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Alfons Macaya Ruíz

Institutions of which they are part

Head of group
Pediatric Neurology
Vall Hebron Institut de Recerca

Alfons Macaya Ruíz

Institutions of which they are part

Head of group
Pediatric Neurology
Vall Hebron Institut de Recerca

Projects

Estudio genético de la migraña hereditaria: Análisis de ligamento y búsqueda de genes responsables en familias españolas

IP: Alfons Macaya Ruíz
Collaborators: -
Funding agency: Ministerio de Ciencia e Innovación-MICINN
Funding:
Reference: FP2000-5484
Duration: 05/07/2001 - 13/10/2004

Ministerio de Ciencia

Estudio genético de la migraña hereditaria: análisis de ligamiento y búsqueda de los genes responsables en familias españolas.

IP: Alfons Macaya Ruíz
Collaborators: -
Funding agency: Ministerio de Ciencia y Tecnología
Funding: 70198.21
Reference: SAF2000-0197
Duration: 01/04/2000 - 01/04/2004

Related news

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

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).

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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