@RiaanResearch
Non-profit hunting for treatments for Cockayne Syndrome. Instagram Links here!
Celebrating our First Year!
Celebrating our First Year!
Riaan Research Initiative Celebrates One Year Fighting For Children with Cockayne Syndrome
Jaipal Singh's Obituary
Jaipal Singh's Obituary
Jaipal Singh Chauhan Jaipal Singh Chauhan, beloved son, brother, and husband left this world Friday, May 13th, 2022 at age 41, after a brief but...
Primer on Genetic Variants (Mutations)
Primer on Genetic Variants (Mutations)
If you want to build a foundational understanding of genomics in both health and disease, it's important to be able to distinguish between the different type of genetic mutations that can occur. Here, we take a look at some of the mutations that can be encountered and the impact they have on the genome.
Interview with Saffron Press
Interview with Saffron Press
Just another WordPress site
Cockayne Syndrome Patient Registry Activation Form
Cockayne Syndrome Patient Registry Activation Form
Donate to #Run4Riaan Campaign
Donate to #Run4Riaan Campaign
RRI Youtube Page
RRI Youtube Page
SheKnows: My Son Was Born With An Incredibly Rare Disease & Fighting for His Life Isn’t Anything Like I Imagined Jo Kaur by JO KAUR
SheKnows: My Son Was Born With An Incredibly Rare Disease & Fighting for His Life Isn’t Anything Like I Imagined Jo Kaur by JO KAUR
On Motherhood and Love: Blog Post
On Motherhood and Love: Blog Post
Happy Valentine's Day!
Donate to #Love4Riaan Campaign (Riaan Research Initiative)
Donate to #Love4Riaan Campaign (Riaan Research Initiative)
Register for Rare Disease Day at the NIH
Register for Rare Disease Day at the NIH
Each year, we support this event to raise awareness about rare diseases, the people they affect, and partnerships that promote research and advance knowledge of new treatments.
FDA Warning for Flagyl
FDA Warning for Flagyl
Nationwide survey of Cockayne syndrome in Japan: Incidence, clinical course and prognosis
Nationwide survey of Cockayne syndrome in Japan: Incidence, clinical course and prognosis
Riaan Research Initiative Blog
Riaan Research Initiative Blog
Sign up for our newsletter and learn more about our journey to find a cure for our son Riaan's rare, fatal, and devastating neurodegenerative genetic disease, Cockayne Syndrome. Visit our foundation page for Riaan Research Initiative at riaanresearch.org. Click to read Riaan's Newsletter, by Riaan Research Initiative, a Substack publication with hundreds of subscribers.
UMass Chan Medical School Research Associate Position
UMass Chan Medical School Research Associate Position
Riaan Research Initiative Website
Riaan Research Initiative Website
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