How 1 dad used AI to advance finding a treatment for his son’s rare disease
Aberrant neurodevelopment in human iPS cell-derived models of Alexander disease
Tadpole Brain Atrophy in Adult-Onset Alexander Disease
A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease
Advances in Ionis' Novel Antisense Technology to be Presented at 2018 Society for Neuroscience Meeting
Father uses AI to learn about son’s illness, connect with scientists
Ionis candidate treatment for AxD granted "orphan drug" status in Europe
2019 Alexander Disease Update
Site-specific phosphorylation and caspase cleavage of GFAP are new markers of Alexander disease severity
Antisense Suppression of glial fibrillary acidic protein as a treatment for Alexander disease
US Army and local boxers fighting for Grayson’s Ladder and a cure for Alexander Disease
2018 Heart of Gold recipient Lauren (LoLo Loredo)
Hundreds Attend Love Hope Cure Gala to Benefit Elise’s Corner
Falls parents seek hope through research for daughter, 3, with fatal disease
The little boy has a disease with no cure. His family is determined to fight back.
Leukodystrophy Patient Featured on Seeking Solutions with Suzanne
Jackson family faces deadly rare diagnosis; 5k planned for therapy, research, wheelchair
Mom fights to bring attention to son’s rare disorder with no cure
