Resultados de búsqueda

Filtrar por sección

05/10/2018
Centros y Servicios

In order to better understand the natural course, risk factors, treatments and reasons for the development of childhood interstitial lung disease (chILD), we will collect and analyse details of symptoms and quality of life, clinical data and also biological material in a Register and Biobank. In the long run, this Register will serve the improved […]

05/10/2018
Centros y Servicios

The principal objective of RaDiCo is prospective collection, in the field of rare diseases (RD), of extensive phenotype data with a view to clinical and epidemiological research in liaison with translational and basic research. The data may be diverse: anatomical (medical imaging), biochemical, molecular, etc.

05/10/2018
Centros y Servicios

Proyecto prioritario del segundo Plan Nacional de Enfermedades Raras, financiado por el Ministerio de Salud, el Banco Nacional de Datos de Enfermedades Raras es un instrumento nacional de epidemiología y salud pública al servicio de las enfermedades raras.

05/10/2018
Centros y Servicios

Iniciativa de Genetic Alliance UK que ofrece apoyo e información a familias de niños con enfermedades genéticas no diagnosticadas.

05/10/2018
Centros y Servicios

EuroGentest2 is a Coordination Action funded by the 7th Framework of the European Commission. The project is organised in 3 Units looking at all aspects of genetic testing. The integration between Unit 1, 2 and 3 will be warranted by two transversal/cross-sectional work packages and one work package dedicated to managerial issues.