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You searched for: Author/Creator Laura, Matilde

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21. MFN2 deletion of exons 7 and 8: founder mutation in the UK population. Issue 2 (June 2015)

22. Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT. (11th April 2017)

23. Natural history of Charcot‐Marie‐Tooth disease during childhood. Issue 3 (22nd September 2017)

27. PO202 Natural history study in hereditary sensory neuropathy type 1. (1st December 2017)

28. Psychometrics evaluation of Charcot‐Marie‐Tooth Neuropathy Score (CMTNSv2) second version, using Rasch analysis. Issue 3 (September 2014)

29. Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS. Issue 9 (6th August 2020)