Behçet’s Disease: Diverse manifestations in both brain and body

Orphanet Journal of Rare Diseases is proud to present this article by Olivia Noone, a runner-up entry in beacon for rare diseases and Medics4RareDiseases' "Student Voice" contest.
Orphanet Journal of Rare Diseases is proud to present this article by Olivia Noone, a runner-up entry in beacon for rare diseases and Medics4RareDiseases' "Student Voice" contest.
Orphanet Journal of Rare Diseases is proud to present this article by Chloe Yallop, a runner-up entry in beacon for rare diseases and Medics4RareDiseases' "Student Voice" contest.
Orphanet Journal of Rare Diseases is proud to present this article by Fiza Javed, a runner-up entry in beacon for rare diseases and Medics4RareDiseases' "Student Voice" contest.
Orphanet Journal of Rare Diseases is proud to present this article by Zheqing Zhang. This blog post is based on the winning essay in beacon for rare diseases and Medics4RareDiseases' "Student Voice" contest, which is accepted for publication in our journal.
For Rare Disease Day 2023, Craig Bodman and Dr Paula Foscarini-Craggs discuss the Enceph-IG study looking at early treatment with intravenous immunoglobulin (IVIG) for autoimmune encephalitis, registered at the ISRCTN registry.
In a blog about a new medical device developed to help predict urinary catheter blockage, Rachel Heylen discusses the study URINOSTICS, a small-scale pilot study which is testing the sensor before the design of a larger randomized trial, registered at the ISRCTN registry.
For World Cancer Day 2023, Monica Dolton, Margaret Horton and Clare Verrill discuss the ARTICULATE PRO study of pathologists using artificial intelligence in the diagnosis of prostate cancer, registered at the ISRCTN registry.