They are Metabolism and disease programme (MetaDis) and Translational research programme for brain disorders
A study jointly led by the Hospital Clínic-IDIBAPS and the Vall d'Hebron Research Institute (VHIR) confirms the effectiveness of neonatal screening i1
The study describes how mutations in the GUK1 gene are responsible for causing this new form of Mitochondrial DNA Depletion-Deletion Syndrome (MDDS),1
Researchers from the Clínic-IDIBAPS have taken part in a study that provides new information on the mechanisms involved in idiopathic inflammatory my1
One of the projects is coordinated by Glòria Garrabou, the head of the group Hereditary metabolic diseases and muscular diseases, and the other by Os1
IDIBAPS looks for talented professionals to meet the needs that appear periodically.
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