{"id":1873,"date":"2016-07-27T05:52:29","date_gmt":"2016-07-27T05:52:29","guid":{"rendered":"http:\/\/sindromecharge.es\/index.php\/2016\/07\/27\/trabajo-en-red-a-favor-de-la-investigacion-en-er\/"},"modified":"2016-07-27T05:52:29","modified_gmt":"2016-07-27T05:52:29","slug":"trabajo-en-red-a-favor-de-la-investigacion-en-er","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2016\/07\/27\/trabajo-en-red-a-favor-de-la-investigacion-en-er\/","title":{"rendered":"Trabajo en red a favor de la investigaci\u00f3n en ER"},"content":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<p>La Federaci\u00f3n Espa\u00f1ola de Enfermedades Raras (FEDER), en su compromiso con la investigaci\u00f3n de estas patolog\u00edas, est\u00e1 trabajando en distintas l\u00edneas con el objetivo de mejorar la calidad de vida de las m\u00e1s de tres millones de personas que conviven con enfermedades poco frecuentes en nuestro pa\u00eds.<\/p>\n<p>Por este motivo, el pasado 22 de Julio tuvo lugar una reuni\u00f3n con la Fundaci\u00f3n Espa\u00f1ola para la Ciencia y la Tecnolog\u00eda (FECYT) a la que acudieron Joaqu\u00edn Arenas, Director del Instituto de Investigaci\u00f3n del Hospital 12 de Octubre; Alba Ancochea, Directora de FEDER; y Patricia Arias, t\u00e9cnico en el \u00e1rea de investigaci\u00f3n de la Federaci\u00f3n.<\/p>\n<p>\u201cSin investigaci\u00f3n no hay futuro. Por ello, es realmente importante para nosotros poder contar con el apoyo de entidades como el FECYT que nos ayudan en nuestro camino para mejorar la realidad de nuestro colectivo, y es que trabajar en red es prioritario para poder avanzar en favor de estas patolog\u00edas\u201d afirm\u00f3 Ancochea&nbsp;<\/p>\n<p>Fuente: FEDER <a href=\"http:\/\/www.enfermedades-raras.org\/index.php\/actualidad\/noticias-eventos\/2-feder\/6547-trabajo-en-red-a-favor-de-la-investigaci%C3%B3n-en-er\" target=\"_blank\">Trabajo en red a favor de la investigaci\u00f3n en ER<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: La Federaci\u00f3n Espa\u00f1ola de Enfermedades Raras (FEDER), en su compromiso con la investigaci\u00f3n de estas patolog\u00edas, est\u00e1 trabajando en distintas l\u00edneas con el objetivo de mejorar la calidad de vida de las m\u00e1s de tres millones de personas que conviven con enfermedades poco [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8],"tags":[36],"class_list":["post-1873","post","type-post","status-publish","format-standard","hentry","category-noticias","tag-enfermedades-raras"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - 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