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Fall Risk Assessment in a Population of Charcot-Marie-Tooth Disease Type 1A (CMT 1A) by Timed Up and Go Test (DeteCTCMT)

• Source: Fall Risk Assessment in a Population of Charcot-Marie-Tooth Disease Type 1A (CMT 1A) by Timed Up and Go TestReilly MM, Shy ME,

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Natural History Study for Charcot Marie Tooth Disease

• Source: Global Registry for Inherited Neuropathies Natural History Study for Charcot Marie Tooth Disease

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Evaluate the Safety and Efficacy of EN001 in Patients With Charcot-Marie-Tooth Disease Type 1A

• Source: An Open, Dose-escalation, Phase 1b Clinical Trial to Evaluate the Safety and Efficacy of EN001 in Patients With Charcot-Marie-Tooth

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Tools for Therapeutic Evaluation in Charcot-Marie-Tooth Disease Type 1A: Outcome Measures and Biomarkers (CMT-TOOLS)

• Source: Tools for Therapeutic Evaluation in Charcot-Marie-Tooth Disease Type 1A: Outcome Measures and Biomarkers

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A Chinese pedigree with a novel mutation in GJB1 gene and a rare variation in DHTKD1 gene for diverse Charcot‑Marie‑Tooth diseases

• Authors : Yin‑Zhou Wang; Zhen‑Hua Zhao; Zhi‑Ting Chen

Subjects: Adult; Male; 0301 basic medicine

• Source: Molecular Medicine Reports.

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Phase III Trial Assessing the Efficacy and Safety of PXT3003 in CMT1A Patients (PLEO-CMT) (PLEO-CMT)

• Source: International, Multi-center, Randomized, Double-blind, Placebo-controlled Phase III Study Assessing in Parallel Groups the Efficacy and Safety of 2 Doses of PXT3003 in Patients With

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Correlation Between Clinical and Electrophysiological Phenotypes in a Population of Patients With Neuropathy Charcot-Marie-Tooth Disease Type 1A (CCA1)

• Source: Correlation Between Clinical and Electrophysiological Phenotypes in a Population of Patients With Neuropathy Charcot-Marie-Tooth Disease

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A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K

• Authors : Arnaud Chevrollier; Marc Ferré; Dominique Bonneau ...

Subjects: Male; inherited peripheral neuropathy; Human Variome Project

• Source: Orphanet Journal of Rare DiseasesOrphanet Journal of Rare Diseases, 2011, 6 (1), pp.87. ⟨10.1186/1750-1172-6-87⟩Orphanet

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Genetic study of demyelinating form of autosomal-recessive Charcot-Marie-tooth diseases in a Turkish family

• Authors : Nilufer Sahin-Calapoglu; Mustafa Soyöz; Mustafa Calapoğlu

Subjects: Adult; Male; congenital, hereditary, and neonatal diseases and abnormalities

• Source: The International journal of neuroscience. 119(8)

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The Charcot-Marie-Tooth diseases: how can we identify and develop novel therapeutic targets?

• Authors : Rhys C. Roberts

Subjects: Genetics; congenital, hereditary, and neonatal diseases and abnormalities; 0303 health sciences

• Source: Brain. 135:3527-3528

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