🙏 Thank you, Multiple Sclerosis News Today, for covering the positive outcome of the interim analysis of our phase 3 #ENSURE program of #vidofludimus calcium in relapsing #MS! ▶ Learn more: bit.ly/4hg0LAS #ClinicalTrials #IMU838 #MultipleScerlosis #RMS #neuroprotection #Nurr1 #DHODH

Spread the word GENETIC NEURODEVELOPMENTAL DISORDERS like autism and cerebral palsy are associated with motor problems!!! Thank you to these collabs and Simons Searchlight for collecting this data! onlinelibrary.wiley.com/doi/epdf/10.10…

🧵 I am very excited to share my postdoc project preprint investigating the role of NR4A2, a transcription factor linked to neuropsychiatric disorders, in the establishment of cell type identities in the claustro-insular region of the brain. 1/9 biorxiv.org/content/10.110…

Today, my son's genetic disorder was listed with the national organization of rare diseases. With this listing, it will help get more attention and more funding. See--rarediseases.org/rare-diseases/…

🚀 Working on your ERDERA 2025 JTC and need patient organisation partners? 🔍 Explore the Orphanet database: loom.ly/kdxJG6w 🤝 Contact EURORDIS: loom.ly/rLIi6-Y 📧 Still stuck? Email [email protected] or [email protected] 🌟

Attention #Oregonians: The #OR House is considering a bill to establish a #RareDisease Advisory Council in your state! Tell your Representative to vote YES on this bill by January 30! Take action (1 min) here: rarediseases.org/driving-policy… #Oregon #RDAC #Oregonian #ORpol #ORleg

Today there’s an article about our journey with NR4A2 in our local newspaper rv-times.com/2025/02/28/doc…

Suboxycontin

Alex Berenson I sell irrigation parts in Oregon and we have noticed that the Chinese have taken over the illegal production of marijuana. We’ve been calling it at work a reverse opium war.

I posted on Facebook this interesting thread about the value money see— facebook.com/share/15HmxHRc…

I just discovered that the producer of the Nightline program that I was on years ago happens to now be the chief scientific writer for UCLA. Where Franklin cells are. youtu.be/7Es-pATepMg?si…

Elon Musk Elon Musk How much have you thought about your vehicles helping special needs children in the future? My daughter has a NR4A2. A rare disease that only 200 people in the world have. CP like symptoms but everyone with the disease is different. Hopefully one day with Tesla she

🧬 Simons Searchlight is proud to join #StartGenetic — a new movement raising awareness for genetic testing ahead of #GeneticTestingActionDay on July 25, honoring Rosalind Franklin. Let’s help shorten the diagnostic journey. 💙💛 🔗 startgenetic.org #RareGenetics

Rare mutation in autism risk gene connects family with researcher | UCLA Health This is my son and myself with participated in this. uclahealth.org/news/article/r…

After years of unanswered questions, a rare NR4A2 gene mutation gave Franklin Henry and his family clarity, and sparked new research into the genetic roots of #autism. Now, he's helping UCLA Health researchers better understand how the brain develops. uclahealth.org/news/article/r…