Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Reilly, M. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Reilly, M. M.
Related Collections
Right arrow Peripheral neuropathy
Right arrow All Genetics
Right arrowRelated Articles
Neurology, Vol. 65, Issue 2, 186-187, July 26, 2005

EDITORIALS

Axonal Charcot–Marie–Tooth disease: The fog is slowly lifting!

Mary M. Reilly

You have reached the most complete version of this article accessible without further authentication.
More complete versions are available.
Link to article

Article topics:


Related Articles

July 26 Highlights
Neurology 2005 65: 184-185. [Full Text] [PDF]

Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene
Victoria H. Lawson, Brad V. Graham, and Kevin M. Flanigan
Neurology 2005 65: 197-204. [Abstract] [Full Text] [PDF]



This article has been cited by other articles:


Home page
Hum Mol GenetHome page
V. Lupo, M. I. Galindo, D. Martinez-Rubio, T. Sevilla, J. J. Vilchez, F. Palau, and C. Espinos
Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway
Hum. Mol. Genet., December 1, 2009; 18(23): 4603 - 4614.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
G. M. Fabrizi, M. Ferrarini, T. Cavallaro, I. Cabrini, R. Cerini, L. Bertolasi, and N. Rizzuto
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease
Neurology, July 17, 2007; 69(3): 291 - 295.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
G. M. Fabrizi, T. Cavallaro, C. Angiari, I. Cabrini, F. Taioli, G. Malerba, L. Bertolasi, and N. Rizzuto
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton
Brain, February 1, 2007; 130(2): 394 - 403.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
R. Del Bo, F. Locatelli, S. Corti, M. Scarlato, S. Ghezzi, A. Prelle, G. Fagiolari, M. Moggio, M. Carpo, N. Bresolin, et al.
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutation
Neurology, March 14, 2006; 66(5): 752 - 754.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Reilly, M. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Reilly, M. M.
Related Collections
Right arrow Peripheral neuropathy
Right arrow All Genetics
Right arrowRelated Articles