The European Medicines Agency (EMA) has validated the marketing authorisation application (MAA) submitted by Soleno ...

In a comprehensive Genomic Press Invited Expert Review, researchers from the University of Haifa have synthesized ...

Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

An illustration of the genetic and expression map of the ... of Haifa have synthesized cutting-edge findings on Prader-Willi syndrome (PWS), revealing how this complex neurodevelopmental disorder ...

In a comprehensive Genomic Press Invited Expert Review, researchers from the University of Haifa have synthesized ...

The former glamour model, 47, took to Instagram on his birthday eve to post a series of throwback snaps with Harvey as she ...

May 15 marks National Prader-Willi Syndrome Awareness Day. For one Virginia father, the date is more than just a spot on the ...

They have Prader-Willi syndrome (PWS) – a rare neurodevelopmental and genetic condition where the “switch” in the brain that signals fullness never gets flipped on. PWS occurs when part of ...

A 5-year-old girl from Bangladesh suffering from Prader-Willi Syndrome, a rare genetic condition leading to extreme childhood obesity, underwent bariatric surgery at a private hospital in Chennai.