|
Muscle disease
Citations 191-200 of 283 total displayed.
|
Past content
(since Jan 2001):
|
- CLINICAL/SCIENTIFIC NOTES
Autoimmune rippling muscle
- Suraj Ashok Muley and John W. Day
Neurology 2003; 61: 869-870.
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Effect of diet on exercise tolerance in carnitine palmitoyltransferase II deficiency
- Mette C. Ørngreen, Rasmus Ejstrup, and John Vissing
Neurology 2003; 61: 559-561.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene
- D. Figarella–Branger, J. Pouget, R. Bernard, M. Krahn, C. Fernandez, N. Lévy, and J. F. Pellissier
Neurology 2003; 61: 562-564.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Response to sumatriptan in headache of MELAS syndrome
- Takahiro Iizuka, Fumihiko Sakai, Motoi Endo, and Norihiro Suzuki
Neurology 2003; 61: 577-578.
[Full text]
[PDF]
- EDITORIALS
Unicorns, dragons, polymyositis, and other mythological beasts
- Anthony A. Amato and Robert C. Griggs
Neurology 2003; 61: 288-289.
[Full text]
[PDF]
- ARTICLES
Polymyositis: An overdiagnosed entity
- M. F.G. van der Meulen, I. M. Bronner, J. E. Hoogendijk, H. Burger, W. J. van Venrooij, A. E. Voskuyl, H. J. Dinant, W. H.J.P. Linssen, J. H.J. Wokke, and M. de Visser
Neurology 2003; 61: 316-321.
[Abstract]
[Full text]
[PDF]
- ARTICLES
MAP kinase phosphatase-1 is induced in abnormal fibers in inclusion body myositis
- S. Nakano, A. Shinde, H. Ito, H. Ito, and H. Kusaka
Neurology 2003; 61: 322-326.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
GNE mutations causing distal myopathy with rimmed vacuoles with inflammation
- I. Yabe, T. Higashi, S. Kikuchi, H. Sasaki, T. Fukazawa, K. Yoshida, and K. Tashiro
Neurology 2003; 61: 384-386.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
A neonatal form of glycogen storage disease type IV
- M. Nambu, K. Kawabe, T. Fukuda, T. B. Okuno, S. Ohta, I. Nonaka, H. Sugie, and I. Nishino
Neurology 2003; 61: 392-394.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2
- L. Palenzuela, A.L. Andreu, J. Gàmez, M.R. Vilà, T. Kunimatsu, A. Meseguer, C. Cervera, I. Fernandez Cadenas, P.F.M. van der Ven, T.G. Nygaard, E. Bonilla, and M. Hirano
Neurology 2003; 61: 404-406.
[Abstract]
[Full text]
[PDF]
|
|
