Is distal motor and/or sensory demyelination a distinctive feature of anti-MAG neuropathy?-Reference-Cited by-同舟云学术

Is distal motor and/or sensory demyelination a distinctive feature of anti-MAG neuropathy?

Published:2016-06-17 Issue:9 Volume:263 Page:1761-1770
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Lozeron Pierre,Ribrag Vincent,Adams David,Brisset Marion,Vignon Marguerite,Baron Marine,Malphettes Marion,Theaudin Marie,Arnulf Bertrand,Kubis Nathalie

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-016-8187-z.pdf

Reference33 articles.

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2. Joint Task Force of the EFNS and the PNS (2010) European Federation of Neurological Societies/Peripheral Nerve Society Guideline on management of paraproteinemic demyelinating neuropathies. Report of a Joint Task Force of the European Federation of Neurological Societies and the Peripheral Nerve Society–first revision. J Periph Nerv Syst 15:185–195

3. Franssen H, Notermans NC (2006) Length dependence in polyneuropathies associated with IgM gammopathy. Ann Neurol 59:365–371

4. Barohn RJ, Kissel JT, Warmolts JR et al (1989) Chronic inflammatory demyelinating polyradiculoneuropathy: clinical characteristics, course and recommendations for diagnostic criteria. Arch Neurol 46:878–884

5. Kaku DA, Parry GJ, Malamut R et al (1993) Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with segmental duplication of chromosome 17. Neurology 43:1806–1808

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