In 2009, HNF partnered with Inspire, a social network for health, to launch a CMT online support community.
Blog Category
Research
Total posts in Category: 95
HNF Presents Research Findings at Three Prestigious Conferences
Read more about the research findings presented at these conferences.
HNF is Now Recruiting Patients for New Gene Therapy Research Projects
HNF has selected its first three types of CMT based on their potential for success…and we need your help!
Orphan Disease Center Million Dollar Bike Ride Pilot Grant Program
The ODC MDBR Pilot Grant Program provides a one‐year grant to support research related to a rare disease represented in the 2019 Million Dollar Bike Ride.
What Is Fast Track?
The FDA has awarded Fast Track designation to two drugs currently in development for CMT.
HNF Featured in Rare Neurological Disease Special Report
HNF is proud to announce that for the fifth year in a row, we have been featured in the annual Rare Neurological Disease Special Report.
StarWise Therapeutics & HNF Form A Strategic Alliance to Bring a NextGen HDAC6 Drug Therapy to CMT2A (MFN2) Patients
HNF has been committed to funding HDAC inhibitor research since 2014.
CMT On The Cloud
HNF takes action and joins genomics revolution for CMT and rare forms of IN.
Exciting News For The CMT Patient Community
Exciting news for the CMT patient community with the first potential treatment ever!
HNF & Athena Diagnostics Form Strategic Alliance
They will collaborate on research and provide access to genetic testing for CMT.
HNF On The Road
HNF presenting and attending prestigious conferences worldwide.
A Letter From HNF’s CEO/Founder
2018 was a pivotal year for the Hereditary Neuropathy Foundation (HNF) and the entire Charcot-MarieTooth (CMT) Community.
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