|
Muscle disease
Citations 101-110 of 281 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations
- E. Ricci, A. Broccolini, T. Gidaro, R. Morosetti, C. Gliubizzi, R. Frusciante, G. M. Di Lella, P. A. Tonali, and M. Mirabella
Neurology 2006; 66: 755-758.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Outcome and effect of pregnancy in myotonic dystrophy type 2
- S. Rudnik-Schöneborn, C. Schneider-Gold, U. Raabe, W. Kress, K. Zerres, and B.G.H. Schoser
Neurology 2006; 66: 579-580.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Course of disability and respiratory function in untreated late-onset Pompe disease
- M.L.C. Hagemans, W. J.C. Hop, P. A. Van Doorn, A. J.J. Reuser, and A. T. Van der Ploeg
Neurology 2006; 66: 581-583.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Oscillatory pallidal local field potential activity correlates with involuntary EMG in dystonia
- C. C. Chen, A. A. Kühn, K. -T. Hoffmann, A. Kupsch, G. -H. Schneider, T. Trottenberg, J. K. Krauss, J. C. Wöhrle, E. Bardinet, J. Yelnik, and P. Brown
Neurology 2006; 66: 418-420.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Coenzyme Q10 deficiency and isolated myopathy
- R. Horvath, P. Schneiderat, B.G.H. Schoser, K. Gempel, E. Neuen-Jacob, H. Plöger, J. Müller-Höcker, D. E. Pongratz, A. Naini, S. DiMauro, and H. Lochmüller
Neurology 2006; 66: 253-255.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Gentamicin treatment in McArdle disease: Failure to correct myophosphorylase deficiency
- A. Schroers, R. A. Kley, A. Stachon, R. Horvath, H. Lochmüller, J. Zange, and M. Vorgerd
Neurology 2006; 66: 285-286.
[Full text]
[PDF]
- ARTICLES
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene
- H. Jungbluth, H. Zhou, L. Hartley, B. Halliger-Keller, S. Messina, C. Longman, M. Brockington, S. A. Robb, V. Straub, T. Voit, M. Swash, A. Ferreiro, G. Bydder, C. A. Sewry, C. Müller, and F. Muntoni
Neurology 2005; 65: 1930-1935.
[Abstract]
[Full text]
[PDF]
- ARTICLES
A mutation in myotilin causes spheroid body myopathy
- T. Foroud, N. Pankratz, A. P. Batchman, M. W. Pauciulo, R. Vidal, L. Miravalle, H. H. Goebel, L. J. Cushman, B. Azzarelli, H. Horak, M. Farlow, and W. C. Nichols
Neurology 2005; 65: 1936-1940.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy
- Edo M. Hoogerwaard, Ieke B. Ginjaar, Egbert Bakker, and Marianne de Visser
Neurology 2005; 65: 1984-1986.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Plasma cells in muscle in inclusion body myositis and polymyositis
- S. A. Greenberg, E. M. Bradshaw, J. L. Pinkus, G. S. Pinkus, T. Burleson, B. Due, L. S. Bregoli, K. C. O’Connor, and A. A. Amato
Neurology 2005; 65: 1782-1787.
[Abstract]
[Full text]
[PDF]
|
|
