168th ENMC International Workshop: Outcome measures and clinical trials in Charcot–Marie–Tooth disease (CMT)
Author:
Funder
NINDS/ORD
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference60 articles.
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2. Treatment for Charcot–Marie–Tooth disease;Young;Cochrane Database Syst Rev,2008
3. Estimation of the mutation frequencies in Charcot–Marie–Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study;Nelis;Eur J Hum Genet,1996
4. DNA duplication associated with Charcot–Marie–Tooth disease type 1A;Lupski;Cell,1991
5. Duplication in chromosome 17p11.2 in Charcot–Marie–Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group;Raeymaekers;Neuromuscul Disord,1991
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1. Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A;Journal of the Peripheral Nervous System;2023-06-13
2. Clinical spectrum and frequency of Charcot–Marie–Tooth disease in Italy: Data from the National CMT Registry;European Journal of Neurology;2023-05-26
3. Quality of life and upper limb disability in Charcot-Marie-Tooth disease: A pilot study;Frontiers in Neurology;2022-10-05
4. A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A;Orphanet Journal of Rare Diseases;2021-10-16
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