
Intravenous immunoglobulin in autoimmune encephalitis – a blog for Rare Disease Day 2023
For Rare Disease Day 2023, Craig Bodman and Dr Paula Foscarini-Craggs discuss the Enceph-IG study looking at early treatment with intravenous… Read more »
For Rare Disease Day 2023, Craig Bodman and Dr Paula Foscarini-Craggs discuss the Enceph-IG study looking at early treatment with intravenous… Read more »
In a blog for Rare Disease Day 2022, Cheney Drew discusses the DOMINO-HD study, registered at the ISRCTN registry, which aims to provide new insights… Read more »
The last day of February marks Rare Disease Day, an initiative that helps increase education, discussion, and improve access to… Read more »
Benoit Coulombe and Marie-Soleil Gauthier of the Montreal Clinical Research Institute (Montréal, Canada), discuss the Rare… Read more »
The last day of February marks Rare Disease Day, an initiative that helps increase education, discussion, and improve access to… Read more »
This piece, our final runner-up entry in Findacure and Medics4RareDiseases' "Student Voice" contest, speaks to the need to… Read more »
The diagnosis and delivery of treatment for rare diseases can vary greatly between different populations or groups within the same… Read more »
This piece, a runner-up entry in Findacure and Medics4RareDiseases' "Student Voice" contest, explores how current methods of… Read more »
As it does every year, Orphanet Journal of Rare Diseases is proud to partner with Findacure in its Student Voice essay contest.… Read more »
Rare Disease Day occurs annually, on the last day of February. It is an awareness day meant to increase cognizance and spark… Read more »