CMT: Genética y Herencia

CMT: Genética y Herencia Los patrones de herencia y CMT Saber cuál de las formas de CMT que tiene es importante para que usted pueda comprender las implicaciones de transmitirles…

CMT Type 1

Charcot-Marie-Tooth disease Type 1 (CMT1) What is CMT Type 1? CMT Type 1 (CMT1) is defined as an autosomal dominant (see inheritance) demyelinating form of CMT. CMT1 accounts for about…

CMTAreportspring24FINALwebSPREADS

…Study (all CMT subtypes) • Finding Your Gene—The Distant Cousin Project • Biomarkers and Outcome Measures (CMT1B, CMTX1 (aka CMT1X/CMTX), CMT2A, CMT2F) • The Inherited Neuropathies Consortium (INC) Study 6601:…

CMTA-STAR Biotech & Alliance Partners

…RESEARCH FOR DEMYELINATING CMT (Click image to enlarge) RESEARCH FOR AXONAL CMT CMTA-STAR ALLIANCE PARTNERS Actio Biosciences Actio Biosciences was founded by leaders in genetics and drug development to push…

Tratamiento y Gestión de CMT

Tratamiento y Gestión de CMT El tratamiento de laCMT se hace en conjunto con los profesionales médicos de distintas especialidades. Después del diagnóstico por un neurólogo, los pacientes de CMT…

CMTAWinter2023webspreads

…CMT2, CMT4, CMTX, dominant intermediate CMT (CMTDI), recessive intermediate CMT (CMTRI), distal hereditary motor neuropathy (dHMN), distal spinal muscular atrophy (dSMA), giant axonal neuropathy (GAN), hereditary motor and sensory neuropathy…

CMTA Report_Winter 2024 – STAR Special Edition_Download

…Toolbox iPSC Licensee CMTA-STAR Advisory Board Member CMTA-STAR Funded Researcher CMTA Center of Excellence INC-Affiliated CMTA Center of Excellence Aarhus, Denmark Drug Developer, CMTA-STAR Alliance Partner, Conducting CMT-SYNAPSE Clinical Trial…