Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation-Reference-Cited by-同舟云学术

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Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation

Published:2008-06-17 Issue:7 Volume:255 Page:986-992
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Gallardo E.,Claeys K. G.,Nelis E.,García A.,Canga A.,Combarros O.,Timmerman V.,Jonghe P.,Berciano J.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-008-0808-8.pdf

Reference29 articles.

1. Berciano J, Combarros O, Figols J, Calleja J, Cabello A, Silos I, et al. (1986) Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family. Brain 109:897–914

2. Berciano J, García A, Calleja J, Combarros O (2000) Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot-Marie-Tooth disease 1A duplication. Neuromuscul Disord 10:419–424

3. Berciano J, Gallardo E, García A, Infante J, Mateo I, Combarros O (2006) Charcot-Marie-Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles. A longterm follow-up study. J Neurol Neurosurg Psychiatry 77:1169–1176

4. Bitoun M, Maugenre S, Jeannet PY, Lacène E, Ferrer X, Laforrêt P, et al. (2005) Mutations in dynamin 2 cause dominant centronuclear myopathy. Nat Genet 37:1207–1209

5. Combarros O, Calleja J, Polo JM, Berciano J (1987) Prevalence of hereditary motor and sensory neuropathy in Cantabria, Spain. Acta Neurol Scand 75:9–12

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