Charcot Marie Tooth disease (CMT): historical perspectives and evolution-Reference-Cited by-同舟云学术

Charcot Marie Tooth disease (CMT): historical perspectives and evolution

Published:2014-09-09 Issue:4 Volume:262 Page:801-805
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Kazamel Mohamed,Boes Christopher J.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-014-7490-9.pdf

Reference26 articles.

1. Herskovitz S, Scelsa S, Schaumberg H (2010) Peripheral neuropathies in clinical practice. Oxford University Press, Oxford

2. Smith AG (2001) Charcot-Marie-tooth disease. Arch Neurol 58:1014–1016

3. Pearce JMS (2003) Fragments of neurological history. Imperial College Press, London

4. Dyck PJ, Lambert EH (1968) Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Arch Neurol 18:619–625

5. Charcot JM, Marie P (1886) Sur une forme particulière d’atrophie musculaire progressive souvent familiale débutant par les pieds et les jambes et atteignant plus tard les mains. Rev Méd Paris 6:97–138

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