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All Neuromuscular Disease
Citations 11-20 of 158 total displayed.
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Past content
(since Jan 2000):
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- ARTICLES
Bilaterally symmetric form of Hirayama disease
- Sunil Pradhan
Neurology 2009; 72: 2083-2089.
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- EDITORIALS
Abnormal glycosylation of the  -dystroglycan: Deficient sugars are no good
- Haluk Topaloglu
Neurology 2009; 72: 1798-1799.
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- ARTICLES
Congenital muscular dystrophies with defective glycosylation of dystroglycan: A population study
- E. Mercuri, S. Messina, C. Bruno, M. Mora, E. Pegoraro, G. P. Comi, A. D'Amico, C. Aiello, R. Biancheri, A. Berardinelli, P. Boffi, D. Cassandrini, A. Laverda, M. Moggio, L. Morandi, I. Moroni, M. Pane, R. Pezzani, A. Pichiecchio, A. Pini, C. Minetti, T. Mongini, E. Mottarelli, E. Ricci, A. Ruggieri, S. Saredi, C. Scuderi, A. Tessa, A. Toscano, G. Tortorella, C. P. Trevisan, C. Uggetti, G. Vasco, F. M. Santorelli, and E. Bertini
Neurology 2009; 72: 1802-1809.
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- ARTICLES
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
- M. Fanin, A. C. Nascimbeni, S. Aurino, E. Tasca, E. Pegoraro, V. Nigro, and C. Angelini
Neurology 2009; 72: 1432-1435.
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- NEUROIMAGES
The small, spastic, and furrowed tongue of Allgrove syndrome
- Henry Houlden
Neurology 2009; 72: 1366.
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- RESIDENT AND FELLOW SECTION
Teaching Video NeuroImages: Tongue myokymia following head and neck radiotherapy for nasopharyngeal carcinoma
- Richard A. Rison and Said R. Beydoun
Neurology 2009; 72: e65.
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- ARTICLES
Brain atrophy in primary lateral sclerosis
- M. C. Tartaglia, V. Laluz, A. Rowe, K. Findlater, D. H. Lee, K. Kennedy, J. H. Kramer, and M. J. Strong
Neurology 2009; 72: 1236-1241.
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- CLINICAL/SCIENTIFIC NOTES
GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY
- B. Segarane, A. Li, R. Paudel, S. Scholz, J. Neumann, A. Lees, T. Revesz, J. Hardy, C. J. Mathias, N. W. Wood, J. Holton, and H. Houlden
Neurology 2009; 72: 1185-1186.
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- ARTICLES
Fat metabolism during exercise in patients with McArdle disease
- M. C. Ørngreen, T. D. Jeppesen, S. Tvede Andersen, T. Taivassalo, S. Hauerslev, N. Preisler, R. G. Haller, G. van Hall, and J. Vissing
Neurology 2009; 72: 718-724.
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- ARTICLES
A novel Frabin (FGD4) nonsense mutation p.R275X associated with phenotypic variability in CMT4H
- Henry Houlden, Simon Hammans, Haider Katifi, and Mary M. Reilly
Neurology 2009; 72: 617-620.
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