Myasthenia

Citations 51-60 of 67 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Myasthenia gravis: A higher than expected incidence in the elderly

J. M. Aragonès, I. Bolíbar, X. Bonfill, E. Bufill, A. Mummany, F. Alonso, and I. Illa
Neurology 2003; 60: 1024-1026. [Abstract] [Full text] [PDF]  

VIEWS & REVIEWS
Thymoma in patients with MG: Characteristics and long-term outcome

A. Evoli, C. Minisci, C. Di Schino, F. Marsili, C. Punzi, A. P. Batocchi, P. A. Tonali, G. B. Doglietto, P. Granone, L. Trodella, A. Cassano, and L. Lauriola
Neurology 2002; 59: 1844-1850. [Abstract] [Full text] [PDF]  

ARTICLES
Congenital myasthenic syndrome caused by low-expressor fast-channel AChR subunit mutation

X.-M. Shen, K. Ohno, T. Fukudome, A. Tsujino, J.M. Brengman, D.C. De Vivo, R.J. Packer, and A.G. Engel
Neurology 2002; 59: 1881-1888. [Abstract] [Full text] [PDF]  

ARTICLES
AChR phosphorylation and indirect inhibition of AChR function in seronegative MG

C.P. Plested, T. Tang, I. Spreadbury, E.T. Littleton, U. Kishore, and A. Vincent
Neurology 2002; 59: 1682-1688. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Paraneoplastic neurological autoimmunity associated with ANNA-1 autoantibody and thymoma

Steven Vernino, Eric R. Eggenberger, Lisa R. Rogers, and Vanda A. Lennon
Neurology 2002; 59: 929-932. [Abstract] [Full text] [PDF]  

ARTICLES
The final month of life in patients with ALS

Linda Ganzini, Wendy S. Johnston, and Maria J. Silveira
Neurology 2002; 59: 428-431. [Abstract] [Full text] [PDF]  

VIEWS & REVIEWS
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes

R. Croxen, C. Hatton, C. Shelley, M. Brydson, G. Chauplannaz, H. Oosterhuis, A. Vincent, J. Newsom-Davis, D. Colquhoun, and D. Beeson
Neurology 2002; 59: 162-168. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Increased serum levels of the interferon-–inducing cytokine interleukin-18 in myasthenia gravis

Sebastian Jander and Guido Stoll
Neurology 2002; 59: 287-289. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Myasthenia gravis in a woman with congenital AChR deficiency due to -subunit mutations

Rebecca Croxen, Angela Vincent, John Newsom–Davis, and David Beeson
Neurology 2002; 58: 1563-1565. [Abstract] [Full text] [PDF]  

ARTICLES
Three novel COLQ mutations and variation of phenotypic expressivity due to G240X

Y.A. Shapira, M.E. Sadeh, M.P. Bergtraum, A. Tsujino, K. Ohno, X.-M. Shen, J. Brengman, S. Edwardson, I. Matoth, and A.G. Engel
Neurology 2002; 58: 603-609. [Abstract] [Full text] [PDF]  

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