Rare Diseases
News
Foundation Develops Congenital Myopathy Guide for Families
News
CurePSP Is Accepting Proposals for Research Projects
News
Drug Approved for LAM Illustrates How Patient Organizations Can Partner With Researchers
News
NIH Will Not Fund Gene-Editing Technologies in Human Embryos
News
Canada Adopts First-Ever Rare Disease Strategy
News
Foundation for Prader-Willi Research and NORD Launch Global Registry
News
NORD Issues Statement on Approval of 21st Century Cures Initiative and Introduction of OPEN Act
News
NORD, EURORDIS, and Rare Disease Organizations in 30 Nations Announce an International Rare Diseases Alliance (copy 1)
Conference Coverage
Research Illuminates Genetic Forms of Epilepsy
Conference Coverage
A New Symptomatic Treatment for Lambert-Eaton Myasthenic Syndrome?
Conference Coverage
AAN: Largest neuroleptic malignant syndrome study finds predictors of poor outcome
Key clinical point: Patients diagnosed with neuroleptic malignant syndrome may be at increased risk of a poor outcome if they are older and have...