The Snow Foundation is proud to be a PLATINUM MEMBER of The National Organization of Rare Disorders. Check out their Website: https://rarediseases.org/
Wolfram Syndrome Poster Presentation by Brianna Carman-Washington University School of Medicine-Urano Lab
https://medicalxpress.com/news/2023-03-febrile-urinary-tract-infections-common.html
Wolfram Syndrome Poster Presentation by William An and Megha Verma-Washington University School of Medicine-Urano Lab
Publication: Amylyx Pharmaceuticals, Inc. | Publication Date: April 13, 2023
Authors: Amylyx Pharmaceuticals, Inc.
Significance
Recently published preclinical data demonstrate initial proof-of-concept for the therapeutic development of AMX0035 (sodium phenylbutyrate and taurursodiol) in Wolfram syndrome
Wolfram Syndrome Poster Presentation by Nila Palaniappan-Washington University School of Medicine-Urano Lab
About the Snow Foundation
The Snow Foundation is a collective voice for Wolfram syndrome patients, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss and neurodegeneration.
Rare Diseases…Common Problems
P.O. Box 50224 Clayton, MO 63105
(402) 694-1354
You must be logged in to post a comment.