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
The study, published by the Journal of Cachexia, Sarcopenia and Muscle, concludes that skin fibroblast cultures derived from patients reproduce the g1
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