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You searched for: Author/Creator Pareyson, D.

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1. Altered TDP‐43‐dependent splicing in HSPB8‐related distal hereditary motor neuropathy and myofibrillar myopathy. (2nd December 2017)

4. Nerve conduction velocity in CMT1A: what else can we tell?. (14th July 2016)

5. No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype. (June 2016)

6. Novel outcome measures for Charcot−Marie−Tooth disease: validation and reliability of the 6‐min walk test and StepWatch™ Activity Monitor and identification of the walking features related to higher quality of life. (10th May 2016)

7. Responsiveness of clinical outcome measures in Charcot−Marie−Tooth disease. (31st July 2015)

8. Treadmill training in patients affected by Charcot–Marie–Tooth neuropathy: results of a multicenter, prospective, randomized, single‐blind, controlled study. (25th September 2019)