The most recent Success stories from EU Research. Select a theme or country from the menus on the left to see more articles
Health & life sciences - Rare & orphan diseases
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EU-funded researchers have conducted the first successful trials of an innovative gene therapy to treat a rare and debilitating metabolic disorder, using a small and innocuous virus as a carrier for genetic information to correct the functioning of liver and muscle cells.
Published: 3 April 2019
EU-funded researchers are close to developing a cure for Crigler-Najjar syndrome, an extremely rare, life-threatening liver disease. The groundbreaking research, currently being validated in clinical trials, could also pave the way for the treatment of other genetic disorders.
Published: 27 February 2019
Virus collections are vital resources for understanding the basis of diseases and formulating control strategies. An EU-funded project is developing an easily accessible global archive of pathogens - a way of boosting research into protecting human and animal health.
Published: 11 December 2018
Management and treatment of neurological diseases is one of the biggest challenges facing medicine today. EU-funded researchers are developing computational tools to improve understanding of how such diseases progress as a means to help treat patients.
Published: 22 June 2018
For patients with rare genetic mutations of the debilitating disease cystic fibrosis, there are few options for effective treatment. EU-funded researchers are working to meet their needs, using new developments in personalised medicine to advance the testing of novel and promising drugs.
Published: 19 June 2018
Published: 12 June 2018