Advertisement
Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
 QUICK SEARCH:   [advanced]


     


Muscle disease

Citations 11-20 of 283 total displayed.

Past content (since Jan 2001):

ARTICLES
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
E. Matthews, R. Labrum, M. G. Sweeney, R. Sud, A. Haworth, P. F. Chinnery, G. Meola, S. Schorge, D. M. Kullmann, M. B. Davis, and M. G. Hanna
Neurology 2009; 72: 1544-1547. [Abstract] [Full text] [PDF]  

ARTICLES
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
M. Fanin, A. C. Nascimbeni, S. Aurino, E. Tasca, E. Pegoraro, V. Nigro, and C. Angelini
Neurology 2009; 72: 1432-1435. [Abstract] [Full text] [PDF]  

NEUROIMAGES
Scotosensitive myoclonic seizures in MERRF
Mohamad Z. Koubeissi, Chaiyos Khongkhatithum, Annette I. Janus, and Hans Lüders
Neurology 2009; 72: 858. [Full text] [PDF]  

ARTICLES
Fat metabolism during exercise in patients with McArdle disease
M. C. Ørngreen, T. D. Jeppesen, S. Tvede Andersen, T. Taivassalo, S. Hauerslev, N. Preisler, R. G. Haller, G. van Hall, and J. Vissing
Neurology 2009; 72: 718-724. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
SUPERFICIAL SIDEROSIS: SEALING THE DEFECT
Neeraj Kumar, John I. Lane, and David G. Piepgras
Neurology 2009; 72: 671-673. [Full text] [PDF]  

EDITORIALS
How much expansion to be diseased?: Toward repeat size and myotonic dystrophy type 2
Benedikt Schoser and Tetsuo Ashizawa
Neurology 2009; 72: 484-485. [Full text] [PDF]  

ARTICLES
Premutation allele pool in myotonic dystrophy type 2
L. L. Bachinski, T. Czernuszewicz, L. S. Ramagli, T. Suominen, M. D. Shriver, B. Udd, M. J. Siciliano, and R. Krahe
Neurology 2009; 72: 490-497. [Abstract] [Full text] [PDF]  

ARTICLES
Effect of aerobic training in patients with spinal and bulbar muscular atrophy (Kennedy disease)
N. Preisler, G. Andersen, F. Thøgersen, C. Crone, T. D. Jeppesen, F. Wibrand, and J. Vissing
Neurology 2009; 72: 317-323. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
LINEZOLID INDUCING COMPLEX PARTIAL STATUS EPILEPTICUS IN A PATIENT WITH EPILEPSY
Bassel F. Shneker, Peggy D. Baylin, and Michael E. Nakhla
Neurology 2009; 72: 378-379. [Full text] [PDF]  

ARTICLES
New morphologic and genetic findings in cap disease associated with β-tropomyosin (TPM2) mutations
M. Ohlsson, S. Quijano-Roy, N. Darin, G. Brochier, E. Lacène, D. Avila-Smirnow, M. Fardeau, A. Oldfors, and H. Tajsharghi
Neurology 2008; 71: 1896-1901. [Abstract] [Full text] [PDF]  

[First page]   [Previous page]   [Next page]
Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29

* Collected Resources Home

* Related collections:
 Neuromuscular disease
 All Neuromuscular Disease
 Anterior nerve cell disease
 Amyotrophic lateral sclerosis
 Myasthenia
 Lambert-Eaton syndrome
 Peripheral neuropathy
 Carpal tunnel syndrome
 Cranial neuropathy
 Guillain-Barre syndrome
 Chronic inflammatory demyelinating polyneuropathy
 Transverse myelitis
 Muscle disease


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
Copyright © 2009 by AAN Enterprises, Inc.
Advertisement