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Neurology
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Myasthenia

Citations 21-30 of 68 total displayed.

Past content (since Jan 2001):

ARTICLES
Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations
J. S. Müller, S. K. Baumeister, V. M. Rasic, S. Krause, S. Todorovic, K. Kugler, W. Müller-Felber, A. Abicht, and H. Lochmüller
Neurology 2006; 67: 1159-1164. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Occurrence of CNS demyelinating disease in patients with myasthenia gravis
Marc Gotkine, Yakov Fellig, and Oded Abramsky
Neurology 2006; 67: 881-883. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Anti-MuSK antibodies: Correlation with myasthenia gravis severity
E. Bartoccioni, F. Scuderi, G. M. Minicuci, M. Marino, F. Ciaraffa, and A. Evoli
Neurology 2006; 67: 505-507. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Strong association of MuSK antibody–positive myasthenia gravis and HLA-DR14-DQ5
E. H. Niks, J.B.M. Kuks, B. O. Roep, G. W. Haasnoot, W. Verduijn, B. E.P.B. Ballieux, M. H. De Baets, A. Vincent, and J. J.G.M. Verschuuren
Neurology 2006; 66: 1772-1774. [Abstract] [Full text] [PDF]  

ARTICLES
Novel congenital myasthenic syndromes associated with defects in quantal release
M. Milone, T. Fukuda, X. M. Shen, A. Tsujino, J. Brengman, and A. G. Engel
Neurology 2006; 66: 1223-1229. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
MuSK Ab described in seropositive MG sera found to be Ab to alkaline phosphatase
K. Ohta, K. Shigemoto, S. Kubo, N. Maruyama, Y. Abe, N. Ueda, A. Fujinami, and M. Ohta
Neurology 2005; 65: 1988. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Primary CNS lymphoma complicating treatment of myasthenia gravis with mycophenolate mofetil
Steven Vernino, Diva R. Salomao, Thomas M. Habermann, and Brian P. O’Neill
Neurology 2005; 65: 639-641. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome
J. S. Müller, R. Stucka, S. Neudecker, S. Zierz, C. Schmidt, A. Huebner, H. Lochmüller, and A. Abicht
Neurology 2005; 65: 463-465. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Congenital endplate acetylcholinesterase deficiency responsive to ephedrine
M. Bestue-Cardiel, A. Sáenz de Cabezón-Alvarez, J. L. Capablo-Liesa, J. López-Pisón, J. L. Peña-Segura, J. Martin-Martinez, and A. G. Engel
Neurology 2005; 65: 144-146. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Treatment with botulinum toxin in a patient with myasthenia gravis and cervical dystonia
A. Fasano, A. R. Bentivoglio, T. Ialongo, F. Soleti, and A. Evoli
Neurology 2005; 64: 2155-2156. [Full text] [PDF]  

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* 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


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