Cure Mito Foundation and Hope for PDCD Foundation announce a patient registry collaboration
NEWS
- Jan 31
- 1 min
New Paper: Interoperability of Leigh Syndrome Patient Registry Data with Regulatory Submission Standards
- Jan 13
- 1 min
C-Path to Lead New Task Force Aimed at Accelerating Drug Development for Mitochondrial and Inherited Metabolic Diseases
- Nov 21, 2023
- 1 min
Newsletters
- Nov 21, 2023
- 1 min
Teamwork makes the dream work: our new paper
- Nov 14, 2023
- 1 min
Their son may never be cured. But these McKinney parents aren’t giving up
- Sep 11, 2023
- 2 min
Leigh syndrome patient registry paper is published!
- Aug 28, 2023
- 1 min
COLOR FOR MITO AND WIN PRIZES
- Jul 12, 2023
- 1 min
Sanford Health Rare Disease Data Registry Partners with C-Path’s RDCA-DAP, Cure Mito Foundation
- Jun 6, 2023
- 1 min
Cure Mito Foundation releases the first-of-its-kind online resource about Leigh syndrome
- May 21, 2023
- 1 min
Our story is featured on WebMD!
- Mar 1, 2023
- 1 min
Leigh syndrome medical network
- Feb 23, 2023
- 1 min
Patient registries FAQ
- Feb 23, 2023
- 1 min
FAMILY PLANNING GUIDE
- Jan 23, 2023
- 1 min
Cure Mito Foundation announces a formation of a Corporate Advisory Council
- Jan 6, 2023
- 1 min
December 2022 newsletter
- Dec 11, 2022
- 1 min
New resource for Leigh syndrome community is coming soon!
- Nov 29, 2022
- 1 min
Drug Repurposing News!
- Nov 9, 2022
- 1 min
Shop and support Leigh Syndrome Research!
- Oct 25, 2022
- 1 min
Genetic testing opportunity for those with suspected mitochondrial disease