Mouse Models of Human CNTNAP1 Mutations: Strategies to Rescue and Restore Functions
January 20, 2021
Research with the Department of Cellular and Integrative Physiology UT Health San Antonio, TX
News from the Hereditary Neuropathy Foundation: research updates, clinical trial progress, partnerships, and advocacy wins for the Charcot-Marie-Tooth community.
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January 20, 2021
Research with the Department of Cellular and Integrative Physiology UT Health San Antonio, TX
January 18, 2021
What GRIN is and why you should join
September 15, 2020
The FDA has agreed with the key elements of Pharnext’s approach for the developmental pathway to approval for PXT3003.
September 9, 2020
The Hereditary Neuropathy Foundation (HNF) would like to advance preclinical research as quickly as possible if it aligns with our key objectives.
July 23, 2020
Helixmith, specializing in gene therapy research for over 20 years, has kicked off its phase I and 2a clinical trial for using VM202 (Engensis) to treat CMT1A.
June 10, 2020
US Food and Drug Administration has agreed with Pharnext and provided clear guidance on the regulatory pathway to approval for PXT3003, including key design elements of a single pivotal Phase III study
January 20, 2020
Addie rewrote Try by Pink into a song about her disease and recorded it to raise awareness.
November 7, 2019
Where do the top CMT researchers in the world unite to share leading-edge research? The Peripheral Nerve Society (PNS) meeting!
November 5, 2019
Read more about the research findings presented at these conferences.
September 20, 2019
HNF has selected its first three types of CMT based on their potential for success…and we need your help!
December 29, 2018
HNF has been committed to funding HDAC inhibitor research since 2014.
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