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The Research Group on Neuromuscular and Mitochondrial Diseases is investigating to improve Antonio's quality of life
Antonio is a three-year-old child who has a rare disease called mitochondrial myopathy due to thymidine kinase 2 (TK2) deficiency. This is a genetic disease that affects very few people in the world. The Research Group on Neuromuscular and Mitochondrial Diseases of VHIR, which studies and seeks for new treatments ...
VHIR, committed to the research on rare diseases
The 28th of February is Rare Disease Day with the theme “Day by Day, Hand in Hand”, to raise awareness about this diseases that, only in Spain, affect more than 3 million people. The Vall d’Hebron Institute of Research (VHIR) wants to join in the campaign to give patients and families a feeling of hope and the possibility ...
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Fundació Institut de Recerca Hospital Universitari Vall d'Hebron 2014
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