UnravelingRare
A podcast produced by Unravel Biosciences to highlight patients, families, and other stakeholders critical to addressing orphan disorders.
Episode 16:
100 Program Milestone on Rare Disease Day
Episode 15:
Unravel Biosciences Team
Episode 14:
CSNK2A1 Conference 2025
Episode 13:
Clinical success in Malan Syndrome
Episode 12:
Forming a rare disease foundation - KMT2B Dystonia Foundation
Episode 11:
Meeting Rare Disease Stakeholders at the World Orphan Drug Congress
Episode 10:
Exponentially scaling drug discovery with COMBINED Brain
Episode 09:
Changing the drug discovery paradigm
Episode 08:
Exciting Progress at the CHOPS Foundation Symposium
Episode 07:
SPATA5L1 and the SPATA Foundation
Episode 06:
SPATA Disorder
Episode 05:
Story of successful repurposing for KMT2B syndrome
Episode 04:
CHOPS Syndrome and Synergies in Drug Development
Episode 03:
AP-4 Hereditary Spastic Paraplegia: solving multiple disorders at once
Episode 02:
Boys with Rett Syndrome
Episode 01:
Rett Syndrome in Latin America
