Hereditary Neuropathy Foundation
Highly Engaged Employees
Non-Profit & Charitable Organizations · Virginia, United States · 1-10 Employees
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Overview
Headquarters
PO Box 1922, Midlothian, Virginia, 23113...Phone Number
(212) 722-8396Website
www.hnf-cure.orgRevenue
<$5 MillionIndustry
About Hereditary Neuropathy Foundation
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Debt
$20K
Hereditary Neuropathy Foundation Tech Stack
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Hereditary Neuropathy Foundation News & Media
Hereditary Neuropathy Foundation & University of Missouri Present The Nerve to Cure: CMT Social + Science Day and Dinner
Uniting Research, Care, and Community for Charcot-Marie-Tooth Awareness and Progress COLUMBIA , MO, UNITED STATES, August 28, 2025 /EINPresswire.com/ -- The Hereditary Neuropathy Foundation (HNF), in partnership with Dr. Ryan Castoro, Dr. Kathryn Moss …Hereditary Neuropathy Foundation (HNF) Expands Charcot-Marie-Tooth (CMT) Biobank Inventory Now Available to Researchers
HNF expands CMT Biobank with immediate access to biospecimens to accelerate biomarker and translational research. Calling researchers, industry and patients. NEW YORK, NY, UNITED STATES, October 8, 2024 /EINPresswire.com/ -- The Hereditary Neuropathy …HNF’s Team CMT Partners with Rock 'n' Roll Running Series to Raise Funds for Charcot-Marie-Tooth (CMT) Research
The Hereditary Neuropathy Foundation (HNF) is thrilled to announce a new partnership with the Rock 'n' Roll Running Series to raise funds for CMT Research. NEW YORK, NY, UNITED STATES, September 19, 2024 /EINPresswire.com/ -- The Hereditary …HNF participates in inaugural Critical Path Institute (C-Path) Global Impact Conference in Washington
Allison Moore, Founder/CEO will participate in the the session, titled “Navigating the Patient-Focused Drug Development Roadmap.” NEW YORK, NEW YORK , UNITED STATES , August 20, 2024 /EINPresswire.com/ -- Hereditary Neuropathy Foundation (HNF) is proud …
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Frequently Asked Questions Regarding Hereditary Neuropathy Foundation
The Hereditary Neuropathy Foundation (HNF) is dedicated to increasing awareness and accurate diagnosis of Charcot-Marie-Tooth (CMT) disease and related inherited neuropathies. They provide critical information and resources to support individuals and families affected by CMT, while also funding research aimed at developing effective treatments and... Read More