Acceso libre a la Opinión del Experto en Medicamentos Huérfanos hasta el 26 de diciembre |||| EODD Landing page, Informa Healthcare

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¿QUÉ ES NUEVO EN EURORDIS?

Descubre nuestros últimos anuncios Lee ahora: Acceso libre a la Opinión del Experto en Medicamentos Huérfanos hasta el 26 de diciembre This themed issue has been organised in partnership with EURORDIS (European Organisation for Rare Diseases) and NORD (National Organization for Rare Disorders). The purpose of this themed issue is to improve the scientific community’s understanding of the important issues surrounding rare diseases and the impact they have on the lives of patients. The issue includes pieces covering the importance of raising awareness and sharing family experiences on coping and caring for a child affected by a complex rare disease; creating patient communities; promoting policies and support in favour of research on rare and genetic diseases; promoting better standards of diagnosis and care; and easier access to cross-border care for patients affected by rare diseases. Throughout, it will highlight areas where it makes sense to work collaboratively and  at the international level. For a limited time, you can access content from this themed issue for Free below Working collaboratively and internationally to improve the lives of people affected by rare disease (Interview) A hidden priority: the paradox of rarity (EURORDIS perspective) (Editorial) A hidden priority: the paradox of rarity (NORD perspective) (Editorial) Adventures of an advocate: Annette De Bow’s big journeys (Patient Story) The diagnostic gap – an expert opinion (Editorial) Knowing more about Noonan, by Samantha Scheer (Patient Story) Pulmonary arterial hypertension: a rare disease that encourages the development of multiple treatments (Review) Access and availability of orphan drugs in the United States: advances or cruel hoaxes? (Editorial) A US perspective on newborn screening: a powerful tool for prevention (Editorial) Working with the NHS to develop the Alström multi-disciplinary clinic service (Editorial) Stiff person syndrome, by Liz Blows (Patient Story) Genethon: patient-empowered research (Editorial) Partnering in medical education: rare disease organizations bring experts and a patient voice to the conversation (Editorial) Findacure: empowering patient groups for drug development (Editorial) The orphan framework as a new opportunity: an expert opinion (Editorial) The Progeria Research Foundation: its remarkable journey from obscurity to treatment (Editorial) The emergence of gene therapy for rare diseases (Review) The impact of integrated omics technologies for patients with rare diseases (Review) How close are we to a cure for Duchenne muscular dystrophy? (Editorial) Resources PLEASE NOTE THESE ARTICLES ARE FREE TO ACCESS UNTIL DECEMBER 26TH 2014 Read More: http://informahealthcare.com/page/free_access_EODD