Researchers have identified a promising strategy to improve memory and brain cell function in models of 22q11.2 Deletion ...

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

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

They have Prader-Willi syndrome (PWS ... a senior consultant with the Genetics Service at KK Women’s and Children’s Hospital (KKH). Complications associated with morbid obesity include ...

In a comprehensive Genomic Press Invited Expert Review, researchers from the University of Haifa have synthesized cutting-edge findings on Prader-Willi syndrome (PWS), revealing how this complex ...

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

VYKAT XR was approved by the U.S. Food and Drug Administration (FDA) on March 26, 2025, and is now commercially available to ...

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

Details of the presentations are as follows: The Prader-Willi Syndrome Association USA estimates that PWS occurs in one in every 15,000 live births. The hallmark symptom of this disorder is ...

Relmada Therapeutics is a clinical-stage biotechnology company focused on developing transformative therapies for central nervous system and oncology-related conditions. Its lead candidates, NDV-01 ...

The Prader-Willi Syndrome Association USA estimates that PWS occurs in one in every 15,000 live births. The hallmark symptom of this disorder is hyperphagia, a chronic and life-threatening ...