Webb22 juni 2024 · Riaan Research Initiative is one of the few women of color-led patient organizations and one of the first known Sikh-led rare disease patient advocacy organizations. Talking about this... Webb215 Followers, 151 Following, 279 Posts - See Instagram photos and videos from Riaan Research Initiative (@riaanresearch) riaanresearch. Follow. 279 posts. 215 followers. 151 following. Riaan Research Initiative. 501(c)(3) working to get treatments developed for #CockayneSyndrome, as fast as humanly possible. linktr.ee/RiaanResearch. Posts.
Riaan Research Initiative funds Cockayne syndrome gene …
Webb12 aug. 2024 · The #Ride4Riaan campaign will help support Riaan Research Initiative’s existing programs to accelerate the development of treatments for Cockayne Syndrome, an ultra-rare and fatal genetic disorder. These include a CSA gene replacement therapy program at the University of Massachusetts Medical School, and drug repurposing … WebbDr. Riaan F. Rifkin is an anthropological archaeologist by training and his expertise straddles multiple areas including cognitive and cultural … sonic 3 the trailer
Florida State University Announces $20 Million-Plus Investment in ...
Webb21 sep. 2024 · I am a research and editorial assistant at Georgetown University’s Institute for the Study of Diplomacy (ISD) and a final-year M.A. student in European Studies in the … Webb25 juni 2024 · Cassidy also quoted Jo Kaur, founder of the Riaan Research Initiative, to ask: “If Roe v Wade is overturned: How many Savitas will die in the US?” THREAD: As Roe v Wade trends. The people of Ireland deeply remember Savita Halappanavar. If the people of the United States have not heard this story, please read. If you feel comfortable. WebbCarolina Bologna wrote a piece for The Huffington Post entitled, "Parents Who Lost A Child Share What They Wish More People Understood." We thought the advice offered here might resonate with the Cockayne syndrome community and the larger rare disease community. sonic 3 \u0026 knuckles genesis online