…
Scientists have uncovered over 5,000 genetic variations that allow some…
For the first time, new research explains the relationship between…
Hirschsprung disease patients may benefit from stem cell therapy, according…
Researchers from Indiana University and the University of South Florida…
For patients with locally advanced, unresectable non-small cell lung cancer…
The network of blood channels and tissues known as the…
For the first time in 50 years, a phase 3…
Autism spectrum disease has yet to be attributed to a…
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