Literature DB >> 24503586

New and evolving rare diseases research programs at the National Institutes of Health.

S C Groft1, Y R Rubinstein.   

Abstract

Research emphasis on rare diseases and orphan products remains a major focus of the research Institutes and Centers of National Institutes of Health (NIH). NIH provides more than USD 31 billion annually in biomedical research and research support. This research is the basis of many of the health advances in rare and common diseases. Numerous efforts and a major emphasis by the public and private sector initiatives have resulted in an increase of interventions and diagnostics for rare diseases. Newer translational research programs provide a more systematic and coordinated approach to rare diseases research and orphan products development. The approach that is offered requires extensive public-private partnerships with the pharmaceutical industry, contract research organizations, philanthropic foundations, medical and scientific advisory boards, patient advocacy groups, the academic research community, research and regulatory scientists, government funding agencies, and the public. Each program is unique and requires lengthy planning and collaborative efforts to reach programmatic goals.
© 2013 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2014        PMID: 24503586     DOI: 10.1159/000355929

Source DB:  PubMed          Journal:  Public Health Genomics        ISSN: 1662-4246            Impact factor:   2.000


  6 in total

Review 1.  Common data elements for spinal cord injury clinical research: a National Institute for Neurological Disorders and Stroke project.

Authors:  F Biering-Sørensen; S Alai; K Anderson; S Charlifue; Y Chen; M DeVivo; A E Flanders; L Jones; N Kleitman; A Lans; V K Noonan; J Odenkirchen; J Steeves; K Tansey; E Widerström-Noga; L B Jakeman
Journal:  Spinal Cord       Date:  2015-02-10       Impact factor: 2.772

2.  Multiple system atrophy: the case for an international collaborative effort.

Authors:  Lucy Norcliffe-Kaufmann; Jose-Alberto Palma; Florian Krismer
Journal:  Clin Auton Res       Date:  2015-04-11       Impact factor: 4.435

3.  The involvement of patient organisations in rare disease research: a mixed methods study in Australia.

Authors:  Deirdre Pinto; Dominique Martin; Richard Chenhall
Journal:  Orphanet J Rare Dis       Date:  2016-01-12       Impact factor: 4.123

4.  Composite CDE: modeling composite relationships between common data elements for representing complex clinical data.

Authors:  Hye Hyeon Kim; Yu Rang Park; Suehyun Lee; Ju Han Kim
Journal:  BMC Med Inform Decis Mak       Date:  2020-07-03       Impact factor: 2.796

5.  Comprehensive Functional Evaluation of the Spectrum of Multi-System Atrophy with 18F-FDG PET/CT and 99mTc TRODAT-1 SPECT: 5 Year's Experience from a Tertiary Care Center.

Authors:  Nikhil Seniaray; Ritu Verma; Rajeev Ranjan; Ethel Belho; Harsh Mahajan
Journal:  Ann Indian Acad Neurol       Date:  2021-05-21       Impact factor: 1.383

6.  A first description of the Colombian national registry for rare diseases.

Authors:  Heidi Eliana Mateus; Ana María Pérez; Martha Lucía Mesa; Germán Escobar; Jubby Marcela Gálvez; José Ivo Montaño; Martha Lucía Ospina; Paul Laissue
Journal:  BMC Res Notes       Date:  2017-10-26
  6 in total

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