Welcome to the Walk4CMT Toolbox
Welcome to the Walk4CMT Toolbox We are grateful that you have taken on a Walk 4 CMT event! This timeline will help you organize and promote your event, give you…
Wilmington, NC CMTA Branch Meeting (In-Person) with Guest Speaker
05/04/2024 @ 10:00 am – 12:00 pm – Please join us for a CMT get-together on Saturday, May 4 from 10 am – 12 pm at the Northeast Library near Landfall Country Club (see library address below). This will be a fun get together combining a bit of education and a bit of social time. We will welcome special guest speaker, Kelsey Komyathy, […]
Gene Therapy for CMT1A, 1B, and X1: Progress in Nanoparticles
…the use of nanoparticles to deliver gene therapies directly to Schwann cells to treat CMTX1 (aka CMTX1, CMTX), the second most common type of CMT. This research focuses on using…
CMTA Announces New Center of Excellence in Kentucky
The Charcot-Marie-Tooth Association (CMTA), the world’s largest philanthropic funder of research aimed at bringing treatments to patients and improving the lives of those living with Charcot-Marie-Tooth disease (CMT), is excited…
CMTA Announces New Center of Excellence at Virginia Commonwealth University
The Charcot-Marie-Tooth Association (CMTA), the world’s largest philanthropic funder of research aimed at bringing treatments to patients and improving the lives of those living with Charcot-Marie-Tooth disease (CMT), is proud…
2020_CMT_PFC_Pediatric_Neurology_transcript
…axonal form of CMT, CMT2, tend to progress a little bit faster than those with CMT1, but that’s just an average. There are certainly patients with CMT2 who stay about…
Voice_of_the_Patient_Report_8-19-2019
…PMP22 (CMT1A/HNPP), GJB1 (CMT1X), MFN2 (CMT2A), and MPZ (CMT1B). There are rarer forms of CMT that are autosomal recessive demyelinating motor and sensory neuropathies that include several genes categorized as…
CMT-and-Genetic-Testing-Why-Is-It-Important
…type of CMT is autosomal dominant demyelinating CMT, or CMT1. The most common genes in this type are PMP22 (CMT1A) and MPV (CMT1B). CMT2 refers to axonal CMT with autosomal…
The 2020 Winter CMTA Report
…see in the world of CMT. Be the Change: A Message from CEO Amy Gray Swimming Uphill with Jamal Hill CMTA Funds Cutting-Edge Gene Editing Studies for Type 2 CMT…
CMTA Appoints Science and Technology Veteran, Patricia Verduin, PhD, to the Board of Directors
The Charcot-Marie-Tooth Association (CMTA), the largest philanthropic funder of Charcot-Marie-Tooth disease (CMT) research aimed at bringing treatments and a cure to patients, is pleased to announce the appointment of a…