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Equipo de Investigación Dr. Juan Vilchez. Instituto de Investigación Sanitaria Hospital Universitario y Politécnico La Fe de Valencia
/en ComitéLíneas de investigación y publicaciones Caracterización clínica y genética de algunas distrofias musculares distales y de cinturas como la miopatía […]
Noticia de Mujer Hoy: “Siempre tuve conciencia social por mis orígenes humildes”
/en ActualLa revista Mujer Hoy publica una entrevista de Ana García Lozano a Isabel Gemio que aborda la labor de la […]
Equipo de Investigación Dr. Francesc Palau. Institut de Recerca Sant Joan de Déu de Barcelona
/en ComitéPalau F. La relevancia de las enfermedades raras. Investigación y Ciencia 2016 octubre; 481: 62 Yubero D, Brandi N, Ormazabal […]
Noticia de NCYT: Identifican un gen causante del síndrome de Opitz C
/en Científicas, Sin categorizarEl síndrome de Opitz C es una enfermedad genética que causa graves discapacidades en los afectados y que se ha […]
Noticia de Genética Médica News: Duplicación de todos los exones del gen TBX5 en una familia española con síndrome de Holt-Oram
/en Científicas, Sin categorizarEl Síndrome de Holt-Oram es una enfermedad ultra rara que asocia trastornos durante la embriogénesis del corazón y miembros superiores […]
Isabel Gemio Premio Talento Extraordinario de la Academia de Televisión
/en Actual, Sin categoríaIsabel Gemio ha sido distinguida con el Premio Talento Extraordinario a los primeros fundadores de la Academia de Televisión. De esta forma, […]
Una línea de investigación de la Fundación Isabel Gemio podría hallar el primer tratamiento para una grave enfermedad rara
/en Científicas, Sin categorizarEl equipo de investigación de la Dra. Belén Pérez del Centro de Diagnóstico de Enfermedades Moleculares (CEDEM) y del Centro de Biología […]
Isabel Gemio participa en el documental «Somos pocos, sumamos mucho» del programa 52 Minutos de Canal Extremadura
/en ActualEl programa «52 Minutos» de Canal Extremadura emitió, el pasado 2 de marzo, el documental «Somos pocos, sumamos mucho» en […]
La proteína responsable de una distrofia muscular podría curar el SIDA
/en Científicas, Sin categorizarUn grupo de investigadores españoles y extranjeros está llevando a cabo un proyecto de investigación para estudiar la proteína implicada […]
Asistencia al Acto oficial por el Día Mundial de las enfermedades raras 2/03/2017
/en EventosLa Fundación Isabel Gemio ha asistido hoy, 2 de marzo de 2017, al Acto Oficial por el Día Mundial de […]