Kick-off meeting of the Erasmus+ project ‘THE VALUE OF FACING SCHOOL’
The kick-off meeting of ‘THE VALUE OF FACING SCHOOL: THE INCLUSION OF YOUTH WITH NEUROMUSCULAR DISEASES, MUSCULAR DYSTROPHIES AND OTHER […]
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The kick-off meeting of ‘THE VALUE OF FACING SCHOOL: THE INCLUSION OF YOUTH WITH NEUROMUSCULAR DISEASES, MUSCULAR DYSTROPHIES AND OTHER […]
Here are the protagonists of the initiative co-funded by the #erasmusplus programme: Laura (@laura.sanchez.92) highlights the importance of professionalized personal […]
The first transnational meeting of the initiative YOUTH WITH RARE DISEASES, co-financed by the Erasmus+ Programme of the European Union, […]
Descifrado el mecanismo molecular de una enfermedad rara que causa inmunodeficiencias graves. Investigadores del Consejo Superior de Investigaciones Científicas (CSIC), […]
2341, 36 € destinados a la investigación. Mil gracias a todos, a la Comisión de Fiestas Patronales de Sant Vicent […]
Get to know all the people that have participated in the initiative #YouthWithCourage in April. Carolina is 28 years old and […]
INVESTIGACIÓN Diseñado un ‘chip de tejido’ para estudiar enfermedades neuromusculares raras Los ‘chips de tejido’ ayudan a los científicos a […]
The kick-off meeting of “YOUNG PEOPLE WITH RARE DISEASES: THE VALUE OF FACING LIFE” was hold last Tuesday, March 29th, […]
En el documento adjunto podéis encontrar los resultados de las siete líneas de investigación financiadas por la Fundación. Enlace: LINEAS […]
La Comisión Europea ha abierto la consulta sobre la evaluación final del tercer Programa de Salud, que se desarrolló entre […]