Chicago, IL CMTA Branch Social (IN-PERSON)
06/15/2024 @ 1:00 pm – 3:00 pm – Please join us (in person) for the Chicago Branch social on Saturday, June 15th at 1:00 am Central Time. Our meeting will be held at the Peace Lutheran Church. The address is 1900 E Lincoln Highway New Lenox, IL 60451. During our meeting, we will hear CMTA updates, discuss our upcoming Walk 4 CMT on […]
Progress in CMT2D Research
…identifying new targets for CMT treatments”. If you would like to support the CMTA’s research efforts, please consider making a donation in support of the CMTA’s Strategy to Accelerate Research….
Type 2 Update: One Patient’s Diagnostic Odyssey with SORD
…the drug basically cured CMT in fruit flies. “This is a remarkable discovery only possible due to large scale genomic data aggregation from volunteering CMT patients,” he added. Dr. Züchner,…
CMT_Fact_Sheet
…development of new drugs to treat CMT, to improve the quality of life for people with CMT, and, ultimately, to find a cure. Our vision is a world without CMT….
CMT Fact sheet_1-2020
…development of new drugs to treat CMT, to improve the quality of life for people with CMT, and, ultimately, to find a cure. Our vision is a world without CMT….
CMTA_2011_Annual_Report
…Suter, ETH Institute, Zurich Dr. Vincent Timmerman, University of Antwerp Dr. Larry Wrabetz, SUNY Buffalo Charcot-Marie-Tooth Association PO Box 105 Glenolden, PA 19036 1-800-606-CMTA www.cmtausa.org www.facebook.com/CMTAssociation Twitter @CMTASTAR https://www.cmtausa.org http://www.facebook.com/CMTAssociation…
Modafinil_Reduces_Fatigue_in_CMT1A_Dr_Gregory_Carter
…in the myelin sheath that also eventually lead to secondary axonal loss.4,5 CMT 1A is passed on in an autosomal dominant pattern.1,5 Most of the descriptive phenotypic studies in CMT…
Genetic Testing
…found have had one of five conditions, caused by mutations in four genes: CMT1A (PMP22 gene duplication), CMT1X (GJB1 gene mutation), CMT1B (MPZ gene mutation), HNPP (PMP22 gene deletion), or…
What is STAR?
…special emphasis on the more prevalent types – CMT1A, CMT2A, CMT2E, CMT1X, CMT1B and CMT4.) Advanced team efforts take place in consortia involving multiple partners with expertise in assay development,…
INC Research Study 6602: Genetics of Charcot Marie Tooth Disease
CMTA-Funded Research Database for CMT2 Identifies New Disease-Causing Mutations While researchers have identified more than 90 mutated genes that cause CMT, approximately 50 percent of CMT2 patients do not yet…