|
All Neuromuscular Disease
Citations 101-110 of 158 total displayed.
|
Past content
(since Jan 2000):
|
- BRIEF COMMUNICATIONS
Creatine monohydrate in DM2/PROMM: A double-blind placebo-controlled clinical study
- C. Schneider–Gold, M. Beck, C. Wessig, A. George, H. Kele, K. Reiners, and K. V. Toyka
Neurology 2003; 60: 500-502.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Deafness and CMT disease associated with a novel four amino acid deletion in the PMP22 gene
- Nyamkhishig Sambuughin, Astrid de Bantel, Shona McWilliams, and Kumaraswamy Sivakumar
Neurology 2003; 60: 506-508.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Obstacles in the diagnosis and treatment of syphilitic amyotrophy
- T. Etgen, C. Bischoff, M. Resch, K. Winbeck, B. Conrad, and D. Sander
Neurology 2003; 60: 509-511.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Sera from Guillain-Barré patients enhance leakage in blood–nerve barrier model
- Takashi Kanda, Masanaga Yamawaki, and Hidehiro Mizusawa
Neurology 2003; 60: 301-306.
[Abstract]
[Full text]
[PDF]
- VIEWS & REVIEWS
The morbidity of Guillain-Barré syndrome admitted to the intensive care unit
- R.D. Henderson, N.D. Lawn, D.D. Fletcher, R.L. McClelland, and E.F.M. Wijdicks
Neurology 2003; 60: 17-21.
[Abstract]
[Full text]
[PDF]
- EXPEDITED ARTICLES
Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C
- V. A. Street, C. L. Bennett, J. D. Goldy, A. J. Shirk, K. A. Kleopa, B. L Tempel, H. P. Lipe, S. S. Scherer, T. D. Bird, and P. F. Chance
Neurology 2003; 60: 22-26.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Fatigue and depression are associated with poor quality of life in ALS
- Jau-Shin Lou, Alexa Reeves, Theodore Benice, and Gary Sexton
Neurology 2003; 60: 122-123.
[Abstract]
[Full text]
[PDF]
- EDITORIALS
GDAP1 mutations in CMT4: Axonal and demyelinating phenotypes?: The exception "proves the rule"
- Garth Nicholson and Robert Ouvrier
Neurology 2002; 59: 1835-1836.
[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
Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy
- E. Nelis, S. Erdem, P. Y.K. Van den Bergh, M.-C. Belpaire–Dethiou, C. Ceuterick, V. Van Gerwen, A. Cuesta, L. Pedrola, F. Palau, A. A.W.M. Gabreëls–Festen, C. Verellen, E. Tan, M. Demirci, C. Van Broeckhoven, P. De Jonghe, H. Topaloglu, and V. Timmerman
Neurology 2002; 59: 1865-1872.
[Abstract]
[Full text]
[PDF]
|
|
