The Coyle Family Story - Living with Hereditary ATTR (hATTR) amyloidosis
This video was created for audiences in the UK & Ireland. Cousins James and Pat recall the story of their family’s experience of hATTR amyloidosis, including genetic testing and their hopes for the future of those diagnosed with the disease. NP IRL 00012
▶︎
Sophia's experience living with hATTR amyloidosis
▶︎
Alnylam & RNAi Therapeutics: Making our Medicines
▶︎
Chen (Brazil) – Living with hATTR Amyloidosis
▶︎
Alnylam Act - No Charge, Third Party Genetic Testing & Counseling
▶︎
Alnylam & RNAi Therapeutics: Silencing Disease. Amplifying Life.
▶︎
Alnylam & RNAi Therapeutics: Making our Medicines
▶︎
Marc – Living with Wild-Type ATTR Amyloidosis with Cardiomyopathy
▶︎
Ben, Lebt Mit AHP
▶︎
Physiopathologie de la PHA
▶︎
Alnylam's siRELIS(TM) Enzymatic Ligation Platform
▶︎
Stephanie, Atteinte de PHA
▶︎
Alnylam Challengers: Improving Access to Healthcare in Boston by Investing in Care Navigators
▶︎
A Message from Alnylam CEO Yvonne Greenstreet - Reflecting on 2025 and Looking forward to 2026
▶︎
RNAi, a promising platform for drug development
▶︎