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Myasthenia
Citations 51-60 of 68 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Treatment of slow-channel congenital myasthenic syndrome with fluoxetine
- C. Michel Harper, Takayasu Fukodome, and Andrew G. Engel
Neurology 2003; 60: 1710-1713.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- ARTICLES
The final month of life in patients with ALS
- Linda Ganzini, Wendy S. Johnston, and Maria J. Silveira
Neurology 2002; 59: 428-431.
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- 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.
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- 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.
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- BRIEF COMMUNICATIONS
Myasthenia gravis in a woman with congenital AChR deficiency due to -subunit mutations
- Rebecca Croxen, Angela Vincent, John NewsomDavis, and David Beeson
Neurology 2002; 58: 1563-1565.
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