Discapacidad
ADPLA. Asociación de Personas con Linfedema en Aragón
…The Immune Tolerance Network is an international clinical research consortium sponsored by NIAID, part of the National Institutes of Health, whose mission is to accelerate the clinical development of immune tolerance therapies through a unique development model.
…The European Hematology Association (EHA) promotes excellence in patient care, research and education in hematology. By organizing an annual congress, providing an educational program based on the European Hematology Curriculum, publishing a journal, lobbying for hematology and promoting research the association supports hematologists in- and outside Europe to further improve hematology patient care.
…ENERCA is an acronym for European Network for Rare and Congenital Anaemias. It started back in 2002, funded by the European Commission, with the purpose of offering an improved public health service to professional medical practitioners and patients in every aspect of rare anaemias.
…Euro-Histio-Net ha sido constituido para aunar esfuerzos en el aumento del conocimiento de la enfermedad, la mejora en la cantidad y calidad del intercambio de conocimientos, la elaboración de recomendaciones y la creación de una base de datos internacional. Cualquier nueva información adquirida será distribuida por este portal web para los profesionales de la HCL, […]
…Página web con información sobre la enfermedad de Wilson.
…Here you will find information about iron disorders: Hemochromatosis Juvenile Hemochromatosis Dysmetabolic Iron Overload Syndrome African Siderosis Iron Avidity Anemia of Inflammatory Response Iron Deficiency, with or without Anemia
…EFAPH’s targets 1.To Inform patients, the general public and medical doctors in Europe about this disease and to guide individual and family screening through reliable testing. 2. To increase awareness. To educate the general public and health professionals about the dangers of the disease. To promote and share the best practices so that patients can […]
…The Scleroderma Research Foundation (SRF) was established in 1987 by patient turned activist Sharon Monsky, when research on this potentially life threatening illness was nearly nonexistent. Since our founding, we’ve stood firm in our belief that the best way to help scleroderma patients is to fund medical research aimed at improved therapies and a cure. […]
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