News

Research March 20 2023 2023-03-19

Merger approved of two IDIBAPS groups, Hereditary metabolic diseases and Muscle research and mitochondrial function

On the retirement of Antònia Ribes, leader of the Hereditary metabolic diseases group, Glòria Garrabou, leader of the Muscle research and mitochondri1

Research October 7 2022 2022-10-14

Glòria Garrabou replaces Josep M. Grau-Junyent as head of the Muscular search and mitochondrial function

Research June 29 2022 2022-06-29

Clínic-IDIBAPS researchers organise an information day for International Phenylketonuria Day

During the “PKU”liar day, held on 28 June, the latest advances in the disease were presented and workshops were organised aimed at patients and famil1

Health Topics March 15 2022 2022-03-15

Neonatal diagnosis is key in patients with phenylketonuria (PKU)

Early diagnosis, a protein-free diet and treatment with a cofactor called BH4 make it possible for patients with this disease to develop normally. A1