Mechanisms and Treatments in Demyelinating CMT
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Neurology (clinical),Pharmacology
Link
https://link.springer.com/content/pdf/10.1007/s13311-021-01145-z.pdf
Reference325 articles.
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2. Harding AE, Thomas PK. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain. 1980;103(2):259-80.
3. Magy L, Mathis S, Le Masson G, Goizet C, Tazir M, Vallat JM. Updating the classification of inherited neuropathies: Results of an international survey. Neurology. 2018;90(10):e870-e6.
4. Manganelli F, Pisciotta C, Reilly MM, Tozza S, Schenone A, Fabrizi GM, et al. Nerve conduction velocity in CMT1A: what else can we tell? Eur J Neurol. 2016;23(10):1566-71.
5. Li J. Caveats in the Established Understanding of CMT1A. Ann Clin Transl Neurol. 2017;4(8):601-7.
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