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Samanes Agreda, Gloria

Samanes Agreda, Gloria

Institutions of which they are part

Research technician
Pediatric Neurology
Vall Hebron Institut de Recerca
Samanes Agreda, Gloria

Samanes Agreda, Gloria

Samanes Agreda, Gloria

Institutions of which they are part

Research technician
Pediatric Neurology
Vall Hebron Institut de Recerca

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ImpulsaT association awards €20,000 for research into LAMA2-deficient muscular dystrophy

The donation will enable further characterisation of patients with this rare disease, the identification of new biomarkers and the exploration of innovative therapies.

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The FDA approves a treatment co-created at Vall d’Hebron for a rare muscle disease

The clinical trial, which also involved Vall d’Hebron, shows that the new therapy improves survival by 86% in patients with thymidine kinase 2 deficiency (TK2d).

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A new clinical algorithm increases the diagnosis rate of rare diseases

The ClinPrior algorithm achieved a positive diagnosis rate of 70% in two minority diseases of neurodegenerative origin, which represents double the number of cases that are diagnosed with current tools.

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