NORD is dedicated to supporting education, elevating care, advancing research, and driving policy for rare diseases
—Regina Bogar, Association for Creatine Deficiencies Make a Donation Finding SupportThrough Advocacy Organizations Patient advocacy organizations play a vital role in helping people with rare diseases live their best and fullest lives. We can help you find one or even start your own. ...
MedicalThe National Organization for Rare Disorders. Tarlov Cysts [internet].2012, June [citado el 7 de Nov. de 2014]. Disponible desde: http://www.National Organization for Rare Disorders (NORD). http://www.rarediseases.org/docs/NewsletterFall2010.pdf (accessed January 8, 2012)....
The Relationship between Oral Health and Brain Function WATANABE Makoto 日本歯科医学会誌 = Journal of the Japanese Association for Dental Science : JJDS (28), 60-63, 2009-03-31Maud GancelWassilios MeissnerFrançois Tison日本歯科医学会誌 ...
As far back as 1972, measures to combat rare diseases have been part of the Japanese national health system. Thanks to extensive support from the government, measures to combat rare diseases in Japan have made considerable progress over the past 40 years, including specific orphan drug legislation...
National Plans for Rare Diseases (RDs) are the common denominator of current public health policy concerns on RDs across the EU. With the aim of a better d... Taruscio,A E,Gentile,... - 《Public Health Genomics》 被引量: 15发表: 2013年 Tackling rare diseases at European level: why ...
The European Commission, recognizing that a number of healthcare and knowledge issues are common to all rare diseases in spite of the wide variety of their clinical manifestation, has recently initiated the promotion of national plans and comprehensive strategies for improving the provision of care ...
Neglected Diseases National Institutes of Health Announces New Program To Develop Therapeutics For Rare And Neglected DiseasesNational Institutes of Health Announces New Program To Develop Therapeutics For Rare And Neglected DiseasesGeoffrey Spencer
The meeting discussed herein is of the advisory committee for this grant. Its focus is on the development of a national collaborative study group system for rare genetic diseases including database needs, and group structures that would be amenable to the broadly multidisci- plinary nature of ...
Shaw-Smith C: Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature. Eur J Med Genet. 2010, 53: 6-13. 10.1016/j.ejmg.2009.10.001. Article PubMed Pu...