Charcot Marie Tooth Disease - CMT Disease - Hereditary Neuropathy

THE FOUNDATION TO SUPPORT THOSE LIVING WITH CMT (CHARCOT-MARIE-TOOTH)
HNF

Bernadette

An Upcoming Documentary about Living with CMT

View Trailer !

 

 

 

 

Arlene has Plans... Big Plans!

Read all about Arlene in  Arlene on the Scene... available in September

Pre-Order your copy now !

 

 

 

 

MEMBER LOGIN

button_become_member
Hereditary Neuropathy Foundation, Inc.
1751 2nd Avenue, Suite 103, NY NY 10128
NY Tel: 212-722-8396
Toll Free: 877-463-1287
info@hnf-cure.org
Register with iGive and shop at brand name online stores through the iGive Mall. A portion of each purchase is donated to your favorite cause.
logo_igive

HNF SCIENTIFIC ADVISORY BOARD

Comprised of world-renowned researchers from all over the country, the Hereditary Neuropathy Foundation’s Scientific Advisory Committee reviews research proposals and oversees on-going research on a regular basis. The members of our Scientific Advisory Committee are noted researchers with expertise in a variety of CMT-related and translational research. Hailing from institutions such as Emory University, Stanford University, Harvard School of Medicine, and Columbia University, the Scientific Advisory Committee brings a wealth of knowledge to the search for a cure for Charcot Marie Tooth.

The Scientific Advisory Committee reviews submitted proposals, provides critiques to the researchers, and makes recommendations to the Medical Advisory Board who then reviews the proposals and provides recommendations to the Board of Directors. Once they are funded, each researcher is required to submit results to the Scientific Advisory Committee at regular intervals to insure that the research is achieving its goals and furthering the search for drug targets. This process guarantees that HNF funds innovative and cutting-edge research with the best possibility for developing a therapeutic.


Links  |  Site Map