Wij zijn onze website aan het vernieuwen.

Ontdekt u nog een pagina die niet klopt of hebt u een goede suggestie, laat het ons dan weten via webmedia@umcutrecht.nl.

Deze website maakt gebruik van cookies

Deze website toont video’s van o.a. YouTube. Dergelijke partijen plaatsen cookies (third party cookies). Als u deze cookies niet wilt kunt u dat hier aangeven. Lees meer over het cookiebeleid.

News

EU H2020 grant for unique HIT-CYSTIC FIBROSIS project

Monday 15 January 2018

The EU has granted 6.7 M€ from the Horizon 2020 research program to a broad collaborative group of researchers, doctors, pharmaceutical companies and patient representatives. The aim is to develop ‘personalized treatments’ for Cystic Fibrosis (CF) patients with uncommon genetic profiles throughout Europe. These patients with extremely rare gene mutations can otherwise never get access to possibly life-saving treatment. Once this concept has been proven, the methodology can extend to all patients with CF and other rare genetic diseases, so that HIT-CF will impact the entire field of orphan diseases

Child Health researcher Henk Schipper is nominated for the new scientist talent award 2016.

Friday 26 August 2016

Child Health researcher Henk Schipper is nominated for the new scientist talent award 2016. Vote for him!

Lab-grown mini-guts open door to personalised medicine

Tuesday 21 June 2016

Organoid technology is changing lives by allowing a more personalised approach to medicine.

Up